降级(电信)
生态毒性
异质结
光催化
沉积(地质)
碳纤维
氮化碳
材料科学
氮化物
化学工程
环境化学
化学
纳米技术
光电子学
复合材料
计算机科学
复合数
有机化学
图层(电子)
工程类
催化作用
生物
电信
古生物学
沉积物
毒性
作者
Jie Zhang,Xu Wang,Chunlan Xu,Deping Huang,Yongsheng Chang,Delu Cao,Xueying Wang,Changyu Lu,Jianwei Zhao,Wei Huang
标识
DOI:10.1016/j.apsusc.2024.162133
摘要
• Constructing lightweight hollow sponge carbon nitride (LHSCN) by calcination method. • Depositing BiVO 4 on the floating LHSCN (BVO/LHSCN) by hydrothermal method . • The light capture capacity of BVO/LHSCN is enhanced by its floatability in water. • The S-scheme charge transfer path was verified by DFT calculation and in situ XPS . • The reaction sites during TC degradation were analyzed by the Fukui index. • During the degradation process of TC, the ecotoxicity decreased. In this study, the floating lightweight hollow sponge carbon nitride containing BiVO 4 (BVO/LHSCN) was constructed using calcination and hydrothermal methods. Experiments and DFT theoretical calculations show that the S-scheme charge transfer path of BVO/LHSCN and its unique porous network floating structure achieve BVO/LHSCN excellent light capture ability, photogenerated carrier separation efficiency and recycling performance. After 180 min of illumination, BVO/LHSCN can degrade 94.9 % of tetracycline (TC), with a rate constant as high as 0.06235 min −1 , which was 4.35 times and 7.7 times higher than that of pure BVO (0.01433 min −1 ) and LHSCN (0.00807 min −1 ), respectively. After 5 cycles of experiment, BVO/LHSCN still exhibited excellent TC degradation performance, demonstrating outstanding stability. Subsequently, the site of TC attack was predicted by Fukui index, the intermediate product and degradation pathway during the TC degradation were analyzed by LC-MS. The possible ecological risks of the intermediate and final products were assessed, determining a low environmental risk in the degradation process of tetracycline. This study provides a novel method to improve the light-capturing ability of S-scheme heterojunction photocatalysts.
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