Parameters influencing charge separation in solid-state dye-sensitized solar cells using novel hole conductors

被引:167
作者
Kroeze, Jessica E.
Hirata, Narukuni
Schmidt-Mende, Lukas
Orizu, Charles
Ogier, Simon D.
Carr, Kathryn
Graetzel, Michael
Durrant, James R.
机构
[1] Univ London Imperial Coll Sci Technol & Med, Ctr Elect Mat & Devices, London SW7 2AY, England
[2] Swiss Fed Inst Technol, Inst Chem Sci & Engn, Lab Photon & Interfaces, CH-1015 Lausanne, Switzerland
[3] Merck Chem Ltd, Manchester Tech Ctr, Manchester M9 8ZS, Lancs, England
关键词
D O I
10.1002/adfm.200500748
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Solid-state dye-sensitized solar cells employing a solid organic hole-transport material (HTM) are currently under intensive investigation, since they offer a number of practical advantages over liquid-electrolyte junction devices. Of particular importance to the design of such devices is the control of interfacial charge transfer. In this paper, the factors that determine the yield of hole transfer at the dye/HTM interface and its correlation with solid-state-cell performance are identified. To this end, a series of novel triarylamine type oligomers, varying in molecular weight and mobility, are studied. Transient absorption spectroscopy is used to determine hole-transfer yields and pore-penetration characteristics. No correlation between hole mobility and cell performance is observed. However, it is found that the photocurrent is directly proportional to the hole-transfer yield. This hole-transfer yield depends on the extent of pore penetration in the dye-sensitized film as well as on the thermodynamic driving force Delta G(dye-HTM) for interfacial charge transfer. Future design of alternative solid-state HTMs should focus on the optimization of pore-filling properties and the control of interfacial energetics rather than on increasing material hole mobilities.
引用
收藏
页码:1832 / 1838
页数:7
相关论文
共 41 条
[1]   Charge separation in solid-state dye-sensitized heterojunction solar cells [J].
Bach, U ;
Tachibana, Y ;
Moser, JE ;
Haque, SA ;
Durrant, JR ;
Grätzel, M ;
Klug, DR .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1999, 121 (32) :7445-7446
[2]   Solid-state dye-sensitized mesoporous TiO2 solar cells with high photon-to-electron conversion efficiencies [J].
Bach, U ;
Lupo, D ;
Comte, P ;
Moser, JE ;
Weissörtel, F ;
Salbeck, J ;
Spreitzer, H ;
Grätzel, M .
NATURE, 1998, 395 (6702) :583-585
[3]  
Barbe CJ, 1997, J AM CERAM SOC, V80, P3157, DOI 10.1111/j.1151-2916.1997.tb03245.x
[4]   A SOLID-STATE, DYE-SENSITIZED PHOTOELECTROCHEMICAL CELL [J].
CAO, F ;
OSKAM, G ;
SEARSON, PC .
JOURNAL OF PHYSICAL CHEMISTRY, 1995, 99 (47) :17071-17073
[5]   Solid-state Ru-dye solar cells using polypyrrole as a hole conductor [J].
Cervini, R ;
Cheng, YB ;
Simon, G .
JOURNAL OF PHYSICS D-APPLIED PHYSICS, 2004, 37 (01) :13-20
[6]   Spectroscopic determination of electron and mole effective masses in a nanocrystalline semiconductor film [J].
Enright, B ;
Fitzmaurice, D .
JOURNAL OF PHYSICAL CHEMISTRY, 1996, 100 (03) :1027-1035
[7]   Dye-sensitized solid-state heterojunction solar cells [J].
Grätzel, M .
MRS BULLETIN, 2005, 30 (01) :23-27
[8]   Transient optical studies of interfacial energetic disorder at nanostructured dye-sensitised inorganic/organic semiconductor heterojunctions [J].
Haque, SA ;
Park, T ;
Holmes, AB ;
Durrant, JR .
CHEMPHYSCHEM, 2003, 4 (01) :89-+
[9]   Charge separation versus recombination in dye-sensitized nanocrystalline solar cells: the minimization of kinetic redundancy [J].
Haque, SA ;
Palomares, E ;
Cho, BM ;
Green, ANM ;
Hirata, N ;
Klug, DR ;
Durrant, JR .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2005, 127 (10) :3456-3462
[10]   Interface engineering for solid-state dye-sensitized nanocrystalline solar cells: The use of ion-solvating hole-transporting polymers [J].
Haque, SA ;
Park, T ;
Xu, C ;
Koops, S ;
Schulte, N ;
Potter, RJ ;
Holmes, AB ;
Durrant, JR .
ADVANCED FUNCTIONAL MATERIALS, 2004, 14 (05) :435-440