Molecular engineering of organic sensitizers for dye-sensitized solar cell applications

被引:655
作者
Hagberg, Daniel P. [1 ]
Yum, Jun-Ho [2 ]
Lee, HyoJoong [2 ]
De Angelis, Filippo [3 ]
Marinado, Tannia
Karlsson, Karl Martin [1 ]
Humphry-Baker, Robin [2 ]
Sun, Licheng [1 ]
Hagfeldt, Anders
Graetzel, Michael [2 ]
Nazeeruddin, Md. K. [2 ]
机构
[1] Royal Inst Technol, Ctr Mol Devices, S-10044 Stockholm, Sweden
[2] Swiss Fed Inst Technol, Sch Basic Sci, Inst Chem Sci & Engn, Lab Photon & Interfaces, CH-1015 Lausanne, Switzerland
[3] Univ Perugia, Dipartimento Chim, Ist CNR Sci & Tecnol Mol, I-06123 Perugia, Italy
关键词
D O I
10.1021/ja800066y
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Novel unsymmetrical organic sensitizers comprising donor, electron-conducting, and anchoring groups were engineered at a molecular level and synthesized for sensitization of mesoscopic titanium dioxide injection solar cells. The unsymmetrical organic sensitizers 3-(5-(4-(diphenylamino)styryl)thiophen-2-yl)-2-cyanoacrylic acid (D5), 3-(5-bis(4-(diphenylamino)styryl)thiophen-2-yl)-2-cyanoacrylic acid (D7), 5-(4-(bis(4-methoxyphenylamino)styryl)thiophen-2-yl)-2-cyanoacrylic acid (D9), and 3-(5-bis(4,4'-dimethoxydiphenylamino)styryl)thiophen-2-yl)-2-cyanoacrylic acid (D11) anchored onto TiO2 and were tested in dye-sensitized solar cell with a volatile electrolyte. The monochromatic incident photon-to-current conversion efficiency of these sensitizers is above 80%, and D11-sensitized solar cells yield a short-circuit photocurrent density of 13.90 +/- 0.2 mA/cm(2), an open-circuit voltage of 740 +/- 10 mV, and a fill factor of 0.70 +/- 0.02, corresponding to an overall conversion efficiency of 7.20% under standard AM 1.5 sun light. Detailed investigations of these sensitizers reveal that the long electron lifetime is responsible for differences in observed open-circuit potential of the cell. As an alternative to liquid electrolyte cells, a solid-state organic hole transporter is used in combination with the D9 sensitizer, which exhibited an efficiency of 3.25%. Density functional theory/time-dependent density functional theory calculations have been employed to gain insight into the electronic structure and excited states of the investigated species.
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页码:6259 / 6266
页数:8
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