材料科学
光催化
兴奋剂
苯酚
白钨矿
降级(电信)
带隙
可见光谱
密度泛函理论
光化学
吸附
化学工程
X射线光电子能谱
单斜晶系
纳米技术
光电子学
计算化学
分子
催化作用
化学
物理化学
有机化学
计算机科学
电信
工程类
钨
冶金
作者
M Zadiranov Yu.,Yiming Tang,Yuxin Liao,Wanhan He,Xinxin Lu,Xin Li
标识
DOI:10.1016/j.jmst.2023.06.002
摘要
The monoclinic scheelite BiVO4 has impressive properties such as a narrow energy band gap, exceptional stability, and extended absorption in visible light, making it a suitable photoanode. Nevertheless, the BiVO4 material encounters challenges such as the high recombination rate of photogenerated electron-hole pairs and poor photoelectron conductivity, which limits photocatalytic activity. To address this problem, we developed Mo-doped BiVO4 films on FTO substrates for photoelectrocatalytic degradation of phenol. When exposed to visible light, the Mo-BiVO4 film attained a 70% degradation of phenol in 120 min with a 1.2 V vs. Ag/AgCl bias—a 3.7 times improvement from pristine BiVO4. Mo-doping facilitates better migration and separation of electron-hole pairs and increases the concentration of photogenerated carriers, leading to an upward shift of the valence band potential direction, and an improvement in oxidation capacity. Furthermore, density-functional theory (DFT) calculations were used to explain how Mo-doping with BiVO4 improves the adsorption energy to phenol degradation intermediates, emphasizing its effectiveness in promoting phenol degradation. Therefore, with the inclusion of DFT calculations, this work provides a more comprehensive understanding of the mechanism underlying the enhancement of photocatalytic activity by Mo-doped BiVO4, which is crucial information for the further development of effective and efficient photoanodes.
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