.elementor-1798 .elementor-element.elementor-element-a0a1602{--display:flex;--min-height:305px;--flex-direction:column;--container-widget-width:100%;--container-widget-height:initial;--container-widget-flex-grow:0;--container-widget-align-self:initial;--justify-content:center;--gap:10px 10px;--background-transition:0.3s;--margin-block-start:145px;--margin-block-end:0px;--margin-inline-start:0px;--margin-inline-end:0px;}.elementor-1798 .elementor-element.elementor-element-a0a1602:not(.elementor-motion-effects-element-type-background), .elementor-1798 .elementor-element.elementor-element-a0a1602 > .elementor-motion-effects-container > .elementor-motion-effects-layer{background-image:url("https://pathosion-wp.com/matsuo-lab-nagoya/wp-content/uploads/2023/09/header_research.jpg");background-position:center center;background-size:cover;}.elementor-1798 .elementor-element.elementor-element-a0a1602, .elementor-1798 .elementor-element.elementor-element-a0a1602::before{--border-transition:0.3s;}.elementor-1798 .elementor-element.elementor-element-2b87cdc{text-align:center;}.elementor-1798 .elementor-element.elementor-element-2b87cdc .elementor-heading-title{color:var( --e-global-color-astglobalcolor5 );font-size:52px;font-weight:700;}.elementor-1798 .elementor-element.elementor-element-d7466f7{--display:flex;--min-height:100vh;--flex-direction:column;--container-widget-width:100%;--container-widget-height:initial;--container-widget-flex-grow:0;--container-widget-align-self:initial;--background-transition:0.3s;--overlay-opacity:0.5;--padding-block-start:30px;--padding-block-end:50px;--padding-inline-start:0px;--padding-inline-end:0px;}.elementor-1798 .elementor-element.elementor-element-d7466f7::before, .elementor-1798 .elementor-element.elementor-element-d7466f7 > .elementor-background-video-container::before, .elementor-1798 .elementor-element.elementor-element-d7466f7 > .e-con-inner > .elementor-background-video-container::before, .elementor-1798 .elementor-element.elementor-element-d7466f7 > .elementor-background-slideshow::before, .elementor-1798 .elementor-element.elementor-element-d7466f7 > .e-con-inner > .elementor-background-slideshow::before, .elementor-1798 .elementor-element.elementor-element-d7466f7 > .elementor-motion-effects-container > .elementor-motion-effects-layer::before{--background-overlay:'';background-image:url("https://pathosion-wp.com/matsuo-lab-nagoya/wp-content/uploads/2023/09/bg_pattern.png");background-size:auto;}.elementor-1798 .elementor-element.elementor-element-234f23e{--display:flex;--background-transition:0.3s;}.elementor-1798 .elementor-element.elementor-element-7343cb4{--display:flex;--background-transition:0.3s;--margin-block-start:30px;--margin-block-end:0px;--margin-inline-start:0px;--margin-inline-end:0px;--padding-block-start:50px;--padding-block-end:80px;--padding-inline-start:80px;--padding-inline-end:80px;}.elementor-1798 .elementor-element.elementor-element-7343cb4:not(.elementor-motion-effects-element-type-background), .elementor-1798 .elementor-element.elementor-element-7343cb4 > .elementor-motion-effects-container > .elementor-motion-effects-layer{background-color:var( --e-global-color-astglobalcolor5 );}.elementor-1798 .elementor-element.elementor-element-7343cb4, .elementor-1798 .elementor-element.elementor-element-7343cb4::before{--border-transition:0.3s;}.elementor-1798 .elementor-element.elementor-element-b9e5ae4{text-align:center;}.elementor-1798 .elementor-element.elementor-element-b9e5ae4 .elementor-heading-title{color:var( --e-global-color-accent );font-size:35px;font-weight:900;letter-spacing:0.1em;}.elementor-1798 .elementor-element.elementor-element-57477d7 > .elementor-widget-container{margin:-10px 0px 20px 0px;padding:0px 0px 0px 0px;}.elementor-1798 .elementor-element.elementor-element-e7c54d1{--display:flex;--background-transition:0.3s;}.elementor-1798 .elementor-element.elementor-element-6e0583f .elementor-heading-title{font-size:24px;font-weight:600;}.elementor-1798 .elementor-element.elementor-element-6e0583f > .elementor-widget-container{margin:0px 0px 20px 0px;padding:5px 0px 5px 15px;border-style:solid;border-width:0px 0px 1px 5px;border-color:var( --e-global-color-primary );}.elementor-1798 .elementor-element.elementor-element-ff4322c{--display:flex;--background-transition:0.3s;}.elementor-1798 .elementor-element.elementor-element-31f27bb .elementor-heading-title{font-size:24px;font-weight:600;}.elementor-1798 .elementor-element.elementor-element-31f27bb > .elementor-widget-container{margin:0px 0px 20px 0px;padding:5px 0px 5px 15px;border-style:solid;border-width:0px 0px 1px 5px;border-color:var( --e-global-color-primary );}.elementor-1798 .elementor-element.elementor-element-363e882{--display:flex;--background-transition:0.3s;}.elementor-1798 .elementor-element.elementor-element-215066c .elementor-heading-title{font-size:24px;font-weight:600;}.elementor-1798 .elementor-element.elementor-element-215066c > .elementor-widget-container{margin:0px 0px 20px 0px;padding:5px 0px 5px 15px;border-style:solid;border-width:0px 0px 1px 5px;border-color:var( --e-global-color-primary );}.elementor-1798 .elementor-element.elementor-element-2450396{--display:flex;--background-transition:0.3s;}.elementor-1798 .elementor-element.elementor-element-d2e3ecf .elementor-heading-title{font-size:24px;font-weight:600;}.elementor-1798 .elementor-element.elementor-element-d2e3ecf > .elementor-widget-container{margin:0px 0px 20px 0px;padding:5px 0px 5px 15px;border-style:solid;border-width:0px 0px 1px 5px;border-color:var( --e-global-color-primary );}.elementor-1798 .elementor-element.elementor-element-ab647ef{--display:flex;--background-transition:0.3s;}.elementor-1798 .elementor-element.elementor-element-5ed4231 .elementor-heading-title{font-size:24px;font-weight:600;}.elementor-1798 .elementor-element.elementor-element-5ed4231 > .elementor-widget-container{margin:0px 0px 20px 0px;padding:5px 0px 5px 15px;border-style:solid;border-width:0px 0px 1px 5px;border-color:var( --e-global-color-primary );}.elementor-1798 .elementor-element.elementor-element-14ad2f1{--display:flex;--background-transition:0.3s;}.elementor-1798 .elementor-element.elementor-element-4739a57 .elementor-heading-title{font-size:24px;font-weight:600;}.elementor-1798 .elementor-element.elementor-element-4739a57 > .elementor-widget-container{margin:0px 0px 20px 0px;padding:5px 0px 5px 15px;border-style:solid;border-width:0px 0px 1px 5px;border-color:var( --e-global-color-primary );}.elementor-1798 .elementor-element.elementor-element-b60a444{--display:flex;--background-transition:0.3s;}.elementor-1798 .elementor-element.elementor-element-5a7c10c .elementor-heading-title{font-size:24px;font-weight:600;}.elementor-1798 .elementor-element.elementor-element-5a7c10c > .elementor-widget-container{margin:0px 0px 20px 0px;padding:5px 0px 5px 15px;border-style:solid;border-width:0px 0px 1px 5px;border-color:var( --e-global-color-primary );}.elementor-1798 .elementor-element.elementor-element-59662b3{--display:flex;--background-transition:0.3s;}.elementor-1798 .elementor-element.elementor-element-35b57d3 .elementor-heading-title{font-size:24px;font-weight:600;}.elementor-1798 .elementor-element.elementor-element-35b57d3 > .elementor-widget-container{margin:0px 0px 20px 0px;padding:5px 0px 5px 15px;border-style:solid;border-width:0px 0px 1px 5px;border-color:var( --e-global-color-primary );}.elementor-1798 .elementor-element.elementor-element-6495ab9{--display:flex;--background-transition:0.3s;}.elementor-1798 .elementor-element.elementor-element-76ac579 .elementor-heading-title{font-size:24px;font-weight:600;}.elementor-1798 .elementor-element.elementor-element-76ac579 > .elementor-widget-container{margin:0px 0px 20px 0px;padding:5px 0px 5px 15px;border-style:solid;border-width:0px 0px 1px 5px;border-color:var( --e-global-color-primary );}.elementor-1798 .elementor-element.elementor-element-42eb1a1{--display:flex;--background-transition:0.3s;}.elementor-1798 .elementor-element.elementor-element-585b6fb .elementor-heading-title{font-size:24px;font-weight:600;}.elementor-1798 .elementor-element.elementor-element-585b6fb > .elementor-widget-container{margin:0px 0px 20px 0px;padding:5px 0px 5px 15px;border-style:solid;border-width:0px 0px 1px 5px;border-color:var( --e-global-color-primary );}.elementor-1798 .elementor-element.elementor-element-5147003{--display:flex;--background-transition:0.3s;}.elementor-1798 .elementor-element.elementor-element-aadff23 .elementor-heading-title{font-size:24px;font-weight:600;}.elementor-1798 .elementor-element.elementor-element-aadff23 > .elementor-widget-container{margin:0px 0px 20px 0px;padding:5px 0px 5px 15px;border-style:solid;border-width:0px 0px 1px 5px;border-color:var( --e-global-color-primary );}.elementor-1798 .elementor-element.elementor-element-a49f793{--display:flex;--background-transition:0.3s;}.elementor-1798 .elementor-element.elementor-element-34c9f40 .elementor-heading-title{font-size:24px;font-weight:600;}.elementor-1798 .elementor-element.elementor-element-34c9f40 > .elementor-widget-container{margin:0px 0px 20px 0px;padding:5px 0px 5px 15px;border-style:solid;border-width:0px 0px 1px 5px;border-color:var( --e-global-color-primary );}@media(max-width:767px){.elementor-1798 .elementor-element.elementor-element-a0a1602{--min-height:215px;--margin-block-start:120px;--margin-block-end:0px;--margin-inline-start:0px;--margin-inline-end:0px;}.elementor-1798 .elementor-element.elementor-element-2b87cdc .elementor-heading-title{font-size:38px;}.elementor-1798 .elementor-element.elementor-element-7343cb4{--padding-block-start:0px;--padding-block-end:50px;--padding-inline-start:20px;--padding-inline-end:20px;}.elementor-1798 .elementor-element.elementor-element-b9e5ae4 .elementor-heading-title{font-size:28px;}.elementor-1798 .elementor-element.elementor-element-e7c54d1{--padding-block-start:0px;--padding-block-end:0px;--padding-inline-start:0px;--padding-inline-end:0px;}.elementor-1798 .elementor-element.elementor-element-ff4322c{--padding-block-start:0px;--padding-block-end:0px;--padding-inline-start:0px;--padding-inline-end:0px;}.elementor-1798 .elementor-element.elementor-element-363e882{--padding-block-start:0px;--padding-block-end:0px;--padding-inline-start:0px;--padding-inline-end:0px;}.elementor-1798 .elementor-element.elementor-element-2450396{--padding-block-start:0px;--padding-block-end:0px;--padding-inline-start:0px;--padding-inline-end:0px;}.elementor-1798 .elementor-element.elementor-element-ab647ef{--padding-block-start:0px;--padding-block-end:0px;--padding-inline-start:0px;--padding-inline-end:0px;}.elementor-1798 .elementor-element.elementor-element-14ad2f1{--padding-block-start:0px;--padding-block-end:0px;--padding-inline-start:0px;--padding-inline-end:0px;}.elementor-1798 .elementor-element.elementor-element-b60a444{--padding-block-start:0px;--padding-block-end:0px;--padding-inline-start:0px;--padding-inline-end:0px;}.elementor-1798 .elementor-element.elementor-element-59662b3{--padding-block-start:0px;--padding-block-end:0px;--padding-inline-start:0px;--padding-inline-end:0px;}.elementor-1798 .elementor-element.elementor-element-6495ab9{--margin-block-start:0px;--margin-block-end:0px;--margin-inline-start:0px;--margin-inline-end:0px;--padding-block-start:0px;--padding-block-end:0px;--padding-inline-start:0px;--padding-inline-end:0px;}.elementor-1798 .elementor-element.elementor-element-42eb1a1{--padding-block-start:0px;--padding-block-end:0px;--padding-inline-start:0px;--padding-inline-end:0px;}.elementor-1798 .elementor-element.elementor-element-5147003{--padding-block-start:0px;--padding-block-end:0px;--padding-inline-start:0px;--padding-inline-end:0px;}.elementor-1798 .elementor-element.elementor-element-a49f793{--padding-block-start:0px;--padding-block-end:0px;--padding-inline-start:0px;--padding-inline-end:0px;}}/* Start custom CSS */<div class="block">
<h4>2023</h4>
<p>6.&nbsp;Single-walled Carbon Nanotubes Supported Pt Electrocatalyst as Cathode Catalyst of a Single Fuel Cell with High Durability Against Start-up/Shut-down Potential Cycling</p>
<p>Miftakhul Huda, Tomoya Kawahara, Jae-Hyeok Park, Masaya Kawasumi, Yutaka Matsuo</p>
<p><em>ACS Appl. Energy Mater.</em> <strong>2023</strong>, accepted.</p>
<p>&nbsp;</p>
<p>5.&nbsp;Highly Durable Graphene-encapsulated Platinum-based Electrocatalyst for Oxygen Reduction Reactions Synthesized by Solution Plasma Process</p>
<p>Jae-Hyeok Park, Kyusung Kim, Xiaoyang Wang, Miftakhul Huda, Yasuyuki Sawada, Yutaka Matsuo, Nagahiro Saito, Masaya Kawasumi</p>
<p><em>J. Power Sources</em>&nbsp;<strong>2023</strong>, <em>580</em>,&nbsp;233419. [<a href="https://doi.org/10.1016/j.jpowsour.2023.233419" target="_blank">DOI: 10.1016/j.jpowsour.2023.233419</a>]&nbsp;</p>
<p>&nbsp;</p>
<p>4.&nbsp;Cationic Nitrogen-doped Graphene Coated Silver as Low-work Function Electrode for Inverted Perovskite Solar Cells</p>
<p>Kento Yokoyama, Hao-Sheng Lin, Qing-Jun Shui, Xiaoyang Wang, Nagahiro Saito, Yutaka Matsuo</p>
<p><em>Appl. Phys. Express</em> <strong>2023</strong>, <em>16</em>, 081001. [<a href="https://doi.org/10.35848/1882-0786/acea18" target="_blank">DOI: 10.35848/1882-0786/acea18</a>]</p>
<p>&nbsp;</p>
<p>3.&nbsp;Evaporable Indano[60]fullerene Ketone for the Electron Transport Layer of Inverted Perovskite Solar Cells</p>
<p>Yutaka Matsuo, Soma Ishikawa, Hirofumi Amada, Kento Yokoyama, Qing-jun Shui, Miftakhul Huda, Naoki Ueoka, Hao-Sheng Lin</p>
<p><em>Chem. Lett.</em> <strong>2023</strong>, <em>52</em>, 685&ndash;687. [<a href="https://doi.org/10.1246/cl.230217" target="_blank">DOI: 10.1246/cl.230217</a>]</p>
<p>&nbsp;</p>
<p>2.&nbsp;Spiro-OMeTAD Versus PTAA for Single-walled Carbon Nanotubes Electrode in Perovskite Solar Cells</p>
<p>Bo-Wen Zhang, Hao-Sheng Lin, Yang Qiu, Qing-Jun Shui, Yong-Ji Zheng, Mohamad Almesfer, Esko I. Kauppinen, Yutaka Matsuo, Shigeo Maruyama</p>
<p><em>Carbon</em> <strong>2023</strong>, <em>205</em>, 321&ndash;327. [<a href="https://doi.org/10.1016/j.carbon.2023.01.011" target="_blank">DOI: 10.1016/j.carbon.2023.01.011</a>]</p>
<p>&nbsp;</p>
<p>1.&nbsp;Sequential Click Modification of a Lithium-ion Endohedral Fullerene Connecting Small Molecules Through a Dieneazide Linker</p>
<p>Shogo Fujiki, Takumi Takada, Shota Nagasawa, Hiroshi Okada, Yusuke Sasano, Eunsang Kwon, Yutaka Matsuo and Yoshiharu Iwabuchi</p>
<p><em>Chem. Commun.</em> <strong>2023</strong>, <em>59</em>, 1237&ndash;1240. [<a href="https://doi.org/10.1039/D2CC06301H" target="_blank">DOI: 10.1039/D2CC06301H</a>]&nbsp;</p>
</div>

<div class="block">
<h4>2022</h4>
<p>10.&nbsp;A Mechanistic Study on Enhanced PEDOT:PSS for Organic Solar Cells Using Semiconducting Single-walled Carbon Nanotubes in Different Diameters</p>
<p>Hao-Sheng Lin,&nbsp;Daisuke Miyata, Mizuki Yagisawa, Miftakhul Huda, Satoru Hashimoto, Takeshi Hashimoto, Yutaka Matsuo</p>
<p><em>Applied Physics Express</em>&nbsp;<strong>2022</strong>,&nbsp;<em>15</em>, 121001.&nbsp;[<a href="https://doi.org/10.35848/1882-0786/ac9d80" target="_blank">DOI: 10.35848/1882-0786/ac9d80</a>]</p>
<p>&nbsp;</p>
<p>9.&nbsp;Inkjet Printing of Mechanochromic Fluorenylidene-Acridane</p>
<p>Keisuke Ogumi, Kohki Nagata, Yuki Takimoto, Kentaro Mishiba, Yutaka Matsuo</p>
<p><em>Sci. Rep.</em> <strong>2022</strong>, <em>12</em>, 16997. [<a href="https://doi.org/10.1038/s41598-022-21600-x" target="_blank">DOI: 10.1038/s41598-022-21600-x</a>]</p>
<p>&nbsp;</p>
<p>8.&nbsp;Synthesis of Neutral Li-endohedral PCBM: An n-Dopant for Fullerene Derivatives</p>
