A comparison of water photo-oxidation and photo-reduction using photoelectrodes surface-modified by deposition of co-catalysts: Insights from photo-electrochemical impedance spectroscopy

被引:11
作者
Antuch, M. [1 ]
El Rouby, W. M. A. [1 ,2 ]
Millet, P. [1 ]
机构
[1] Paris Sud Univ, ICMMO Eriee, CNRS, UMR 8182, F-91405 Orsay, France
[2] Beni Suef Univ, Mat Sci & Nanotechnol Dept, Fac Postgrad Studies Adv Sci, Bani Suwayf 62511, Egypt
关键词
Water photo-oxidation; Water photo-reduction; Titanium dioxide nanorods; Strontium titanate; ZIF-67; MOF; CHARGE-TRANSFER; EVOLUTION; TIO2; PHOTOANODES; OXIDATION; KINETICS; CATALYST; GROWTH; ZIF-67; CUWO4;
D O I
10.1016/j.ijhydene.2018.11.214
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 purpose of this research paper is to highlight the similarities in the kinetic treatment between water photo-oxidation into molecular oxygen and water photo-reduction into molecular hydrogen, using photoelectrodes surface modified by deposition of co-catalysts. Photo-anodes made of TiO2 nanorods surface-covered by crystals of cobalt Zeolitic Imidazolate Framework (ZIF-67), and photo-cathodes made of Rh:SrTiO3 particles surface modified by adsorption of molecules of trisdioximate hexa-chlorine cobalt (II) clathrochelate (Co(Cl(2)Gm)(3)(BCH3)(2)), have been prepared and used for water photo-oxidation and photo-reduction experiments, respectively. Both photoelectrodes have been characterized by SEM and cyclic voltammetry under illumination conditions. Charge transfer mechanisms have been investigated by photo-electrochemical impedance spectroscopy (PEIS). It is shown that for both systems, the presence of a co-catalyst increases the charge transfer kinetics, and that the trapping resistance is larger than the charge transfer resistance, at any operating potential. (C) 2018 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:9970 / 9977
页数:8
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