Embedding ZnCdS@ZnIn2S4 into thiazole-modified g-C3N4 by electrostatic self-assembly to build dual Z-scheme heterojunction with spatially separated active centers for photocatalytic H2 evolution and ofloxacin degradation

噻唑 光催化 降级(电信) 对偶(语法数字) 异质结 材料科学 嵌入 方案(数学) 化学工程 光电子学 化学 电子工程 有机化学 计算机科学 工程类 催化作用 人工智能 艺术 数学分析 文学类 数学
作者
Linlin Hou,Wei Li,Zhiliang Wu,Q. Wei,Huixing Yang,Yangyang Jiang,Teng Wang,Yinzhen Wang,Qinyu He
出处
期刊:Separation and Purification Technology [Elsevier BV]
卷期号:290: 120858-120858 被引量:87
标识
DOI:10.1016/j.seppur.2022.120858
摘要

• The dual Z-scheme heterojunction improves the separation and migration efficiency of electron-hole pairs. • The space separation between the oxidation center and the reduction center improves the utilization rate of carriers. • Thiazoles as an electron acceptor to reconstruct electrons on the g-C 3 N 4 surface and adjust its HOMO and LUMO dispersion to improve electron mobility. • ZnCdS@ZnIn 2 S 4 @g-C 3 N 4 -vTA prepared by electrostatic self-assembly, and its intimate interfacial contact shortens the migration distance of carriers. The structural design of the photocatalyst has a great influence on photocatalytic performance. Here, the ZnCdS@ZnIn 2 S 4 @g-C 3 N 4 -vTA with a dual Z-scheme heterojunction structure is prepared by electrostatic self-assembly. It has high photocatalytic hydrogen evolution (11359.9 μmol g −1 h −1 ), excellent OFX degradation performance (95.7%), and good reusability under visible light. The hydrogen production performance of ZnCdS@ZnIn 2 S 4 @g-C 3 N 4 -vTA is about 56, 7, 2 times higher than g-C 3 N 4 , ZnCdS, and ZnIn 2 S 4 , respectively. The excellent photocatalytic performance mainly depends on the following aspects: (1) The dual Z-scheme heterojunction with spatial separation of active centers improves the migration and separation efficiency and utilization of electron-hole pairs. (2) The 4-methyl-5-vinylthiazole (vTA) molecular is grafted to the edge of g-C 3 N 4 by visible light to reconstruct the surface electrons so that the electrons can be transferred to the ZnIn 2 S 4 surface more efficiently to increase the overall carrier transport rate; (3) ZnCdS@ZnIn 2 S 4 @g-C 3 N 4 -vTA prepared by electrostatic self-assembly, and its intimate interfacial contact shortens the migration distance of carriers. In addition, the high specific surface area and pore size of ZnCdS@ZnIn 2 S 4 @g-C 3 N 4 -vTA improves the migration and separation of carriers. Our research provides an expandable idea for designing molecular engineering-based dual Z-scheme heterojunction photocatalysts and nanomaterial composite methods.
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