光催化
催化作用
可见光谱
氧气
光化学
化学
材料科学
傅里叶变换红外光谱
无机化学
化学工程
有机化学
光电子学
工程类
作者
Wendong Zhang,Xiaoli Liu,Xing’an Dong,Yuxin Zhang
出处
期刊:Chinese Journal of Catalysis
[China Science Publishing & Media Ltd.]
日期:2017-12-01
卷期号:38 (12): 2030-2038
被引量:56
标识
DOI:10.1016/s1872-2067(17)62941-3
摘要
Bi12O17Br2 and Bi4O5Br2 visible-light driven photocatalysts, were respectively fabricated by hydrothermal and room-temperature deposition methods with the use of BiBr3 and NaOH as precursors. Both Bi12O17Br2 and Bi4O5Br2 were composed of irregular nanosheets. The Bi4O5Br2 nanosheets exhibited high and stable visible-light photocatalytic efficiency for ppb-level NO removal. The performance of Bi4O5Br2 was markedly higher than that of the Bi12O17Br2 nanosheets. The hydroxyl radical (•OH) was determined to be the main reactive oxygen species for the photo-degradation processes of both Bi12O17Br2 and Bi4O5Br2. However, in situ diffuse reflectance infrared Fourier transform spectroscopy analysis revealed that Bi12O17Br2 and Bi4O5Br2 featured different conversion pathways for visible light driven photocatalytic NO oxidation. The excellent photocatalytic activity of Bi4O5Br2 resulted from a high surface area and large pore volumes, which facilitated the transport of reactants and intermediate products, and provided more active sites for photochemical reaction. Furthermore, the Bi4O5Br2 nanosheets produced more •OH and presented stronger valence band hole oxidation. In addition, the oxygen atoms of NO could insert into oxygen-vacancies of Bi4O5Br2, which provided more active sites for the reaction. This work gives insight into the photocatalytic pollutant-degradation mechanism of bismuth oxyhalide.
科研通智能强力驱动
Strongly Powered by AbleSci AI