光催化
光化学
可见光谱
催化作用
氧气
材料科学
空位缺陷
吸附
激进的
带隙
反应机理
降级(电信)
化学
光电子学
物理化学
有机化学
结晶学
计算机科学
电信
作者
Yanjuan Sun,Hong Wang,Xing Qian,Wen Cui,Jieyuan Li,Sujuan Wu,Lidong Sun
出处
期刊:Chinese Journal of Catalysis
[China Science Publishing & Media Ltd.]
日期:2019-05-01
卷期号:40 (5): 647-655
被引量:86
标识
DOI:10.1016/s1872-2067(19)63277-8
摘要
Bi2MoO6, a typical Bi-based photocatalyst, has received increasing interests and been widely applied in various fields. However, the visible light photocatalytic activity of Bi2MoO6 is still restricted by some obstacles, such as limited photo-response and low charge separation efficiency. In this work, we developed a facile method to introduce artificial oxygen vacancy into Bi2MoO6 microspheres, which could effectively address these problems and realize highly efficient visible light photocatalysis. The experimental and theoretical methods were combined to explore the effects of oxygen vacancy on the electronic structure, photocatalytic activity and the reaction mechanism toward NO removal. The results showed that the addition of NaBH4 during catalyst preparation induced the formation of oxygen vacancy in Bi2MoO6, which plays a significant role in extending the visible light absorption of Bi2MoO6. The visible light photocatalytic activity of Bi2MoO6 with oxygen vacancy was obviously enhanced with a NO removal ratio of 43.5%, in contrast to that of 25.0% with the pristine Bi2MoO6. This can be attributed to the oxygen vacancy that creates a defect energy level in the band gap of Bi2MoO6, thus facilitating the charge separation and transfer processes. Hence, more reactive radicals were generated and participated in the photocatalytic NO oxidation reaction. The in situ FT-IR was used to dynamically monitor the photocatalytic NO oxidation process. The reaction intermediates were observed and the adsorption-reaction mechanism was proposed. It was found that the reaction mechanism was unchanged by introducing the oxygen vacancy in Bi2MoO6. This work could provide new insights into the understanding of the oxygen vacancy in photocatalysis and gas-phase photocatalytic reaction mechanism.
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