<p>Hiroshi Ueno, Daiki Kitabatake, Hao-Sheng Lin, Yue Ma, Il Jeon, Seiichiro Izawa, Masahiro Hiramoto, Fuminori Misaizu, Shigeo Maruyama, Yutaka Matsuo</p>
<p><em>Chem. Commun.</em> <strong>2022</strong>, <em>58</em>, 10190&ndash;10193. [<a href="https://doi.org/10.1039/D2CC03678A" target="_blank">DOI: 10.1039/D2CC03678A</a>]</p>
<p>&nbsp;</p>
<p>7.&nbsp;Synthesis of n-Type [60]Fullerene Derivatives with Sterically Bulky <em>tert</em>-Butyl Groups for Vacuum Deposition Processes</p>
<p>Hiromasa Shibuya, Yeong Suk Choi, Taejin Choi, Sungyoung Yun, Juhee Moon, Yutaka Matsuo</p>
<p><em>Chem. Asian J.</em> <strong>2022</strong>, <em>17</em>, e202200609. [<a href="https://doi.org/10.1002/asia.202200609" target="_blank">DOI: 10.1002/asia.202200609</a>]</p>
<p>&nbsp;</p>
<p>6.&nbsp;Quantitative and High-resolution Mechanical Pressure Sensing Functions of Mechanochromic Fluorenylidene-acridane</p>
<p>Keisuke Ogumi, Kohki Nagata, Yuki Takimoto, Kentaro Mishiba, Yutaka Matsuo</p>
<p><em>J. Mater. Chem. C</em> <strong>2022</strong>, <em>10</em>, 11181&ndash;11186. [<a href="https://doi.org/10.1039/D2TC01988D" target="_blank">DOI: 10.1039/D2TC01988D</a>]</p>
<p>&nbsp;</p>
<p>5.&nbsp;Triarylamine/Bithiophene Copolymer with Enhanced Quinoidal Character as Hole-Transporting Material for Perovskite Solar Cells</p>
<p>Hao-Sheng Lin, Takahiro Doba, Wataru Sato, Yutaka Matsuo, Rui Shang, Eiichi Nakamura</p>
<p><em>Angew. Chem. Int. Ed.</em> <strong>2022</strong>, <em>61</em>, e202203949. [<a href="https://doi.org/10.1002/anie.202203949" target="_blank">DOI: 10.1002/anie.202203949</a>]</p>
<p>&nbsp;</p>
<p>4.&nbsp;Multi-Functional MoO3 Doping of Carbon-Nanotube Top Electrodes for Highly Transparent and Efficient Semi-Transparent Perovskite Solar Cells</p>
<p>Seungju Seo, Kosuke Akino, Jeong-Seok Nam, Ahmed Shawky, Hao-Sheng Lin, Hiroki Nagaya, Esko I. Kauppinen, Rong Xiang, Yutaka Matsuo, Il Jeon, Shigeo Maruyama</p>
<p><em>Advanced Materials Interfaces</em>&nbsp;<strong>2022</strong>, 9, 2101595. [DOI : <a href="https://doi.org/10.1002/admi.202101595">10.1002/admi.202101595</a>]</p>
<p>&nbsp;</p>
<p>3.&nbsp;Scalable eDIPS-based Single-walled Carbon Nanotube Films for Conductive Transparent Electrodes in Organic Solar Cells</p>
<p>Hao-Sheng Lin, Riku Hatomoto, Daisuke Miyata, Miftakhul Huda, Il Jeon, Satoru Hashimoto, Takeshi Hashimoto, Yutaka Matsuo</p>
<p><em>Applied Physics Express</em>&nbsp;<strong>2022</strong>, <em>15</em>, 046505. [DOI：<a href="https://iopscience.iop.org/article/10.35848/1882-0786/ac5c02">10.35848/1882-0786/ac5c02</a>]</p>
<p>&nbsp;</p>
<p>2. Facile Multiple Alkylations of C60 Fullerene</p>
<p>Kazuhira Miwa, Shinobu Aoyagi, Takahiro Sasamori, Shogo Morisako, Hiroshi Ueno, Yutaka Matsuo, Hideki Yorimitsu</p>
<p><em>Molecules</em> <strong>2022</strong>, <em>27</em>, 450. [DOI: 10.3390/molecules27020450]&nbsp;</p>
<p>&nbsp;</p>
<p>1. Synthesis of Conjugated Donor-Acceptor Antiaromatic Porphyrin and Their Application to Perovskite Solar Cells</p>
<p>Xue-Lin Zheng, Hao-Sheng Lin, Bo-Wen Zhang, Shigeo Maruyama, Yutaka Matsuo</p>
<p><em>J. Org. Chem.</em>&nbsp;<strong>2022</strong>, <em>87</em>, 5457&ndash;5463. [<a href="https://pubs.acs.org/doi/10.1021/acs.joc.1c01947" target="_blank">DOI: 10.1021/acs.joc.1c01947</a>]</p>
</div>

<div class="block">
<h4>2021</h4>
<p>11. An Adamantane Capsule and Efficient Uptake of Spherical Guests upto 3 nm in Water</p>
<p>Yuri Katagiri, Yamato Tsuchida, Yutaka Matsuo, Michito Yoshizawa</p>
<p><em>J. Am. Chem. Soc.</em>&nbsp;<strong>2021</strong>, <em>143</em>, 21492&ndash;21496. [<a href="https://pubs.acs.org/doi/10.1021/jacs.1c11021" target="_blank">DOI: 10.1021/jacs.1c11021</a>]</p>
<p>&nbsp;</p>
<p>10.&nbsp;Recent Progress in Porphyrin Derivatives Used in Organic Thin-film Solar Cells, in "Applications of Porphyrinoids as Functional Materials"</p>
<p>Yutaka Matsuo, Keisuke Ogumi [<a href="https://doi.org/10.1039/9781839164149-00204" target="_blank">DOI: 10.1039/9781839164149-00204</a>]</p>
<p>&nbsp;</p>
<p>9.&nbsp;Lithium Endohedral Fullerenes, in "Handbook of Fullerene Science and Technology"</p>
<p>Yue Ma, Yutaka Matsuo [<a href="https://doi.org/10.1007/978-981-13-3242-5_31-1" target="_blank">DOI: 10.1007/978-981-13-3242-5_31-1</a>]</p>
<p>&nbsp;</p>
<p>8.&nbsp;Fullerenes in Photovoltaics, in "Handbook of Fullerene Science and Technology"</p>
<p>Hao-Sheng Lin, Yutaka Matsuo [<a href="https://doi.org/10.1007/978-981-13-3242-5_37-1" target="_blank">DOI: 10.1007/978-981-13-3242-5_37-1</a>]</p>
<p>&nbsp;</p>
<p>7. Multi-Walled Carbon Nanotube-Assisted Encapsulation Approach for Stable Perovskite Solar Cells</p>
<p>Jin-Myung Choi, Hiroki Suko, Kyusun Kim, Jiye Han, Sangsu Lee, Yutaka Matsuo, Shigeo Maruyama, Il Jeon, Hirofumi Daiguji</p>
<p><em>Molecules</em> <strong>2021</strong>, 26, 5060. [<a href="https://www.mdpi.com/1420-3049/26/16/5060" target="_blank">DOI: 10.3390/molecules26165060</a>]</p>
<p>&nbsp;</p>
<p>6.&nbsp;One-step Direct Oxidation of Alkoxy to Ketone for Evaporable Fullerene-fused Ketone as Efficient Electron-transport Materials</p>
<p>Hao-Sheng Lin, Yue Ma, Rong Xiang, Sergei Manzhos, Il Jeon, Shigeo Maruyama, Yutaka Matsuo</p>
<p><em>Communications Chemistry</em>&nbsp;<strong>2021</strong>, <em>4</em>, 74. [<a href="https://doi.org/10.1038/s42004-021-00511-4" target="_blank">DOI: 10.1038/s42004-021-00511-4</a>]</p>
<p>&nbsp;</p>
<p>5.&nbsp;Cationic Nitrogen-doped Graphene as p-Type Modifier for High-performance PEDOT:PSS Hole-transporters in Organic Solar Cells</p>
<p>Hao-Sheng Lin, Takuhei Kaneko,&nbsp;Soma Ishikawa, Il Jeon, Sangwoo Chae, Takumi Yana, Nagahiro Saito, Yutaka Matsuo</p>
<p><em>Jpn. J. Appl. Phys.</em> <strong>2021</strong>, <em>60</em>, 070902 1-5. [DOI: <a href="https://doi.org/10.35848/1347-4065/ac00fc">10.35848/1347-4065/ac00fc</a>]</p>
<p>&nbsp;</p>
<p>4.&nbsp;Synthesis of 5,15-<em>meso</em>-Bis(2-chlorothiophen-3-yl)porphyrin as a Building Block for Further Functional Materials</p>
<p>Safi Ullah, Keisuke Ogumi, Xuelin Zheng, Huan Wang, Yutaka Matsuo</p>
<p><em>J. Porphyrins Phthalocyanines</em>&nbsp;<strong>2021</strong>, <em>25</em>, 944&ndash;950. [DOI: <a href="https://www.worldscientific.com/doi/abs/10.1142/S1088424621500590" target="_blank">10.1142/S1088424621500590</a>]</p>
<p>&nbsp;</p>
<p>3.&nbsp;Controlled Removal of Surfactants from Double‐Walled Carbon Nanotubes for Stronger p‐Doping Effect and Its Demonstration in Perovskite Solar Cells</p>
<p>Ahmed Shawky, Jeong‐Seok Nam, Kyusun Kim, Jiye Han, Jungjin Yoon, Seungju Seo, Chang Soo Lee, Rong Xiang, Yutaka Matsuo, Hyuck Mo Lee, Shigeo Maruyama, Il Jeon</p>
<p><em>Small Method</em>&nbsp;<strong>2021</strong>, <em>5</em>, 210080 1-10. [<a href="https://doi.org/10.1002/smtd.202100080" target="_blank">DOI: 10.1002/smtd.202100080</a>]</p>
<p>&nbsp;</p>
<p>2.&nbsp;Creation of Highly Efficient and Durable Organic and Perovskite Solar Cells Using Nanocarbon Materials</p>
<p>Yutaka Matsuo</p>
<p><em>Bull. Chem. Soc. Jpn.</em> <strong>2021</strong>, <em>94</em>, 1080&ndash;1089. [<a href="https://doi.org/10.1246/bcsj.20200404" target="_blank">DOI: 10.1246/bcsj.20200404</a>]</p>
<p>(Prof. Eiichi Nakamura special issue on his 70th birthday)</p>
<p>&nbsp;</p>
<p>1. Magnesium Diethynylporphyrin Derivatives with Strong Near-Infrared Absorption for Solution-process Bulk Heterojunction Organic Solar Cells</p>
<p>Keisuke Ogumi, Takafumi Nakagawa, Masahiro Nakano, Yutaka Matsuo</p>
<p><em>J. Porphyrins Phthalocyanines</em>&nbsp;<strong>2021</strong>,&nbsp;<em>25</em>, 128&ndash;134. [<a href="https://doi.org/10.1142/S1088424621500036" target="_blank">DOI: 10.1142/S1088424621500036</a>]&nbsp;</p>
</div>

<div class="block">
<h4>2020</h4>
<p>9.&nbsp;Recent Progress in Porphyrin- and Phthalocyanine-containing Perovskite Solar Cells</p>
<p>Yutaka Matsuo, Keisuke Ogumi, Il Jeon, Huan Wang, Takafumi Nakagawa</p>
<p><em>RSC Adv.</em> <strong>2020</strong>,&nbsp;<em>10</em>, 32678&ndash;32689. [<a href="https://doi.org/10.1039/D0RA03234D" target="_blank">DOI: 10.1039/D0RA03234D</a>]</p>
<p>&nbsp;</p>
<p>8.&nbsp;Solvation-Free Li<sup>+</sup>&nbsp;Lewis Acid Enhancing Reaction: Kinetic Study of [5,6]-Li<sup>+</sup>@PCBM to [6,6]-Li<sup>+</sup>@PCBM</p>
<p>Yue Ma, Hiroshi Ueno, Hiroshi Okada, Sergei Manzhos, Yutaka Matsuo</p>
<p><em>Org. Lett.</em> <strong>2020</strong>, <em>22</em>, 18, 7239&ndash;7243. [<a href="https://pubs.acs.org/doi/10.1021/acs.orglett.0c02570" target="_blank">DOI: 10.1021/acs.orglett.0c02570</a>]</p>
<p>&nbsp;</p>
<p>7.&nbsp;Equilibrium and Thermodynamic Studies of Chromic Overcrowded Fluorenylidene-Acridanes with Modified Fluorene Moieties</p>
<p>Ya Wang, Yue Ma, Keisuke Ogumi, Bing Wang, Takafumi Nakagawa, Yao Fu, Yutaka Matsuo</p>
<p><em>Communications Chemistry</em>&nbsp;<strong>2020</strong>, <em>3</em>, 93. [<a href="https://www.nature.com/articles/s42004-020-00345-6" target="_blank">DOI: 10.1038/s42004-020-00345-6</a>]</p>
<p>&nbsp;</p>
<p>6. Denatured M13 Bacteriophage-Templated Perovskite Solar Cells Exhibiting High Efficiency</p>
<p>Hao-Sheng Lin, Jong-Min Lee, Jiye Han, Changsoo Lee, Seungju Seo, Shaun Tan, Hyuck Mo Lee, Eun Jung Choi, Michael S. Strano, Yang Yang, Shigeo Maruyama, Il Jeon, Yutaka Matsuo, Jin-Woo Oh</p>
<p><em>Adv. Sci.</em>&nbsp;<strong>2020</strong>, <em>7</em>, 2000782. [<a href="https://onlinelibrary.wiley.com/doi/full/10.1002/advs.202000782" target="_blank">DOI: 10.1002/advs.202000782</a>]</p>
<p>&nbsp;</p>
<p>5.&nbsp;MoS<sub>2</sub>-Carbon Nanotube Heterostructure as Efficient Hole Transporters and Conductors in Perovskite Solar Cells</p>
<p>Yang Qian, Seungju Seo, Il Jeon, Haosheng Lin, Shuhei Okawa, Yongjia Zheng, Ahmed Shawky, Anton Anisimov, Esko I. Kauppinen, Jing Kong, Rong Xiang, Yutaka Matsuo, Shigeo Maruyama</p>
<p><em>Appl. Phys. Express</em> <strong>2020</strong>, <em>13</em> 075009. [<a href="https://iopscience.iop.org/article/10.35848/1882-0786/ab9efa" target="_blank">DOI: 10.35848/1882-0786/ab9efa</a>]</p>
<p>&nbsp;</p>
<p>4. Carbon Nanotubes to Outperform Metal Electrodes in Perovskite Solar Cells via Dopant Engineering and Hole-Selectivity Enhancement</p>
<p>Il Jeon, Ahmed Shawky, Seungju Seo, Yang Qian, Anton Anisimov, Esko I. Kauppinen, Yutaka Matsuo, Shigeo Maruyama</p>
<p><em>J. Mater. Chem. A</em> <strong>2020</strong>, <em>8</em>, 11141&ndash;11147. [<a href="https://pubs.rsc.org/en/content/articlelanding/2020/ta/d0ta03692g" target="_blank">DOI: 10.1039/D0TA03692G</a>]</p>
<p style="text-align: center;"><img src="http://www.matsuo-lab.net/img/Get.jpeg.gif" alt="" width="378" height="161" /></p>
<p>&nbsp;</p>
<p>3. Polyaromatic Nanotweezers on Semiconducting Carbon Nanotubes for the Growth and Interfacing of Lead Halide Perovskite Crystal Grains in Solar Cells</p>
<p>Hao-Sheng Lin, Shunhei Okawa, Yue Ma, Satoshi Yotsumoto, Changsoo Lee, Shaun Tan, Sergei Manzhos, Michito Yoshizawa, Shohei Chiashi, Hyuck Mo Lee, Takeshi Tanaka, Hiromichi Kataura, Il Jeon, Yutaka Matsuo, Shigeo Maruyama</p>
<p><em>Chem. Mater.</em> <strong>2020</strong>, <em>32</em>, 5125&ndash;5133. [<a href="https://pubs.acs.org/doi/10.1021/acs.chemmater.0c01011" target="_blank">DOI: 10.1021/acs.chemmater.0c01011</a>]</p>
<p>&nbsp;</p>
<p>2.&nbsp;Nickel-Catalyzed Deaminative Acylation of Activated Aliphatic Amines with Aromatic Amides via C&ndash;N Bond Activation</p>
<p>Chu-guo Yu, Yutaka Matsuo</p>
<p><em>Org. Lett.</em> <strong>2020</strong>, <em>22</em>, 950&ndash;955. [<a href="https://pubs.acs.org/doi/10.1021/acs.orglett.9b04497" target="_blank">DOI: 10.1021/acs.orglett.9b04497</a>]</p>
<p style="text-align: center;"><img src="http://www.matsuo-lab.net/img/ol9b04497_0006.gif" alt="" width="500" height="199" /></p>
<p>&nbsp;</p>
<p>1.&nbsp;Multifunctional Effect of p-Doping, Anti-Reflection, and Encapsulation by Polymeric Acid for High Efficiency and Stable Carbon Nanotube-based Silicon Solar Cells</p>
<p>Yang Qian, Il Jeon, Ya-Lun Ho, Changhyun Lee, Sujeong Jeong, Clement Delacou, Anton Anisimov, Esko I. Kaupinnen, Yutaka Matsuo, Yoonmook Kang, Hae-Seok Lee, Donghwan Kim, Jean-Jacques Delaunay, Shigeo Maruyama</p>
<p><em>Adv. Energy Mater.</em>&nbsp;<strong>2020</strong>, <em>10</em>, 1902389. [<a href="https://doi.org/10.1002/aenm.201902389" target="_blank">DOI: 10.1002/aenm.201902389</a>]</p>
<p style="text-align: center;"><img src="http://www.matsuo-lab.net/img/aenm201902389-gra-0001-m.jpg" alt="" width="394" height="336" /></p>
</div>

<div class="block">
<h4>2019</h4>
<p>26.&nbsp;Highly Selective Synthesis of Tetrahydronaphthaleno[60]fullerenes via Fullerene-Cation-Mediated Intramolecular Cyclization</p>
<p>Xiao-Yu Yang, Hao-Sheng Lin, Yutaka Matsuo</p>
<p><em>J. Org. Chem.</em>&nbsp;<strong>2019</strong>,&nbsp;<em>84</em>, 16314&ndash;16322. [<a href="https://doi.org/10.1021/acs.joc.9b02618" target="_blank">DOI: 10.1021/acs.joc.9b02618</a>]</p>
<p style="text-align: center;"><img src="http://www.matsuo-lab.net/img/jo9b02618_0007.gif" alt="" width="500" height="185" /></p>
<p>&nbsp;</p>
<p>25.&nbsp;Prediction of Magnesium Tetraethynylporphyrin&rsquo;s Solubility by Theoretical Calculation</p>
<p>Keisuke Ogumi, Yutaka Matsuo</p>
<p><em>J. Porphyrins Phthalocyanines</em>&nbsp;<strong>2019</strong>, <em>23</em>, 1144&ndash;1148. [<a href="https://doi.org/10.1142/S1088424619501475" target="_blank">DOI: 10.1142/S1088424619501475</a>]</p>
<p>&nbsp;</p>
<p>24.&nbsp;High-yielding Pd<sub>2</sub>(dba)<sub>3</sub>&middot;C<sub>6</sub>H<sub>6</sub>-based Four-fold Sonogashira Coupling with Selenophene-conjugated Magnesium Tetraethynylporphyrin for Organic Solar Cells</p>
<p>Huan Wang, Takafumi Nakagawa, Meng-Meng Zhang, Keisuke Ogumi, Shangfeng Yang, Yutaka Matsuo</p>
<p><em>RSC Adv.</em> <strong>2019</strong>, <em>9</em>, 32562&ndash;32572. [<a href="https://pubs.rsc.org/en/content/articlelanding/2019/ra/c9ra07393k" target="_blank">DOI: 10.1039/C9RA07393K</a>]</p>
<p style="text-align: center;"><img src="http://www.matsuo-lab.net/img/Se-DPP-Por.jpg" alt="" width="394" height="228" /></p>
<p>&nbsp;</p>
<p>23.&nbsp;Controlled Redox of Lithium-ion Endohedral Fullerene for Efficient and Stable Metal Electrode-Free Perovskite Solar Cells</p>
<p>Il Jeon, Ahmed Shawky, Hao-Sheng Lin, Seungju Seo, Hiroshi Okada, Jin-Wook Lee, Amrita Pal, Shaun Tan, Anton Anisimov, Esko I. Kauppinen, Yang Yang, Sergei Manzhos, Shigeo Maruyama, Yutaka Matsuo</p>
<p><em>J. Am. Chem. Soc.</em> <strong>2019</strong>, <em>141</em>, 16553&ndash;16558. [<a href="https://pubs.acs.org/doi/full/10.1021/jacs.9b06418" target="_blank">DOI: 10.1021/jacs.9b06418</a>]</p>
<p style="text-align: center;"><img src="http://www.matsuo-lab.net/img/CNT-LiC60-PSC.png" alt="" width="472" height="323" /></p>
<p>&nbsp;</p>
<p>22. Highly Selective and Scalable Fullerene-Cation-Mediated Synthesis accessing Cyclo[60]fullerenes with 5-Membered-Carbon-Ring and their Application to Perovskite Solar Cells</p>
<p>Hao-Sheng Lin, Il Jeon, Yingqian Chen, Xiao-Yu Yang, Takafumi Nakagawa, Shigeo Maruyama, Sergei Manzhos, Yutaka Matsuo</p>
<p><em>Chem. Mater.</em> <strong>2019</strong>, <em>31</em>, 8432&ndash;8439. [<a href="https://pubs.acs.org/doi/abs/10.1021/acs.chemmater.9b02468" target="_blank">DOI: 10.1021/acs.chemmater.9b02468</a>]</p>
<p style="text-align: center;"><img src="http://www.matsuo-lab.net/img/FIF-PSC.png" alt="" width="472" height="425" /></p>
<p>&nbsp;</p>
<p>21.&nbsp;Investigation of Charge Interaction between Fullerene Derivatives and Single-Walled Carbon Nanotubes</p>
<p>Cl&eacute;ment Delacou, Il Jeon, Keigo Otsuka, Taiki Inoue, Anton Anisimov, Takenori Fujii, Esko I. Kauppinen, Shigeo Maruyama, Yutaka Matsuo</p>
