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BiVO光阳极与过一硫酸盐耦合增强光电催化降解双酚A

Enhanced photoelectrocatalytic degradation of bisphenol a by BiVO photoanode coupling with peroxymonosulfate.

作者信息

Shao Huixin, Wang Yanbin, Zeng Huabin, Zhang Juanjuan, Wang Yan, Sillanpää Mika, Zhao Xu

机构信息

Key Laboratory of Drinking Water Science and Technology, Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences, Beijing, 100085, PR China; University of Chinese Academy of Sciences, Beijing, 100049, PR China.

School of Environment, Henan Key Laboratory for Environmental Pollution Control, Key Laboratory for Yellow River and Huai River Water Environmental Pollution Control, Ministry of Education, Henan Normal University, Xinxiang, Henan, 453007, PR China.

出版信息

J Hazard Mater. 2020 Jul 15;394:121105. doi: 10.1016/j.jhazmat.2019.121105. Epub 2019 Aug 27.

Abstract

Peroxymonosulfate (PMS) was introduced into a photoelectrocatalytic (PEC) system with a bismuth vanadate (BiVO) photoanode to enhance the PEC oxidation of bisphenol A (BPA). With the addition of 5 mM PMS, the degradation efficiency of 10 mg/L BPA was significantly improved from 24.2% to 100.0% within 120 min and the side reaction of O evolution was avoided at a potential as low as 0.25 V. The electron spin resonance and radicals quenching results suggested that photogenerated holes instead of SO and OH were primarily responsible for the BPA degradation. To further explore the role of PMS, a photocatalytic fuel cell with the structure of BiVO (photoanode)|10 mg/L BPA|proton exchange membrane (separator)|5 mM PMS|Pt (cathode) was constructed and demonstrated that PMS played a key role as electrons acceptor instead of the precursor of SO. The PEC tests including open-circuit potential, linear sweep voltammetry and electrochemical impedance spectroscopy indicated that a more efficient separation of photogenerated charges was achieved in the PEC process with the help of PMS, thus generating more photogenerated holes for enhanced BPA degradation. This work may provide a novel way to enhance the separation of photogenerated charges at the photoanode.

摘要

将过一硫酸盐(PMS)引入到具有钒酸铋(BiVO)光阳极的光电催化(PEC)体系中,以增强双酚A(BPA)的PEC氧化。添加5 mM PMS后,10 mg/L BPA的降解效率在120分钟内从24.2%显著提高到100.0%,并且在低至0.25 V的电位下避免了析氧副反应。电子自旋共振和自由基猝灭结果表明,光生空穴而非SO和OH是BPA降解的主要原因。为了进一步探究PMS的作用,构建了具有BiVO(光阳极)|10 mg/L BPA|质子交换膜(分离器)|5 mM PMS|Pt(阴极)结构的光催化燃料电池,证明PMS作为电子受体而非SO的前体发挥关键作用。包括开路电位、线性扫描伏安法和电化学阻抗谱在内的PEC测试表明,在PMS的帮助下,PEC过程中实现了更有效的光生电荷分离,从而产生更多光生空穴以增强BPA降解。这项工作可能为增强光阳极处光生电荷的分离提供一种新方法。

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