Dual electron transfer path and LSPR photothermal enhancement in BiOCl@ZnIn2S4 heterojunction for enhanced photocatalytic H2 evolution, H2O2 production and tetracycline removal†

IF 6.1 1区 化学 Q1 CHEMISTRY, INORGANIC & NUCLEAR Inorganic Chemistry Frontiers Pub Date : 2025-01-03 DOI:10.1039/D4QI02806F
Fan Wu, Guangyu Wu, Yonggong Tang, Yuwei Pan, Jiangang Han, Jin Zhang, Weinan Xing and Yudong Huang
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Abstract

A well-designed catalyst structure can significantly enhance the efficiency of photocatalytic light-trapping. Herein, the local surface plasmon resonance effect (LSPR) generated by introducing BiOCl nanosheets effectively broadened the photoresponsive range of ZnIn2S4 (ZIS), and the photothermal effect of BiOCl increased the temperature of the reaction system of the BiOCl@ZIS-1% composites, which in turn improved the photo-thermal performance and light-harvesting efficiency of the catalyst. The improved photothermal effect promoted the transfer rate of charge carriers across the heterojunction and enhanced the surface reaction kinetics. In addition, Kelvin probe force microscopy and density functional theory (DFT) calculations showed that the difference of merit between BiOCl and ZIS led to the generation of an internal electric field, which not only enhanced the efficiency of photogenerated charges to separate and migrate but also promoted the photocatalytic H2 production (13.69 mmol g−1 h−1), H2O2 generation (9670 μM g−1 h−1) and tetracycline degradation performance (86.2%). In addition, a possible reaction mechanism for photothermal-assisted photocatalysis was presented. Thus, this research proposes a possible direction for constructing a visible photothermal-assisted photocatalytic reaction system.

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BiOCl@ZnIn2S4异质结的双电子转移路径和LSPR光热增强对光催化H2演化、H2O2生成和四环素去除的促进作用
设计良好的催化剂结构可以显著提高光催化捕光效率。其中,引入BiOCl纳米片产生的局部表面等离子体共振效应(LSPR)有效地拓宽了ZnIn2S4 (ZIS)的光响应范围,BiOCl的光热效应提高了BiOCl@ZIS-1%复合材料反应体系的温度,从而提高了催化剂的光热性能和光收集效率。光热效应的改善提高了载流子在异质结上的转移速率,增强了表面反应动力学。此外,开尔文探针力显微镜和密度功能理论(DFT)计算表明,BiOCl和ZIS之间的性能差异导致了内部电场的产生,这不仅提高了光生电荷的分离和迁移效率,而且还促进了光催化H2生成(13.69 mmol g−1 h−1),H2O2生成(9670 μ g−1 h−1)和四环素降解性能(86.2%)。此外,还提出了光热辅助光催化的可能反应机理。因此,本研究为构建可见光光热辅助光催化反应体系提供了可能的方向。
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来源期刊
Inorganic Chemistry Frontiers
Inorganic Chemistry Frontiers CHEMISTRY, INORGANIC & NUCLEAR-
CiteScore
10.40
自引率
7.10%
发文量
587
审稿时长
1.2 months
期刊介绍: The international, high quality journal for interdisciplinary research between inorganic chemistry and related subjects
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