Control of Molecular Arrangement and/or Orientation of D-π-A Fluorescent Dyes for Dye-sensitized Solar Cells

被引:18
作者
Ooyama, Yousuke [1 ]
Ohshita, Joji [1 ]
Harima, Yutaka [1 ]
机构
[1] Hiroshima Univ, Grad Sch Engn, Dept Appl Chem, Hiroshima 7398527, Japan
基金
日本科学技术振兴机构;
关键词
SOLID-STATE FLUORESCENCE; ORGANIC-DYES; STRUCTURAL ISOMERS; ENERGY-CONVERSION; ANCHORING GROUP; PYRIDINE RING; RUTHENIUM SENSITIZERS; EFFICIENCY; TIO2; DESIGN;
D O I
10.1246/cl.2012.1384
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Dye-sensitized solar cells (DSSCs) based on organic dyes adsorbed on TiO2 electrodes, which emerged as a new generation of sustainable photovoltaic devices, have received considerable attention because of high incident solar light-to-electricity conversion efficiency and low cost of production. The aim of this Highlight Review is to indicate the importance of creating effective D-pi-A dye sensitizers capable of controlling not only photophysical and electrochemical properties of the dyes themselves but also molecular arrangement and/or orientation of the dyes on TiO2 surface to provide a good electron communication between the dye and TiO2 electrode, for developing high-performance DSSCs.
引用
收藏
页码:1384 / 1396
页数:13
相关论文
共 81 条
[41]   Kinetic and Energetic Paradigms for Dye-Sensitized Solar Cells: Moving from the Ideal to the Real [J].
O'Regan, Brian C. ;
Durrant, James R. .
ACCOUNTS OF CHEMICAL RESEARCH, 2009, 42 (11) :1799-1808
[42]   New Photovoltaic Devices Based on the Sensitization of p-type Semiconductors: Challenges and Opportunities [J].
Odobel, Fabrice ;
Le Pleux, Loic ;
Pellegrin, Yann ;
Blart, Errol .
ACCOUNTS OF CHEMICAL RESEARCH, 2010, 43 (08) :1063-1071
[43]  
Ooyama Y., 2010, EUR J ORG CHEM, P92
[44]  
Ooyama Y., 2012, CHEMPHYSCHE IN PRESS, DOI [10.1002/cphc.201200218, DOI 10.1002/CPHC.201200218]
[45]  
Ooyama Y., 2011, Angew. Chemie., V123, P7567, DOI [DOI 10.1002/ANGE.201102552, 10.1002/ange.201102552]
[46]   Synthesis of new-type donor-acceptor π-conjugated benzofuro[2,3-c]oxazolo[4,5-a]carbazole fluorescent dyes and their photovoltaic performances of dye-sensitized solar cells [J].
Ooyama, Yousuke ;
Shimada, Yoshihito ;
Kagawa, Yusuke ;
Yamada, Yuuki ;
Imae, Ichiro ;
Komaguchi, Kenji ;
Harima, Yutaka .
TETRAHEDRON LETTERS, 2007, 48 (52) :9167-9170
[47]   Dye-sensitized solar cells based on novel donor-acceptor π-conjugated benzofuro[2,3-c]oxazolo[4,5-a]carbazole-type fluorescent dyes exhibiting solid-state fluorescence [J].
Ooyama, Yousuke ;
Ishii, Akihiro ;
Kagawa, Yusuke ;
Imae, Ichiro ;
Harima, Yutaka .
NEW JOURNAL OF CHEMISTRY, 2007, 31 (12) :2076-2082
[48]   Synthesis and solid-state fluorescence properties of structural isomers of novel benzofuro[2,3-c]oxazolocarbazole-type fluorescent dyes [J].
Ooyama, Yousuke ;
Kagawa, Yusuke ;
Harima, Yutaka .
EUROPEAN JOURNAL OF ORGANIC CHEMISTRY, 2007, 2007 (22) :3613-3621
[49]   Photovoltaic performance of dye-sensitized solar cells based on donor acceptor π-conjugated benzofuro[2,3-c]oxazolo[4,5-a] carbazole-type fluorescent dyes with a carboxyl group at different positions of the chromophore skeleton [J].
Ooyama, Yousuke ;
Shimada, Yoshihito ;
Kagawa, Yusuke ;
Imae, Ichiro ;
Harima, Yutaka .
ORGANIC & BIOMOLECULAR CHEMISTRY, 2007, 5 (13) :2046-2054
[50]   Dramatic effects of the substituents on the solid-state fluorescence properties of structural isomers of novel benzofuro[2,3-c]oxazolocarbazole-type fluorophores [J].
Ooyama, Yousuke ;
Harima, Yutaka .
CHEMISTRY LETTERS, 2006, 35 (08) :902-903