Phase control of MoWS2 nanostructures via oxalic acid-assisted electron injection: From molybdenum disulfide to tungsten disulfide

IF 13.2 1区 工程技术 Q1 ENGINEERING, CHEMICAL Chemical Engineering Journal Pub Date : 2025-03-28 DOI:10.1016/j.cej.2025.162031
Xiao-Yu Chen, Yuan Zhao, Zi-Han Liu, Yi-Tong Pang, Di-Gen Wei, Jing-Yi Wangchen, Cheng-Bao Yao
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Abstract

Metallic-phase molybdenum disulfide (1T-MoS2) and tungsten disulfide (1T-WS2) have attracted great attention due to their excellent performance in the field of electrochemical hydrogen evolution catalysis. Recent studies have demonstrated that reducing the potential barrier of lattice distortion and injecting electrons into materials are the keys to synthesizing 1T phase transition metal dichalcogenides (1T-TMDs) materials with long-term stability. Here, a novel synthesis strategy for 1T-TMDs was proposed. With the assistance of oxalic acid, the continuous synthesis from semiconductor-phase (2H) MoS2 to 1T-MoWS2 and then to 2H-WS2 was achieved by changing the proportion of precursors. The 1T-phase of MoWS2 has a proportion of 74.36 %. Phase transformation mechanism analysis shows that the construction of the ternary structure reduces the lattice distortion barrier, and oxalic acid directly injects electrons into the ternary structure, providing a driving force for the formation and stabilization of the 1T-phase. Compared with the 2H-phase, the 1T-phase MoWS2 has significantly optimized electrochemical catalytic performance. Density functional calculations and transient absorption results revealed that the origin of the efficient catalytic performance of 1T-phase MoWS2, with special electronic structure being the main reason. This study provides a new strategy for the structural design and synthesis of high-efficiency 1T phase catalysts

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草酸辅助电子注入MoWS2纳米结构的相控制:从二硫化钼到二硫化钨
金属相二硫化钼(1T-MoS2)和二硫化钨(1T-WS2)因其在电化学析氢催化领域的优异性能而备受关注。近年来的研究表明,降低晶格畸变势垒和向材料中注入电子是合成具有长期稳定性的1T相变金属二硫族化合物(1T- tmds)材料的关键。本文提出了一种新的1t - tmd合成策略。在草酸的辅助下,通过改变前驱体的比例,实现了从半导体相(2H) MoS2到1T-MoWS2再到2H- ws2的连续合成。MoWS2的1t相比例为74.36 %。相变机理分析表明,三元结构的构建降低了晶格畸变势垒,草酸直接向三元结构注入电子,为1t相的形成和稳定提供了驱动力。与2h相相比,1t相MoWS2的电化学催化性能明显优化。密度函数计算和瞬态吸收结果揭示了1t相MoWS2高效催化性能的来源,其特殊的电子结构是主要原因。本研究为高效1T相催化剂的结构设计和合成提供了新的思路
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来源期刊
Chemical Engineering Journal
Chemical Engineering Journal 工程技术-工程:化工
CiteScore
21.70
自引率
9.30%
发文量
6781
审稿时长
2.4 months
期刊介绍: The Chemical Engineering Journal is an international research journal that invites contributions of original and novel fundamental research. It aims to provide an international platform for presenting original fundamental research, interpretative reviews, and discussions on new developments in chemical engineering. The journal welcomes papers that describe novel theory and its practical application, as well as those that demonstrate the transfer of techniques from other disciplines. It also welcomes reports on carefully conducted experimental work that is soundly interpreted. The main focus of the journal is on original and rigorous research results that have broad significance. The Catalysis section within the Chemical Engineering Journal focuses specifically on Experimental and Theoretical studies in the fields of heterogeneous catalysis, molecular catalysis, and biocatalysis. These studies have industrial impact on various sectors such as chemicals, energy, materials, foods, healthcare, and environmental protection.
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