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铋基异质结协同光催化氧化和过一硫酸盐还原活化用于高效降解有机污染物

Synergistic Photocatalytic Oxidation and Reductive Activation of Peroxymonosulfate by Bi-Based Heterojunction for Highly Efficient Organic Pollutant Degradation.

作者信息

Zhao Xiaopeng, Wang Yang, Liu Fangning, Ye Xiaobin, Wei Shangxiong, Sun Yilin, He Jinghui

机构信息

College of Chemistry, Chemical Engineering and Materials Science, Soochow University, Suzhou 215123, China.

State Key Laboratory of Silicate Materials for Architectures, Wuhan University of Technology, Wuhan 430070, China.

出版信息

Nanomaterials (Basel). 2025 Mar 20;15(6):471. doi: 10.3390/nano15060471.

DOI:10.3390/nano15060471
PMID:40137644
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11944557/
Abstract

Organic pollutants present a substantial risk to both ecological systems and human well-being. Activation of peroxymonosulfate (PMS) have emerged as an effective strategy for the degradation of organic pollutants. Bi-based heterojunction is commonly used as a photocatalyst for reductively activating PMS, but single-component Bi-based heterojunction frequently underperforms due to its restricted absorption spectrum and rapid combination of photogenerated electron-hole pairs. Herein, BiVO was selected as the oxidative semiconductor to form an S-type heterojunction with CuBiO-x-CuBiO/BiVO (x = 0.2, 0.5, and 0.8) for PMS photoactivation. The built-in electric field (BEF) in x-CuBiO/BiVO promoted electron transfer to effectively activate PMS. The x-CuBiO/BiVO heterojunctions also demonstrate stronger adsorption of the polar PMS than pure CuBiO or BiVO. In addition, the BEF prompts photoelectrons able to reduce O to •O and photogenerated holes in the valence band of BiVO able to oxidize HO to generate •OH. Therefore, under visible light irradiation, 95.1% of ciprofloxacin (CIP) can be degraded. The 0.5-CuBiO/BiVO demonstrated the best degradation efficiency and excellent stability in cyclic tests, as well as a broad applicability in degrading other common pollutants. The present work demonstrates the high-efficiency S-type heterojunctions in the coupled photocatalytic and PMS activation technology.

摘要

有机污染物对生态系统和人类福祉都构成重大风险。过一硫酸盐(PMS)的活化已成为降解有机污染物的有效策略。基于铋的异质结通常用作光催化剂来还原活化PMS,但单组分基于铋的异质结由于其受限的吸收光谱和光生电子 - 空穴对的快速复合而经常表现不佳。在此,选择BiVO作为氧化半导体,与CuBiO - x - CuBiO/BiVO(x = 0.2、0.5和0.8)形成S型异质结用于PMS光活化。x - CuBiO/BiVO中的内建电场(BEF)促进电子转移以有效活化PMS。x - CuBiO/BiVO异质结还表现出比纯CuBiO或BiVO对极性PMS更强的吸附。此外,BEF促使光电子能够将O还原为•O,并且BiVO价带中的光生空穴能够氧化HO以产生•OH。因此,在可见光照射下,95.1%的环丙沙星(CIP)可以被降解。0.5 - CuBiO/BiVO在循环测试中表现出最佳的降解效率和优异的稳定性,并且在降解其他常见污染物方面具有广泛的适用性。本工作展示了耦合光催化和PMS活化技术中的高效S型异质结。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b85b/11944557/8a6406a01eed/nanomaterials-15-00471-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b85b/11944557/6e2f2950a935/nanomaterials-15-00471-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b85b/11944557/fcf66ec58885/nanomaterials-15-00471-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b85b/11944557/aadd9bf69469/nanomaterials-15-00471-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b85b/11944557/838616c47340/nanomaterials-15-00471-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b85b/11944557/c16ebf1aece1/nanomaterials-15-00471-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b85b/11944557/cf4f8c844acc/nanomaterials-15-00471-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b85b/11944557/8a6406a01eed/nanomaterials-15-00471-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b85b/11944557/6e2f2950a935/nanomaterials-15-00471-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b85b/11944557/fcf66ec58885/nanomaterials-15-00471-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b85b/11944557/aadd9bf69469/nanomaterials-15-00471-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b85b/11944557/838616c47340/nanomaterials-15-00471-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b85b/11944557/c16ebf1aece1/nanomaterials-15-00471-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b85b/11944557/cf4f8c844acc/nanomaterials-15-00471-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b85b/11944557/8a6406a01eed/nanomaterials-15-00471-g007.jpg

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