Electron transport and back reaction in nanocrystalline TiO2 films prepared by hydrothermal crystallization

被引:191
作者
Oekermann, T
Zhang, D
Yoshida, T
Minoura, H
机构
[1] Gifu Univ, Grad Sch Engn, ERES Div, Gifu 5011193, Japan
[2] Leibniz Univ Hannover, Inst Phys Chem & Elektrochem, D-30167 Hannover, Germany
关键词
D O I
10.1021/jp034918z
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
The electron transport and back reaction in nanocrystalline TiO2 films prepared at low temperature using a new hydrothermal crystallization method on conductive glass and plastic substrates have been investigated by intensity modulated photocurrent spectroscopy (IMPS) and intensity modulated photovoltage spectroscopy (IMVS). The hydrothermal method enables the preparation of crack-free TiO2 thick films and at the same time enhances the electron transport compared to films prepared by low-temperature sintering, providing a path towards efficient photoelectrode materials for flexible dye-sensitized solar cells. UV/ozone treatment of the films enables the removal of residual organics left from the hydrothermal preparation process. Since these organics represent surface states that mediate the back reaction of electrons, the electron lifetime is increased by their removal, while the electron transport is not enhanced significantly. High-temperature sintering of the hydrothermally prepared films leads to both a removal of the surface states and a significant enhancement of the electron transport properties. Interestingly, the electron lifetimes are not changed by high-temperature sintering, since faster electron transport and less surface states have opposite effects on the back reaction process. These films showed improved electron transport properties and efficiencies even if compared with films prepared by conventional high-temperature methods, which shows the high potential for the further development of the hydrothermal method.
引用
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页码:2227 / 2235
页数:9
相关论文
共 34 条
[21]  
Peter L. M., 1999, ADV ELECTROCHEMICAL, V6
[22]   Intensity dependence of the electron diffusion length in dye-sensitised nanocrystalline TiO2 photovoltaic cells [J].
Peter, LM ;
Wijayantha, KGU .
ELECTROCHEMISTRY COMMUNICATIONS, 1999, 1 (12) :576-580
[23]   Electron transport and back reaction in dye sensitised nanocrystalline photovoltaic cells [J].
Peter, LM ;
Wijayantha, KGU .
ELECTROCHIMICA ACTA, 2000, 45 (28) :4543-4551
[24]  
Pichot F, 2000, LANGMUIR, V16, P5626, DOI [10.1021/la000095i, 10.1021/1a000095i]
[25]   Titania nanostructured films derived from a titania nanosheet/polycation multilayer assembly via heat treatment and UV irradiation [J].
Sasaki, T ;
Ebina, Y ;
Fukuda, K ;
Tanaka, T ;
Harada, M ;
Watanabe, M .
CHEMISTRY OF MATERIALS, 2002, 14 (08) :3524-3530
[26]   ANOMALOUS TRANSIT-TIME DISPERSION IN AMORPHOUS SOLIDS [J].
SCHER, H ;
MONTROLL, EW .
PHYSICAL REVIEW B, 1975, 12 (06) :2455-2477
[27]   Band edge movement and recombination kinetics in dye-sensitized nanocrystalline TiO2 solar cells: A study by intensity modulated photovoltage spectroscopy [J].
Schlichthorl, G ;
Huang, SY ;
Sprague, J ;
Frank, AJ .
JOURNAL OF PHYSICAL CHEMISTRY B, 1997, 101 (41) :8141-8155
[28]   THEORETICAL-MODELS FOR THE ACTION SPECTRUM AND THE CURRENT-VOLTAGE CHARACTERISTICS OF MICROPOROUS SEMICONDUCTOR-FILMS IN PHOTOELECTROCHEMICAL CELLS [J].
SODERGREN, S ;
HAGFELDT, A ;
OLSSON, J ;
LINDQUIST, SE .
JOURNAL OF PHYSICAL CHEMISTRY, 1994, 98 (21) :5552-5556
[29]   Electron transport in the nanostructured TiO2-electrolyte system studied with time-resolved photocurrents [J].
Solbrand, A ;
Lindstrom, H ;
Rensmo, H ;
Hagfeldt, A ;
Lindquist, SE ;
Sodergren, S .
JOURNAL OF PHYSICAL CHEMISTRY B, 1997, 101 (14) :2514-2518
[30]  
SOMMELING PM, 2001, 16 EUR PHOT SOL EN C, V1, P67