Molecular engineering of new phenothiazine-based D-A-π-A dyes for dye-sensitized solar cells

被引:13
|
作者
Zhang, Xiaofeng [1 ]
Gou, Faliang [1 ]
Shi, Jian [1 ]
Gao, Hong [1 ]
Xu, Cailing [1 ]
Zhu, Zhenping [2 ]
Jing, Huanwang [1 ,2 ]
机构
[1] Lanzhou Univ, Coll Chem & Chem Engn, State Key Lab Appl Organ Chem, Lanzhou 730000, Gansu, Peoples R China
[2] Chinese Acad Sci, Inst Coal Chem, State Key Lab Coal Convers, Taiyuan 030001, Shanxi, Peoples R China
基金
中国国家自然科学基金;
关键词
TRIDENTATE ANCHORING GROUP; ORGANIC-DYES; AUXILIARY ACCEPTOR; ELECTROCHEMICAL PROPERTIES; PHOTOVOLTAIC PERFORMANCE; CHARGE RECOMBINATION; FEATURED SENSITIZERS; SALICYLIC-ACID; ENERGY-LEVELS; ABSORPTION;
D O I
10.1039/c6ra20769c
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A new series of phenothiazine-based D-A-pi-A dyes PZ-1-4 have been designed, synthesized and fully characterized by H-1, C-13 NMR, HRMS, UV-vis, fluorescence, and cyclic voltammetry spectroscopy. Benzothiadiazole was introduced into the D-pi-A dyes as an additional acceptor. Various donors and new pi-spacers have been connected to phenothiazine skeleton on opposite sides to generate PZ-2-4 dyes. The DSSC devices have been systematically investigated by photoelectrochemical experiments, the solar cell of PZ-4 with a simple hexyloxyphenyl group achieves the highest photoelectric conversion efficiency of 6.35%. Density functional theory (DFT) calculation results demonstrate that the large dihedral angle (36.3 degrees) between the pi-spacer and phenothiazine in PZ-4 induces better charge separation. Its largest semicircle at intermediate frequencies in electrochemical impedance spectroscopy (EIS) prevents the recombination of photoelectrons injected into the titanium dioxide (TiO2) conductive band with I-3(-) in electrolyte, which might be caused by the blocking interaction of the hexyloxy group dye.
引用
收藏
页码:106380 / 106386
页数:7
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