<p><em>InfoMat</em>&nbsp;<strong>2019</strong>, <em>1</em>, 559&ndash;570. [<a href="https://onlinelibrary.wiley.com/doi/full/10.1002/inf2.12045" target="_blank">DOI: 10.1002/inf2.12045</a>]</p>
<p style="text-align: center;"><img src="http://www.matsuo-lab.net/img/C60CNTCle.png" alt="" width="338" height="196" /></p>
<p>&nbsp;&nbsp;</p>
<p>20. Li@C<sub>60</sub>&nbsp;Endohedral Fullerene as Supraatomic Dopant for C<sub>60</sub>&nbsp;Electron-transporting Layer Promoting Efficiency of Perovskite Solar Cells</p>
<p>Hiroshi Ueno, Il Jeon, Hao-sheng Lin, Abhishek Thote, Takafumi Nakagawa, Hiroshi Okada, Seiichiro Izawa, Masahiro Hiramoto, Hirofumi Daiguji, Shigeo Maruyama, Yutaka Matsuo</p>
<p><em>Chem. Commun.</em> <strong>2019</strong>, <em>55</em>, 11837&ndash;11839. [<a href="https://pubs.rsc.org/en/content/articlelanding/2019/CC/C9CC06120G" target="_blank">DOI: 10.1039/c9cc06120g</a>]</p>
<p style="text-align: center;"><img src="http://www.matsuo-lab.net/img/LiC60-PSC.png" alt="" width="472" height="408" /></p>
<p>&nbsp;&nbsp;</p>
<p>19.&nbsp;Synergic Catalysts of Polyoxometalate@Cationic Porous Aromatic Framework: Reciprocal Modulation of Both Capture and Conversion Materials</p>
<p>Jian Song, Yue Li, Ping Cao, Xiaofei Jing, Muhammad Faheem, Yutaka Matsuo, Youliang Zhu, Yuyang Tian, Xiaohong Wang, Guangshan Zhu</p>
<p><em>Adv. Mater.</em> <strong>2019</strong>, <em>31</em>, 1902444. [<a href="https://onlinelibrary.wiley.com/doi/full/10.1002/adma.201902444" target="_blank">DOI: 10.1002/adma.201902444</a>]</p>
<p>&nbsp;</p>
<p>18.&nbsp;Dialkoxymethano[60]fullerenes as Electron Acceptors in Thin-film Organic Solar Cell&nbsp;</p>
<p>Mohammed Y. Suleiman, Yue Ma, Takafumi Nakagawa, Hiroshi Ueno, Yutaka Matsuo</p>
<p><em>Tetrahedron</em> <strong>2019</strong>, <em>75</em>, 130514. [<a href="https://doi.org/10.1016/j.tet.2019.130514" target="_blank">DOI:&nbsp;10.1016/j.tet.2019.130514</a>]</p>
<p>&nbsp;</p>
<p>17.&nbsp;Chemical Reduction of Li<sup>+</sup>@C<sub>60</sub>&nbsp;by Decamethylferrocene to Produce Neutral Li<sup>+</sup>@C<sub>60</sub><sup>&bull;&ndash;</sup></p>
<p>Hiroshi Okada, Hiroshi Ueno, Yasuhiro Takabayashi, Takeshi Nakagawa, Martina Vranki&#263;, John Arvanitidis, Tetsuro Kusamoto, Kosmas Prassides, Yutaka Matsuo</p>
<p><em>Carbon</em> <strong>2019</strong>, <em>153</em>, 467&ndash;471. [<a href="https://www.sciencedirect.com/science/article/pii/S0008622319307158" target="_blank">DOI: 10.1016/j.carbon.2019.07.028</a>]</p>
<p style="text-align: center;"><img src="http://www.matsuo-lab.net/img/carbonLiC60.png" alt="" width="320" /></p>
<p>&nbsp;</p>
<p>16.&nbsp;High-Performance Solution-Processed Double-Walled Carbon Nanotube Transparent Electrode for Perovskite Solar Cells</p>
<p>Il Jeon, Jungjin Yoon, Unsoo Kim, Changsoo Lee, Rong Xiang, Ahmed Shawky, Jun Xi, Junseop Byeon, Hyuck Mo Lee, Mansoo Choi, Shigeo Maruyama, Yutaka Matsuo</p>
<p><em>Adv. Energy Mater.</em> <strong>2019</strong>, <em>9</em>, 1901204. [<a href="https://onlinelibrary.wiley.com/doi/abs/10.1002/aenm.201901204" target="_blank">DOI: 10.1002/aenm.201901204</a>] (<a href="https://onlinelibrary.wiley.com/doi/10.1002/aenm.201970105" target="_blank">Selected as a Cover Art</a>)</p>
<p style="text-align: center;"><img src="http://www.matsuo-lab.net/img/223_DWNT.png" alt="" width="350" /></p>
<p>&nbsp;</p>
<p>15. Semiconducting Carbon Nanotubes as Crystal Growth Templates and Grain Bridges in Perovskite Solar Cells</p>
<p>Seungju Seo, Il Jeon, Rong Xiang, Changsoo Lee, Hao Zhang, Takeshi Tanaka, Jin-Wook Lee, Donguk Suh, Tatsuro Ogamoto, Ryosuke Nishikubo, Akinori Saeki, Shohei Chiashi, Junichiro Shiomi, Hiromichi Kataura, Hyuck Mo Lee, Yang Yang, Yutaka Matsuo, Shigeo Maruyama</p>
<p><em>J. Mater. Chem. A</em>&nbsp;<strong>2019</strong>, <em>7</em>, 12987&ndash;12992. [<a href="https://doi.org/10.1039/C9TA02629K%20" target="_blank">DOI: 10.1039/C9TA02629K</a>]</p>
<p style="text-align: center;"><img src="http://www.matsuo-lab.net/img/222_s-SWCT.jpg" alt="" width="400" /></p>
<p>&nbsp;</p>
<p>14. Improved Solubility of Asymmetric Tetraethynylporphyrin Derivatives for Solution-processed Organic Solar Cells</p>
<p>Keisuke Ogumi, Takafumi Nakagawa, Hiroshi Okada, Yutaka Matsuo</p>
<p><em>Org. Electron.</em> <strong>2019</strong>, <em>71</em>, 50&ndash;57. [<a href="https://doi.org/10.1016/j.orgel.2019.04.036" target="_blank">DOI: 10.1016/j.orgel.2019.04.036</a>]</p>
<p style="text-align: center;"><img src="http://www.matsuo-lab.net/img/221_assymPor.png" alt="" width="400" /></p>
<p>&nbsp;</p>
<p>13. Synthesis of Benzothieno[60]fullerenes Through Fullerenyl Cation Intermediate&nbsp;</p>
<p>Yutaka Matsuo, Yun Yu, Xiao-Yu Yang, Hiroshi Ueno, Hiroshi Okada, Hiromasa Shibuya, Yeong Suk Choi, Yong Wan Jin</p>
<p><em>J. Org. Chem.</em> <strong>2019</strong>, <em>84</em>, 6270&ndash;6277. [<a href="https://doi.org/10.1021/acs.joc.9b00549" target="_blank">DOI: 10.1021/acs.joc.9b00549</a>]</p>
<p style="text-align: center;"><img src="http://www.matsuo-lab.net/img/220_benzothieno.png" alt="" width="400" /></p>
<p>&nbsp;</p>
<p>12. Mechanochromism, Twisted/Folded Structure Determination, and Derivatization of (<em>N</em>‐Phenylfluorenylidene)acridane</p>
<p>Yutaka Matsuo, Ya Wang, Hiroshi Ueno, Takafumi Nakagawa, Hiroshi Okada</p>
<p><em>Angew. Chem. Int. Ed.</em> <strong>2019</strong>, <em>58</em>, 8762&ndash;8767. [<a href="https://doi.org/10.1002/anie.201902636" target="_blank">DOI: 10.1002/anie.201902636</a>]</p>
<p style="text-align: center;"><img src="http://www.matsuo-lab.net/img/219_PhFA.png" alt="" width="400" /></p>
<p>&nbsp;</p>
<p>11. Stable and Reproducible 2D/3D Formamidinium&ndash;Lead&ndash;Iodide Perovskite Solar Cells</p>
<p>Abhishek Thote, Il Jeon, Jin-Wook Lee, Seungju Seo, Hao-Sheng Lin, Yang Yang, Hirofumi Daiguji, Shigeo Maruyama, Yutaka Matsuo</p>
<p><em>ACS Appl. Energy Mater.</em> <strong>2019</strong>, <em>2</em>, 2486&ndash;2493. [<a href="https://pubs.acs.org/doi/10.1021/acsaem.8b01964" target="_blank">DOI : 10.1021/acsaem.8b01964</a>] (<a href="https://pubs.acs.org/toc/aaemcq/2/4" target="_blank">Selected as a Cover Art</a>)</p>
<p style="text-align: center;"><img src="http://www.matsuo-lab.net/img/217_2D3D.png" alt="" width="400" /></p>
<p>&nbsp;</p>
<p>10. High-Working-Pressure Sputtering of ZnO for Stable and Efficient Perovskite Solar Cells</p>
<p>Abhishek Thote, Il Jeon, Hao-Sheng Lin, Sergei Manzhos, Takafumi Nakagawa, Donguk Suh, Junho Hwang, Makoto Kashiwagi, Junichiro Shiomi, Shigeo Maruyama, Hirofumi Daiguji, Yutaka Matsuo</p>
<p><em>ACS Appl. Electron. Mater.</em> <strong>2019</strong>, <em>1</em>, 389&ndash;396. [<a href="https://pubs.acs.org/doi/10.1021/acsaelm.8b00105" target="_blank">DOI: 10.1021/acsaelm.8b00105</a>] (<a href="https://pubs.acs.org/toc/aaembp/1/3" target="_blank">Selected as a Cover Art</a>)</p>
<p style="text-align: center;"><img src="http://www.matsuo-lab.net/img/218_HWP_SputterZnO.png" alt="" width="400" />&nbsp;</p>
<p>&nbsp;</p>
<p>9. Effects of Optical Interference and Optimized Crystallinity in Organic Photovoltaic Cells with a Low-bandgap Small Molecule Fabricated by Dry Process</p>
<p>Kohei Yamamoto, Tetsuhiko Miyadera, Yutaka Matsuo, Takayuki Kuwabara, Kohshin Takahashi, Tetsuya Taima, Masayuki Chikamatsu</p>
<p><em>Jpn. J. Appl. Phys.</em> <strong>2019</strong>, <em>58</em>, SBBG12. [<a href="https://doi.org/10.7567/1347-4065/aafe6b" target="_blank">DOI: 10.7567/1347-4065/aafe6b</a>]</p>
<p>&nbsp;</p>
<p>8. Highly Soluble <em>C</em><sub>2<em>v</em></sub> -symmetrical Fullerene Derivatives: Efficient Synthesis, Characterization, and Electrochemical Study</p>
<p>Yue Ma, Kouya Uchiyama, Hiroshi Ueno, Hiroshi Okada, Hiroshi Moriyama, Yutaka Matsuo</p>
<p><em>Org. Chem. Front.</em> <strong>2019</strong>, <em>6</em>, 1372&ndash;1377. [<a href="https://pubs.rsc.org/en/content/articlelanding/2019/qo/c9qo00056a" target="_blank">DOI: 10.1039/c9qo00056a</a>]</p>
<p style="text-align: center;"><img src="http://www.matsuo-lab.net/img/215_octa.png" alt="" width="350" /></p>
<p>&nbsp;</p>
<p>7. Fluorescein-based Fluorescent Porous Aromatic Framework for Fe<sup>3+</sup> Detection with High Sensitivity<br />Tingting Ma, Xue Zhao, Yutaka Matsuo, Jian Song, Rui Zhao, Muhammad Faheem, Mo Chen, Yunfeng Zhang, Yuyang Tian, Guangshan Zhu<br /><em>J. Mater. Chem. C</em> <strong>2019</strong>, <em>7</em>, 2327&ndash;2332. [<a href="https://pubs.rsc.org/en/content/articlelanding/2019/tc/c8tc06288a" target="_blank">DOI: 10.1039/C8TC06288A</a>]</p>
<p>&nbsp;&nbsp;</p>
<p>6. Polarity Engineering of Porous Aromatic Frameworks for Specific Water Contaminants Capture<br />Xiaoshan Shen, Muhammad Faheem, Yutaka Matsuo, Saba Aziz, Xu Zhang, Yuhan Li, Jian Song , Yuyang Tian, Guangshan Zhu<br /><em>J. Mater. Chem. A</em> <strong>2019</strong>, <em>7</em>, 2507&ndash;2512. [<a href="https://pubs.rsc.org/en/content/articlelanding/2019/ta/c8ta11343b" target="_blank">DOI: 10.1039/C8TA11343B</a>]</p>
<p>&nbsp;</p>
<p>5. Star-shaped Magnesium Tetraethynylporphyrin Bearing Four Peripheral Electron-accepting Diketopyrrolopyrrole Functionalities for Organic Solar Cells</p>
<p>Huan Wang, Qihui Yue, Takafumi Nakagawa, Anna Zieleniewska, Hiroshi Okada, Keisuke Ogumi, Hiroshi Ueno, Dirk M. Guldi, Xiaozhang Zhu, Yutaka Matsuo&nbsp;</p>
<p><em>J. Mater. Chem. A</em> <strong>2019</strong>, <em>7</em>, 4072&ndash;4083. [<a href="https://pubs.rsc.org/en/Content/ArticleLanding/2019/TA/C8TA10710F" target="_blank">DOI: 10.1039/c8ta10710f</a>]</p>
<p style="text-align: center;"><img src="http://www.matsuo-lab.net/img/214_DPP4.png" alt="" width="400" /></p>
<p>&nbsp;</p>
<p>4. Reduced Knoevenagel Reaction of Acetetracenylene-1,2-dione with Acceptor Units for Luminescent Tetracene Derivatives</p>
<p>Yutaka Matsuo, Chu-Guo Yu, Takafumi Nakagawa, Hiroshi Okada, Hiroshi Ueno, Tian-Ge Sun, Yu-Wu Zhong</p>
<p><em>J. Org. Chem.</em> <strong>2019</strong>, <em>84</em>, 2339&ndash;2345. [<a href="http://dx.doi.org/10.1021/acs.joc.8b03083" target="_blank">DOI: 10.1021/acs.joc.8b03083</a>]</p>
<p style="text-align: center;"><img src="http://www.matsuo-lab.net/img/213_tetracene-RHA.png" alt="" width="400" /></p>
<p>&nbsp;</p>
<p>3. Formation of Environmentally Stable Hole-doped Graphene Films: Instantaneous and High-density Carrier Doping by a Boron-Based Oxidant</p>
<p>Kaito Kanahashi, Naoki Tanaka, Yoshiaki Shoji, Mina Maruyama, Il Jeon, Kenji Kawahara, Masatou Ishihara, Masataka Hasegawa, Hiromichi Ohta, Hiroki Ago, Yutaka Matsuo, Susumu Okada, Takanori Fukushima, Taishi Takenobu</p>
<p>npj 2D Materials and Applications&nbsp;<strong>2019</strong>, <em>3</em>, 7. [<a href="https://www.nature.com/articles/s41699-019-0090-x" target="_blank">DOI: 10.1038/s41699-019-0090-x</a>]</p>
<p>&nbsp;</p>
<p>2. Vapor-Assisted <em>Ex-Situ</em> Doping of Carbon Nanotube towards Efficient and Stable Perovskite Solar Cells</p>
<p>Jin-Wook Lee, Il Jeon, Hao-Sheng Lin, Seungju Seo, Tae-Hee Han, Anton Anisimov, Esko I. Kauppinen, Yutaka Matsuo, Shigeo Maruyama, Yang Yang</p>
<p><em>Nano Lett.</em> <strong>2019</strong>, <em>19</em>, 2223&ndash;2230. [<a href="https://doi.org/10.1021/acs.nanolett.8b04190" target="_blank">DOI: 10.1021/acs.nanolett.8b04190</a>] (<a href="https://pubs.acs.org/toc/nalefd/19/4" target="_blank">Selected as a Cover Art</a>)</p>
<p style="text-align: center;"><img src="http://www.matsuo-lab.net/img/209_CNT_TFMS.png" alt="" width="400" /></p>
<p>&nbsp;</p>
<p>1. Single-Walled Carbon Nanotubes in Emerging Solar Cells: Synthesis and Electrode Applications</p>
<p>Il Jeon, Rong Xiang, Ahmed Shawky, Yutaka Matsuo, Shigeo Maruyama</p>
<p><em>Adv. Energy Mater.</em> <strong>2019</strong>, <em>9</em>, 1801312. (Review Article) [<a href="https://onlinelibrary.wiley.com/doi/abs/10.1002/aenm.201801312" target="_blank">DOI: 10.1002/aenm.201801312</a>]</p>
<p style="text-align: center;"><img src="http://www.matsuo-lab.net/img/2019_AEM.png" alt="" width="394" height="199" /></p>
</div>

<div class="block">
<h4>2018</h4>
<p>17. Achieving High Efficiency in Solution-Processed Perovskite Solar Cells using C<sub>60</sub>/C<sub>70</sub> Mixed Fullerenes</p>
<p>Hao-Sheng Lin, Il Jeon, Rong Xiang, Seungju Seo, Jin-Wook Lee, Chao Li, Amrita Pal, Sergei Manzhos, Mark Goorsky, Yang Yang, Shigeo Maruyama, Yutaka Matsuo</p>
<p><em>ACS Appl. Mater. Interfaces</em> <strong>2018</strong>, <em>10</em>, 39590&ndash;39598. [<a href="https://pubs.acs.org/doi/abs/10.1021/acsami.8b11049" target="_blank">DOI: 10.1021/acsami.8b11049</a>] (<a href="https://pubs.acs.org/toc/aamick/10/46" target="_blank">Selected as a Cover Art</a>)</p>
<p style="text-align: center;"><img src="http://www.matsuo-lab.net/img/208_C60C70ETL.png" alt="" width="300" /></p>
<p>&nbsp;</p>
<p>16. Functionalization of [60]Fullerene through Fullerene Cation Intermediates</p>
<p>Hao-Sheng Lin, Yutaka Matsuo</p>
<p><em>Chem. Commun.</em> <strong>2018</strong>, <em>54</em>, 11244&ndash;11259. [<a href="https://pubs.rsc.org/en/content/articlelanding/2018/cc/c8cc05965a#!divAbstract" target="_blank">DOI: 10.1039/C8CC05965A</a>] (Feature Article)</p>
<p style="text-align: center;"><img src="http://www.matsuo-lab.net/img/2018_cation_review.png" alt="" width="300" /></p>
<p>&nbsp;</p>
<p>15. Octaalkoxyfullerenes: Widely LUMO-Tunable <em>C</em><sub>2<em>v</em></sub>-Symmetric Fullerene Derivatives</p>
<p>Hiroshi Ueno, Kouya Uchiyama, Yue Ma, Keita Watanabe, Kenji Yoza, Yutaka Matsuo, Hiroshi Moriyama</p>
<p><em>J. Org. Chem.</em> <strong>2018</strong>, <em>83</em>, 10655&ndash;10659. [<a href="https://pubs.acs.org/doi/10.1021/acs.joc.8b01485" target="_blank">DOI: 10.1021/acs.joc.8b01485</a>]</p>
<p style="text-align: center;"><img src="http://www.matsuo-lab.net/img/212_C60R8.gif" alt="" width="400" /></p>
<p>&nbsp;</p>
<p>14. Magnesium Tetra(phenylethynyl)porphyrin: Stepwise Synthetic Route, Crystal Structures, and Longer Singlet Excited State Lifetime than Zinc Congener</p>
<p>Takafumi Nakagawa, Huan Wang, Anna Zieleniewska, Hiroshi Okada, Shinobu Aoyagi, Dirk M. Guldi, Yutaka Matsuo</p>
<p><em>Chem. Asian J.</em> <strong>2018</strong>, <em>13</em>, 3032&ndash;3039. [<a href="https://onlinelibrary.wiley.com/doi/abs/10.1002/asia.201800994" target="_blank">DOI: 10.1002/asia.201800994</a>]</p>
<p style="text-align: center;"><img src="http://www.matsuo-lab.net/img/211_MgPorPh4.jpg" alt="" width="400" /></p>
<p>&nbsp;</p>
<p>13. Enhanced Electrical Conduction in Anatase TaON via Soft Chemical Lithium Insertion towards Electronics Application</p>
<p>Atsushi Suzuki, Yasushi Hirose, Takafumi Nakagawa, Satoshi Fujiwara, Shoichiro Nakao, Yutaka Matsuo, Isao Harayama, Daiichiro Sekiba, Tetsuya Hasegawa</p>
<p><em>ACS Appl. Nano Mater.</em> <strong>2018</strong>, <em>1</em>, 3981&ndash;3985. [<a href="https://pubs.acs.org/doi/10.1021/acsanm.8b00750" target="_blank">DOI: 10.1021/acsanm.8b00750</a>]</p>
<p style="text-align: center;"><img src="http://www.matsuo-lab.net/img/210_TaON.gif" alt="" width="300" /></p>
<p>&nbsp;</p>
<p>12. Non-doped and Unsorted Single-walled Carbon Nanotubes as Carrier-selective, Transparent, and Conductive Electrode for Perovskite Solar Cells</p>
<p>Takahiro Sakaguchi, Il Jeon, Takaaki Chiba, Ahmed Shawky, Rong Xiang, Shohei Chiashi, Esko I. Kauppinen, Nam-Gyu Park, Yutaka Matsuo, Shigeo Maruyama</p>
<p><em>MRS Commun.</em> <strong>2018</strong>, <em>8</em>, 1058&ndash;1063. [<a href="https://doi.org/10.1557/mrc.2018.142" target="_blank">DOI: 10.1557/mrc.2018.142</a>]</p>
<p style="text-align: center;"><img src="http://www.matsuo-lab.net/img/204_CNTPMMA.jpeg" alt="" width="300" /></p>
<p>&nbsp;</p>
