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Improving the photoelectrochemical catalytic ability of bismuth vanadate electrodes by depositing efficient Co-catalysts

钒酸铋 光电流 电极 可逆氢电极 催化作用 材料科学 化学工程 光催化 电化学 无机化学 分解水 化学 工作电极 光电子学 冶金 物理化学 工程类 生物化学
作者
Shan-Lung Chen,Lu‐Yin Lin,Yu-Shiang Chen
出处
期刊:Electrochimica Acta [Elsevier BV]
卷期号:295: 507-513 被引量:28
标识
DOI:10.1016/j.electacta.2018.10.174
摘要

Depositing effective co-catalysts with an excellent electrocatalytic ability is one of the most efficient ways to solve the serious surface charge recombination for BiVO4 as the photocatalyst toward water oxidation. Five cheap co-catalysts based on nickel, cobalt and iron were synthesized and deposited on BiVO4 electrodes using hydrothermal synthesis and electrodeposition methods. The negatively shifted onset potentials and higher photocurrent densities were obtained for the BiVO4 electrodes with co-catalyst depositions. The best photoelectrochemical performance toward catalysing water oxidation was attained for the NiOOH/BiVO4 electrode, owing to the better intrinsic properties of NiOOH and the continuous film on the BiVO4 surface to improve the connection between nanoparticles. The loading amount of NiOOH on the BiVO4 electrode was optimized by varying the photo-assisted electrodeposition times. The NiOOH/BiVO4 electrode prepared using 15 min for the photo-assisted electrodeposition showed the highest photocurrent density of 2.10 mA/cm2 at 1.23 V versus reversible hydrogen electrode under air mass 1.5 global illumination. The BiVO4 electrode without the co-catalyst deposition only presented a photocurrent density of 0.30 mA/cm2 measured at the same conditions. The negatively shifted onset potential, smaller charge transfer resistance and the better long-term stability were also attained for the NiOOH/BiVO4 electrode. The excellent photoelectrochemical catalytic ability for the NiOOH/BiVO4 electrode is primarily owing to the reduced surface charge recombination and the continuous film of NiOOH on the BiVO4 electrode for achieving better connection between nanoparticles. This study confirms the function of co-catalysts and provides a systematic comparison of cheap co-catalysts deposited on the promising monoclinic BiVO4 electrode on the enhancement of the photoelectrochemical catalytic performance toward water oxidation. It is also suggested that the adequate deposition amount of the co-catalyst is of the great importance for improving the catalytic ability of the co-catalyst/photocatalyst system.
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