X射线光电子能谱
光催化
甲基橙
光降解
异质结
可见光谱
漫反射红外傅里叶变换
材料科学
扫描电子显微镜
光电子学
光致发光
透射电子显微镜
光化学
光谱学
热液循环
纳米技术
核化学
化学工程
化学
催化作用
有机化学
复合材料
物理
工程类
量子力学
作者
Jin Luo,Xiaosong Zhou,Lin Ma,Xuyao Xu
出处
期刊:Journal of Molecular Catalysis A-chemical
[Elsevier BV]
日期:2015-10-03
卷期号:410: 168-176
被引量:83
标识
DOI:10.1016/j.molcata.2015.09.019
摘要
Novel visible-light-driven WO3/BiOI heterojuncted photocatalysts were fabricated by a facile hydrothermal method and were characterized by scanning electron microscopy (SEM), transmission electron microscopy (TEM), X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), UV–vis diffuse reflectance spectroscopy (UV–vis DRS) and photoluminescence spectroscopy (PL). The photocatalytic activity of the as-prepared samples was evaluated by photocatalytic degradation of methyl orange (MO) under visible light irradiation (λ > 420 nm). The results indicated that the optimum rate constant of the WO3/BiOI heterojunction catalyst at a weight content of 1.0% WO3 for the degradation of MO was 1.6 times as high as that of pure BiOI and 54 times larger than that of pure WO3, respectively. The enhancement could be attributed predominantly to improving photogenerated electron–hole pairs separation and migration efficiency because of the p–n heterojunction formed between p-type BiOI and n-type WO3. Additionally, the superoxide radical anions (O2−) and holes (h+) were considered as the dominant reactive species during the photodegradation MO process, and a possible photocatalytic mechanism was proposed.
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