光催化
生物炭
异质结
降级(电信)
光化学
环境修复
污染物
化学工程
化学
材料科学
猝灭(荧光)
激进的
电子转移
催化作用
污染
有机化学
荧光
热解
光电子学
物理
工程类
生态学
生物
电信
量子力学
计算机科学
作者
Kemin Qi,Zirun Wang,Xiaoyun Xie,Zhaowei Wang
标识
DOI:10.1016/j.cej.2023.143424
摘要
Biochar-based photocatalysts have attracted widespread attention for the remediation of organic pollutants in water. Herein, we have successfully prepared Bi2WO6/TiO2 heterojunction photocatalysts modified by pyrochar (HC) and hydrochar (PC) to illustrate the role of two different biochar in the system. HC had a higher O elemental content and a larger specific surface area compared to PC. Under the visible light irradiation, PC with persistent radicals could facilitate the production of ·OH during the photocatalytic reaction, while the HC promoted the production of ·O2– due to the presence of oxygen-containing functional groups, which made the Bi2WO6/TiO2/HC exhibit superior photocatalytic property for sulfathiazole (STZ) degradation. The results of characterization revealed that PC could act as an electron shuttle to facilitate photo-excited electron transfer. For HC, the oxygen-containing functional groups (OFGs) could act as photosensitizers while the particles with rod structure function as an electron carrier, which could synergistically promote the photocatalytic degradation of sulfathiazole with Bi2WO6/TiO2 heterojunction. Surprisingly, the real water experiments, luminescent bacterial test, and Toxicity Estimation Software Tool program indicated that Bi2WO6/TiO2/HC and Bi2WO6/TiO2/PC exhibited excellent practicality and reduced toxicity, which could provide a prospering strategy and insight into the design of efficient biochar-based photocatalysts for environmental remediation.
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