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Space-Confinement and in Situ Reduction of Pt with 1T-MoS for Exceptional Hydrogen Evolution Reaction in Simulated Seawater.

作者信息

Li Mengyao, Min Jie, Huang Yixuan, Meng Linghui, Dong Zekun, Wang Shuangyue, Wan Tao, Guan Peiyuan, Hu Long, Zhou Yingze, Han Zhaojun, Ni Bingjie, Chu Dewei

机构信息

School of Materials Science and Engineering, University of New South Wales, Sydney, NSW 2052, Australia.

School of Chemical Engineering, University of New South Wales, Sydney, NSW 2052, Australia.

出版信息

ACS Appl Mater Interfaces. 2024 Dec 18;16(50):69199-69209. doi: 10.1021/acsami.4c13270. Epub 2024 Dec 9.

DOI:10.1021/acsami.4c13270
PMID:39653014
Abstract

Efficient catalysts for hydrogen generation from seawater are essential for advancing clean energy technologies. In this study, we present a straightforward method for producing Pt nanoparticles enclosed within metallic 1T-phase MoS nanosheets on graphite paper as a promising catalyst for the hydrogen evolution reaction (HER). The resulting 14.3 wt % Pt-MoS nanosheets demonstrate an ultralow onset potential of 65.6 mV vs the reversible hydrogen electrode (RHE) and a minimal Tafel slope of 64 mV/dec with remarkable stability and durability in simulated seawater, offering comparable catalytic performance to the 40 wt % Pt/C commercial catalyst at a lower cost. This exceptional hydrogen production is attributed to the robust reducing ability of 1T-phase MoS and the confinement of Pt nanoparticles within the MoS interlayers and nanosheets. Our findings highlight the significance of this approach in developing practical and sustainable electrocatalysts for seawater splitting. This research represents a crucial step toward a greener and more sustainable future, leveraging innovative catalyst design strategies for clean energy production.

摘要

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