Desin of Chemical Structure Based on D-A copolymers via Tuning the Alkyl Side Chain in Efficient Polymer Solar Cells
Sung Jae Jeon a, Doo Hun Kim a, Jeong Eun Yu a, Ye Jin Lee a, Yong Woon Han a, Young Hun Kim a, Doo Kyung Moon a
a Nano and Information Materials Lab. (NIMs Lab.), Department of Materials Chemistry and Engineering, Konkuk University, 1 Hwayang-dong, Gwangjin-gu, Seoul, Republic of Korea.
Asia-Pacific International Conference on Perovskite, Organic Photovoltaics and Optoelectronics
Proceedings of International Conference Asia-Pacific Hybrid and Organic Photovoltaics 2018 (AP-HOPV18)
Kitakyūshū-shi, Japan, 2018 January 28th - 30th
Organizers: Shuzi Hayase, Juan Bisquert and Hiroshi Segawa
Poster, Sung Jae Jeon, 104
Publication date: 27th October 2017

 Polymer solar cells (PSCs) are in the spotlight as a potential technology for the development of flexible and portable photovoltaic devices because of their superior mechanical flexibility and ability to allow low-cost solution processing on a plastic substrate. Lately, bulk heterojunction (BHJ) polymer solar cells consisting of polymer donor-fullerene acceptor blends have been reported to exhibit high power conversion efficiencies (PCEs) of greater than over 10%. A fine morphology that forms an interpenetrating donor-acceptor (D-A) networks is specifically necessary to obtain highly efficient PSCs. In the study, we designed and synthesized D-A copolymers via tuning the shape and length of alkyl side chain in the backbone. Synthesized D-A copolymers exhibited each different behaviour of their properties as kind of alkyl side chain. The among of polymers, we reached the nearly 9% of PCE in optimized polymer structure.

 

Keywords: Polymer solar cells (PSCs), Organic solar cells (OSCs), Organic Photovoltaics (OPVs), Fullerene, side chain engineering

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