<p>11. Polymeric Acid-doped Transparent Carbon Nanotube Electrodes in Organic Solar Cells with the Longest Doping Durability</p>
<p>Il Jeon, Clement Delacou, Hiroshi Okada, Graham E. Morse, Tae-Hee Han, Yuta Sato, Anton Anisimov, Kazu Suenaga, Esko I. Kauppinen, Shigeo Maruyama, Yutaka Matsuo</p>
<p><em>J. Mater. Chem. A</em> <strong>2018</strong>, <em>6</em>, 14553&ndash;14559. [<a href="http://pubs.rsc.org/en/content/articlelanding/2018/ta/c8ta03383h#!divAbstract" target="_blank">DOI: 10.1039/C8TA03383H</a>]</p>
<p>(Selected as <a href="http://pubs.rsc.org/en/journals/articlecollectionlhttp://pubs.rsc.org/en/journals/articlecollectionlanding?sercode=ta&amp;themeid=f7d0c2cb-4131-4611-8a14-f0c78308057d" target="_blank">2018 Journal of Materials Chemistry A HOT Papers</a>)</p>
<p style="text-align: center;"><img src="http://www.matsuo-lab.net/img/203_NafionCNTOSC.gif" alt="" width="242" height="189" /></p>
<p>&nbsp;</p>
<p>10. Structure of [60]Fullerene with Mobile Lithium Cation Inside</p>
<p>Shinobu Aoyagi, Kazuhira Miwa, Hiroshi Ueno, Hiroshi Okada, Yutaka Matsuo, Ken Kokubo</p>
<p><em>Royal Soc. Open Sci.</em> <strong>2018</strong>, <em>5</em>, 180337. [<a href="http://dx.doi.org/10.1098/rsos.180337" target="_blank">DOI: 10.1098/rsos.180337</a>]</p>
<p style="text-align: center;"><img src="http://www.matsuo-lab.net/img/202_LiC60TFSI.png" alt="" width="300" /></p>
<p>&nbsp;</p>
<p>9. Electronic Structure and Cohesive Energy of Silyl-methyl-fullerene and Methano-indene-fullerene Solids</p>
<p>Sho Furutani, Yutaka Matsuo, Susumu Okada</p>
<p><em>Jpn. J. Appl. Phys.</em> <strong>2018</strong>, 57, 085102. [<a href="http://iopscience.iop.org/article/10.7567/JJAP.57.085102" target="_blank">DOI: 10.7567/JJAP.57.085102</a>]</p>
<p>&nbsp;</p>
<p>8. Fullerene-Cation-Mediated Noble-Metal-Free Direct Introduction of Functionalized Aryl Groups onto [60]Fullerene</p>
<p>Xiao-Yu Yang, Hao-Sheng Lin, Il Jeon, Yutaka Matsuo</p>
<p><em>Org. Lett.</em> <strong>2018</strong>, <em>20</em>, 3372&ndash;3376. [<a href="https://pubs.acs.org/doi/10.1021/acs.orglett.8b01295" target="_blank">DOI: 10.1021/acs.orglett.8b01295</a>]</p>
<p style="text-align: center;"><img src="http://www.matsuo-lab.net/img/200_cation_boronic.png" alt="" width="400" /></p>
<p>&nbsp;</p>
<p>7. Anthracene-based Organic Small-molecule Electron-injecting Material for Inverted Organic Light-emitting Diodes</p>
<p>Yutaka Matsuo, Hiroshi Okada, Yasuhiro Kondo, Il Jeon, Huan Wang, Yun Yu, Takeshi Matsushita, Motoki Yanai, Toshiaki Ikuta</p>
<p><em>ACS Appl. Mater. Interfaces</em> <strong>2018</strong>, <em>10</em>, 11810&ndash;11817. [<a href="https://pubs.acs.org/doi/abs/10.1021/acsami.8b00603" target="_blank">DOI: 10.1021/acsami.8b00603</a>]</p>
<p style="text-align: center;"><img src="http://www.matsuo-lab.net/img/199_DPAMA.png" alt="" width="394" height="156" /></p>
<p>&nbsp;</p>
<p>6. Engineering High-performance and Air-stable PBTZT-stat-BDTT-8:PC<sub>61</sub>BM/PC<sub>71</sub>BM Organic Solar Cells</p>
<p>Il Jeon, Ryohei Sakai, Seungju Seo, Graham E. Morse, Hiroshi Ueno, Takafumi Nakagawa, Yang Qian, Shigeo Maruyama, Yutaka Matsuo</p>
<p><em>J. Mater. Chem. A</em> <strong>2018</strong>, <em>6</em>, 5746&ndash;5751. [<a href="http://pubs.rsc.org/en/content/articlelanding/2018/ta/c7ta11095b#!divAbstract" target="_blank">DOI: 10.1039/C7TA11095B</a>]</p>
<p style="text-align: center;"><img src="http://www.matsuo-lab.net/img/198_MerckOSC.png" alt="" width="354" height="189" /></p>
<p>&nbsp;</p>
<p>5. Lithium-Ion Endohedral Fullerene (Li<sup>+</sup>@C<sub>60</sub>) Dopant in Stable Perovskite Solar Cells Inducing Anti-Oxidation</p>
<p>Il Jeon [+], Hiroshi Ueno [+], Seungju Seo, Kerttu Aitola, Ryosuke Nishikubo, Akinori Saeki, Hiroshi Okada, Gerrit Boschloo, Shigeo Maruyama, Yutaka Matsuo ([+], contributed equally)</p>
<p><em>Angew. Chem. Int. Ed.</em> <strong>2018</strong>, <em>57</em>, 4607&ndash;4611. [<a href="https://onlinelibrary.wiley.com/doi/abs/10.1002/anie.201800816" target="_blank">DOI: 10.1002/anie.201800816</a>]</p>
<p style="text-align: center;"><img src="http://www.matsuo-lab.net/img/197_LiC60PSC.jpg" alt="" width="354" height="352" /></p>
<p>&nbsp;</p>
<p>4. A Helically-Twisted Ladder Based on 9,90-Bifluorenylidene: Synthesis, Characterization, and Charge Transport Properties</p>
<p>Jinjia Xu, Atsuro Takai, Alisa Bannaron, Takafumi Nakagawa, Yutaka Matsuo, Manabu Sugimoto, Yoshitaka Matsushita, Masayuki Takeuchi</p>
<p><em>Mater. Chem. Front.</em> <strong>2018</strong>, <em>2</em>, 780&ndash;784 . [<a href="http://pubs.rsc.org/en/content/articlelanding/2018/qm/c7qm00583k#!divAbstract" target="_blank">DOI: 10.1039/c7qm00583k</a>]</p>
<p>&nbsp;</p>
<p>3. Single-walled Carbon Nanotubes in Solar Cells</p>
<p>Il Jeon, Yutaka Matsuo, Shigeo Maruyama<em></em></p>
<p><em>Topics Curr. Chem.</em> <strong>2018</strong>, <em>376</em>, 4. [<a href="https://link.springer.com/article/10.1007%2Fs41061-017-0181-0" target="_blank">DOI: 10.1007/s41061-017-0181-0</a>]</p>
<p style="text-align: center;"><img src="http://www.matsuo-lab.net/img/SWCNTsSC.jpeg" alt="" width="150" /></p>
<p>&nbsp;</p>
<p>2. Carbon-Sandwiched Perovskite Solar Cell</p>
<p>Namyoung Ahn, Il Jeon, Jungjin Yoon, Esko I. Kauppinen, Yutaka Matsuo, Shigeo Maruyama, Mansoo Choi</p>
<p><em>J. Mater. Chem. A</em> <strong>2018</strong>, <em>6</em>, 1382&ndash;1389. [<a href="http://pubs.rsc.org/en/Content/ArticleLanding/2018/TA/C7TA09174E" target="_blank">DOI: 10.1039/C7TA09174E</a>]</p>
<p><img style="display: block; margin-left: auto; margin-right: auto;" src="http://www.matsuo-lab.net/img/CarbonSandwich.png" alt="" width="344" height="141" /></p>
<p>&nbsp;</p>
<p>1. A Fluorenylidene-Acridane That Becomes Dark in Color upon Grinding &ndash; Ground State Mechanochromism by Conformational Change</p>
<p>Tsuyoshi Suzuki, Hiroshi Okada, Takafumi Nakagawa, Kazuki Komatsu, Chikako Fujimoto, Hiroyuki Kagi, Yutaka Matsuo</p>
<p><em>Chem. Sci.</em><strong></strong> <strong>2018</strong>, <em>9</em>, 475&ndash;482. [<a href="http://pubs.rsc.org/en/Content/ArticleLanding/2018/SC/C7SC03567E" target="_blank">DOI: 10.1039/c7sc03567e</a>]</p>
<p style="text-align: center;"><img src="http://www.matsuo-lab.net/img/193FA100.png" alt="" width="394" height="156" /></p>
</div>

<div class="block">
<h4>2017</h4>
<p>17. Perovskite Solar Cells Using Carbon Nanotubes Both as Cathode and as Anode</p>
<p>Il Jeon, Seungju Seo, Yuta Sato, Clement Delacou, Anton Anisimov, Kazutomo Suenaga, Esko Kauppinen, Shigeo Maruyama, Yutaka Matsuo</p>
<p><em>J. Phys. Chem. C</em> <strong>2017</strong>, <em>121</em>, 25743&ndash;25749. [<a href="http://pubs.acs.org/doi/full/10.1021/acs.jpcc.7b10334" target="_blank">DOI: 10.1021/acs.jpcc.7b10334</a>]</p>
<p style="text-align: center;"><img src="http://www.matsuo-lab.net/img/194bothCNT.png" alt="" width="406" height="152" /></p>
<p>&nbsp;</p>
<p>16. Synthesis and Crystal Structure of Li<sup>+</sup>@Fluoreno[60]fullerene: Effect of Encapsulated Lithium Ion on Electrochemistry of Spiroannelated Fullerene</p>
<p>Hiroshi Ueno, Hiroshi Okada, Shinobu Aoyagi, Yutaka Matsuo</p>
<p><em>J. Org. Chem.</em> <strong>2017</strong>, <em>82</em>, 11631&ndash;11635. [<a href="http://pubs.acs.org/doi/abs/10.1021/acs.joc.7b01893" target="_blank">DOI: 10.1021/acs.joc.7b01893</a>]</p>
<p style="text-align: center;"><img src="http://www.matsuo-lab.net/img/192fluorenoLiC60.png" alt="" width="368" height="184" /></p>
<p>&nbsp;</p>
<p>15. Carbon Nanotubes Versus Graphene as Flexible Transparent Electrodes in Inverted Perovskite Solar Cells</p>
<p>Il Jeon, Jungjin Yoon, Namyoung Ahn, Mohamed Atwa, Clement Delacou, Anton Anisimov, Esko Kauppinen, Mansoo Choi, Shigeo Maruyama, Yutaka Matsuo</p>
<p><em>J. Phys. Chem. Lett.</em> <strong>2017</strong>, <em>8</em>, 5395&ndash;5401. [<a href="http://pubs.acs.org/doi/abs/10.1021/acs.jpclett.7b02229" target="_blank">DOI: 10.1021/acs.jpclett.7b02229</a>]</p>
<p style="text-align: center;"><img src="http://www.matsuo-lab.net/img/191CNTvsGraphene.png" alt="" width="271" height="207" /></p>
<p>&nbsp;</p>
<p>14. Substituent Effect in Magnesium Tetraethynylporphyrin with Two Diketopyrrolopyrrole Units for Bulk Heterojunction Organic Solar Cells</p>
<p>Keisuke Ogumi (+), Takafumi Nakagawa (+), Hiroshi Okada, Ryohei Sakai, Huan Wang, Yutaka Matsuo ([+], contributed equally)</p>
<p><em>J. Mater. Chem.</em> <em>A</em> <strong>2017</strong>, <em>5</em>, 23067&ndash;23077. [<a href="http://pubs.rsc.org/en/content/articlelanding/2017/ta/c7ta07576f#!divAbstract" target="_blank">DOI: 10.1039/C7TA07576F</a>]</p>
<p style="text-align: center;"><img src="http://www.matsuo-lab.net/img/190TEPDPP2.png" alt="" width="394" height="212" /></p>
<p>&nbsp;</p>
<p>13. Comparative Density Functional Theory &ndash; Density Functional Tight Binding Study of Fullerene Derivatives: Effects Due to Fullerene Size, Addends, and Crystallinity on Bandstructure, Charge Transport and Optical Properties</p>
<p>Amrita Pal, Lai Kai Wen, Chia Yao Jun, Il Jeon, Yutaka Matsuo, Sergei Manzhos</p>
<p><em>Phys. Chem. Chem. Phys.</em> <strong>2017</strong>, <em>19</em>, 28330&ndash;28343. [<a href="http://pubs.rsc.org/en/content/articlelanding/2017/cp/c7cp05290a#!divAbstract" target="_blank">DOI: 10.1039/C7CP05290A</a>]</p>
<p>&nbsp;</p>
<p>12. Endohedral Lithium-containing Fullerenes: Preparation, Derivatization, and Application</p>
<p>Yutaka Matsuo, Hiroshi Okada, Hiroshi Ueno</p>
<p>Springer<strong></strong>, Singapore, 2017. [DOI: 10.1007/978-981-10-5004-6] [ISBN: 978-981-10-5003-9] [<a href="http://www.springer.com/jp/book/9789811050039" target="_blank">LINK</a>]</p>
<p style="text-align: center;"><img src="http://www.matsuo-lab.net/img/SpringerLiC60.jpg" alt="" width="210" height="310" /></p>
<p>&nbsp;</p>
<p>11. Highly Conductive and Transparent Large-Area Bilayer Graphene Realized by MoCl<sub>5</sub> Intercalation</p>
<p>Hiroki Kinoshita, Il Jeon, Mina Maruyama, Kenji Kawahara, Yuri Terao, Dong Ding, Rika Matsumoto, Yutaka Matsuo, Susumu Okada, Hiroki Ago</p>
<p><em>Adv. Mater.</em> <strong>2017</strong>, <em></em>1702141. [<a href="http://onlinelibrary.wiley.com/doi/10.1002/adma.201702141/abstract" target="_blank">DOI: 10.1002/adma.201702141</a>]</p>
<p style="text-align: center;"><img src="http://www.matsuo-lab.net/img/BLGopv.png" alt="" width="455" height="231" /></p>
<p>&nbsp;</p>
<p>10. Regiocontrolled Electrosynthesis of [60]Fullerene Bisadducts: Photovoltaic Performance and Crystal Structures of C<sub>60</sub> <em>o</em>‐Quinodimethane Bisadducts</p>
<p>Zong-Jun Li, Sisi Wang, Shu-Hui Li, Tao Sun, Wei-Wei Yang, Kazutaka Shoyama, Takafumi Nakagawa, Il Jeon, Xiaoniu Yang, Yutaka Matsuo, Xiang Gao</p>
<p><em>J. Org. Chem.</em> <strong>2017</strong>, <em>82</em>, 8676&ndash;8685. [<a href="http://pubs.acs.org/doi/abs/10.1021/acs.joc.7b01732" target="_blank">DOI: 10.1021/acs.joc.7b01732</a>]</p>
<p>&nbsp;</p>
<p>9. Crystallographic Structure Determination of Both [5,6]- and [6,6]-Isomers of Lithium-ion-containing Diphenylmethano[60]fullerene</p>
<p>Hiroshi Okada, Hiroki Kawakami, Shinobu Aoyagi, Yutaka Matsuo</p>
<p><em>J. Org. Chem.</em> <strong>2017</strong>, <em>82</em>, 5868&ndash;5872. [<a href="http://pubs.acs.org/doi/abs/10.1021/acs.joc.7b00730" target="_blank">DOI: 10.1021/acs.joc.7b00730</a>]</p>
<p style="text-align: center;"><img src="http://www.matsuo-lab.net/img/186_LiC60Ph2-2.png" alt="" width="394" height="156" /></p>
<p>&nbsp;</p>
<p>8. Indium Tin Oxide-free Small Molecule Organic Solar Cells using Single-Walled Carbon Nanotube Electrodes</p>
<p>Cl&eacute;ment Delacou, Il Jeon, Seungju Seo, Takafumi Nakagawa, Esko I. Kauppinen, Shigeo Maruyama, Yutaka Matsuo</p>
<p><em>ECS J. Solid State Sci. Technol.</em> <strong>2017</strong>, 6, M3181&ndash;M3184. (Sir Harry Kroto memorial issue) [<a href="http://jss.ecsdl.org/cgi/content/abstract/6/6/M3181" target="_blank">DOI: 10.1149/2.0311706jss</a>]</p>
<p>&nbsp;</p>
<p>7. Scalable and Solid-state Redox Functionalization of Transparent Single-walled Carbon Nanotube Films for Highly Efficient and Stable Solar Cells</p>
<p>Kehang Cui, Yang Qian, Il Jeon, Anton Anisimov, Yutaka Matsuo, Esko I. Kauppinen, Shigeo Maruyama</p>
<p><em>Adv. Energy Mater.</em> <strong>2017</strong>, <em>7</em>, 1700449. [<a href="http://dx.doi.org/10.1002/aenm.201700449" target="_blank">DOI: 10.1002/aenm.201700449</a>]</p>
<p>&nbsp;</p>
<p>6. Regioselective Acylation and Carboxylation of [60]Fulleroindoline via Electrochemical Synthesis</p>
<p>Hao-Sheng Lin, Yutaka Matsuo, Jun-Jie Wang, Guan-Wu Wang</p>
<p><em>Org. Chem. Front.</em> <strong>2017</strong>, <em>4</em>, 603&ndash;607. [<a href="http://pubs.rsc.org/en/Content/ArticleLanding/2017/QO/C6QO00654J#!divAbstract" target="_blank">DOI: 10.1039/C6QO00654J</a>]</p>
<p>&nbsp;</p>
<p>5. Fullerene Cation-mediated Demethylation/Cyclization to 5- and 7-Membered Cyclo[60]fullerene Derivatives</p>
<p>Yutaka Matsuo, Keisuke Ogumi, Ying Zhang, Hiroshi Okada, Takafumi Nakagawa, Hiroshi Ueno, Akiko Gocho, Eiichi Nakamura<br /><em>J. Mater. Chem. A</em> <strong>2017</strong>, <em>5</em>, 2774&ndash;2783 . [<a href="http://pubs.rsc.org/en/content/articlelanding/2014/ta/c6ta10319g" target="_blank">DOI: 10.1039/C6TA10319G</a>]</p>
<p style="text-align: center;"><img src="http://www.matsuo-lab.net/img/SIOF.png" alt="" width="394" height="162" /></p>
<p>&nbsp;</p>
<p>4. An Efficient Organic Solvent-free Solution-processing Strategy for High-mobility Metal Chalcogenide Film Growth</p>
<p>Jie Zhao, Il Jeon, Qinghua Yi, Menka Jain, Mark H. Rummeli, Pingyuan Song, Yutaka Matsuo, Guifu Zou</p>
<p><em>Green Chem.</em> <strong>2017</strong>, <em>19</em>, 946&ndash;951. [<a href="http://pubs.rsc.org/en/content/articlelanding/2016/gc/c6gc02489k" target="_blank">DOI: 10.1039/C6GC02489K</a>]</p>
<p>&nbsp;</p>
<p>3. Polymer-Fullerene Solar Cells</p>
<p>Il Jeon, Yutaka Matsuo</p>
<p><em>Encyclopedia of Polymer Science and Technology</em> <strong>2017</strong>, 1&ndash;17. [<a href="http://onlinelibrary.wiley.com/doi/10.1002/0471440264.pst650/abstract" target="_blank">DOI: 10.1002/0471440264.pst650</a>]</p>
<p><br />2. Structures and Properties of Saturn-Like Complexes Composed of Oligothiophene Macrocycle with Methano[60]fullerene and [70]Fullerene<br />Masahiko Iyoda, Hideyuki Shimizu, Shinobu Aoyagi, Hiroshi Okada, Biao Zhou, Yutaka Matsuo<br /><em>Can. J. Chem.</em> <strong>2017</strong>, <em>95</em>, 315&ndash;319. [<a href="http://www.nrcresearchpress.com/doi/abs/10.1139/cjc-2016-0461" target="_blank">DOI: 10.1139/cjc-2016-0461</a>]</p>
<p>&nbsp;</p>
<p style="text-align: center;"><img src="http://www.matsuo-lab.net/img/C61H2atSaturn.png" alt="" width="244" height="237" /></p>
<p>&nbsp;</p>
<p>1. Dual Interfacial Modifications Enable High Performance Semitransparent Perovskite Solar Cells with Large Open Circuit Voltage and Fill Factor<br />Qifan Xue, Yang Bai, Meiyue Liu, Ruoxi Xia, Ziming Chen, Zhicheng Hu, Xiao-Fang Jiang, Fei Huang, Shihe Yang, Yutaka Matsuo, Hin-Lap Yip, Yong Cao<br /><em>Adv. Energy Mater.</em> <strong>2017</strong>, <em>7</em>, 1602333. [<a href="http://onlinelibrary.wiley.com/doi/10.1002/aenm.201602333/full" target="_blank">DOI: 10.1002/aenm.201602333</a>] [<a href="http://onlinelibrary.wiley.com/doi/10.1002/aenm.201770047/full" target="_blank">cover picture</a>]</p>
<p style="text-align: center;"><img src="http://www.matsuo-lab.net/img/MIFpsc.png" alt="" width="394" height="260" /></p>
</div>

<div class="block">
<h4>2016</h4>
