Current density versus potential characteristics of dye-sensitized nanostructured semiconductor photoelectrodes. 1. Analytical expressions

被引:57
作者
Lee, JJ
Coia, GM
Lewis, NS
机构
[1] Portland State Univ, Dept Chem, Portland, OR 97207 USA
[2] CALTECH, Noyes Lab, Div Chem & Chem Engn, Pasadena, CA 91125 USA
关键词
D O I
10.1021/jp035194u
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
A closed-form analytical model is developed to describe the steady-state current density-potential (J-E) characteristics of dye-sensitized nanostructured semiconductor photoelectrodes. The basic components of the model are a set of differential equations that describe the generation, recombination, and transport of charge carriers in mesoporous semiconductor electrode systems. Charge-carrier transport is treated as a diffusion process, and semiclassical Marcus theory is used to describe the kinetics at the interfaces between the semiconductor and the contacting phase as well as the kinetics at the interfaces with adsorbed dye. The model relates explicitly, within a single formalism, the rate constants for charge transfer of the mesoporous membrane electrode system to conventional intramolecular and intermolecular electron-transfer rate constant expressions and to interfacial electron-transfer processes at planar metal or semiconductor electrodes. The near-equilibrium situation is considered by including the reverse electron-transfer pathways for each rate process of interest. The underlying physical and chemical factors that form the basis of the model are completely parameterized to facilitate input into a numerical simulation algorithm, thereby allowing facile generation of simulated J-E Curves for a wide range of experimental conditions.
引用
收藏
页码:5269 / 5281
页数:13
相关论文
共 42 条
[1]   THE TRANSPORT AND KINETICS OF PHOTOGENERATED CARRIERS IN COLLOIDAL SEMICONDUCTOR ELECTRODE PARTICLES [J].
ALBERY, WJ ;
BARTLETT, PN .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 1984, 131 (02) :315-325
[2]   Nature of photovoltaic action in dye-sensitized solar cells [J].
Cahen, D ;
Hodes, G ;
Grätzel, M ;
Guillemoles, JF ;
Riess, I .
JOURNAL OF PHYSICAL CHEMISTRY B, 2000, 104 (09) :2053-2059
[3]   Electron transport in porous nanocrystalline TiO2 photoelectrochemical cells [J].
Cao, F ;
Oskam, G ;
Meyer, GJ ;
Searson, PC .
JOURNAL OF PHYSICAL CHEMISTRY, 1996, 100 (42) :17021-17027
[4]   Does interfacial charge transfer compete with charge carrier recombination? A femtosecond diffuse reflectance investigation of TiO2 nanoparticles [J].
Colombo, DP ;
Bowman, RM .
JOURNAL OF PHYSICAL CHEMISTRY, 1996, 100 (47) :18445-18449
[5]   Dynamic response of dye-sensitized nanocrystalline solar cells: Characterization by intensity-modulated photocurrent spectroscopy [J].
Dloczik, L ;
Ileperuma, O ;
Lauermann, I ;
Peter, LM ;
Ponomarev, EA ;
Redmond, G ;
Shaw, NJ ;
Uhlendorf, I .
JOURNAL OF PHYSICAL CHEMISTRY B, 1997, 101 (49) :10281-10289
[6]   An electrical model of the dye-sensitized solar cell [J].
Ferber, J ;
Stangl, R ;
Luther, J .
SOLAR ENERGY MATERIALS AND SOLAR CELLS, 1998, 53 (1-2) :29-54
[7]   Modeling of photovoltage and photocurrent in dye-sensitized titanium dioxide solar cells [J].
Ferber, J ;
Luther, J .
JOURNAL OF PHYSICAL CHEMISTRY B, 2001, 105 (21) :4895-4903
[8]   Intensity dependence of the back reaction and transport of electrons in dye-sensitized nanacrystalline TiO2 solar cells [J].
Fisher, AC ;
Peter, LM ;
Ponomarev, EA ;
Walker, AB ;
Wijayantha, KGU .
JOURNAL OF PHYSICAL CHEMISTRY B, 2000, 104 (05) :949-958
[9]   TRANSIENT NEAR-INFRARED SPECTROSCOPY OF VISIBLE-LIGHT SENSITIZED OXIDATION OF I- AT COLLOIDAL TIO2 [J].
FITZMAURICE, DJ ;
FREI, H .
LANGMUIR, 1991, 7 (06) :1129-1137
[10]  
GERISCHER H, 1970, PHYSICAL CHEMISTRY A, V9, P463