Effects of anchoring groups in multi-anchoring organic dyes with thiophene bridge for dye-sensitized solar cells

被引:62
作者
Yang, Yu Seok [1 ]
Do Kim, Hyung [1 ]
Ryu, Jang-Hyun [2 ]
Kim, Kyung Kon [2 ]
Park, Sung Soo [3 ]
Ahn, Kwang-Soon [1 ]
Kim, Jae Hong [1 ]
机构
[1] Yeungnam Univ, Dept Display & Chem Engn, Kyongsan 712749, Gyeongbuk, South Korea
[2] Korea Inst Sci & Technol, Solar Cell Res Ctr, Seoul 136791, South Korea
[3] Samsung Electromech, CAE Grp, Suwon 443743, South Korea
基金
新加坡国家研究基金会;
关键词
Dye-sensitized solar cells; Organic dyes; Multi-anchoring groups; Short-circuit current enhancement; Thiophene bridge; Structure optimization; HIGH-EFFICIENCY; COUMARIN DYES; MOLECULAR DESIGN; MOIETY;
D O I
10.1016/j.synthmet.2011.02.012
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Organic photo-sensitizers were designed and synthesized based on a phenothiazine framework containing single- and double-electron acceptors that were bridged with thiophene for the dye sensitized solar cells (DSSCs). The optimized geometries were determined with density functional theory (DFT) calculations to estimate the photovoltaic properties of the dyes in the design stage. The organic dye with the double electron acceptors exhibited a better light absorption at long wavelength and an effective electron extraction pathway from the electron donor to the TiO2 surface, leading to an improved short-circuit current (11.6 mA cm(-2)), compared with that of the dye with the single electron acceptor (10.2 mA cm(-2)) and the conventional N3 Ru-dye (10.4 mA cm(-2)). Contrarily, the open-circuit voltage of the organic dye with the double electron acceptors decreased because the additional protonated carboxylic groups caused a positive shift in the Fermi level of TiO2. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:850 / 855
页数:6
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