Novel Alkoxyanthracene Donor and Benzothiadiazole Acceptor for Organic Thin Film Transistor and Bulk Heterojunction Organic Photovoltaic Cells
- Authors
- Ma, Jae Yeol; Yun, Hui-Jun; Kim, Seul-Ong; Lee, Gi Back; Cha, Hyojung; Park, Chan Eon; Kwon, Soon-Ki; Kim, Yun-Hi
- Issue Date
- May-2014
- Publisher
- John Wiley & Sons Inc.
- Keywords
- alkoxy anthracene; benzothiadiazole; charge transfer; organic photovoltaic cell
- Citation
- Journal of Polymer Science, Part A: Polymer Chemistry, v.52, no.9, pp 1306 - 1314
- Pages
- 9
- Indexed
- SCI
SCIE
SCOPUS
- Journal Title
- Journal of Polymer Science, Part A: Polymer Chemistry
- Volume
- 52
- Number
- 9
- Start Page
- 1306
- End Page
- 1314
- URI
- https://scholarworks.gnu.ac.kr/handle/sw.gnu/18993
- DOI
- 10.1002/pola.27119
- ISSN
- 0887-624X
1099-0518
- Abstract
- 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
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