4.7 Article

Effect of side chain position and conformation of quinacridone-quinoxaline based conjugated polymers on photovoltaic properties

期刊

出版社

ELSEVIER SCIENCE INC
DOI: 10.1016/j.jiec.2015.10.029

关键词

Quinacridone; Quinoxaline; Side-chain; Suzuki coupling reaction; Bulk heterojunction polymer solar cells

资金

  1. Energy Efficiency & Resources Core Technology Program of the Korea Institute of Energy Technology Evaluation and Planning (KETEP) from the Ministry of Trade, Industry & Energy, Republic of Korea [20142020103970]
  2. Korea Evaluation Institute of Industrial Technology (KEIT) [20142020103970] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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Poly[quinacridone-alt-dithienylquinoxaline](PQCDTQx)s series with alkoxy chains at different anchoring positions (meta- or para-) in quinoxaline were synthesized via Suzuki coupling reaction. The ICT effects were stronger at the meta than para. Meta-polymers had enhanced pi-pi stacking of the polymer main chains and showed a lower HOMO energy level than those of the para, from -5.26 to -5.16 eV, because of the greater electron-withdrawing effects of the alkoxy groups. As a result, the photovoltaic device comprising a PQCDTQx-mEH/PC71 BM (1:4) blend system exhibited performance, with a PCE,J(sc), V-oc, and FF of 2.1%, 4.8 mA/cm(2), 0.73 V, and 59.3%, respectively. (C) 2015 The Korean Society of Industrial and Engineering Chemistry. Published by Elsevier B.V. All rights reserved.

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