Photoelectrochemical Oxidation of Water Using Nanostructured BiVO4 Films

被引:214
作者
Berglund, Sean P. [1 ]
Flaherty, David W. [1 ]
Hahn, Nathan T. [1 ]
Bard, Allen J. [2 ,3 ]
Mullins, C. Buddie [1 ,2 ,3 ]
机构
[1] Univ Texas Austin, Texas Mat Inst, Ctr Electochem, Dept Chem Engn, Austin, TX 78712 USA
[2] Univ Texas Austin, Texas Mat Inst, Ctr Electochem, Dept Chem & Biochem, Austin, TX 78712 USA
[3] Univ Texas Austin, Ctr Nano & Mol Sci, Austin, TX 78712 USA
基金
美国国家科学基金会;
关键词
REACTIVE BALLISTIC DEPOSITION; VISIBLE-LIGHT IRRADIATION; THIN-FILMS; HYDROTHERMAL PREPARATION; ASSISTED SYNTHESIS; PHOTOCATALYSTS; CRYSTALLINE; OXIDE; PHOTOOXIDATION; DECOMPOSITION;
D O I
10.1021/jp1109459
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
Nanostructured BiVO4 films were synthesized by coevaporation of bismuth and vanadium in an oxygen ambient, a process referred to as reactive ballistic deposition (RBD). The films were tested in various electrolyte solutions to assess their activity for photoelectrochemical water oxidation. Deposition parameters, including the V/Bi atomic flux ratio and the incident angle of deposition, were adjusted. Films deposited with excess vanadium (V/Bi = 2) and incident angles of deposition at 65 degrees showed the highest initial photocurrents with IPCE values above 21% for light wavelengths of 340-460 nm (in 0.5 M Na2SO4 at 1.0 V vs Ag/AgCl). With continued illumination the excess vanadium in these films dissolved into the electrolyte and the photocurrents dropped by 60-75% before reaching steady state. The steady-state photocurrent and IPCE values (above 14% for 340-460 nm light) were higher than the initial values for films synthesized with stoichiometric amounts of vanadium and bismuth (V/Bi = 1) and incident angles of deposition at 65 degrees. Stoichiometric BiVO4 films remained stable under illumination but their photocurrents were limited by surface reaction kinetics. The addition of cobalt as an electrocatalyst to the surface of these films increased their photocurrent by a factor of 3.
引用
收藏
页码:3794 / 3802
页数:9
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