Unravelling the Potential for Dithienopyrrole Sensitizers in Dye-Sensitized Solar Cells

被引:45
|
作者
Polander, Lauren E. [1 ]
Yella, Aswani [1 ]
Teuscher, Joel [1 ]
Humphry-Baker, Robin [1 ]
Curchod, Basile F. E. [2 ]
Astani, Negar Ashari [2 ]
Gao, Peng [1 ]
Moser, Jacques-E. [3 ]
Tayernelli, Ivano [2 ]
Rothlisberger, Ursula [2 ]
Graetzel, Michael [1 ]
Nazeeruddin, Md. Khaja [1 ]
Frey, Julien [1 ]
机构
[1] Ecole Polytech Fed Lausanne, Lab Photon & Interfaces, CH-1015 Lausanne, Switzerland
[2] Ecole Polytech Fed Lausanne, Lab Computat Chem & Biochem, CH-1015 Lausanne, Switzerland
[3] Ecole Polytech Fed Lausanne, Grp Photochem Dynam, Inst Chem Sci & Engn, Sch Basic Sci, CH-1015 Lausanne, Switzerland
基金
新加坡国家研究基金会; 瑞士国家科学基金会;
关键词
dye-sensitized solar cells; D-pi-A; dithienopyrrole; DENSITY FUNCTIONALS; ORGANIC-DYES; EFFICIENCY; RECOMBINATION; DESIGN;
D O I
10.1021/cm401144j
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Two D-pi-A dyes based on the dithieno[3,2-b:2',3'-d]pyrrole pi-bridge (DTP) were synthesized, characterized using UV-vis absorption spectroscopy and electrochemistry, modeled using quantum chemical calculations, and used as sensitizers in dye-sensitized solar cells (DSCs). The photoelectrochemical properties and DSC performance are thoroughly compared with their cyclopenta[1,2-b:5,4-b']dithiophene (CPDT) analogues. The use of DTP results in a small increase in the zero zero transition energy reflecting the higher lying lowest unoccupied molecular orbital that is commonly reported for DTP relative to CPDT systems. This increased optical gap manifests in slightly blue-shifted incident photon-to-collected electron conversion efficiency (IPCE) responses; however, increased open-circuit photovoltage values and improved charge-transfer kinetics relative to the CPDT systems result in comparable power conversion efficiencies. The present report highlights the potential of DTP for the development of tailored sensitizers employing stronger acceptors.
引用
收藏
页码:2642 / 2648
页数:7
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