The Influence of Charge Transport and Recombination on the Performance of Dye-Sensitized Solar Cells

被引:257
作者
Wang, Mingkui [1 ]
Chen, Peter [1 ]
Humphry-Baker, Robin [1 ]
Zakeeruddin, Shaik M. [1 ]
Graetzel, Michael [1 ]
机构
[1] Swiss Fed Inst Technol, Inst Chem Sci & Engn, Lab Photon & Interfaces, CH-1015 Lausanne, Switzerland
基金
瑞士国家科学基金会;
关键词
charge-carrier recombination; dye-sensitized solar cells; electron transport; impedance; nanocrystalline TiO(2); POROUS FILM ELECTRODES; NANOPOROUS TIO2; IMPEDANCE SPECTROSCOPY; CONVERSION EFFICIENCY; ENERGY-LEVELS; DIFFUSION; KINETICS; SEMICONDUCTOR; MICROSCOPY; CONSTANTS;
D O I
10.1002/cphc.200800708
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
Electrochemical impedance spectroscopy (EIS) and transient voltage decay measurements are applied to compare the performance of dye sensitized solar cells (DSCs) using organic electrolytes, ionic liquids and organic-hole conductors as hole transport materials (HTM). Nano-crystalline titania films sensitized by the some heteroleptic ruthenium complex NaRu(4-carboxylic acid-4'-carboxylate) (4,4'-dinonyl-2,2'-bipyridyl)(NCS)(2), coded Z-907Na are employed as working electrodes. The influence of the nature of the HTM on the photovoltaic figures of merit, that is, the open circuit voltage, short circuit photocurrent and fill factor is evaluated. In order to derive the electron lifetime, as well as the electron diffusion coefficient and charge collection efficiency, EIS measurements are performed in the dark and under illumination corresponding to realistic photovoltaic operating conditions of these mesoscopic solar cells. A theoretical model is established to interpret the frequency response off the impedance under open circuit conditions, which is conceptually similar to photovoltage transient decay measurements. Important information on factors that govern the dynamics of electron transport within the nanocrystalline TiO(2) film and charge recombination across the dye sensitized heterojunction is obtained.
引用
收藏
页码:290 / 299
页数:10
相关论文
共 49 条
[1]   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
[2]  
BACH U, 2000, THESIS SWISS FEDERAL
[3]  
Bard A.J., 2001, ELECTROCHEMICAL METH
[4]  
Benkstein KD, 2003, J PHYS CHEM B, V107, P7759, DOI 10.1021/jp0226811
[5]  
Bisquert J, 2002, J PHYS CHEM B, V106, P325, DOI 10.1021/jp01194lg
[6]   Physical chemical principles of photovoltaic conversion with nanoparticulate, mesoporous dye-sensitized solar cells [J].
Bisquert, J ;
Cahen, D ;
Hodes, G ;
Rühle, S ;
Zaban, A .
JOURNAL OF PHYSICAL CHEMISTRY B, 2004, 108 (24) :8106-8118
[7]   Determination of rate constants for charge transfer and the distribution of semiconductor and electrolyte electronic energy levels in dye-sensitized solar cells by open-circuit photovoltage decay method [J].
Bisquert, J ;
Zaban, A ;
Greenshtein, M ;
Mora-Seró, I .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2004, 126 (41) :13550-13559
[8]   Interpretation of the time constants measured by kinetic techniques in nanostructured semiconductor electrodes and dye-sensitized solar cells [J].
Bisquert, J ;
Vikhrenko, VS .
JOURNAL OF PHYSICAL CHEMISTRY B, 2004, 108 (07) :2313-2322
[9]   Analysis of the mechanisms of electron recombination in nanoporous TiO2 dye-sensitized solar cells.: Nonequilibrium steady-state statistics and interfacial electron transfer via surface states [J].
Bisquert, J ;
Zaban, A ;
Salvador, P .
JOURNAL OF PHYSICAL CHEMISTRY B, 2002, 106 (34) :8774-8782
[10]   Influence of the boundaries in the impedance of porous film electrodes [J].
Bisquert, J .
PHYSICAL CHEMISTRY CHEMICAL PHYSICS, 2000, 2 (18) :4185-4192