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A visible light active, carbon–nitrogen–sulfur co-doped TiO(2)/g-C(3)N(4) Z-scheme heterojunction as an effective photocatalyst to remove dye pollutants

Heterojunction formation and heteroatom doping could be viewed as promising strategies for constructing composite photocatalysts with high visible light catalytic activity. In this work, we fabricated a carbon, nitrogen and sulfur co-doped TiO(2)/g-C(3)N(4) (CNS-TiO(2)/g-C(3)N(4)) Z-scheme heterojun...

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Detalles Bibliográficos
Autores principales: Huang, Zhen, Jia, Shuai, Wei, Jie, Shao, Ziqiang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9032027/
https://www.ncbi.nlm.nih.gov/pubmed/35479154
http://dx.doi.org/10.1039/d1ra01890f
Descripción
Sumario:Heterojunction formation and heteroatom doping could be viewed as promising strategies for constructing composite photocatalysts with high visible light catalytic activity. In this work, we fabricated a carbon, nitrogen and sulfur co-doped TiO(2)/g-C(3)N(4) (CNS-TiO(2)/g-C(3)N(4)) Z-scheme heterojunction photocatalyst composite via one-step hydrothermal and calcination methods. Compared with pure TiO(2) and g-C(3)N(4), the CNS-TiO(2)/g-C(3)N(4) Z-scheme heterojunction photocatalyst possessed excellent degradation performance under visible light irradiation. Due to the formation of the Z-scheme heterostructure, the utilization rate of the photogenerated electrons–holes generated by the catalyst was increased, which enhanced the catalytic activity. Moreover, the heteroatom doping (C, N and S) could efficiently tailor the band gap of TiO(2) and facilitate electron transition, contributing to enhancing the degradation ability under visible light. The CNS-TiO(2)/g-C(3)N(4)-2 exhibited a superior photocatalytic degradation efficiency (k = 0.069 min(−1)) for methyl orange dye (MO), which is higher than those of pure TiO(2) (k = 0.001 min(−1)) and g-C(3)N(4) (k = 0.012 min(−1)), showing excellent photocatalytic activity against organic pollutants.