Article
Synthesis and applications of 2,7-carbazole-based conjugated main-chain copolymers containing electron deficient bithiazole units for organic solar cells
Article first published online: 5 OCT 2010
DOI: 10.1002/pola.24356
Copyright © 2010 Wiley Periodicals, Inc.
Issue

Journal of Polymer Science Part A: Polymer Chemistry
Volume 48, Issue 23, pages 5479–5489, 1 December 2010
Additional Information
How to Cite
Patra, D., Sahu, D., Padhy, H., Kekuda, D., Chu, C.-W. and Lin, H.-C. (2010), Synthesis and applications of 2,7-carbazole-based conjugated main-chain copolymers containing electron deficient bithiazole units for organic solar cells. J. Polym. Sci. A Polym. Chem., 48: 5479–5489. doi: 10.1002/pola.24356
Publication History
- Issue published online: 28 OCT 2010
- Article first published online: 5 OCT 2010
- Manuscript Accepted: 21 AUG 2010
- Manuscript Received: 11 JUL 2010
Funded by
- National Science Council of Taiwan (ROC). Grant Number: NSC 97-2113-M-009-006-MY2
- National Chiao Tung University. Grant Number: 97W807
- Energy and Environmental Laboratories (charged by Dr. Chang-Chung Yang) in Industrial Technology Research Institute (ITRI)
- Abstract
- Article
- References
- Cited By
Keywords:
- bithiazole units;
- bulk heterojunction;
- copolymers;
- donor–acceptor
Abstract
A series of low-band-gap (LBG) donor–accepor conjugated main-chain copolymers (P1–P4) containing planar 2,7-carbazole as electron donors and bithiazole units (4,4′-dihexyl-2,2′-bithiazole and 4,4′-dihexyl-5,5′-di(thiophen-2-yl)-2,2′-bithiazole) as electron acceptors were synthesized and studied for the applications in bulk heterojunction (BHJ) solar cells. The effects of electron deficient bithiazole units on the thermal, optical, electrochemical, and photovoltaic (PV) properties of these LBG copolymers were investigated. Absorption spectra revealed that polymers P1–P4 exhibited broad absorption bands in UV and visible regions from 300 to 600 nm with optical band gaps in the range of 1.93–1.99 eV, which overlapped with the major region of the solar emission spectrum. Moreover, carbazole-based polymers P1–P4 showed low values of the highest occupied molecular orbital (HOMO) levels, which provided good air stability and high open circuit voltages (Voc) in the PV applications. The BHJ PV devices were fabricated using polymers P1–P4 as electron donors and (6,6)-phenyl-C61-butyric acid methyl ester (PC61BM) or (6,6)-phenyl-C71-butyric acid methyl ester (PC71BM) as electron acceptors in different weight ratios. The PV device bearing an active layer of polymer blend P4:PC71BM (1:1.5 w/w) showed the best power conversion efficiency value of 1.01% with a short circuit current density (Jsc) of 4.83 mA/cm2, a fill factor (FF) of 35%, and Voc = 0.60 V under 100 mW/cm2 of AM 1.5 white-light illumination. © 2010 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2010

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