Modulation of Exposed Active Sites and Electronic Structure of Co-Doped Carbon Nitride Achieving Enhanced Activity toward Peroxymonosulfate Activation for Antibiotic Degradation

被引:1
|
作者
Liu, Ziwei [1 ]
Wu, Jiaming [1 ]
Li, Keyan [1 ]
Song, Chunshan [1 ,2 ]
Guo, Xinwen [1 ]
机构
[1] Dalian Univ Technol, State Key Lab Fine Chem, Frontiers Sci Ctr Smart Mat, PSU DUT Joint Ctr Energy Res,Sch Chem Engn, Dalian 116024, Peoples R China
[2] Chinese Univ Hong Kong, Fac Sci, Dept Chem, Hong Kong 999077, Peoples R China
基金
中国国家自然科学基金;
关键词
PHOTOCATALYTIC DEGRADATION; ENVIRONMENTAL REMEDIATION; G-C3N4; TETRACYCLINE; PERSULFATE; PHOTODEGRADATION; HETEROJUNCTIONS; PHOTOSYNTHESIS; FABRICATION; EFFICIENCY;
D O I
10.1021/acs.iecr.4c00877
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
Co-doped carbon nitride (CoCN-6NH(4)Cl) was prepared through an NH4Cl-assisted pyrolysis method. The catalyst exhibits enhanced and persistent activity toward peroxymonosulfate (PMS) activation for antibiotic degradation under visible light. The levofloxacin (LEV) removal efficiency reaches 89.1% within 60 min, much higher than that of the catalyst (CoCN) prepared without addition of NH4Cl (65.0%). Moreover, the decay of the LEV removal efficiency after four cycles over CoCN-6NH(4)Cl is only 7.6%, in contrast to 21.8% over CoCN. The enhanced activity of CoCN-6NH(4)Cl can be attributed to the remarkably increased specific surface area to expose more active sites as well as the modified electronic structure caused by Cl doping. The improved charge separation efficiency of CoCN-6NH(4)Cl results in the generation of more photogenerated holes (h(+)), superoxide radicals (<middle dot>O-2(-)), and singlet oxygen (O-1(2)) as main active species participating in the LEV degradation, thus greatly promoting the degradation efficiency. This work provides a facile and effective strategy to develop high-performance catalysts in advanced oxidation processes.
引用
收藏
页码:9082 / 9092
页数:11
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