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发布时间：2019-03-09

论文类型：期刊论文

发表时间：2013-12-01

发表刊物：JOURNAL OF MOLECULAR MODELING

收录刊物：Scopus、PubMed、SCIE

卷号：19

期号：12

页面范围：5317-5325

ISSN号：1610-2940

关键字：Dye-sensitized solar cell; Organic sensitizer; TDDFT; Absorption spectrum; Charge transfer; Charge difference density

摘要：The electronic structures of three D-A-pi-A indoline dyes (WS-2, WS-6, and WS-11) used in dye-sensitized solar cells (DSSCs) were studied by performing quantum chemistry calculations. The coplanarity of the A-pi-A segment and distinct noncoplanarity of the indoline donor part of each dye were confirmed by checking the calculated geometric parameters. The relationships between molecular modifications and the optical properties of the dyes were derived in terms of the partial density of states, absorption spectrum, frontier molecular orbital, and excited-state charge transfer. 3D real-space analysis of the transition density (TD) and charge difference density (CDD) was also performed to further investigate the excited-state features of the molecular systems, as they provide visualized physical pictures of the charge separation and transfer. It was found that modifying the alkyl chain of the bridge unit near the acceptor unit is an efficient way to decrease dye aggregation and improve DSSC efficiency. Inserting a hexylthiophene group next to the donor unit leads to a complicated molecular structure and a decrease in the charge-transfer ability of the system, which has an unfavorable impact on DSSC performance.