<p>11. Room Temperature-processed Inverted Organic Solar Cells using High Working-pressure-sputtered ZnO Film<br />Il Jeon, Yang Qian, Shoichiro Nakao, Daisuke Ogawa, Rong Xiang, Taiki Inoue, Shohei Chiashi, Tetsuya Hasegawa, Shigeo Maruyama,* Yutaka Matsuo*<br /><em>J. Mater. Chem. A</em> <strong>2016</strong>, <em>4</em>, 18763&ndash;18768. [<a href="http://pubs.rsc.org/en/content/articlelanding/2016/ta/c6ta08068e" target="_blank">DOI: 10.1039/C6TA08068E</a>]</p>
<p>&nbsp;</p>
<p>10. Regio- and Stereo-selective Intermolecular [2+2] Cycloaddition of Allenol Esters with C<sub>60</sub> leading to Alkylidenecyclobutane-annulated Fullerenes<br />Mitsuhiro Ueda,* Tsukasa Sakaguchi, Miho Hayama, Takafumi Nakagawa, Yutaka Matsuo,* Aiko Munechika, Shunsuke Yoshida, Hiroshi Yasuda, Ilhyong Ryu*<br /><em>Chem. Commun.</em> <strong>2016</strong>, <em>52</em>, 13175&ndash;13178. [<a href="http://pubs.rsc.org/is/content/articlelanding/2016/cc/c6cc07320d" target="_blank">DOI: 10.1039/c6cc07320d</a>]</p>
<p style="text-align: center;"><img src="http://www.matsuo-lab.net/img/2plus2allenol.gif" alt="" width="378" height="171" /></p>
<p>&nbsp;</p>
<p>9. Interface Engineering of Metal Oxides using Ammonium Anthracene in Inverted Organic Solar Cells</p>
<p>Il Jeon, Sasa Zeljkovic, Kei Kondo, Michito Yoshizawa, Yutaka Matsuo*</p>
<p><em>ACS Appl. Mater. Interfaces</em>, <strong>2016</strong>, <em>8</em>, 29866&ndash;29871. [<a href="http://pubs.acs.org/doi/abs/10.1021/acsami.6b09684" target="_blank">DOI: 10.1021/acsami.6b09684</a>]</p>
<p style="text-align: center;"><img src="http://www.matsuo-lab.net/img/C60catchingAA.gif" alt="" width="311" height="223" /></p>
<p>&nbsp;</p>
<p>8. Metal-electrode-free Window-like Organic Solar Cells with p-Doped Carbon Nanotube Thin-film Electrodes</p>
<p>Il Jeon, Clement Delacou, Antti Kaskela, Esko I. Kauppinen, Shigeo Maruyama, Yutaka Matsuo*</p>
<p><em>Sci. Rep.</em> <strong>2016</strong>, <em>6</em>, 31348. [<a href="http://www.nature.com/articles/srep31348" target="_blank">DOI: 10.1038/srep31348</a>]</p>
<p style="text-align: center;"><img src="http://www.matsuo-lab.net/img/windowlikeCNTOSC.png" alt="" width="429" height="216" /></p>
<p>&nbsp;</p>
<p>7. Enhancement of Low-field Magnetoresistance in Self-Assembled Epitaxial La<sub>0.67</sub>Ca<sub>0.33</sub>MnO<sub>3</sub>:NiO and La<sub>0.67</sub>Ca<sub>0.33</sub>MnO<sub>3</sub>:Co<sub>3</sub>O<sub>4</sub> Composite Films via Polymer-Assisted Deposition</p>
<p>Meng Zhou, Yuling Li, Il Jeon, Qinghua Yi, Xuebin Zhu, Xianwu Tang, Haiyan Wang, Ling Fei, Yuping Sun, Shuguang Deng, Yutaka Matsuo,* Hongmei Luo,* Guifu Zou*</p>
<p><em>Sci. Rep.</em> <strong>2016</strong>, <em>6</em>, 26390. [<a href="http://www.nature.com/articles/srep26390" target="_blank">DOI:10.1038/srep26390</a>]</p>
<p>&nbsp;</p>
<p>6. Enhancement of Fill Factor in Air-processed Inverted Organic Solar Cells using Self-Assembled Monolayer of Fullerene Catechol</p>
<p>Il Jeon, Keisuke Ogumi, Takafumi Nakagawa, Yutaka Matsuo*</p>
<p><em>Jpn J. Appl. Phys.</em> <strong>2016</strong>, <em>55</em>, 082301. [<a href="http://iopscience.iop.org/article/10.7567/JJAP.55.082301/pdf" target="_blank">DOI: 10.7567/JJAP.55.082301</a>]</p>
<p>&nbsp;</p>
<p>5. Electrochemical Reduction of Cationic Li<sup>+</sup>@C<sub>60</sub> to Neutral Li<sup>+</sup>@C<sub>60</sub><sup>&bull;&ndash;</sup>: Isolation and Characterisation of Endohedral [60]Fulleride</p>
<p>Hiroshi Ueno, Shinobu Aoyagi, Yu Yamazaki, Kei Ohkubo, Naohiko Ikuma, Hiroshi Okada, Tatsuhisa Kato, Yutaka Matsuo, Shunichi Fukuzumi, Ken Kokubo*</p>
<p><em>Chem. Sci.</em> <strong>2016</strong>, <em>7</em>, 5770&ndash;5774. [<a href="http://pubs.rsc.org/en/content/articlelanding/2016/sc/c6sc01209d" target="_blank">DOI: 10.1039/C6SC01209D</a>]</p>
<p style="text-align: center;"><img src="http://www.matsuo-lab.net/img/neutralLiC60.gif" alt="" width="278" height="189" /></p>
<p>&nbsp;</p>
<p>4. Multifunctionalization of C<sub>70</sub> at the Two Polar Regions with a High Regioselectivity via Oxazolination and Benzylation Reactions</p>
<p>Shu-Hui Li, Zong-Jun Li, Takafumi Nakagawa, Il Jeon, Zheng Ju, Yutaka Matsuo,* Xiang Gao*</p>
<p><em>Chem. Commun.</em> <strong>2016</strong>, <em>52</em>, 5710&ndash;5713. [<a href="http://pubs.rsc.org/en/Content/ArticleLanding/2016/CC/C6CC00997B" target="_blank">DOI: 10.1039/C6CC00997B</a>]</p>
<p>&nbsp;</p>
<p>3. Stability of Diketopyrrolopyrrole Small-Molecule Inverted Organic Solar Cells</p>
<p>Il Jeon, Ryohei Sakai, Takafumi Nakagawa, Hiroki Setoguchi, Yutaka Matsuo*</p>
<p><em>Org. Electron.</em> <strong>2016</strong>, <em>35</em>, 193&ndash;198. [<a href="http://www.sciencedirect.com/science/article/pii/S156611991630218X" target="_blank">DOI: 10.1016/j.orgel.2016.05.022</a>]</p>
<p><img style="display: block; margin-left: auto; margin-right: auto;" src="http://www.matsuo-lab.net/img/stableDPPmPCBM.jpg" alt="" width="398" height="175" /></p>
<p>&nbsp;</p>
<p>2. Enhancement of Open-Circuit Voltage by Using the 58-&pi; Silylmethyl Fullerenes in Small-Molecule Organic Solar Cells</p>
<p>Il Jeon, Cl&eacute;ment Delacou, Takafumi Nakagawa, Yutaka Matsuo*</p>
<p><em>Chem. Asian J.</em> <strong>2016</strong>, <em>11</em>, 1268&ndash;1272. [<a href="http://onlinelibrary.wiley.com/doi/10.1002/asia.201501400/abstract" target="_blank">DOI: 10.1002/asia.201501400</a>]</p>
<p><img style="display: block; margin-left: auto; margin-right: auto;" src="http://www.matsuo-lab.net/img/SIMEFDPPcryst.png" alt="" width="317" height="228" /></p>
<p>&nbsp;</p>
<p>1. Indium-free Inverted Organic Solar Cells Using Niobium-doped Titanium Oxide with Integrated Dual Function of Transparent Electrode and Electron Transport Layer</p>
<p>Il Jeon, Shoichiro Nakao, Yasushi Hirose, Tetsuya Hasegawa, Yutaka Matsuo*</p>
<p><em>Adv. Electron. Mater.</em> <strong>2016</strong>, <em>2</em>, 1500341. [<a href="http://onlinelibrary.wiley.com/doi/10.1002/aelm.201500341/full" target="_blank">DOI: 10.1002/aelm.201500341</a>]</p>
<p><img style="display: block; margin-left: auto; margin-right: auto;" src="http://www.matsuo-lab.net/img/TNOtoc.png" alt="" width="310" height="174" /></p>
</div>

<div class="block">
<h4>2015</h4>
<p>11. Chemical Pathways Connecting Lead(II) Iodide and Perovskite via Polymeric Plumbate(II) Fiber</p>
<p>Yunlong Guo, Kazutaka Shoyama, Wataru Sato, Yutaka Matsuo, Kento Inoue, Koji Harano, Chao Liu, Hideyuki Tanaka, Eiichi Nakamura*</p>
<p><em>J. Am. Chem. Soc.</em><strong><em></em></strong><em></em> <strong>2015</strong>, <em>137</em>, 15907&ndash;15914. [<a href="http://pubs.acs.org/doi/10.1021/jacs.5b10599" target="_blank">DOI: 10.1021/jacs.5b10599</a>]</p>
<p>&nbsp;</p>
<p>10. An Enantiopure Hydrogen-Bonded Octameric Tube: Self-Sorting and Guest-Induced Rearrangement</p>
<p>Dovil&#279; Ra&#269;kauskait&#279;, Rokas Gegevi&#269;ius, Yutaka Matsuo, Kenneth W&auml;rnmark*, Edvinas Orentas*</p>
<p><em>Angew. Chem. Int. Ed.</em> <strong>2015</strong>, <em>55</em>, 208&ndash;212. [<a href="http://onlinelibrary.wiley.com/doi/10.1002/anie.201508362/abstract" target="_blank">DOI: 10.1002/anie.201508362</a>]</p>
<p>&nbsp;</p>
<p>9. Single-Walled Carbon Nanotube Film as Electrode in Indium-Free Planar Heterojunction Perovskite Solar Cells: Investigation of Electron-Blocking Layers and Dopants</p>
<p>Il Jeon, Takaaki Chiba, Clement Delacou, Yunlong Guo, Antti Kaskela, Olivier Reynaud, Esko I. Kauppinen, Shigeo Maruyama, Yutaka Matsuo*</p>
<p><em>Nano Lett.</em> <strong>2015</strong>, <em>15</em>, 6665&ndash;6671. [<a href="http://pubs.acs.org/doi/10.1021/acs.nanolett.5b02490" target="_blank">DOI: 10.1021/acs.nanolett.5b02490</a>]</p>
<p>&nbsp;</p>
<p style="text-align: center;"><img src="http://www.matsuo-lab.net/img/CNT_Perovskite.png" alt="" width="411" height="149" /></p>
<p>&nbsp;</p>
<p>8. Direct and Dry Deposited Single-Walled Carbon Nanotube Films Doped with MoOx as Electron-Blocking Transparent Electrodes for Flexible Organic Solar Cells</p>
<p>Il Jeon, Kehang Cui, Takaaki Chiba, Anton Anisimov, Albert Nasibulin, Esko Kauppinen, Shigeo Maruyama*, Yutaka Matsuo*</p>
<p><em>J. Am. Chem. Soc.</em> <strong>2015</strong>, <em>137</em>, 7982&ndash;7985. [<a href="http://pubs.acs.org/doi/abs/10.1021/jacs.5b03739" target="_blank">DOI: 10.1021/jacs.5b03739</a>]</p>
<p>&nbsp;</p>
<p style="text-align: center;"><img src="http://www.matsuo-lab.net/img/CNT_OPV.gif" alt="" width="406" height="157" /></p>
<p>&nbsp;</p>
<p>7. A V-Shaped Polyaromatic Amphiphile: Solubilization of Various Nanocarbons in Water and Enhanced Photostability</p>
<p>Kei Kondo, Munetaka Akita, Takafumi Nakagawa, Yutaka Matsuo, Michito Yoshizawa*</p>
<p><em>Chem. Eur. J.</em> <strong>2015</strong>, <em>21</em>, 12741&ndash;12746. [<a href="http://onlinelibrary.wiley.com/doi/10.1002/chem.201501414/abstract" target="_blank">DOI: 10.1002/chem.201501414</a>]</p>
<p>&nbsp;</p>
<p>6. Vertical Phase Separation and Light-soaking Effect Improvements by Photoactive Layer Spin Coating Initiation Time Control in Air-processed Inverted Organic Solar Cells</p>
<p>Il Jeon and Yutaka Matsuo*</p>
<p><em>Sol. Energy Mater. Sol. Cells</em> <strong>2015</strong>, <em>140</em>, 335&ndash;343. [<a href="http://www.sciencedirect.com/science/article/pii/S0927024815001725" target="_blank">10.1016/j.solmat.2015.04.017</a>]</p>
<p>&nbsp;</p>
<p style="text-align: center;"><img src="http://www.matsuo-lab.net/img/ZnO_vertical.png" alt="" width="377" height="168" /></p>
<p>&nbsp;</p>
<p>5. Organic Solid Solution Composed of Two Structurally Similar Porphyrins for Organic Solar Cells</p>
<p>Yonggang Zhen, Hideyuki Tanaka*, Koji Harano, Satoshi Okada, Yutaka Matsuo*, Eiichi Nakamura*</p>
<p><em>J. Am. Chem. Soc.</em> <strong>2015</strong>, <em>137</em>, 2247&ndash;2252. [<a href="http://pubs.acs.org/doi/abs/10.1021/ja513045a" target="_blank">DOI: 10.1021/ja513045a</a>]</p>
<p>&nbsp;</p>
<p style="text-align: center;"><img src="http://www.matsuo-lab.net/img/Por_solid_solution.gif" alt="" width="380" height="182" /></p>
<p>&nbsp;</p>
<p>4. Increased Efficiency in Small Molecule Organic Solar Cells Through the Use of a 56-&pi; Electron Acceptor - Methano Indene Fullerene</p>
<p>James W. Ryan and Yutaka Matsuo*</p>
<p><em>Sci. Rep.</em> <strong>2015</strong>, <em>5</em>, 8319. [<a href="http://www.nature.com/srep/2015/150209/srep08319/full/srep08319.html" target="_blank">DOI: 10.1038/srep08319</a>]</p>
<p>&nbsp;</p>
<p style="text-align: center;"><img src="http://www.matsuo-lab.net/img/DPP_MIF.png" alt="" width="244" height="212" /></p>
<p>&nbsp;</p>
<p>3. Diporphyrin Magnesium Complex with Long-Wavelength Light Absorption for Organic Solar Cells</p>
<p>Takenari Sato, Takafumi Nakagawa, Hiroshi Okada, Yutaka Matsuo*</p>
<p><em>J. Porphyrins Phthalocyanines</em> <strong>2015</strong>, <em>19</em>, 451. (Prof. Shunichi Fukuzumi special issue) [<a href="http://www.worldscientific.com/doi/abs/10.1142/S1088424615500303?src=recsys&amp;journalCode=jpp" target="_blank">DOI: 10.1142/S1088424615500303</a>]</p>
<p>&nbsp;</p>
<p style="text-align: center;"><img src="http://www.matsuo-lab.net/img/diporphyrin.png" alt="" width="333" height="133" /></p>
<p>&nbsp;</p>
<p>2. Multilayered MoS<sub>2</sub> Nanoflakes Bound to Carbon Nanotubes as Electron Acceptors in Bulk Heterojunction Inverted Organic Solar Cells</p>
<p>Il Jeon, Dai Kutsuzawa, Yu Hashimoto, Takashi Yanase, Taro Nagahama, Toshihiro Shimada*, Yutaka Matsuo*</p>
<p><em>Org. Electron.</em> <strong>2015</strong>, <em>17</em>, 275&ndash;280. [<a href="http://www.sciencedirect.com/science/article/pii/S1566119914005734" target="_blank">DOI: 10.1016/j.orgel.2014.12.025</a>]</p>
<p style="text-align: center;"><img src="http://www.matsuo-lab.net/img/CNT_MoS2_P3HT.png" alt="" width="311" height="197" /></p>
<p>&nbsp;</p>
<p>1. Approach to High Open-circuit Voltage in Organic Solar Cells Utilizing Structural Change of Oxazolino-C<sub>70</sub> Derivative</p>
<p>Shu-Hui Li, Zong-Jun Li, Takafumi Nakagawa, James W. Ryan, Yutaka Matsuo*, Xiang Gao*</p>
<p><em>Chem. Eur. J.</em> <strong>2015</strong>, <em>21</em>, 1894&ndash;1899. [<a href="http://onlinelibrary.wiley.com/doi/10.1002/chem.201405890/abstract" target="_blank">DOI:&nbsp;10.1002/chem.201405890</a>]</p>
<p style="text-align: center;"><img src="http://www.matsuo-lab.net/img/High_LUMO_struct_change.png" alt="" width="418" height="143" /></p>
</div>

<div class="block">
<h4>2014</h4>
<p>17. Ferromagnetic Ordering in Superatomic Solids</p>
<p>Chul-Ho Lee, Lian Liu, Christopher Bejger, Ari Turkiewicz, Tatsuo Goko, Carlos J. Arguello, Benjamin A. Frandsen, Sky C. Cheung, Teresa Medina, Timothy J. S. Munsie, Robert D&rsquo;Ortenzio, Graeme M. Luke, Tiglet Besara, Roger A. Lalancette, Theo Siegrist, Peter W. Stephens, Andrew C. Crowther, Louis E. Brus, Yutaka Matsuo, Eiichi Nakamura, Yasutomo J. Uemura, Philip Kim, Colin Nuckolls, Michael L. Steigerwald, Xavier Roy*</p>
<p><em>J. Am. Chem. Soc.</em> <strong>2014</strong>, <em>136</em>, 16926&ndash;16931. [<a href="http://pubs.acs.org/doi/abs/10.1021/ja5098622" target="_blank">DOI: 10.1021/ja5098622</a>]&nbsp;</p>
<p>&nbsp;</p>
<p>16. Air-Processed Inverted Organic Solar Cells Utilizing a 2-Aminoethanol-Stabilized ZnO Nanoparticle Electron Transport Layer That Requires No Thermal Annealing</p>
<p>Il Jeon, James W. Ryan, Tafu Nakazaki, Kee Sheng Yeo, Yuichi Negishi, Yutaka Matsuo*</p>
<p><em>J. Mater. Chem. A</em> <strong>2014</strong>, <em>2</em>, 18754&ndash;18760. [<a href="http://pubs.rsc.org/en/content/articlelanding/2014/ta/c4ta04595e" target="_blank">DOI: 10.1039/C4TA04595E</a>] (<a href="http://pubs.rsc.org/en/content/articlepdf/2014/ta/c4ta04595e" target="_blank">Inside Cover Picture</a>)</p>
<p><img style="display: block; margin-left: auto; margin-right: auto;" src="http://www.matsuo-lab.net/img/AE_ZnONPs.png" alt="" width="328" height="158" /></p>
<p>&nbsp;</p>
<p>15. Electronic Infrared Light Absorption of a Tri-palladium Complex Containing Two &pi;-Expanded Tetracene Ligands</p>
<p>Tsuyoshi Suzuki, Takafumi Nakagawa, Kei Ohkubo, Shunichi Fukuzumi, Yutaka Matsuo*</p>
<p><em>Chem. Sci.</em> <strong>2014</strong>, <em>5</em>, 4888&ndash;4894. [<a href="http://pubs.rsc.org/en/content/articlelanding/2014/sc/c4sc02018a" target="_blank">DOI: 10.1039/C4SC02018A</a>]</p>
<p><img style="display: block; margin-left: auto; margin-right: auto;" src="http://www.matsuo-lab.net/img/Pd3TIDS2-IR.png" alt="" width="363" height="218" /></p>
<p>&nbsp;</p>
<p>14. Influence of Additives in Bulk Heterojunction Solar Cells Using Magnesium Tetraethynylporphyrin with Triisopropylsilyl and Anthryl Substituents</p>
<p>Takafumi Nakagawa, Junichi Hatano, Yutaka Matsuo*</p>
<p><em>J. Porphyrins Phthalocyanines</em> <strong>2014</strong>, <em>18</em>, 735&ndash;740. (Prof. Nagao Kobayashi special issue [<a href="http://www.worldscientific.com/doi/abs/10.1142/S1088424614500655" target="_blank">DOI: 10.1142/S1088424614500655</a>]</p>
<p>&nbsp;</p>
<p>13. Supramolecular Formation of Lithium-Ion-Encapsulated PCBM Fullerene with Sulfonated meso-Tetraphenylporphyrins and Long-Lived Charge Separation</p>
<p>Yuki Kawashima, Kei Ohkubo, Hiroshi Okada, Yutaka Matsuo*, Shunichi Fukuzumi*</p>
<p><em>ChemPhysChem</em>, <strong>2014</strong>, <em>15</em>, 3782&ndash;3790. [<a href="http://onlinelibrary.wiley.com/doi/10.1002/cphc.201402512/abstract" target="_blank">DOI: 10.1002/cphc.201402512</a>]</p>
<p>&nbsp;</p>
<p>12. Kinetic Study of the Diels&ndash;Alder Reaction of Li<sup>+</sup>@C<sub>60</sub> with Cyclohexadiene: Greatly Increased Reaction Rate by Encapsulated Li<sup>+</sup></p>
<p>Hiroshi Ueno, Hiroki Kawakami, Koji Nakagawa, Hiroshi Okada, Naohiko Ikuma, Shinobu Aoyagi, Ken Kokubo*, Yutaka Matsuo*, Takumi Oshima</p>
