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用于提高过渡金属硫化物自支撑电极析氢反应催化性能的调制策略综述。

A review of modulation strategies for improving the catalytic performance of transition metal sulfide self-supported electrodes for the hydrogen evolution reaction.

作者信息

Liu Qianqian, Liu Kehan, Huang Jianfeng, Hui Chiyuan, Li Xiaoyi, Feng Liangliang

机构信息

College of Materials Science and Engineering, Xi'an University of Science and Technology, Xi'an 710054, China.

School of Materials Science & Engineering, Shaanxi Key Laboratory of Green Preparation and Functionalization for Inorganic Materials, Shaanxi University of Science and Technology, Xi'an, Shaanxi 710021, P.R. China.

出版信息

Dalton Trans. 2024 Feb 27;53(9):3959-3969. doi: 10.1039/d3dt04244h.

Abstract

Electrocatalytic water splitting is considered to be one of the most promising technologies for large-scale sustained production of H. Developing non-noble metal-based electrocatalytic materials with low cost, high activity and long life is the key to electrolysis of water. Transition metal sulfides (TMSs) with good electrical conductivity and a tunable electronic structure are potential candidates that are expected to replace noble metal electrocatalysts. In addition, self-supported electrodes have fast electron transfer and mass transport, resulting in enhanced kinetics and stability. In this paper, TMS self-supported electrocatalysts are taken as examples and their recent progress as hydrogen evolution reaction (HER) electrocatalysts is reviewed. The HER mechanism is first introduced. Then, based on optimizing the active sites, electrical conductivity, electronic structure and adsorption/dissociation energies of water and intermediates of the electrocatalysts, the article focuses on summarizing five modulation strategies to improve the activity and stability of TMS self-supported electrode electrocatalysts in recent years. Finally, the challenges and opportunities for the future development of TMS self-supported electrodes in the field of electrocatalytic water splitting are presented.

摘要

电催化水分解被认为是大规模持续生产氢气最具前景的技术之一。开发低成本、高活性和长寿命的非贵金属基电催化材料是水电解的关键。具有良好导电性和可调节电子结构的过渡金属硫化物有望成为替代贵金属电催化剂的潜在候选材料。此外,自支撑电极具有快速的电子转移和质量传输,从而增强了动力学和稳定性。本文以过渡金属硫化物自支撑电催化剂为例,综述了其作为析氢反应(HER)电催化剂的研究进展。首先介绍了析氢反应机理。然后,基于优化电催化剂的活性位点、导电性、电子结构以及水和中间体的吸附/解离能,文章重点总结了近年来提高过渡金属硫化物自支撑电极电催化剂活性和稳定性的五种调控策略。最后,介绍了过渡金属硫化物自支撑电极在电催化水分解领域未来发展面临的挑战和机遇。

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