Visible Light Photocatalysis: Efficient S-Scheme γ-Bi2O3/BiOBr Photocatalyst for Phenol Degradation

IF 2.3 4区 化学 Q3 CHEMISTRY, PHYSICAL
Zekui Zhou, Yong Li, Fenrong Liu
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引用次数: 0

Abstract

The development of heterostructures with stabilized heterogeneous structures is crucial for the improvement of photocatalytic activity and practical applications. In this study, a S-type heterojunction of γ-Bi2O3/BiOBr was synthesized by a simple hydrothermal method. Under simulated sunlight, the degradation ratio of phenol can attain nearly 91.75% for 17%-γ-Bi2O3/BiOBr heterojunction after 120 min, while only 2.8% and 52.86% for pure γ-Bi2O3 and BiOBr, respectively. Meanwhile, its first-order reaction rate is 3.46 and 22.81 times more than those of pure BiOBr and γ-Bi2O3, respectively. In addition, the 17%-γ-Bi2O3/BiOBr heterojunction exhibits the excellent cycle stability, as its phenol degradation ratio can retain nearly 86% after five cycle experiments. The heterojunction was analyzed as an S-type heterojunction based on XPS, EPR and free radical trapping experiments. The performance enhancement of the catalyst is thus due to the formation of an S-type heterojunction, which reduces the recombination rate of photogenerated electrons and photogenerated holes and promotes the formation of active species, thus dramatically increasing the efficiency of photocatalytic degradation of phenol.

可见光催化:高效S-Scheme γ-Bi2O3/BiOBr光催化剂降解苯酚
发展具有稳定异质结构的异质结构对于提高光催化活性和实际应用具有重要意义。本研究采用简单的水热法合成了γ-Bi2O3/BiOBr的s型异质结。在模拟阳光下,苯酚对17%-γ-Bi2O3/BiOBr异质结的降解率在120 min后可达到近91.75%,而对纯γ-Bi2O3和BiOBr的降解率分别仅为2.8%和52.86%。同时,其一级反应速率分别是纯BiOBr和γ-Bi2O3的3.46倍和22.81倍。此外,17%-γ-Bi2O3/BiOBr异质结表现出优异的循环稳定性,经过5次循环实验后,其苯酚降解率仍保持在近86%。通过XPS、EPR和自由基捕获实验分析了该异质结为s型异质结。因此,催化剂性能的增强是由于s型异质结的形成,降低了光生电子与光生空穴的复合速率,促进了活性物质的形成,从而大大提高了光催化降解苯酚的效率。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Catalysis Letters
Catalysis Letters 化学-物理化学
CiteScore
5.70
自引率
3.60%
发文量
327
审稿时长
1 months
期刊介绍: Catalysis Letters aim is the rapid publication of outstanding and high-impact original research articles in catalysis. The scope of the journal covers a broad range of topics in all fields of both applied and theoretical catalysis, including heterogeneous, homogeneous and biocatalysis. The high-quality original research articles published in Catalysis Letters are subject to rigorous peer review. Accepted papers are published online first and subsequently in print issues. All contributions must include a graphical abstract. Manuscripts should be written in English and the responsibility lies with the authors to ensure that they are grammatically and linguistically correct. Authors for whom English is not the working language are encouraged to consider using a professional language-editing service before submitting their manuscripts.
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