<p><em>J. Am. Chem. Soc.</em> <strong>2014</strong>, <em>136</em>, 11162&ndash;11167. [<a href="http://pubs.acs.org/doi/abs/10.1021/ja505952y" target="_blank">DOI: 10.1021/ja505952y</a>]</p>
<p>(Highlighted in <a href="http://www.matsuo-lab.net/file/cen20140721pp29.pdf" target="_blank">Chemical &amp; Engineering News</a>)</p>
<p>(Selected in <a href="http://pubs.acs.org/doi/pdf/10.1021/ja507887p" target="_blank">JACS Spotlights</a>)</p>
<p>(プレスリリース：<a href="http://www.s.u-tokyo.ac.jp/ja/press/2014/36.html" target="_blank">東大理学部</a>，<a href="http://resou.osaka-u.ac.jp/ja/research/2014/20140717_1" target="_blank">阪大工学部</a>，<a href="http://www.spring8.or.jp/ja/news_publications/press_release/2014/140717/" target="_blank">SPring-8</a>)</p>
<p><img style="display: block; margin-left: auto; margin-right: auto;" src="http://www.matsuo-lab.net/img/LiC60C6H8.gif" alt="" width="440" height="168" /></p>
<p>&nbsp;</p>
<p>11.&nbsp; Exciton Diffusion Length and Charge Mobility in Donor and Acceptor Materials in Organic Photovoltaics: Tetrabenzoporphyrin and Silylmethyl[60]fullerene<br />Hiroyuki Tamura*, Yutaka Matsuo<br /><em>Chem. Phys. Lett.</em> <strong>2014</strong>, <em>598,</em> 81&ndash;85. [<a href="http://dx.doi.org/10.1016/j.cplett.2014.03.013" target="_blank">DOI: 10.1016/j.cplett.2014.03.013</a>]</p>
<p>&nbsp;</p>
<p>10. Mobility of Long-Lived Fullerene Radical in Solid State and Nonlinear Temperature Dependence<br />Yoko Abe, Hideyuki Tanaka, Yunlong Guo, Yutaka Matsuo*, Eiichi Nakamura*<br /><em>J. Am. Chem. Soc.</em> <strong>2014</strong>, <em>136</em>, 3366&ndash;3369. [<a href="http://pubs.acs.org/doi/abs/10.1021/ja500340f" target="_blank">DOI: 10.1021/ja500340f</a>]</p>
<p>(Selected in JACS Spotlights, <a href="http://pubs.acs.org/doi/full/10.1021/ja502363z" target="_blank"><em>J. Am. Chem. Soc.</em> <strong>2014</strong>, <em>136</em>, 4091.</a>)</p>
<p><img style="display: block; margin-left: auto; margin-right: auto;" src="http://www.matsuo-lab.net/img/dimer-FET.png" alt="" width="269" height="131" /><br />9. Direct Probing of the Structure and Electron Transfer of Fullerene/ Ferrocene Hybrid on Au(111) Electrodes by in Situ Electrochemical STM<br />Ting Chen, Dong Wang*, Li-Hua Gan, Yutaka Matsuo*, Jing-Ying Gu, Hui-Juan Yan, Eiichi Nakamura, Li-Jun Wan*<br /><em>J. Am. Chem. Soc.</em> <strong>2014</strong>, <em>136</em>, 3184&ndash;3191. [DOI: <a href="http://pubs.acs.org/doi/abs/10.1021/ja411813r" target="_blank">10.1021/ja411813r</a>]</p>
<p style="text-align: center;"><img src="http://www.matsuo-lab.net/img/BF-STM.gif" alt="" width="423" height="137" /></p>
<p>&nbsp;<br />8. Divergent Synthesis and Tuning of the Electronic Structures of Cobalt&ndash;Dithiolene&ndash;Fullerene Complexes for Organic Solar Cells<br />Yutaka Matsuo*, Keisuke Ogumi, Masashi Maruyama, Takafumi Nakagawa<br /><em>Organometallics</em> <strong>2014</strong>, <em>33</em>, 659&ndash;664. [<a href="http://pubs.acs.org/doi/abs/10.1021/om400796p" target="_blank">DOI: 10.1021/om400796p</a>]<br /><br />7. 1,8-Diazabicycloundecene-mediated Separation of Singly bonded Fullerene Dimer and Application to Facile Preparation of C<sub>61</sub>H<sub>2</sub><br />Yoko Abe, Yutaka Matsuo*<br /><em>Fullerenes, Nanotubes and Carbon Nanostructures</em>, <strong>2014</strong>, <em>23</em>, 259&ndash;262.</p>
<p>[DOI:10.1080/1536383X.2014.894026]</p>
<p>&nbsp;</p>
<p>6. FeCl<sub>3</sub>-Mediated Retro-Reactions of Fullerene Derivatives to C<sub>60</sub></p>
<p>Masahiko Hashiguchi*, Takao Ueno, Yutaka Matsuo*</p>
<p><em>Fullerenes, Nanotubes and Carbon Nanostructures</em><strong></strong>, <strong>2014</strong>, <em>22</em>, 845&ndash;852.</p>
<p>[DOI:10.1080/1536383X.2012.742429]</p>
<p>&nbsp;</p>
<p>5. Anion Exchange of Li<sup>+</sup>@C<sub>60</sub> Salt for Improved Solubility</p>
<p>Hiroshi Okada, Yutaka Matsuo*</p>
<p><em>Fullerenes, Nanotubes and Carbon Nanostructures</em> <strong>2014</strong>, <em>22,</em> 262&ndash;268.</p>
<p>[<a href="http://www.tandfonline.com/doi/full/10.1080/1536383X.2013.812639" target="_blank">DOI:10.1080/1536383X.2013.812639</a>] (Prof. Takeshi Akasaka special issue).</p>
<p style="text-align: center;"><img src="http://www.matsuo-lab.net/img/anion_exchange.png" alt="" width="333" height="216" /></p>
<p>&nbsp;</p>
<p>4. Acceleration of Tri-addition to [70]Fullerene by "Nanom Black" Fullerene Soot</p>
<p>Yutaka Matsuo*, Shigeo Yasuda, Koji Suemura, Eiichi Nakamura*</p>
<p><em>Fullerenes, Nanotubes and Carbon Nanostructures</em> <strong>2014</strong>, <em>22</em>, 196&ndash;201.</p>
<p>[<a href="http://www.tandfonline.com/doi/full/10.1080/1536383X.2013.798727" target="_blank">DOI:10.1080/1536383X.2013.798727</a>] (Prof. Takeshi Akasaka special issue).</p>
<p style="text-align: center;"><img src="http://www.matsuo-lab.net/img/nanom_black.png" alt="" width="258" height="135" /></p>
<p>&nbsp;<br />3. <em>cis</em>-Substituted Tetraethynylporphyrin Derivatives for Small Molecule Organic Solar Cells<br />Yutaka Matsuo*, Junichi Hatano, Takafumi Nakagawa<br /><em>J. Phys. Org. Chem.</em> <strong>2014</strong>, <em>27</em>, 87&ndash;93. [<a href="http://dx.doi.org/10.1002/poc.3241" target="_blank">DOI: 10.1002/poc.3241</a>]</p>
<p><img style="display: block; margin-left: auto; margin-right: auto;" src="http://www.matsuo-lab.net/img/cis-Por.png" alt="" width="360" height="198" /></p>
<p>&nbsp;<br />2. Solvent-dependent Morphology of Thermally Converted Copper Phthalocyanine for Solution-processed Small Molecule Organic Photovoltaic Devices<br />Huihui Wang, Takamitsu Fukuda, Naoto Ishikawa, Yutaka Matsuo*<br /><em>Org. Electron.</em> <strong>2014</strong>, <em>15</em>, 139&ndash;143. [<a href="http://dx.doi.org/10.1016/j.orgel.2013.10.023" target="_blank">DOI: 10.1016/j.orgel.2013.10.023</a>]</p>
<p style="text-align: center;"><img src="http://www.matsuo-lab.net/img/CuPcPOMe2.png" alt="" width="428" height="115" /></p>
<p>&nbsp;<br />1. Friedel&ndash;Crafts Functionalization of the Cyclopentadienyl Ligand in Buckymetallocenes<br />Yutaka Matsuo*, Yoichiro Kuninobu, Shingo Ito, Masaya Sawamura, Eiichi Nakamura*<br /><em>Dalton Trans.</em> <strong>2014</strong>, <em>43</em>, 7407&ndash;7412. [<a href="http://dx.doi.org/10.1039/C3DT52002A" target="_blank">DOI: 10.1039/C3DT52002A</a>]</p>
<p style="text-align: center;"><img src="http://www.matsuo-lab.net/img/acylBF.png" alt="" width="333" height="147" /></p>
</div>

<div class="block">
<h4>2013</h4>
<p>18. Low-LUMO 56&pi;-Electron Fullerene Acceptors Bearing Electron-withdrawing Cyano Groups for Small-Molecule Organic Solar Cells</p>
<p>Yoko Abe, Takamichi Yokoyama, Yutaka Matsuo*</p>
<p><em>Org. Electron.</em> <strong>2013</strong>, <em>14</em>, 3306&ndash;3311. [DOI: 10.1016/j.orgel.2013.09.012]</p>
<p>&nbsp;</p>
<p>17. 56&pi;-Electron Hydrofullerene Derivatives as Electron Acceptors for Organic Solar Cells</p>
<p>Yoko Abe, Rieko Hata, Yutaka Matsuo*</p>
<p><em>Chem. Lett.</em> <strong>2013</strong>, <em>42</em>, 1525&ndash;1527. [DOI: 10.1246/cl.130753]</p>
<p><img style="display: block; margin-left: auto; margin-right: auto;" src="http://www.matsuo-lab.net/img/hydrofullerene.png" alt="" width="401" height="139" /></p>
<p>&nbsp;</p>
<p>16. Synthesis, Photophysical Properties, and Excited State Dynamics of Platinum Complex of Tetracene Imide Disulfide</p>
<p>Takafumi Nakagawa, Tsuyoshi Suzuki, Matthias K&ouml;nig, Dirk M. Guldi,* Yutaka Matsuo*</p>
<p><em>Chem. Commun.</em> <strong>2013</strong>, <em>49</em>, 10394&ndash;10396. [<a href="http://dx.doi.org/10.1039/C3CC46068A" target="_blank">DOI: 10.1039/C3CC46068A</a>]</p>
<p style="text-align: center;"><img src="http://www.matsuo-lab.net/img/PtTIDS_GA.gif" alt="" width="354" height="189" /></p>
<p>&nbsp;</p>
<p>15. Efficient Diels&ndash;Alder Addition of Cyclopentadiene to Lithium Ion Encapsulated [60]Fullerene<br />Hiroki Kawakami, Hiroshi Okada, Yutaka Matsuo*<br /><em>Org. Lett.</em> <strong>2013</strong>, <em>15</em>, 4466&ndash;4469. [<a href="http://pubs.acs.org/doi/abs/10.1021/ol4020046" target="_blank">DOI: 10.1021/ol4020046</a>]</p>
<p style="text-align: center;"><img src="http://www.matsuo-lab.net/img/ol-2013-020046_0005.gif" alt="" width="327" height="122" /></p>
<p>&nbsp;</p>
<p>14. Mixture of [60] and [70]PCBM Giving Morphological Stability in Organic Solar Cells</p>
<p>Yoshihide Santo, Il Jeon, Kee Sheng Yeo, Takafumi Nakagawa, Yutaka Matsuo*</p>
<p><em>Appl. Phys. Lett.</em> <strong>2013</strong>, <em>103</em>, 073306. [<a href="http://dx.doi.org/10.1063/1.4818726" target="_blank">DOI: 10.1063/1.4818726</a>]</p>
<p style="text-align: center;"><img src="http://www.matsuo-lab.net/img/mixPCBM_s.png" alt="" width="413" height="156" /></p>
<p>&nbsp;</p>
<p>13. Selective Synthesis of Co<sub>8</sub>S<sub>15</sub> Cluster in Bowl-shaped Template of the Pentaaryl[60]fullerene Ligand</p>
<p>Masashi Maruyama, Kenta Imoto, Matthias K&ouml;nig, Dirk M. Guldi,* Shin-ichi Ohkoshi, Eiichi Nakamura, Yutaka Matsuo*</p>
<p><em>J. Am. Chem. Soc.</em> <strong>2013</strong>, <em>135</em>, 10914&ndash;10917. [<a href="http://pubs.acs.org/doi/abs/10.1021/ja405045t" target="_blank">DOI: 10.1021/ja405045t</a>]</p>
<p style="text-align: center;"><img src="http://www.matsuo-lab.net/img/Co8S15-s.png" alt="" width="442" height="209" /></p>
<p>&nbsp;</p>
<p>12. Addition of Dihydromethano Group to Fullerenes for Improving the Performance of Bulk Heterojunction Organic Solar Cells</p>
<p>Yutaka Matsuo,* Junya Kawai, Hiroshi Inada, Takafumi Nakagawa, Hitoshi Ota, Saika Otsubo, Eiichi Nakamura*</p>
<p><em>Adv. Mater.</em> <strong>2013</strong>, <em>25</em>, 6266&ndash;6269. [<a href="http://onlinelibrary.wiley.com/doi/10.1002/adma.201302607/abstract" target="_blank">DOI: 10.1002/adma.201302607</a>]</p>
<p style="text-align: center;">&nbsp;<img src="http://www.matsuo-lab.net/img/methanoindenefullerene.png" alt="" width="386" height="215" /></p>
<p>&nbsp;</p>
<p>11. First-principles Investigation on Structural and Optical Properties of M<sup>+</sup>@C<sub>60</sub> (where M = H, Li, Na, and K)</p>
<p>Yoshifumi Noguchi,* Osamu Sugino, Hiroshi Okada, Yutaka Matsuo</p>
<p><em>J. Phys. Chem. C</em> <strong>2013</strong>, <em>117</em>, 15362&ndash;15368. [<a href="http://pubs.acs.org/doi/abs/10.1021/jp4041259" target="_blank">DOI: 10.1021/jp4041259</a>]</p>
<p><img style="display: block; margin-left: auto; margin-right: auto;" src="http://www.matsuo-lab.net/img/LiC60calc_jpcc_s.png" alt="" width="364" height="104" /></p>
<p>&nbsp;</p>
<p>10. Solution-Phase Synthesis of Dumbbell-Shaped C<sub>120</sub> by FeCl<sub>3</sub>-Mediated Dimerization of C<sub>60</sub></p>
<p>Masahiko Hashiguchi,* Hiroshi Inada, Yutaka Matsuo*</p>
<p><em>Carbon</em> <strong>2013</strong>, <em>61</em>, 418&ndash;422. [<a href="http://dx.doi.org/10.1016/j.carbon.2013.04.101" target="_blank">DOI: 10.1016/j.carbon.2013.04.101</a>]</p>
<p style="text-align: center;"><img src="http://www.matsuo-lab.net/img/C120_solution_phase.png" alt="" width="365" height="93" /></p>
<p>&nbsp;</p>
<p>9. Regioselective [2 + 2] Cycloaddition of Fullerene Dimer with Alkyne Triggered by Thermolysis of Inter-fullerene C&ndash;C Bond</p>
<p>Zuo Xiao, Yutaka Matsuo,* Masashi Maruyama, Eiichi Nakamura*</p>
<p><em>Org. Lett.</em> <strong>2013</strong>, <em>15</em>, 2176&ndash;2178. [<a href="http://pubs.acs.org/doi/abs/10.1021/ol400713t" target="_blank">DOI: 10.1021/ol400713t</a>]</p>
<p style="text-align: center;"><img src="http://www.matsuo-lab.net/img/dimer_alkyne.png" alt="" width="385" height="149" /></p>
<p>&nbsp;</p>
<p>8. Application of Sputter-deposited Amorphous and Anatase TiO<sub>2</sub> as Electron-collecting Layers in Inverted Organic Photovoltaics</p>
<p>Kee Sheng Yeo, Shoichiro Nakao, Yasushi Hirose, Tetsuya Hasegawa, Yutaka Matsuo*</p>
<p><em>Org. Electron.</em> <strong>2013</strong>, <em>14</em>, 1715&ndash;1719. [<a href="http://dx.doi.org/10.1016/j.orgel.2013.04.007" target="_blank">DOI: 10.1016/j.orgel.2013.04.007</a>]</p>
<p style="text-align: center;"><img src="http://www.matsuo-lab.net/img/sputterTiO2.png" alt="" width="419" height="154" /></p>
<p>&nbsp;</p>
<p>7. Magnetic Properties of Decamethyl Fullerenes: Radical Spin Interactions in Chemically Functionalized Fullerenes</p>
<p>Haruna Nitta, Yutaka Matsuo, Eiichi Nakamura, Susumu Okada*</p>
<p><em>Appl. Phys. Express</em> <strong>2013</strong>, <em>6</em>, 045102. [<a href="http://apex.jsap.jp/link?APEX/6/045102/" target="_blank">DOI: 10.7567/APEX.6.045102</a>]</p>
<p>&nbsp;</p>
<p>6. Formation of Photoconductive Nanowires of Tetracene Derivative in Composite Thin Film</p>
<p>Tsuyoshi Suzuki, Toshihiro Okamoto,* Akinori Saeki, Shu Seki, Hiroyasu Sato, Yutaka Matsuo*</p>
<p><em>ACS Appl. Mater. Interfaces</em> <strong>2013</strong>, <em>5</em>, 1937&ndash;1942. [<a href="http://pubs.acs.org/doi/abs/10.1021/am302914w" target="_blank">DOI: 10.1021/am302914w</a>]</p>
<p style="text-align: center;"><img src="http://www.matsuo-lab.net/img/TIDS_nanowires.png" alt="" width="390" height="223" /></p>
<p>&nbsp;</p>
<p>5. Reactivity of a Metastable Cobalt(III) Trisulfide Complex: Multiple C&ndash;H Functionalization of <em>p</em>-Xylene and Disulfides to Afford Photofunctional Cobalt Complexes</p>
<p>Masashi Maruyama, Matthias K&ouml;nig, Dirk M. Guldi,* Eiichi Nakamura, Yutaka Matsuo*</p>
<p><em>Angew. Chem. Int. Ed.</em> <strong>2013</strong>, <em>52</em>, 3015&ndash;3018. [<a href="http://onlinelibrary.wiley.com/doi/10.1002/anie.201209046/abstract" target="_blank">DOI: 10.1002/anie.201209046</a>]</p>
<p><img style="display: block; margin-left: auto; margin-right: auto;" src="http://www.matsuo-lab.net/img/tripleC-H_activation_Co.png" alt="" width="393" height="201" /></p>
<p>&nbsp;</p>
<p>4. Small Molecule Solution-Processed Bulk Heterojunction Solar Cells with Inverted Structure Using Porphyrin Donor</p>
<p>Takaki Yamamoto, Junichi Hatano, Takafumi Nakagawa, Shigeru Yamaguchi, Yutaka Matsuo*</p>
<p><em>Appl. Phys. Lett.</em> <strong>2013</strong>, <em>102</em>, 013305. [<a href="http://dx.doi.org/10.1063/1.4773910" target="_blank">DOI: 10.1063/1.4773910</a>]</p>
<p><img style="display: block; margin-left: auto; margin-right: auto;" src="http://www.matsuo-lab.net/img/inverted_MgPor.png" alt="" width="374" height="203" /></p>
<p>&nbsp;</p>
<p>3. Photostability of a Dyad of Magnesium Porphyrin and Fullerene and Its Application to Photocurrent Conversion</p>
<p>Takahiko Ichiki, Yutaka Matsuo,* Eiichi Nakamura*</p>
<p><em>Chem. Commun.</em><strong></strong> <strong>2013</strong>, <em>49</em>, 279&ndash;281. [<a href="http://pubs.rsc.org/en/content/articlelanding/2013/CC/C2CC36988E" target="_blank">DOI: 10.1039/C2CC36988E</a>]</p>
<p><img style="display: block; margin-left: auto; margin-right: auto;" src="http://www.matsuo-lab.net/img/MgPorC60_supraSAM.png" alt="" width="404" height="299" /></p>
<p>&nbsp;</p>
<p>2. Benzopyrazine-Fused Tetracene Derivatives: Thin-film Formation at the Crystalline Mesophase for Solution-Processed Hole Transporting Devices</p>
<p>Shungo Kojima, Toshihiro Okamoto,* Kazumoto Miwa, Hiroyasu Sato, Jun Takeya,* Yutaka Matsuo*</p>
<p><em>Org. Electron.</em><strong></strong> <strong>2013</strong>, <em>14</em>, 437&ndash;444. [<a href="http://dx.doi.org/10.1016/j.orgel.2012.10.029" target="_blank">DOI: 10.1016/j.orgel.2012.10.029</a>]</p>
<p>&nbsp;</p>
<p style="text-align: center;"><img src="http://www.matsuo-lab.net/img/TBPyS_OrgElectron.jpg" alt="" width="319" height="125" /></p>
<p>&nbsp;</p>
<p>1. 1-Aryl-4-Silylmethyl[60]fullerenes: Synthesis, Properties, and Photovoltaic Performance</p>
