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Synthesis and photovoltaic properties of a star-shaped molecule based on a triphenylamine core and branched terthiophene end groups 被引量:4

Synthesis and photovoltaic properties of a star-shaped molecule based on a triphenylamine core and branched terthiophene end groups
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摘要 A new star-shaped donor-acceptor molecule has been synthesized for application as the donor material in solution-processed bulk-heterojunction organic solar cells (OSCs). The molecule consists of a triphenylamine (TPA) unit as the core and a donor unit with three arms containing benzo[1,2,5]thiadiazole (BT) acceptor units and 5,5''-dihexyl-2,2′:3′,2″-terthiophene (tTh) end groups. The molecule, denoted S(TPA-BT-tTh), exhibits a broad absorption band in the wavelength range 300-650 nm and high hole mobility of 1.1×10 -4 cm2 V -1 s 1 . An OSC device based on S(TPA-BT-tTh) as donor and [6,6]-phenyl C71 -butyric acid methyl ester (PC 70 BM) as the acceptor (1:3, w/w) exhibited a power conversion efficiency of 2.28% with a short circuit current density of 6.39 mA/cm2 under illumination of AM.1.5, 100 mW/cm2 . A new star-shaped donor-acceptor molecule has been synthesized for application as the donor material in solution-processed bulk-heterojunction organic solar cells (OSCs). The molecule consists of a triphenylamine (TPA) unit as the core and a donor unit with three arms containing benzo[1,2,5]thiadiazole (BT) acceptor units and 5,5'-dihexyl-2,2':3',2'-terthiophene (tTh) end groups. The molecule, denoted S(TPA-BT-tTh), exhibits a broad absorption band in the wavelength range 300-650 nm and high hole mobility of 1.1×10^-4 cm2 V^-1 s^-1. An OSC device based on S(TPA-BT-tTh) as donor and [6,6]-phenyl C71-butyric acid methyl ester (PC70BM) as the acceptor (1:3, w/w) exhibited a power conversion efficiency of 2.28% with a short circuit current density of 6.39 mA/cm2 under illumination of AM. 1.5, 100 mW/cm2.
出处 《Science China Chemistry》 SCIE EI CAS 2013年第7期997-1003,共7页 中国科学(化学英文版)
基金 supported by the National Natural Science Foundation of China (50933003 and 21021091) the support from MOE, Jiangsu Province, and SEU (NCET-09-0294, 20100092120037,XNY-48-037 and Seujq201103)
关键词 受体分子 三苯胺 三噻吩 光伏性能 星形 合成 端基 有机太阳能电池 organic solar cells, star-shaped photovoltaic organic molecules, solution-processability
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  • 1Chen JW, Cao Y. Development of novel conjugated donor poly- mers for high-efficiency bulk-heterojunction photovoltaic devices. Acc Chem Res, 2009, 42: 1709-1718.
  • 2Cheng YJ, Yang SH, Hsu CS. Synthesis of conjugated polymers for organic solar cell ap- plications. Chem Rev, 2009, 109: 5868-5923.
  • 3Li YF. Molecular design of photovoltaic materials for polymer solar cells: Toward suitable electronic energy levels and broad absorption. Acc Chem Res, 2012.45:723-733.
  • 4He YJ, Li YF. Fullerene derivative acceptors for high performance polymer solar cells. Phys Chem Chem Phys, 2011, 13:1970-1983.
  • 5Liang YY, Xu Z, Xia JB, Tsai ST, Wu Y, Li G, Ray C, Yu LP. For the bright future-bulk heterojunction polymer solar cells with power conversion efficiency of 7.4%. Adv Mater, 2010, 22: E135- E138.
  • 6Chen HY, Hou JH, Zhang SQ, Liang YY, Yang GW, Yang Y, Yu LP, Wu Y, Li G. Polymer solar cells with enhanced open- circuit voltage and efficiency Nat Photonics, 2009, 3:649-653.
  • 7Huo LJ, Zhang SQ, Guo X, Xu F, Li YF, Hou JH. Replacing alkoxy groups with alkylthienyl groups: A feasible approach to improve the properties of photovoltaic polymers. Angew Chem lnt Ed, 2011, 50: 9697-9702.
  • 8Roncali J. Molecular bulk heterojunctions: An emerging approach to organic solar cells. Acc Chem Res, 2009, 42:1719-1730.
  • 9Li YW, Guo Q, Li ZF, Pei JN, Tian WJ. Solution processable D-A small molecules for bulk-heterojunction solar cells. Energy Environ Sci, 2010, 3:1427-1436.
  • 10Walker B, Kim C, Nguyen TQ. Small molecule solution-processed bulk heterojunction solar cells. Chem Mater, 2011, 23:470-482.

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