电化学(中英文) ›› 2024, Vol. 30 ›› Issue (1): 2305101. doi: 10.13208/j.electrochem.2305101
收稿日期:
2023-05-10
修回日期:
2023-08-08
接受日期:
2023-08-22
出版日期:
2024-01-28
发布日期:
2023-09-09
Hai-Bin Ma, Xiao-Yan Zhou, Jia-Yi Li, Hong-Fei Cheng*(), Ji-Wei Ma*()
Received:
2023-05-10
Revised:
2023-08-08
Accepted:
2023-08-22
Published:
2024-01-28
Online:
2023-09-09
Contact:
*Hong-Fei Cheng, E-mail: 摘要:
在碱性介质中,由于电极材料的较高的稳定性,电催化析氢反应(HER)具有实现大规模制氢的巨大潜力。然而,即使对于最突出的铂催化剂,HER在碱性介质中的反应动力学也比在酸性介质中慢2-3个数量级,这是由于碱性环境下质子的浓度较低。异质结构催化剂具有多种结构优势,研究表明,构建异质结构电催化剂是促进碱性HER动力学的有效策略。协同效应是异质结构的一个独特特征,这意味着一个功能活性位点作为水解离的促进剂,另一个活性位点则负责适度的氢吸附,从而协同提高HER催化性能。此外,异质结构中的每个构建模块都是可调节的,为构建最佳催化剂提供了更多的灵活性和可能性。同时,由于界面处两个组分之间存在费米能级差,可以合理地调控每个组分的电子结构,从而大幅度提高碱性介质中的HER催化性能。随着对纳米结构的深入理解,人们开发了更先进的设计策略来构建高性能异质结构电催化剂。本文综述了异质结构催化剂在碱性HER方面的最新发展,以及构建界面异质结构以促进碱性HER动力学性能的合理设计原则。我们首先介绍了HER在碱性介质中的基本反应途径,然后详细讨论了促进碱性HER动力学的新兴有效策略,包括协同效应、应变效应、电子相互作用、相工程和结构工程,最后提出了未来面向实际应用的新型异质结构催化剂设计所面临的挑战和研究机遇。
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