共 74 条
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
来源:
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.
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页码:97 / 104
页数:8
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