Bilayer n-WO3/p-Cu2O photoelectrode with photocurrent enhancement in aqueous electrolyte photoelectrochernical reaction

被引:24
作者
Minggu, Lorna Jeffery [1 ]
Ng, Kim Hang [1 ]
Kadir, Hasmida Abdul [1 ,2 ]
Bin Kassim, Mohammad [1 ,2 ]
机构
[1] Univ Kebangsaan Malaysia, Fuel Cell Inst, Ukm Bangi 43600, Selangor, Malaysia
[2] Univ Kebangsaan Malaysia, Fac Sci & Technol, Sch Chem Sci & Food Technol, Ukm Bangi 43600, Selangor, Malaysia
关键词
Photoelectrochemical; Electrodeposition; WO3; Cu2O; Photoelectrode; P-TYPE CU2O; SOLAR-HYDROGEN; H-2; EVOLUTION; WATER; COMPOSITE; PHOTOANODES; OXIDATION; ELECTRODEPOSITION; HETEROJUNCTION; DEGRADATION;
D O I
10.1016/j.ceramint.2014.07.135
中图分类号
TQ174 [陶瓷工业]; TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Bilayer n-WO3/p-Cu2O photoelectrode films on fluorine-doped tin oxide (FTO) coated glass have been synthesized by consecutive electrodeposition of tungsten trioxide (n-WO3) and cuprous oxide (p-Cu2O) films from acidic aqueous solution of peroxytungstate and basic aqueous solution of copper sulfate-lactic acid by electrodeposition method. The WO3 film was annealed at 350 degrees C for 30 min to obtain a crystalline WO3 before the second layer of Cu2O was incorporated. Photoelectrochemical characterization of the WO3, Cu2O and WO3/Cu2O photoelectrodes were carried out under 100 W xenon light illumination, in 0.5 M Na2SO4 solution with saturated calomel electrode (SCE) as a reference and a platinum wire as the counter electrode. Investigation on the oxidative nature of the Cu2O on both mono and bilayer electrode films was carried out and a mechanism scheme was suggested. The photocurrent generated by n-WO3/p-Cu2O bilayer photoelectrode was much higher compared to the plain n-WO3 and p-Cu2O. (C) 2014 Elsevier Ltd and Techna Group S.r.l. All rights reserved.
引用
收藏
页码:16015 / 16021
页数:7
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