Molecular engineering of quinoxaline dyes toward more efficient sensitizers for dye-sensitized solar cells

被引:28
作者
Yang, Li-Na [1 ]
Li, Shi-Cheng [1 ]
Li, Ze-Sheng [1 ]
Li, Quan-Song [1 ]
机构
[1] Beijing Inst Technol, Beijing Key Lab Photoelect Electrophoton Convers, Beijing Key Lab Chem Power Source & Green Catalys, Key Lab Cluster Sci,Minist Educ,Sch Chem, Beijing 100081, Peoples R China
基金
中国国家自然科学基金;
关键词
A-FEATURED SENSITIZERS; ORGANIC-DYES; ELECTRONIC-PROPERTIES; AUXILIARY ACCEPTOR; CONVERSION EFFICIENCIES; CHARGE RECOMBINATION; HIGHLY EFFICIENT; DONOR; DESIGN; CYCLOPENTADITHIOPHENE;
D O I
10.1039/c5ra00587f
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
D-A-p-A-featured organic dyes incorporating diphenylquinoxaline unit (such as IQ4) have shown great potential in anti-aggregation and broadening spectral response in the field of dye-sensitized solar cells (DSSCs). The crucial restriction for quinoxaline-based cell to attain higher efficiency is the relatively low photocurrent density (J(SC)). In the present work, three novel push-pull dyes only differing in electron donors, have been designed based on the IQ4 backbone, in order to further improve the light-harvesting capability of quinoxaline dyes and to examine the donor influence on dye performance. Theoretical analysis of the factors correlated with the J(SC) and open-circuit photovoltage (V-OC) demonstrate that, relative to the parent IQ4 dye, the NIQ4 dye bearing the elegant N-annulated perylene donor shows a good performance in light harvesting, electron injection, and dye regeneration, indicating an increased J(SC) potential for the related cell. Furthermore, despite possessing a smaller vertical dipole moment, the improved blocking effect of NIQ4 not only prevents unfavorable self-aggregation, but also effectively inhibits the parasitic back-recombination. Therefore, the NIQ4 is proposed to be a potential dye in DSSC applications.
引用
收藏
页码:25079 / 25088
页数:10
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