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    Please use this identifier to cite or link to this item: http://140.128.103.80:8080/handle/310901/23108


    Title: Highly efficient triarylene conjugated dyes for sensitized solar cells
    Authors: Chang, Y.J., Chow, T.J.
    Keywords: Acceptor groups;Donor groups;Dye-sensitized solar cells;Electrochemical measurements;Fill factor;High yield;Incident photon-to-current conversion efficiencies;LUMO energy levels;New series;Organic dye;Overall conversion efficiency;Phenyl group;Photochemical behaviors;Photophysical;Theoretical calculations;Time dependent density functional theory;Triarylamines
    Date: 2011
    Issue Date: 2013-06-04T08:22:40Z (UTC)
    Abstract: A new series of organic dyes containing a triarylamine donor group, a triarylene-linked bridging moiety, and a cyanoacrylic acid acceptor group were synthesized through a simple procedure in high yields. A selected set of substituents were added onto the phenyl group ortho to the cyanoacrylic acid in order to examine their influences on the performance of dye-sensitized solar cells (DSSCs). Their photochemical behaviors were examined under AM1.5 solar condition (100 mW cm -2). A typical device made with a compound containing a -CF 3 substituent (PSP-CF 3) displayed a short-circuit current (J sc) 15.16 mA cm -2, an open-circuit voltage (V oc) 0.68 V, a fill factor (ff) 0.68, corresponding to an overall conversion efficiency of 7.0% and a maximal monochromatic incident photon-to-current conversion efficiency (IPCE) 78%. Their photophysical and electrochemical properties were analyzed with the aid of a time-dependent density functional theory (TDDFT) model with the B3LYP functional. Their HOMO and LUMO energy levels are verified by both electrochemical measurements and theoretical calculations. ? 2011 The Royal Society of Chemistry.
    Relation: Journal of Materials Chemistry 21 (26) , pp. 9523-9531
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