通过 SnS2/TiO2{101} 表面 Z 型电荷分离提高 SnS2/TiO2 复合材料的光催化性能

Catalysts Pub Date : 2024-07-10 DOI:10.3390/catal14070442
Nkenku Carl, Muhammad Fiaz, Hyun-Seok Oh, Yu-Kwon Kim
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引用次数: 0

摘要

为实现高效电荷分离而形成的异质结已被用于制备高效的半导体光催化剂,以应用于制氢和环境修复等领域。在本研究中,我们通过微波辅助水热法合成了 SnS2 和 TiO2 异质结复合结构,其中 SnS2 纳米颗粒优先生长在纳米晶 TiO2 纳米片上暴露的 {101} 面上。复合材料中 TiO2 纳米片的{001}和{101}面适当暴露,SnS2 纳米颗粒优先生长在{101}面上,这是电荷分离直接 Z 型机制的起源,与单独使用 SnS2 和 TiO2 相比,在光降解亚甲基蓝(MB)和罗丹明 B(RhB)等有机染料方面,光催化性能得到了增强。光降解率与复合材料中 SnS2 比例的关系曲线呈现出火山状,在 SnS2 比例约为 33% 时达到最大值,此时具有高表面积(118.2 m2g-1)的 TiO2 纳米片的{101}面上出现了 SnS2 纳米小颗粒。我们的研究结果表明,微波辅助水热法是合成具有优先异质结结构的复合型光催化剂的良好方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Enhanced Photocatalytic Performances of SnS2/TiO2 Composites via a Charge Separation Following Z-Scheme at the SnS2/TiO2{101} Facets
The formation of heterojunctions for efficient charge separation has been practiced for the preparation of efficient semiconductor-based photocatalysts for applications such as hydrogen production and environmental remediation. In this study, we synthesized a composite structure with a heterojunction between SnS2 and TiO2 through a microwave-assisted hydrothermal process, in which SnS2 nanoparticles grew on nanocrystalline TiO2 nanosheets preferentially at the exposed {101} facets. Appropriate exposure of the {001} and {101} facets of the TiO2 nanosheet in the composite with a preferential growth of SnS2 nanoparticles at the {101} facets was the origin of the charge separation following a direct Z-scheme mechanism to result in enhanced photocatalytic performances in photodegradation of organic dyes such as methylene blue (MB) and rhodamine B (RhB) compared to that of SnS2 and TiO2 alone. A plot of photodegradation rates vs. SnS2 ratios in the composites gave an overall volcano-shaped curve with a maximum at the SnS2 ratio of about 33% at which small SnS2 nanoparticles were populated at the {101} facets of the TiO2 nanosheets with a high surface area (118.2 m2g−1). Our results suggest the microwave-assisted hydrothermal process can be a good synthetic approach for composite-based photocatalysts with a preferential heterojunction structure.
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