光催化
埃洛石
材料科学
三元运算
可见光谱
光降解
异质结
煅烧
复合数
复合材料
核化学
化学工程
催化作用
光电子学
有机化学
化学
工程类
计算机科学
程序设计语言
作者
Zongli Ren,Zhongwei Zhao,Zhao Yang,Bin Cheng,Xuan Yang
出处
期刊:NANO
[World Scientific]
日期:2021-07-06
卷期号:16 (09)
被引量:5
标识
DOI:10.1142/s1793292021501009
摘要
Constructing heterojunction photocatalyst is an effective method to enhance the separation of photogenerated electron and hole, which significantly improves ability of visible light response. In this study, calcination methods have been proposed to prepare highly efficient magnetic ternary photocatalyst g-C 3 N 4 /TiO 2 -MnFe 2 O 4 halloysite. It showed an enhanced photocatalytic degradation for dyes (crystal violet) and nonsteroidal anti-inflammatory drugs (acetaminophen) under vision light irradiation. Compared to pure g-C 3 N 4 , TiO 2 , MnFe 2 O 4 halloysite and binary g-C 3 N 4 -MnFe 2 O 4 halloysite, the optimized ternary g-C 3 N 4 /TiO 2 -MnFe 2 O 4 halloysite displayed enhanced photodegradation efficiency with 91.1% removal of crystal violet (10[Formula: see text]ppm) in 90[Formula: see text]min under visible light irradiation, the optimized ternary g-C 3 N 4 /TiO 2 -MnFe 2 O 4 halloysite composite showed significantly enhanced photocatalytic activity with more than 79.1% removal of acetaminophen (10[Formula: see text]ppm) within 90[Formula: see text]min under visible light. The photocatalytic mechanism was identified through the free radical quenching experiment. The heterojunction photocatalyst could be easily recovered by an extra magnetic field and reused several times without any obvious deterioration in catalytic activity. Besides, the ternary heterojunction also exhibited antibacterial ability against Escherichia coli. The superior photocatalytic performance of composite should be mainly attributed to both the improvement of light harvesting as well as the enhanced separation and transfer efficiency. It is expected that this novel ternary visible-light responding composite would be a promising candidate material for organic pollutants degradation and bacteria inactivation.
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