Layered Ti3C2 MXene and silver co-modified g-C3N4 with enhanced visible light-driven photocatalytic activity

被引:110
作者
Huang, Kelei [1 ]
Li, Chunhu [1 ]
Wang, Liang [1 ]
Wang, Wentai [1 ]
Meng, Xiangchao [1 ]
机构
[1] Ocean Univ China, Coll Chem & Chem Engn, Key Lab Marine Chem Theory & Technol, Minist Educ, Qingdao 266100, Peoples R China
基金
中国国家自然科学基金;
关键词
Ti3C2; MXene; Silver; Graphitic carbon nitride; Carriers separation; Tetracycline degradation; IN-SITU CONSTRUCTION; EFFICIENT PHOTOCATALYST; DYE-SENSITIZATION; DEGRADATION; MELAMINE; METAL; HETEROJUNCTION; COMPOSITE; PATHWAYS;
D O I
10.1016/j.cej.2021.131493
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Novel Ag/g-C3N4/Ti3C2 heterojunction (ACN/TC) was synthesized via one-step calcining the mixture of Ag+-melamine superamolecule and Ti3C2. With robust interfacial contact of ACN/TC heterojunction, the introduction of Ag nanoparticles could induce localized surface plasmon resonance and improve the visible light responsivity. Besides, layered Ti3C2 was served as electron sink and co-catalyst to provide rapid charges transfer channel and enhance O-2 adsorption, thereby accelerating the separation of photogenerated charges and production of radicals. The optimized ternary heterojunction (ACN/TC-15) exhibited that the photocatalytic removal rate of Rhodamine B (RhB) and Tetracycline hydrochloride (TC) reached 99.2% and 92.1% under visible light (lambda > 420 nm) irradiation, respectively. Besides, extending to lambda > 510 nm light irradiation, the removal rate of RhB and TC still 85.6% and 79.5%, respectively. During the TC degradation, the superoxide radical (center dot O-2(-)) was determined as the main oxidative species. Besides, the possible degradation pathway of TC was proposed. This work not only showed a simplified method for the preparation of Ag/g-C3N4/Ti3C2 composite, but also provided insights into Ti3C2 MXene as co-catalyst to improve the photocatalytic degradation of organic pollutants.
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页数:12
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