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    Please use this identifier to cite or link to this item: https://irlib.pccu.edu.tw/handle/987654321/24009


    Title: Meta versus para substituent effect of organic dyes for sensitized solar cells
    Authors: Lin, YD (Lin, Yan-Duo)1
    Chien, CT (Chien, Ching-Ting)
    Lin, SY (Lin, Szu-Yu)
    Chang, HH (Chang, Heng-Hsuan)
    Liu, CY (Liu, Ching-Yang)
    Chow, TJ (Chow, Tahsin J.)
    Contributors: Dept Appl Chem
    Keywords: Dye-sensitized solar cell
    Meta substituent effect
    Stilbene
    Charge transfer
    Date: 2011-07
    Issue Date: 2013-01-16 14:14:58 (UTC+8)
    Abstract: A series of new metal-free organic donor-bridge-acceptor dyes comprising a triphenylamine moiety as the electron donor, and a cyanoacrylic acid (dye series A) or a carboxylic acid moiety (dye series B) as the electron acceptor were synthesized and utilized for dye-sensitized solar cells (DSSCs). The triphenylamine moiety was linked to the main chromophore through either a para or a meta position across a phenyl group in order to examine the difference of structural effect. Both types of compounds exhibited apparent solvatochromic shift in their fluorescence spectra, showing the ready formation of charge separated states in both the para and meta-isomers. Quantum mechanical calculations were performed by using the density functional theory (DFT) at the B3LYP/6-31G(d,p) level to gain insight into the electron distributions surrounding the par and meta-substituted triphenylamine groups. The movement of an electron from the donor to the acceptor under the irradiation of light can be depicted by the time-dependent DFT (TDDFT) calculations, and the results were compared with experimental observations. These dyes were used effectively as sensitizers in DSSCs after being absorbed on surface of nanocrystalline TiO(2). The incident photo-to-current conversion efficiency (IPCE) spectra of the para isomers are broader than that of the corresponding meta isomers, and the short-circuit current density (J(sc)) values of the former is also higher than the latter. Dyes of series A exhibited overall conversion efficiencies of 1.27-4.12%, depending on the relative values of J(sc), under AM 1.5G irradiation (100 mW cm(-2)). For dyes of series B, the para isomers showed overall better performance than the meta isomers, i.e., higher values for all three parameters J(sc), V(oc) (open-circuit voltage), and ff (fill factor), thus led to a higher conversion efficiency. (C) 2011 Elsevier B.V. All rights reserved.
    Relation: JOURNAL OF PHOTOCHEMISTRY AND PHOTOBIOLOGY A-CHEMISTRY Volume: 222 Issue: 1 Pages: 192-202
    Appears in Collections:[Department of Chemistry & Graduate Institute of Applied Chemistry ] journal articles

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