期刊
JOURNAL OF POLYMER SCIENCE PART A-POLYMER CHEMISTRY
卷 52, 期 9, 页码 1306-1314出版社
WILEY
DOI: 10.1002/pola.27119
关键词
alkoxy anthracene; benzothiadiazole; charge transfer; organic photovoltaic cell
资金
- National Research Foundation of Korea (NRF)
- Ministry of Education, Science and Technology [2012-047047]
- KRC
- KIST [NAP-08-01]
Novel alkoxy anthracene (ODA)-based polymeric semiconductors were designed for polymer solar cell applications. Alkoxyanthracene, which contains many electrons and electron donating group, was easily synthesized. The copolymers, poly(alkoxy anthracene-alt-thiophene benzothiadiazole thiophene) poly(ODA-TBT) and poly(alkoxy anthracene-alt-benzothiadiazole) poly(ODA-BT), have been obtained by Suzuki coupling polymerization. Both polymers have ODA unit as a donor and benzothiadiazole as an acceptor. ODA-TBT has thiophene linkages between ODA and benzothiadiazole. The optical, thermal, and electrochemical properties have been investigated by UV-visible absorption, thermal gravimetric analysis, differential scanning calorimetry, and CV. Organic thin-film transistor using polymers showed that the hole mobility of poly(ODA-alt-TBT) was around 3.6 x 10(-3) cm(2)/Vs with on/off ratio of 9.91 x 10(5) while that of poly(ODA-alt-BT) was around 1.21 x 10(-2) cm(2)/Vs with on/off ratio of 2.64 x 10(6). Organic photovoltaic performance based on polymers were evaluated with a configuration of ITO/PEDOT:PSS/active layer/LiF/Al. Poly(ODA-TBT) exhibits a short circuit current (J(sc)) of 3.9 mA/cm(2) and power conversion efficiency (PCE) of 1.4%, and poly(ODA-BT) exhibits the J(sc) of 6.4 mA/cm(2) and PCE of 2.2%. The better device performance of poly(ODA-BT) is attributed to its charge transfer ability and enhanced mobility and crystallinity although poly(ODA-BT) does not have extended -conjugation due to twisted structure compared with poly(ODA-TBT). (c) 2014 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2014, 52, 1306-1314
作者
我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。
推荐
暂无数据