Ag-Bridged Z-Scheme 2D/2D Bi5FeTi3O15/g-C3N4 Heterojunction for Enhanced Photocatalysis: Mediator-Induced Interfacial Charge Transfer and Mechanism Insights

异质结 材料科学 光催化 三元运算 降级(电信) 可见光谱 纳米颗粒 电子转移 载流子 化学工程 光电子学 纳米技术 光化学 催化作用 电信 生物化学 计算机科学 工程类 化学 程序设计语言
作者
Kai Wang,Jun Li,Gaoke Zhang
出处
期刊:ACS Applied Materials & Interfaces [American Chemical Society]
卷期号:11 (31): 27686-27696 被引量:196
标识
DOI:10.1021/acsami.9b05074
摘要

Heterojunction photocatalysts have attracted widespread interest in photocatalysis because of their high-efficiency interfacial charge-transfer characteristics of nanoarchitectures. In this study, Ag-bridged 2D/2D Bi5FeTi3O15/ultrathin g-C3N4 Z-scheme heterojunction photocatalysts with powerful interfacial charge transfer has been synthesized via a facile ultrasound method coupled with a photoreduction strategy for efficient photocatalytic degradation of antibiotics. The morphology analysis displays that the bridged Ag nanoparticles were anchored on the interface of layered Bi5FeTi3O15 and ultrathin g-C3N4 nanosheets. Owing to its unique 2D/2D ternary heterostructure, the Bi5FeTi3O15/2%Ag/10% ultrathin g-C3N4 composite exhibited the best tetracycline degradation performance under visible-light and simulated solar irradiation. Meanwhile, the intermediates and degradation pathways were proposed by a liquid-phase mass spectrometry system. Characterizations and density functional theory studies together verify that the matched band structure of Bi5FeTi3O15 and g-C3N4 could induce a superfast Z-scheme interfacial charge-transfer path. More importantly, bridged Ag nanoparticles in the 2D/2D heterojunction extended the light absorption range and prolonged the lifetime of photogenerated electron–holes induced by Bi5FeTi3O15. This work affords a promising approach for designing multicomponent Z-scheme heterojunction photocatalysts for highly efficient photocatalytic application.

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