<p>Yutaka Matsuo,* Hiromi Oyama, Iwao Soga, Toshihiro Okamoto, Hideyuki Tanaka, Akinori Saeki, Shu Seki, Eiichi Nakamura*</p>
<p><em>Chem. Asian J.</em><strong></strong> <strong>2013</strong>, <em>8</em>, 121&ndash;128. [<a href="http://onlinelibrary.wiley.com/doi/10.1002/asia.201200726/abstract" target="_blank">DOI: 10.1002/asia.201200726</a>]</p>
<p>&nbsp;</p>
<p style="text-align: center;"><img src="http://www.matsuo-lab.net/img/1alkyl1arylC60.png" alt="" width="339" height="141" /></p>
<p>&nbsp;</p>
</div>

<div class="block">
<h4>2012</h4>
<p>21. Synthesis of Thieno-Bridged Porphyrins: Changing Antiaromatic Contribution by Direction of the Thiophene Ring</p>
<p>Yusuke Mitsushige, Shigeru Yamaguchi, Byung Sun Lee, Young Mo Sung, Susanne Kuhri, Christoph Schierl, Dirk M. Guldi,* Dongho Kim,* Yutaka Matsuo*</p>
<p><em>J. Am. Chem. Soc.</em> <strong>2012</strong>, <em>134</em>, 16540&ndash;16543. [<a href="http://pubs.acs.org/doi/abs/10.1021/ja3082999" target="_blank">DOI: 10.1021/ja3082999</a>]</p>
<p style="text-align: center;"><img src="http://www.matsuo-lab.net/img/ja-2012-082999_0006.gif" alt="" width="392" height="129" /></p>
<p>&nbsp;</p>
<p>20. Synthesis of Tetradeca- and Pentadeca(organo)[60]fullerenes Containing Unique Photo- and Electroluminescent &pi;-Conjugated Systems</p>
<p>Takeshi Fujita, Yutaka Matsuo,* Eiichi Nakamura*</p>
<p><em>Chem. Mater.</em> <strong>2012</strong>, <em>24</em>, 3972&ndash;3980. [<a href="http://pubs.acs.org/doi/abs/10.1021/cm3024296" target="_blank">DOI: 10.1021/cm3024296</a>]</p>
<p style="text-align: center;"><img src="http://www.matsuo-lab.net/img/cm-2012-024296_0014.gif" alt="" width="430" height="142" /></p>
<p>&nbsp;</p>
<p>19. Preparation of Li-encapsulated [60]Fullerene (Li@C<sub>60</sub>) and Its Derivatization to Hexafluorophosphate Salt [Li<sup>+</sup>@C<sub>60</sub>]PF<sub>6</sub><sup>--</sup></p>
<p>Hiroshi Okada, Takashi Komuro, Takeshi Sakai, Yutaka Matsuo, Yoshihiro Ono, Kenji Omote, Kuniyoshi Yokoo, Kazuhiko Kawachi, Yasuhiko Kasama, Shoichi Ono, Rikizo Hatakeyama, Toshiro Kaneko, Hiromi Tobita*</p>
<p><em>RSC Advances</em> <strong>2012</strong>, <em>2</em>, 10624&ndash;10631. [<a href="http://pubs.rsc.org/en/content/articlelanding/2012/ra/c2ra21244g" target="_blank">DOI: 10.1039/C2RA21244G</a>]</p>
<p style="text-align: center;"><img src="http://www.matsuo-lab.net/img/LiC60PF6.gif" alt="" width="328" height="101" /></p>
<p>&nbsp;</p>
<p>18. Benzo[<em>c</em>]thiophene-C<sub>60</sub> Diadduct: An Electron Acceptor for p&ndash;n Junction Organic Solar Cells Harvesting Visible to Near-IR Light</p>
<p>Yonggang Zhen, Naoki Obata, Yutaka Matsuo,* Eiichi Nakamura*</p>
<p><em>Chem. Asian J.</em> <strong>2012</strong>, <em>7</em>, 2644&ndash;2649. [<a href="http://onlinelibrary.wiley.com/doi/10.1002/asia.201200698/abstract" target="_blank">DOI: 10.1002/asia.201200698</a>]</p>
<p style="text-align: center;"><img src="http://www.matsuo-lab.net/img/BTCDA_CAJ.jpg" alt="" width="368" height="252" /></p>
<p>&nbsp;</p>
<p>17. Soluble Porphyrin Donors for Small Molecule Bulk Heterojunction Solar Cells</p>
<p>Junichi Hatano, Naoki Obata, Shigeru Yamaguchi, Takeshi Yasuda, Yutaka Matsuo*</p>
<p><em>J. Mater. Chem.</em> <strong>2012</strong>, <em>22</em>, 19258&ndash;19263. [<a href="http://dx.doi.org/10.1039/C2JM33956K" target="_blank">DOI: 10.1039/C2JM33956K</a>]</p>
<p style="text-align: center;"><img src="http://www.matsuo-lab.net/img/MgPor.png" alt="" width="468" height="188" /></p>
<p>&nbsp;</p>
<p>16. The Chemistry of Four-Membered Aromatics</p>
<p>Yutaka Matsuo* and Masashi Maruyama</p>
<p><em>Chem. Commun.</em> <strong>2012</strong>, <em>48</em>, 9334&ndash;9342. (Feature Article) [<a href="http://dx.doi.org/10.1039/C2CC34244H" target="_blank">DOI: 10.1039/C2CC34244H</a>]</p>
<p style="text-align: center;"><img src="http://www.matsuo-lab.net/img/4ring.gif" alt="" width="251" height="151" /></p>
<p>&nbsp;</p>
<p>15. Covalently Chemical Modification of Lithium Ion-Encapsulated Fullerene: Synthesis and Characterization of [Li<sup>+</sup>@PCBM]PF<sub>6</sub><sup>--</sup></p>
<p>Yutaka Matsuo*, Hiroshi Okada, Masashi Maruyama, Hiroyasu Sato, Hiromi Tobita, Yoshihiro Ono, Kenji Omote, Kazuhiko Kawachi, Yasuhiko Kasama</p>
<p><em>Org. Lett.</em> <strong>2012</strong>, <em>14</em>, 3784&ndash;3787. [<a href="http://dx.doi.org/10.1021/ol301671n" target="_blank">DOI: 10.1021/ol301671n</a>]</p>
<p style="text-align: center;"><img src="http://www.matsuo-lab.net/img/LiPCBM_toclow2web.png" alt="" width="304" height="157" /></p>
<p>&nbsp;</p>
<p>14. Design Concept for High-LUMO-level Fullerene Electron-acceptors for Organic Solar Cells</p>
<p>Yutaka Matsuo*</p>
<p><em>Chem. Lett.</em> <strong>2012</strong>, <em>41</em>, 754&ndash;759. (Highlight Review) [<a href="http://dx.doi.org/10.1246/cl.2012.754" target="_blank">DOI: 10.1246/cl.2012.754</a>]</p>
<p style="text-align: center;"><img src="http://www.matsuo-lab.net/img/41_CL-120682.gif" alt="" width="292" height="205" /></p>
<p>&nbsp;</p>
<p>13. Electropolymerized Conjugated Polyelectrolytes with Tunable Work Function and Hydrophobicity as an Anode Buffer in Organic Optoelectronics</p>
<p>Sebastian Lacher, Naoki Obata, Shyh-Chyang Luo, Yutaka Matsuo,* Bo Zhu, Hsiao-hua Yu, Eiichi Nakamura*</p>
<p><em>ACS Appl. Mater. Interfaces</em> <strong>2012</strong>, <em>4</em>, 3396&ndash;3404. [<a href="http://pubs.acs.org/doi/abs/10.1021/am300366d" target="_blank">DOI: 10.1021/am300366d</a>]</p>
<p style="text-align: center;"><img src="http://www.matsuo-lab.net/img/am-2012-00366d_0004.gif" alt="" width="368" height="152" /></p>
<p>&nbsp;</p>
<p>12. Structurally Defined High-LUMO-level 66&pi;-[70]Fullerene Derivatives: Synthesis and Application in Organic Photovoltaic Cells</p>
<p>Zuo Xiao, Yutaka Matsuo,* Iwao Soga, Eiichi Nakamura*</p>
<p><em>Chem. Mater.</em> <strong>2012</strong>, <em>24</em>, 2572&ndash;2582. [<a href="http://pubs.acs.org/doi/abs/10.1021/cm301238n" target="_blank">DOI: 10.1021/cm301238n</a>]</p>
<p style="text-align: center;"><img src="http://www.matsuo-lab.net/img/66pi_C70Ar4.png" alt="" width="404" height="148" /></p>
<p>&nbsp;</p>
<p>11. FeCl<sub>3</sub>-mediated Synthesis of Fullerenyl Esters as Low-LUMO Acceptors for Organic Photovoltaic Devices</p>
<p>Masahiko Hashiguchi,* Naoki Obata, Masashi Maruyama, Kee Sheng Yeo, Takao Ueno, Tomohiko Ikebe, Isao Takahashi, Yutaka Matsuo*</p>
<p><em>Org. Lett.</em> <strong>2012</strong>, <em>14</em>, 3276&ndash;3279. [<a href="http://pubs.acs.org/doi/abs/10.1021/ol301186u" target="_blank">DOI:10.1021/ol301186u</a>]</p>
<p style="text-align: center;"><img src="http://www.matsuo-lab.net/img/ol-2012-01186u_0001.gif" alt="" width="376" height="118" /></p>
<p>&nbsp;</p>
<p>10. An Amorphous Mesophase Generated by Thermal Annealing for High-Performance Organic Photovoltaic Devices</p>
<p>Hideyuki Tanaka, Yoko Abe, Yutaka Matsuo,* Junya Kawai, Iwao Soga, Yoshiharu Sato, Eiichi Nakamura*</p>
<p><em>Adv. Mater.</em> <strong>2012</strong>, <em>24</em>, 3521&ndash;3525. [<a href="http://onlinelibrary.wiley.com/doi/10.1002/adma.201200490/abstract" target="_blank">DOI: 10.1002/adma.201200490</a>]</p>
<p style="text-align: center;"><img src="http://www.matsuo-lab.net/img/SIMEF2_TOC.png" alt="" width="426" height="194" /></p>
<p>&nbsp;</p>
<p>9. Facile Purification of C<sub>60</sub>O-containing [60]Fullerene Using Trialkylphosphines at Room Temperature</p>
<p>Masahiko Hashiguchi,* Koichi Nagata, Katsutomo Tanaka, Yutaka Matsuo</p>
<p><em>Org. Process Res. Dev.</em> <strong>2012</strong>, <em>16</em>, 643&ndash;646. [<a href="http://pubs.acs.org/doi/abs/10.1021/op200376w" target="_blank">DOI: 10.1021/op200376w</a>]</p>
<p style="text-align: center;"><img src="http://www.matsuo-lab.net/img/C60O_OPRD.gif" alt="" width="313" height="133" /></p>
<p>&nbsp;</p>
<p>8. Deterioration of Bulk Heterojunction Organic Photovoltaic Devices by a Minute Amount of Oxidized Fullerene</p>
<p>Yutaka Matsuo,* Ayako Ozu, Naoki Obata, Naoya Fukuda, Hideyuki Tanaka, Eiichi Nakamura*</p>
<p><em>Chem. Commun.</em> <strong>2012</strong>, <em>48</em>, 3878&ndash;3880. [<a href="http://pubs.rsc.org/en/Content/ArticleLanding/2012/CC/c2cc30262d" target="_blank">DOI: 10.1039/C2CC30262D</a>]</p>
<p style="text-align: center;"><img src="http://www.matsuo-lab.net/img/simef-O2_web.png" alt="" width="400" height="157" /></p>
<p>&nbsp;</p>
<p>7. Facile Synthesis of Biphenyl-Fused BODIPY and Its Property</p>
<p>Yosuke Hayashi, Naoki Obata, Masatomo Tamaru, Shigeru Yamaguchi, Yutaka Matsuo, Akinori Saeki, Shu Seki, Yuka Kureishi, Shohei Saito, Shigehiro Yamaguchi, Hiroshi Shinokubo*&nbsp;</p>
<p><em>Org. Lett.</em> <strong>2012</strong>, <em>14</em>, 866&ndash;869. [<a href="http://pubs.acs.org/doi/abs/10.1021/ol2033916" target="_blank">DOI: 10.1021/ol2033916</a>]</p>
<p>&nbsp;</p>
<p>6. Development of New Fullerene-based Electron Acceptors for Efficient Organic Photovoltaic Cells</p>
<p>Yutaka Matsuo</p>
<p><em>Proc. MRS</em> <strong>2012</strong>, <em>1390</em>, mrsf11-1390-h13-79. [DOI: 10.1557/opl.2012.652]</p>
<p>&nbsp;</p>
<p>5. Development of Fullerene Derivatives with High LUMO Level through Changes in &pi;-Conjugated System Shape</p>
<p>Yutaka Matsuo</p>
<p><em>Pure Appl. Chem.</em> <strong>2012</strong>, <em>84</em>, 945&ndash;952. (ISNA-14 special issue). [<a href="http://iupac.org/publications/pac/84/4/0945/" target="_blank">DOI: 10.1351/PAC-CON-11-11-01</a>]</p>
<p>&nbsp;</p>
<p>4. Fullerene Acceptor for Improving Open-Circuit Voltage in Inverted Organic Photovoltaic Devices without Accompanying Decrease in Short-Circuit Current Density</p>
<p>Yutaka Matsuo*, Junichi Hatano, Takayuki Kuwabara, Kohshin Takahashi</p>
<p><em>Appl. Phys. Lett.</em> <strong>2012</strong>, <em>100</em>, 063303. [<a href="http://dx.doi.org/10.1063/1.3683469" target="_blank">DOI: 10.1063/1.3683469</a>]</p>
<p style="text-align: center;"><img src="http://www.matsuo-lab.net/img/inverted_simef_APL.png" alt="" width="286" height="184" /></p>
<p>&nbsp;</p>
<p>3. Role of Subsurface Diffusion and Ostwald Ripening in Catalyst Formation for SWNT Forest Growth</p>
<p>Shunsuke Sakurai, Hidekazu Nishino, Don N. Futaba, Satoshi Yasuda, Takeo Yamada, Alan Maigne, Yutaka Matsuo, Eiichi Nakamura, Motoo Yumura, Kenji Hata*</p>
<p><em>J. Am. Chem. Soc.</em> <strong>2012</strong>, <em>134</em>, 2148&ndash;2153. [<a href="http://pubs.acs.org/doi/abs/10.1021/ja208706c" target="_blank">DOI: 10.1021/ja208706c</a>]</p>
<p>&nbsp;</p>
<p>2. Tetracene Dicarboxylic Imide and Its Disulfide: Synthesis of New Ambipolar Organic Semiconductors for Organic Photovoltaic Cells</p>
<p>Toshihiro Okamoto,* Tsuyoshi Suzuki, Hideyuki Tanaka, Daisuke Hashizume, Yutaka Matsuo*<em></em></p>
<p><em>Chem. Asian J.</em> <strong>2012</strong>, <em>7</em>, 105&ndash;111. [<a href="http://onlinelibrary.wiley.com/doi/10.1002/asia.201100590/abstract" target="_blank">DOI: 10.1002/asia.201100590</a>]</p>
<p style="text-align: center;"><img src="http://www.matsuo-lab.net/img/develop_donor_TIDS.png" alt="" width="480" height="367" /></p>
<p>&nbsp;</p>
<p style="text-align: left;">1. Construction of Long-Wavelength-Light Photocurrent Generation System Based on Self-Assembled Monolayer of Cobaltadithiolene [60]Fullerene Complex<br />Yutaka Matsuo and Masashi Maruyama<br /><em>J. Nanosci. Nanotech.</em> <strong>2012</strong>, <em>12</em>, 6869&ndash;6871 (ANM2010 special issue).</p>
</div>

<div class="block">
<h4>2011年</h4>
<p>15. Small-Molecule-Based Organic Photovoltaic Devices Covering Visible and Near-Infrared Absorption through Phase Transition of Titanylphthalocyanine Induced by Solvent Exposure</p>
<p>Naoki Obata, Yoshiharu Sato, Eiichi Nakamura, Yutaka Matsuo*<em></em></p>
<p><em>Jpn. J. Appl. Phys.</em> <strong>2011</strong>, <em>50</em>, 121603. [<a href="http://jjap.jsap.jp/link?JJAP/50/121603/" target="_blank">DOI: 10.1143/JJAP.50.121603</a>]</p>
<p style="text-align: center;"><img src="http://www.matsuo-lab.net/img/solution_exposure_jjap.png" alt="" width="327" height="223" /></p>
<p>&nbsp;</p>
<p>14. Regiocontrolled Synthesis of 1,2-Di(organo)fullerenes via Copper-Assisted 1,4-Aryl Migration from Silicon to Carbon</p>
<p>Ying Zhang, Yutaka Matsuo,* Eiichi Nakamura*</p>
<p><em>Org. Lett.</em> <strong>2011</strong>, <em>13</em>, 6058-6061. [<a href="http://pubs.acs.org/doi/abs/10.1021/ol202511u" target="_blank">DOI: 10.1021/ol202511u</a>]</p>
<p><img style="display: block; margin-left: auto; margin-right: auto;" src="http://www.matsuo-lab.net/img/migration.png" alt="" width="364" height="118" /></p>
<p>&nbsp;</p>
<p>13. Electric Field Dependent Photocurrent Generation in a Thin-film Organic Photovoltaic Device with a [70]Fullerene&ndash;benzodifuranone Dyad</p>
<p>Pirmin A. Ulmann, Hideyuki Tanaka, Yutaka Matsuo,* Zuo Xiao, Iwao Soga, Eiichi Nakamura*<em></em></p>
<p><em>Phys. Chem. Chem. Phys.</em> <strong>2011</strong>, <em>13</em>, 21045-21049. [<a href="http://pubs.rsc.org/en/content/articlelanding/2011/cp/c1cp22886b" target="_blank">DOI: 10.1039/C1CP22886B</a>]</p>
<p style="text-align: center;"><img src="http://www.matsuo-lab.net/img/benzodifuranone_dye.png" alt="" width="289" height="152" /></p>
<p>&nbsp;</p>
<p>12. Molecular and Supramolecular Control of the Work Function of an Inorganic Electrode with Self-assembled Umbrella-shaped Fullerene Derivatives</p>
<p>Sebastian Lacher, Yutaka Matsuo, Eiichi Nakamura*<em></em></p>
<p><em>J. Am. Chem. Soc.</em> <strong>2011</strong>, 133, 16997-17004. [<a href="http://pubs.acs.org/doi/abs/10.1021/ja2067675" target="_blank">DOI: 10.1021/ja206767</a>]</p>
<p style="text-align: center;"><img src="http://www.matsuo-lab.net/img/ja-2011-067675_0014.gif" alt="" width="364" height="164" /></p>
<p>&nbsp;</p>
<p>11. Electron Microscopic Imaging of a Single Group 8 Metal Atom Catalyzing C-C Bond Reorganization of Fullerenes</p>
<p>Eiichi Nakamura,* Masanori Koshino, Takeshi Saito, Yoshiko Niimi, Kazu Suenaga, Yutaka Matsuo</p>
<p><em>J. Am. Chem. Soc.</em> <strong>2011</strong>, <em>133</em>, 14151-14153. [<a href="http://pubs.acs.org/doi/abs/10.1021/ja203225n" target="_blank">DOI: 10.1021/ja203225n</a>]</p>
<p>&nbsp;</p>
<p>10. Regioselective Synthesis of Tetra(aryl)-Mono(silylmethyl)[60]fullerenes and Derivatization to Methanofullerene Compound</p>
<p>Chang-Zhi Li, Yutaka Matsuo,* Eiichi Nakamura*</p>
<p><em>Tetrahedron</em> <strong>2011</strong>, <em>67</em>, 9944-9949. [<a href="http://www.sciencedirect.com/science/article/pii/S0040402011015079" target="_blank">DOI:10.1016/j.tet.2011.09.125</a>]</p>
<p style="text-align: center;"><img src="http://www.matsuo-lab.net/img/4_1methano.png" alt="" width="328" height="95" /></p>
<p>&nbsp;</p>
<p>9. Facile Synthesis of a 56&pi;-electron 1,2-Dihydromethano-[60]PCBM and Its Application for Thermally Stable Polymer Solar Cells</p>
<p>Chang-Zhi Li, Shang-Chieh Chien, Hin-Lap Yip, Chu-Chen Chueh, Fang-Chung Chen, Yutaka Matsuo, Eiichi Nakamura, Alex K.-Y. Jen*</p>
<p><em>Chem. Commun.</em> <strong>2011</strong>, 47, 10082-10084. [<a href="http://pubs.rsc.org/en/Content/ArticleLanding/2011/CC/c1cc14446d" target="_blank">DOI: 10.1039/C1CC14446D</a>]</p>
<p style="text-align: center;"><img src="http://www.matsuo-lab.net/img/methanoPCBM.png" alt="" width="90" height="115" /></p>
<p>&nbsp;</p>
<p>8. Facile Fullerene Modification: FeCl<sub>3</sub>-mediated Quantitative Conversion of C<sub>60</sub> to Polyarylated Fullerenes Containing Pentaaryl(chloro)[60]fullerenes</p>
<p>Masahiko Hashiguchi,* Kazuhiro Watanabe, Yutaka Matsuo*</p>
<p><em>Org. Biomol. Chem.</em> <strong>2011</strong>, <em>9</em>, 6417-6421. [<a href="http://pubs.rsc.org/en/Content/ArticleLanding/2011/OB/C1OB05895A" target="_blank">DOI: 10.1039/C1OB05895A</a>]</p>
