光催化
罗丹明B
甲基橙
光化学
电子顺磁共振
降级(电信)
可见光谱
水溶液
材料科学
异质结
离子键合
化学
化学工程
催化作用
有机化学
光电子学
离子
工程类
物理
电信
核磁共振
计算机科学
作者
Qiuyi Ji,Zhe Xu,Weiming Xiang,Yijie Wu,Xinying Cheng,Chenmin Xu,Chengdu Qi,Huan He,Jiapeng Hu,Shaogui Yang,Shiyin Li,Limin Zhang
出处
期刊:Chemosphere
[Elsevier BV]
日期:2020-04-11
卷期号:253: 126751-126751
被引量:55
标识
DOI:10.1016/j.chemosphere.2020.126751
摘要
A novel n-n type inorganic/organic heterojunction of flaky-like BiOCl/PDI photocatalyst was constructed by water bath heating method. Meanwhile, a simple method - secondary self-assembly was used to prepare the BiOCl/PDI with a special band structure. The photocatalytic activities were evaluated by degrading aqueous organic pollutants under visible light (λ > 420 nm). The removal rates of 5 mg L-1 phenol (non-ionic type), methyl orange (MO, anionic type), rhodamine B (RhB, cationic type) and 10 mg L-1 RhB by secondary self-assembly BiOCl/PDI (BiOCl/PDI-2) were 8.0%, 3.4%, 27.8% and 78.9% higher than self-assembly BiOCl/PDI (BiOCl/PDI-1) under visible light (λ > 420 nm). The better photocatalytic activity for BiOCl/PDI-2 was attributed to the optimization of energy-band structures, which arose from different exposed surfaces, narrower interplanar spacing and stronger visible light absorption performance. Under acidic condition, BiOCl/PDI-2 showed a good photocatalytic activity, which was not affected by neutral ionic intensity and had good recycling properties. Moreover, the photocatalytic mechanism was explored by free radical capture test and electron paramagnetic resonance (EPR), and contribution of active species was calculated. The main active species of BiOCl/PDI-2 were ·O2-, 1O2 and h+. Our work may provide a route to design efficient inorganic/organic heterojunctions for organic pollutants degradation.
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