Efficient Structural Modification of Triphenylamine-Based Organic Dyes for Dye-Sensitized Solar Cells

• Published in: Journal of physical chemistry. C Vol. 112; no. 30; pp. 11591 - 11599
• Main Authors: Li, Gang, Jiang, Ke-Jian, Li, Ying-Feng, Li, Shao-Lu, Yang, Lian-Ming
• Format: Journal Article
• Language: English
• Published: American Chemical Society 31.07.2008
• Subjects: C: Energy Conversion and Storage
• ISSN: 1932-7447; 1932-7455
• DOI: 10.1021/jp802436v

A series of new organic D−π−A dyes, coded as DS-1, DS-2, DS-3, and DS-4, was designed, synthesized, and characterized by 1H NMR,13C NMR, infrared spectroscopy, mass spectrometry, and elemental analysis. These dyes consist of a di(p-tolyl)phenylamine moiety as an electron donor, a cyanoacetic acid moiety as an electron acceptor/anchoring group, and different types of conducting thiophene units as electron spacers to bridge the donor and acceptor. It was found that both the use of di(p-tolyl)phenylamine donor and the variation of electron spacers in the D−π−A dyes played an essential role in modifying and/or tuning physical properties of organic dyes. These dyes were developed as sensitizers for the application in dye-sensitized TiO2 nanocrystalline solar cells (DSSCs), and their photophysical and electrochemical properties were investigated. The DSSCs based on the dyes gave good performance in terms of incident photon-to-current conversion efficiency (IPCE) in the range of 400−700 nm. A solar-energy-to-electricity conversion efficiency (η) of 7.00% was obtained with the DSSC based on 5-[[2-[p-(di-p-tolylamino)]styryl]thiophene-yl]thiophene-2-cyanoacrylic acid (DS-2) under simulated AM 1.5 G irradiation (100 mW/cm2): short-circuit current density (J sc) of 15.3 mA cm−2; open-circuit voltage (V oc) of 0.633 V; fill factor (FF) of 0.725. The density functional theory (DFT) calculation suggests that the electron-transfer distribution moves from the donor unit to the acceptor under light irradiation, which means efficient intramolecular charge transfer.