Electron-Acceptor-Dependent Light Absorption, Excited-State Relaxation, and Charge Generation in Triphenylamine Dye-Sensitized Solar Cells

被引:18
作者
Li, Renzhi [1 ]
Zhang, Min [1 ]
Yan, Cancan [1 ,2 ]
Yao, Zhaoyang [1 ,2 ]
Zhang, Jing [1 ]
Wang, Peng [1 ]
机构
[1] Chinese Acad Sci, Changchun Inst Appl Chem, State Key Lab Polymer Phys & Chem, Changchun 13002, Peoples R China
[2] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
基金
美国国家科学基金会;
关键词
cyclic voltammetry; density functional calculations; dyes/pigments; energy conversion; solar cells; ORGANIC-DYES; HIGH-EFFICIENCY; TRANSFER DYNAMICS; ENERGY-DISSIPATION; FEMTOSECOND; TITANIA; TIO2; RECOMBINATION; PERFORMANCE; MOLECULES;
D O I
10.1002/cssc.201402806
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
By choosing a simple triphenylamine electron donor, we herein compare the influence of electron acceptors benzothiadiazole benzoic acid (BTBA) and cyanoacrylic acid (CA), on energy levels, light absorption, and dynamics of excited-state evolution and electron injection. DFT and time-dependent DFT calculations disclosed remarkable intramolecular conformational changes for the excited states of these two donor-acceptor dyes. Photoinduced dihedral angle variation occurs to the tri-phenylamine unit in the CA dye and backbone planarization happens to conjugated aromatic blocks in the BTBA dye. Femtosecond spectroscopic measurements suggested the crucial role of having a long excited-state lifetime in maintaining a high electron-injection yield because a reduced driving force for a low energy-gap dye can result in slower electron-injection dynamics.
引用
收藏
页码:97 / 104
页数:8
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