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Efficient Interfacial Charge Transfer Based on 2D/2D Heterojunctions of Fe-C(3)N(4)/Ti(3)C(2) for Improving the Photocatalytic Degradation of Antibiotics

Graphitic carbon nitride (g-C(3)N(4)) has shown to be a promising photocatalyst that, however, suffers from strong charge recombination and poor conductivity, while MXenes have shown to be perfect cocatalysts for the photocatalytic process but show poor stability. In this study, we successfully cons...

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Detalles Bibliográficos
Autores principales: Huo, Zhaohui, Liao, Yanmin, He, Yongyi, Zhang, Yifan, Liao, Xiaolin, Zhang, Qitong, Wu, Haojie, Shi, Junjie, Wen, Genglong, Su, Haixia, Yao, Suyang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9168236/
https://www.ncbi.nlm.nih.gov/pubmed/35677594
http://dx.doi.org/10.3389/fchem.2022.865847
Descripción
Sumario:Graphitic carbon nitride (g-C(3)N(4)) has shown to be a promising photocatalyst that, however, suffers from strong charge recombination and poor conductivity, while MXenes have shown to be perfect cocatalysts for the photocatalytic process but show poor stability. In this study, we successfully constructed 2D/2D heterojunctions of Fe-C(3)N(4)/Ti(3)C(2) for the photocatalytic degradation of antibiotics. In this study, multilayer Ti(3)C(2) was obtained by etching Ti(3)AlC(2), and then Fe-C(3)N(4)/Ti(3)C(2) photocatalyst was prepared by the one-pot microwave method and high-temperature calcination method. The synthesized samples were characterized by XRD, SEM, TEM, XPS, TGA, BET, DRS, PL, and other means. The photocatalytic degradation of tetracycline hydrochloride by Fe-C(3)N(4)/Ti(3)C(2) was in accordance with the first-order reaction kinetics model, and the apparent rate constant k was 2.83, 2.06, and 1.77 times that of g-C(3)N(4), Fe-C(3)N(4), and g-C(3)N(4)/Ti(3)C(2), respectively. Through the mechanism study, it was shown that the most active species in the reaction system was • O(2) (−), while h(+) and •OH had a relatively lower effect on the degradation system.