Efficient triphenylamine dyes for solar cells: Effects of alkyl-substituents and π-conjugated thiophene unit

被引:116
作者
Shen, Ping [1 ,2 ]
Liu, Yijiang [1 ,2 ]
Huang, Xianwei [1 ,2 ]
Zhao, Bin [1 ,2 ]
Xiang, Na [1 ,2 ]
Fei, Junjie [1 ,2 ]
Liu, Liming [1 ,2 ]
Wang, Xueye [1 ,2 ,3 ]
Huang, Hui [1 ,2 ]
Tan, Songting [1 ,2 ,3 ]
机构
[1] Xiangtan Univ, Coll Chem, Coll Hunan Prov, Xiangtan 411105, Peoples R China
[2] Xiangtan Univ, Key Lab Adv Funct Polymer Mat, Coll Hunan Prov, Xiangtan 411105, Peoples R China
[3] Xiangtan Univ, Key Lab Environm Friendly Chem & Applicat, Minist Educ, Xiangtan 411105, Peoples R China
关键词
Triphenylamine moiety; Oligothiophenes; pi-Conjugated unit; Solar-to-electricity conversion efficiency; Dye-sensitized solar cells; Photovoltaic performances; NANOCRYSTALLINE TIO2 ELECTRODES; ORGANIC-DYES; CHARGE-TRANSFER; COUMARIN DYES; MOLECULAR PHOTOVOLTAICS; STRUCTURAL MODIFICATION; SENSITIZERS; PERFORMANCE; LIGHT; CHROMOPHORES;
D O I
10.1016/j.dyepig.2009.04.005
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Several triplienylamine dyes, both with and without an n-hexyl-substituted oligothiophene as pi-conjugated linker, were designed, synthesized and utilised in dye-sensitized, nanocrystalline, TiO2 solar cells. The effects of both the length of the pi-conjugated unit and of the alkyl chain upon the photophysical, electrochemical and photovoltaic properties of the dyes were studied. Between I and 3 thiophene units impart superior solar-to-electricity conversion efficiency and the hexyl chains also markedly improve both short-circuit photocurrent density and open-circuit photovoltage, which result in relatively high solar-to-electricity conversion efficiency. In EtOH solution, a dye-sensitized solar cell based on 2-cyano-3-(5-(4-(diphenylamino) phenyl)-4-hexylthioplienyl-2-yl) acrylic acid with one hexyl-substituted thiophene, pi-conjugated unit, exhibited the largest observed maximum solar-to-electricity conversion efficiency of 7.26% under simulated AM 1.5 G solar irradiation (100 mW/cm(2)). (C) 2009 Elsevier Ltd. All rights reserved.
引用
收藏
页码:187 / 197
页数:11
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