<p>&nbsp;</p>
<p>7. Synthesis, Physical Properties, and Crystal Structure of Acetetracenylene-1,2-dione</p>
<p>Toshihiro Okamoto, Tsuyoshi Suzuki, Shungo Kojima, Yutaka Matsuo*</p>
<p><em>Chem. Lett.</em> <strong>2011</strong>, <em>40</em>, 739-741. [<a href="http://dx.doi.org/10.1246/cl.2011.739" target="_blank">DOI: 10.1246/cl.2011.739</a>]</p>
<p style="text-align: center;"><img src="http://www.matsuo-lab.net/img/TDK.png" alt="" width="246" height="111" /></p>
<p>&nbsp;</p>
<p>6. Molecular Photoelectric Switch Using a Mixed SAM of Organic [60]Fullerene and [70]Fullerene Doped with a Single Iron Atom</p>
<p>Yutaka Matsuo,* Takahiko Ichiki, Eiichi Nakamura*</p>
<p><em>J. Am. Chem. Soc.</em> <strong>2011</strong>, <em>133</em>, 9932-9937. [<a href="http://pubs.acs.org/doi/abs/10.1021/ja203224d" target="_blank">DOI: 10.1021/ja203224d</a>]</p>
<p style="text-align: center;"><img src="http://www.matsuo-lab.net/img/photoswitch.png" alt="" width="357" height="138" /></p>
<p>&nbsp;</p>
<p>5. A Scalable Synthesis of Methano[60]fullerene and Congeners by the Oxidative Cyclopropanation Reaction of Silylmethylfullerene</p>
<p>Ying Zhang, Yutaka Matsuo,* Chang-Zhi Li, Hideyuki Tanaka, Eiichi Nakamura*</p>
<p><em>J. Am. Chem. Soc.</em> <strong>2011</strong>, <em>133</em>, 8086-8089. [<a href="http://pubs.acs.org/doi/abs/10.1021/ja201267t" target="_blank">DOI: 10.1021/ja201267t</a>]</p>
<p style="text-align: center;"><img src="http://www.matsuo-lab.net/img/methanofullerene2.png" alt="" width="419" height="116" /></p>
<p>&nbsp;</p>
<p>4. Isolation of Planar 4-Membered Aromatic Systems by Using Confined Spaces of Cobalt Pentaaryl[60]fullerene Complexes</p>
<p>Masashi Maruyama, Jing-Dong Guo, Shigeru Nagase, Eiichi Nakamura, Yutaka Matsuo*</p>
<p><em>J. Am. Chem. Soc.</em> <strong>2011</strong>, <em>133</em>, 6890-6893. [<a href="http://pubs.acs.org/doi/abs/10.1021/ja111474v" target="_blank">DOI: 10.1021/ja111474v</a>]</p>
<p style="text-align: center;"><img src="http://www.matsuo-lab.net/img/CoS3_4ring_aromatics.png" alt="" width="446" height="145" /></p>
<p>&nbsp;</p>
<p>3. Aryl-Perfluoroaryl Substituted Tetracene: Induction of Face-to-Face &pi;-&pi; Stacking and Enhancement of Charge Carrier Properties</p>
<p>Toshihiro Okamoto,* Katsumasa Nakahara, Akinori Saeki, Shu Seki, Joon Hak Oh, Hylke B. Akkerman, Zhenan Bao, Yutaka Matsuo*</p>
<p><em>Chem. Mater.</em> <strong>2011</strong>, <em>23</em>, 1646-1649. [<a href="http://pubs.acs.org/doi/abs/10.1021/cm200356y" target="_blank">DOI: 10.1021/cm200356y</a>]</p>
<p style="text-align: center;"><img src="http://www.matsuo-lab.net/img/85.png" alt="" width="283" height="167" /></p>
<p>&nbsp;</p>
<p>2. Synthesis of 1,4-Diaryl[60]fullerenes by Bis-hydroarylation of C<sub>60</sub> and Their Use in Solution-processable, Thin-film Organic photovoltaic Cells</p>
<p>Yutaka Matsuo,* Ying Zhang, Iwao Soga, Yoshiharu Sato, Eiichi Nakamura*</p>
<p><em>Tetrahedron Lett.</em> <strong>2011</strong>, <em>52</em>, 2240-2242. [<a href="http://dx.doi.org/10.1016/j.tetlet.2011.01.031" target="_blank">DOI:10.1016/j.tetlet.2011.01.031</a>]</p>
<p>&nbsp;</p>
<!-- 画像(中央配置) 終 -->
<p>&nbsp;</p>
<div style="text-align: center;">
<div class="photo-c" style="width: 302px;"><img src="http://www.matsuo-lab.net/img/C60Ar2.jpg" alt="" width="223" height="108" /></div>
</div>
<!-- 画像(中央配置) 終 -->
<p>&nbsp;</p>
<p>1. Simple Formation of C<sub>60</sub> and C<sub>60</sub>-Ferrocene Conjugated Monolayers Anchored onto Silicon Oxide with Five Carboxylic Acids and Their Transistor Applications</p>
<p>Yoshimitsu Itoh,* Bumjung Kim, Raluca I. Gearba, Noah J. Tremblay, Ron Pindak, Yutaka Matsuo, Eiichi Nakamura, Colin Nuckolls</p>
<p><em>Chem. Mater.</em> <strong>2011</strong>, <em>23</em>, 970-975. [<a href="http://pubs.acs.org/doi/abs/10.1021/cm1025975" target="_blank">DOI: 10.1021/cm1025975</a>]</p>
<div style="text-align: center;">
<div class="photo-c" style="width: 500px;"><img src="http://www.matsuo-lab.net/img/cm-2010-025975_0011.gif" alt="" width="277" height="135" /></div>
&nbsp;</div>
</div>

<div class="block">
<h4>2010年</h4>
<p>11. Octupole-like Supramolecular Aggregates of Conical Iron Fullerene Complexes into a Three-dimensional Liquid Crystalline Lattice</p>
<p>Chang-Zhi Li, Yutaka Matsuo,* Eiichi Nakamura*</p>
<p><em>J. Am. Chem. Soc.</em> <strong>2010</strong>, <em>132</em>, 15514-15515. [<a href="http://pubs.acs.org/doi/abs/10.1021/ja1073933" target="_blank">DOI: 10.1021/ja1073933</a>]</p>
<p style="text-align: center;"><img src="http://www.matsuo-lab.net/img/84.gif" alt="" width="302" height="104" /></p>
<p>&nbsp;</p>
<p>10. Face-to-face C<sub>6</sub>F<sub>5</sub>&ndash;[60]Fullerene Interaction for Ordering Fullerene Molecules and Application to Thin-film Organic Photovoltaics</p>
<p>Chang-Zhi Li, Yutaka Matsuo,* Takaaki Niinomi, Yoshiharu Sato, Eiichi Nakamura*</p>
<p><em>Chem. Commun.</em> <strong>2010</strong>, <em>46</em>, 8582-8584. [<a href="http://pubs.rsc.org/en/Content/ArticleLanding/2010/CC/C0CC03028G" target="_blank">DOI: 10.1039/C0CC03028G</a>]</p>
<p style="text-align: center;"><img src="http://www.matsuo-lab.net/img/83.gif" alt="" width="271" height="153" /></p>
<p>&nbsp;</p>
<p>9. Conical Pentaaryl[60]Fullerene Thiols: Self-Assembled Monolayers on Gold and Photocurrent Generating Property</p>
<p>Yutaka Matsuo,* Sebastian Lacher, Aiko Sakamoto, Keiko Matsuo, Eiichi Nakamura*</p>
<p><em>J. Phys. Chem. C</em> <strong>2010</strong>, <em>114</em>, 17741-17752. [<a href="http://pubs.acs.org/doi/abs/10.1021/jp1059402" target="_blank">DOI: 10.1021/jp1059402</a>]</p>
<p style="text-align: center;"><img src="http://www.matsuo-lab.net/img/82.gif" alt="" width="218" height="160" /></p>
<p>&nbsp;</p>
<p>8. Voltammetry of Half-Sandwich Manganese Group Complexes of &eta;<sup>6</sup>-PhC<sub>3</sub>B<sub>7</sub>H<sub>9</sub> and &eta;<sup>5</sup>-C<sub>60</sub>Bn<sub>2</sub>PhH<sub>2</sub>, Two Ligands That Are Cyclopentadienyl Mimicks</p>
<p>Michael P. Stewart, Robert Butterick III, Larry G. Sneddon, Yutaka Matsuo, William E. Geiger*</p>
<p><em>Inorg. Chem. Acta.</em> <strong>2010</strong>, <em>364</em>, 251-254. [<a href="http://dx.doi.org/10.1016/j.ica.2010.05.040" target="_blank">DOI: 10.1016/j.ica.2010.05.040</a>]</p>
<p>&nbsp;</p>
<p>7. Copper-catalyzed Formal [4+2] Annulation between Alkyne and Fullerene Bromide</p>
<p>Zuo Xiao, Yutaka Matsuo,* Eiichi Nakamura*</p>
<p><em>J. Am. Chem. Soc.</em> <strong>2010</strong>, <em>132</em>, 12234-12236. [<a href="http://pubs.acs.org/doi/abs/10.1021/ja1056399" target="_blank">DOI: 10.1021/ja1056399</a>]</p>
<p style="text-align: center;"><img src="http://www.matsuo-lab.net/img/81.gif" alt="" width="307" height="101" /></p>
<p>&nbsp;</p>
<p>6. Loading Pentapod Deca(organo)[60]fullerenes with Electron Donors: From Photophysics to Photoelectrochemical Bilayers</p>
<p>Yutaka Matsuo,* Takahiko Ichiki, Shankara Radhakrishnan, Dirk M. Guldi,* Eiichi Nakamura*</p>
<p><em>J. Am. Chem. Soc.</em> <strong>2010</strong>, <em>132</em>, 6342-6348. [<a href="http://pubs.acs.org/doi/abs/10.1021/ja909970h" target="_blank">DOI: 10.1021/ja909970h</a>]</p>
<p style="text-align: center;"><img src="http://www.matsuo-lab.net/img/80.gif" alt="" width="265" height="115" /></p>
<p>&nbsp;</p>
<p>5. Synthesis of Ruthenium Pentamethyl[60]fullerene Complexes Bearing Monodentate Diphenylphosphino-methane, ferrocene, and -butane Ligands</p>
<p>Yutaka Matsuo,* Bo Keun Park, Yuichi Mitani, Yu-Wu Zhong, Masashi Maruyama, Eiichi Nakamura*</p>
<p><em>Bull. Korean Chem. Soc.</em> <strong>2010</strong>, <em>31</em>, 697-699. [<a href="http://newjournal.kcsnet.or.kr/main/j_search/j_abstract_view.htm?code=B100337&amp;qpage=j_search&amp;spage=b_bkcs&amp;dpage=ar" target="_blank">DOI: 10.5012/bkcs.2010.31.03.697</a>]</p>
<p>&nbsp;</p>
<p>4. C<sub>60</sub> Derivatives Having Self-Assembly Capability</p>
<p>Yutaka Matsuo</p>
<p><em>Fullerene, Nanotubes, and Carbon Nanostructures</em> <strong>2010</strong>, <em>18</em>, 338-352. [<a href="http://www.informaworld.com/smpp/content~db=all~content=a928677994" target="_blank">DOI: 10.1080/1536383X.2010.487395</a>]</p>
<p>&nbsp;</p>
<p>3. Reductive Benzylation of Dimetallo Hexaaryl[70]Fullerenes on the Equatorial Region</p>
<p>Takeshi Fujita, Yutaka Matsuo,* Eiichi Nakamura*</p>
<p><em>Chem. Asian J.</em> <strong>2010</strong>, <em>5</em>, 835-840. [<a href="http://onlinelibrary.wiley.com/doi/10.1002/asia.200900651/abstract" target="_blank">DOI: 10.1002/asia.200900651</a>]</p>
<p style="text-align: center;"><img src="http://www.matsuo-lab.net/img/77.gif" alt="" width="242" height="165" /></p>
<p>&nbsp;</p>
<p>2. Highly Soluble Penta[(alkyl)dimethylsilylmethyl][60]fullerenes and Their Ruthenium and Palladium Complexes</p>
<p>Yutaka Matsuo,* Ayako Muramatsu, Jiang Lu, Eiichi Nakamura*</p>
<p><em>Chem. Lett.</em> <strong>2010</strong>, <em>39</em>, 342-343. [<a href="http://www.jstage.jst.go.jp/article/cl/39/4/39_342/_article" target="_blank">DOI: 10.1246/cl.2010.342</a>]</p>
<p style="text-align: center;"><img src="http://www.matsuo-lab.net/img/76.png" alt="" width="238" height="125" /></p>
<p>&nbsp;</p>
<p>1. Substituent-Dependent Ordering of Adlayer Structure of Fullerene Derivatives: A Scanning Tunneling Microscopy Study</p>
<p>Ting Chen, Ge-Bo Pan, Hui-Juan Yan, Li-Jun Wan,* Yutaka Matsuo,* Eiichi Nakamura*</p>
<p><em>J. Phys. Chem. C</em> <strong>2010</strong>, <em>114</em>, 3170-3174. [<a href="http://pubs.acs.org/doi/abs/10.1021/jp9114173" target="_blank">DOI: 10.1021/jp9114173</a>]</p>
<p style="text-align: center;"><img src="http://www.matsuo-lab.net/img/75.gif" alt="" width="285" height="112" /></p>
<p>&nbsp;</p>
</div>

<div class="block">
<h4>2009年</h4>
<p>11. Luminescent Bow-Tie-Shaped Decaaryl[60]fullerene Mesogens</p>
<p>Chang-Zhi Li, Yutaka Matsuo,* Eiichi Nakamura*</p>
<p><em>J. Am. Chem. Soc.</em> <strong>2009</strong>, <em>131</em>, 17058-17059. [<a href="http://pubs.acs.org/doi/abs/10.1021/ja907908m" target="_blank">DOI: 10.1021/ja907908m</a>]</p>
<p style="text-align: center;"><img src="http://www.matsuo-lab.net/img/74.gif" alt="" width="307" height="137" /></p>
<p>&nbsp;</p>
<p>10. Columnar Structure in Bulk Heterojunction in Solution-processable Three-layered p-i-n Organic Photovoltaic Devices Using Tetrabenzoporphyrin Precursor and Silylmethyl[60]fullerene</p>
<p>Yutaka Matsuo,* Yoshiharu Sato,* Takaaki Niinomi, Iwao Soga, Hideyuki Tanaka, Eiichi Nakamura*</p>
<p><em>J. Am. Chem. Soc.</em> <strong>2009</strong>, <em>131</em>, 16048-16050. [<a href="http://pubs.acs.org/doi/abs/10.1021/ja9048702" target="_blank">DOI: 10.1021/ja9048702</a>]</p>
<p style="text-align: center;"><img src="http://www.matsuo-lab.net/img/73.gif" alt="" width="314" height="119" /></p>
<p>&nbsp;</p>
<p>9. Synthesis of Imino[60]fullerenes Using Nitriles and Trimethylsilylmethyl Triflate</p>
<p>Keiko Matsuo, Yutaka Matsuo,* Akihiko Iwashita, Eiichi Nakamura*</p>
<p><em>Org. Lett.</em> <strong>2009</strong>, <em>11</em>, 4192-4194. [<a href="http://pubs.acs.org/doi/full/10.1021/ol901851g" target="_blank">DOI: 10.1021/ol901851g</a>]</p>
<p style="text-align: center;"><img src="http://www.matsuo-lab.net/img/72.gif" alt="" width="343" height="96" /></p>
<p>&nbsp;</p>
<p>8. &pi;-Conjugated Multi-Donor/Acceptor Arrays of Fullerene-Cobaltadithiolene-Tetrathiafulvalene: From Synthesis and Structure to Electronic Interactions</p>
<p>Yutaka Matsuo,* Masashi Maruyama, S. Shankara Gayathri, Tomoya Uchida, Dirk M. Guldi,* Hideo Kishida,* Arao Nakamura, Eiichi Nakamura*</p>
<p><em>J. Am. Chem. Soc.</em> <strong>2009</strong>, <em>131</em>, 12643-12649. [<a href="http://pubs.acs.org/doi/full/10.1021/ja902312q" target="_blank">DOI: 10.1021/ja902312q</a>]</p>
<p style="text-align: center;"><img src="http://www.matsuo-lab.net/img/71.gif" alt="" width="223" height="149" /></p>
<p>&nbsp;</p>
<p>7. Di- and Trinuclear [70]Fullerene Complexes: Syntheses and Metal-Metal Electronic Interactions</p>
<p>Yutaka Matsuo,* Kazukuni Tahara, Takeshi Fujita, Eiichi Nakamura*</p>
<p><em>Angew. Chem. Int. Ed.</em> <strong>2009</strong>, <em>48</em>, 6239-6241. [<a href="http://onlinelibrary.wiley.com/doi/10.1002/anie.200902185/abstract" target="_blank">DOI: 10.1002/anie.200902185</a>]</p>
<p style="text-align: center;"><img src="http://www.matsuo-lab.net/img/70.gif" alt="" width="343" height="139" /></p>
<p>&nbsp;</p>
<p>6. Efficient Bidirectional Photocurrent Generation by Self-assembled Monolayer of Penta(aryl)[60]fullerene Phosphonic Acid</p>
<p>Aiko Sakamoto, Yutaka Matsuo,* Keiko Matsuo, Eiichi Nakamura*</p>
<p><em>Chem. Asian J.</em> <strong>2009</strong>, <em>4</em>, 1208-1212. [<a href="http://onlinelibrary.wiley.com/doi/10.1002/asia.200900155/abstract" target="_blank">DOI: 10.1002/asia.200900155</a>]</p>
<p style="text-align: center;"><img src="http://www.matsuo-lab.net/img/69.gif" alt="" width="268" height="125" /></p>
<p>&nbsp;</p>
<p>5. Penta(organo)[60]fullerenes as Acceptors for Organic Photovoltaic Cells<br />Takaaki Niinomi, Yutaka Matsuo,* Masahiko Hashiguchi, Yoshiharu Sato, Eiichi Nakamura*</p>
<p><em>J. Mater. Chem.</em> <strong>2009</strong>, <em>19</em>, 5804-5811. [<a href="http://pubs.rsc.org/en/Content/ArticleLanding/2009/JM/b904485j" target="_blank">DOI: 10.1039/b904485j</a>]</p>
<p style="text-align: center;"><img src="http://www.matsuo-lab.net/img/68.gif" alt="" width="378" height="100" /></p>
<p>&nbsp;</p>
<p>4. Random Telegraphic Conductance Fluctuation at Au-Pentacene-Au Nanojunctions</p>
<p>Yuki Kihira, Toshihiro Shimada,* Yutaka Matsuo, Eiichi Nakamura, Tetsuya Hasegawa</p>
<p><em>Nano Lett.</em> <strong>2009</strong>, <em>9</em>, 1442-1446. [<a href="http://pubs.acs.org/doi/abs/10.1021/nl803284t" target="_blank">DOI: 10.1021/nl803284t</a>]</p>
<p style="text-align: center;"><img src="http://www.matsuo-lab.net/img/67.gif" alt="" width="262" height="102" /></p>
<p>&nbsp;</p>
<p>3. Ring-opening Reaction of Tetrahydrofuran on the Penta(organo)[60]fullerenes: Synthesis of Hydroxybutyl, Methacrylate, and Norbornene Derivatives</p>
<p>Yutaka Matsuo,* Akihiko Iwashita, Hiromi Oyama, Eiichi Nakamura*</p>
<p><em>Tetrahedron Lett.</em> <strong>2009</strong>, <em>50</em>, 3411-3413. (50th Anniversary of TL) [<a href="http://dx.doi.org/10.1016/j.tetlet.2009.02.155" target="_blank">DOI: 10.1016/j.tetlet.2009.02.155</a>]</p>
<p style="text-align: center;"><img src="http://www.matsuo-lab.net/img/66.jpg" alt="" width="301" height="111" /></p>
<p>&nbsp;</p>
<p>2. Synthesis, Electrochemical and Photophysical Properties, and Electroluminescent Performance of the Octa- and Deca-aryl [60]Fullerene Derivatives</p>
<p>Yutaka Matsuo,* Yoshiharu Sato, Masahiko Hashiguchi, Keiko Matsuo, Eiichi Nakamura*</p>
<p><em>Adv. Funct. Mater.</em> <strong>2009</strong>, <em>19</em>, 2224-2229. [<a href="http://dx.doi.org/10.1002/adfm.200900021" target="_blank">DOI: 10.1002/adfm.200900021</a>]</p>
<p style="text-align: center;"><img src="http://www.matsuo-lab.net/img/65.png" alt="" width="198" height="179" /></p>
<p>&nbsp;</p>
<p>1. Iron and Ruthenium Nanoparticles in Carbon Prepared by Thermolysis of Buckymetallocenes</p>
<p>Takahiro Nakae, Yutaka Matsuo,* Masatoshi Takagi, Yuta Sato, Kazu Suenaga, Eiichi Nakamura*</p>
<p><em>Chem. Asian J.</em> <strong>2009</strong>, <em>4</em>, 457-465. [<a href="http://dx.doi.org/10.1002/asia.200800331" target="_blank">DOI: 10.1002/asia.200800331</a>]</p>
<p style="text-align: center;"><img src="http://www.matsuo-lab.net/img/64.gif" alt="" width="303" height="109" /></p>
<p>&nbsp;</p>
</div>/* End custom CSS */