Photovoltaic Properties of OPV Devices Using <i>cis</i>- and <i>trans</i>-2,5-Diarylfulleropyrrolidines as Acceptor Partners with P3HT on an ITO Electrode with or without PEDOT:PSS
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- Ken Yoshimura
- Department of Chemistry and Biotechnology, Graduate School of Engineering, Tottori University
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- Kiyotaka Sugawara
- Department of Chemistry and Biotechnology, Graduate School of Engineering, Tottori University
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- Shigeki Sakumichi
- Department of Chemistry and Biotechnology, Graduate School of Engineering, Tottori University
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- Kei Matsumoto
- Department of Chemistry and Biotechnology, Graduate School of Engineering, Tottori University
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- Yasunori Uetani
- Sumitomo Chemical Co., Ltd
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- Shuichi Hayase
- Department of Chemistry and Biotechnology, Graduate School of Engineering, Tottori University
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- Toshiki Nokami
- Department of Chemistry and Biotechnology, Graduate School of Engineering, Tottori University
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- Toshiyuki Itoh
- Department of Chemistry and Biotechnology, Graduate School of Engineering, Tottori University
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<jats:title>Abstract</jats:title> <jats:p>Three types of 2,5-diarylfulleropyrrolidine derivatives, i.e., 2,5-diphenyl, 2,5-di(thiophen-2-yl), and 2,5-di(thiophen-3-yl)fulleropyrrolidines were used as acceptor molecules with P3HT of OPV devices using two types of ITO electrodes. Their PCE depended on both the stereochemistry and nature of the two aryl substituents at the 2,5-positions of the pyrrolidine ring: the PCE of the devices using trans-diphenyl or both cis- and trans-di(thiophen-3-yl) compounds were significantly lowered by using an ITO electrode with PEDOT:PSS, while the cis-diphenyl isomer was not influenced by PSS. Furthermore, both cis- and trans-2,5-di(thiophen-2-yl)fulleropyrrolidine displayed high PCE using PEDOT:PSS.</jats:p>
収録刊行物
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- Chemistry Letters
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Chemistry Letters 42 (10), 1209-1211, 2013-07-17
Oxford University Press (OUP)
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詳細情報 詳細情報について
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- CRID
- 1360283694082128896
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- NII論文ID
- 10031201312
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- NII書誌ID
- AA00603318
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- ISSN
- 13480715
- 03667022
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