基于掺钨 MoS2 的纳米结构在可见光下光催化氢气进化

IF 1.7 4区 化学 Q4 CHEMISTRY, PHYSICAL Reaction Kinetics, Mechanisms and Catalysis Pub Date : 2024-05-02 DOI:10.1007/s11144-024-02627-9
Khursheed Ahmad, Waseem Raza, Mohd Quasim Khan, Rais Ahmad Khan
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引用次数: 0

摘要

在这项工作中,我们引入了一种简单的方法,通过掺杂过渡金属(W)来提高 MoS2 的光催化活性。W-MoS2(10 毫克)的光催化产生 H2 的活性得到了大幅提高,6 小时后达到了约 925 µmol g-1 的惊人速率,是裸 MoS2 的 1.5 倍。50 毫克 W-MoS2 光催化剂 6 小时后的 H2 生成活性最高,达到 1740 µmol g-1。所观察到的活性提高可归因于异质结界面上肖特基势垒的形成,以及在 MoS2 中掺入钨后活性位点得到改善的优势特性。此外,W-MoS2 的活性增强可能是由于钨和钼位点促进了催化动力学,在水解离方面表现出值得称道的活性,在吸附 H+ 方面效率更高。这些因素大大提高了 W-MoS2 光催化剂的整体性能。此外,W-MoS2 + 5 wt% Pt 还使用了铂(Pt)作为协同催化剂,6 小时后观察到 W-MoS2 + 5 wt% Pt 的光催化活性提高到 2145 µmol g-1。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Tungsten-doped MoS2-based nanostructure for photocatalytic hydrogen evolution under visible light

In this work, we introduced a simple approach to boost the photocatalytic activity of MoS2 by introducing transition metal (W) doping. The W-MoS2 (10 mg) exhibited a substantial enhancement in photocatalytic activity for H2 production, achieving an impressive rate of approximately 925 µmol g−1 after 6 h, which is 1.5-fold higher than bare MoS2. The highest H2 production activity of 1740 µmol g−1 after 6 h was obtained for 50 mg W-MoS2 photocatalyst. The observed increase in activity can be ascribed to the formation of a Schottky barrier at the heterojunction interface, along with advantageous properties of improved active sites resulting from tungsten doping into MoS2. Furthermore, the enhanced activity of W-MoS2 may be attributed to the promotion of catalytic kinetics by tungsten and molybdenum sites, exhibiting commendable activity for water dissociation and higher efficiency in H+ adsorption. These factors contribute significantly to the overall improved performance of the W-MoS2 photocatalyst. Further, platinum (Pt) was also used as cocatalyst and enhanced photocatalytic activity of 2145 µmol g−1 after 6 h was observed for W-MoS2 + 5 wt% Pt.

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来源期刊
CiteScore
3.30
自引率
5.60%
发文量
201
审稿时长
2.8 months
期刊介绍: Reaction Kinetics, Mechanisms and Catalysis is a medium for original contributions in the following fields: -kinetics of homogeneous reactions in gas, liquid and solid phase; -Homogeneous catalysis; -Heterogeneous catalysis; -Adsorption in heterogeneous catalysis; -Transport processes related to reaction kinetics and catalysis; -Preparation and study of catalysts; -Reactors and apparatus. Reaction Kinetics, Mechanisms and Catalysis was formerly published under the title Reaction Kinetics and Catalysis Letters.
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