钨酸盐
过电位
动力学
铋
光催化
异质结
氧化锡
交换电流密度
反应速率常数
材料科学
基质(水族馆)
分解水
化学
氧化物
塔菲尔方程
化学工程
无机化学
冶金
催化作用
电极
物理化学
电化学
光电子学
工程类
物理
海洋学
量子力学
生物化学
地质学
作者
Guangming Cao,Jundie Hu,Yuanxing Wang,Jiafu Qu,Dekun Ma,Jiaqi Jin,Wei Sun,Xiaogang Yang,Chang Ming Li
标识
DOI:10.1016/j.apsusc.2022.156081
摘要
Charge separation and transfer kinetics play a significant role in photocatalytic water oxidation, which is sensitive to the crystal facets. Herein, the bismuth tungstate (Bi2WO6) films were used as a model photoanode to investigate how the photogenerated charges react on {1 3 1} and {2 0 0} facets under constantly applied bias in a photoelectrochemical (PEC) cell. On the WO3 electron transport layer, the Bi2WO6 films have a {2 0 0} orientation while possessing a {1 3 1} orientation on the fluorine-doped tin oxide substrate. It is discovered that {2 0 0} facets on the WO3/Bi2WO6 heterojunction display a low overpotential of PEC water oxidation, showing a 1st-order reaction behavior and faster charge transfer rate constant. Differently, water oxidation on the {1 3 1} facet on Bi2WO6 displays a 2nd-order reaction behavior. Further, density functional theory calculations were applied to demonstrate how the rate-determining step and the major formed intermediate correlate with the charge accumulation and reaction orders. The findings of this work shed fundamental light on how to rationally design and precisely modulate surface charge density and reaction kinetics for efficient (photo)electrocatalysts.
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