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定制铜单原子稳定的亚稳态过渡金属二硫属化物用于可持续制氢

Tailoring Copper Single-Atoms-Stabilized Metastable Transition-Metal-Dichalcogenides for Sustainable Hydrogen Production.

作者信息

Yi Lixin, Nie Kunkun, Li Binjie, Zhang Yujia, Hu Chen, Hao Xiaorong, Wang Ziyi, Qu Xiaoyan, Liu Zhengqing, Huang Wei

机构信息

Frontiers Science Center for Flexible Electronics, Xi'an Institute of Flexible Electronics (IFE), Northwestern Polytechnical University, Xi'an, 710129, China.

Frontier Institute of Science and Technology, State Key Laboratory for Manufacturing Systems Engineering, Xi'an Jiaotong University, Xi'an, 710049, China.

出版信息

Angew Chem Int Ed Engl. 2025 Jan 10;64(2):e202414701. doi: 10.1002/anie.202414701. Epub 2024 Oct 31.

DOI:10.1002/anie.202414701
PMID:39275887
Abstract

Unconventional 1T' phase transition metal dichalcogenides (TMDs) show great potential for hydrogen evolution reaction (HER). However, they are susceptible to transitioning into the stable 2H phase, which reduces their catalytic activity and stability. Herein, we present a scalable approach for designing thermally stable 1T'-TMDs hollow structures (HSs) by etching CuS templates from pre-synthesized CuS@TMDs heterostructures, including 1T'-MoS, MoSe, WS, and WSe HSs. Furthermore, taking 1T'-MoS HSs as an example, the etched Cu ions can be firmly adsorbed on their surface in the form of single atoms (SAs) through Cu-S bonds, thereby elevating the phase transition temperature from 149 °C to 373 °C. Due to the advantages conferred by the 1T' phase, hollow structure, and synergistic effect between Cu SAs and 1T'-MoS supports, the fabricated 1T'-MoS HSs demonstrate superior HER performance. Notably, their high-phase stability enables continuous operation of designed 1T'-MoS HSs for up to 200 hours at an ampere-level current density without significant activity decay. This work provides a universal method for synthesizing highly stable 1T'-TMDs electrocatalysts, with a particular focus on the relationship between their phase and catalytic stability.

摘要

非常规的1T'相过渡金属二硫属化物(TMDs)在析氢反应(HER)中显示出巨大潜力。然而,它们容易转变为稳定的2H相,这会降低其催化活性和稳定性。在此,我们提出了一种可扩展的方法,通过从预合成的CuS@TMDs异质结构中蚀刻CuS模板来设计热稳定的1T'-TMDs中空结构(HSs),包括1T'-MoS、MoSe、WS和WSe HSs。此外,以1T'-MoS HSs为例,蚀刻出的铜离子可以通过Cu-S键以单原子(SAs)的形式牢固地吸附在其表面,从而将相转变温度从149℃提高到373℃。由于1T'相、中空结构以及Cu单原子与1T'-MoS载体之间的协同效应所赋予的优势,制备的1T'-MoS HSs表现出优异的HER性能。值得注意的是,它们的高相稳定性使得设计的1T'-MoS HSs能够在安培级电流密度下连续运行长达200小时而无明显活性衰减。这项工作提供了一种合成高度稳定的1T'-TMDs电催化剂的通用方法,特别关注其相与催化稳定性之间的关系。

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