Gold as an efficient hydrogen isotope separation catalyst in proton exchange membrane water electrolysis

被引:0
|
作者
Xue, Xiaochong [1 ,2 ]
Zhang, Mingjun [1 ,2 ]
Wei, Fei [1 ,2 ]
Liang, Chaofei [1 ,2 ]
Liang, Jie [1 ,2 ]
Li, Jinglin [1 ,2 ]
Cheng, Wenyu [1 ,2 ]
Deng, Ke [1 ]
Liu, Wei [1 ,2 ]
机构
[1] Chinese Acad Sci, Shanghai Inst Appl Phys, Shanghai 201800, Peoples R China
[2] Univ Chinese Acad Sc, Beijing 100049, Peoples R China
基金
中国国家自然科学基金;
关键词
Hydrogen isotope separation; PEM water electrolysis; Hydrogen evolution reaction; Kinetic isotope effect; Gold catalyst; SOLID-POLYMER-ELECTROLYTE; EVOLUTION REACTION; DEUTERIUM; TRITIUM; TEMPERATURE; ENRICHMENT; DENSITY; OPTIMIZATION; IRON;
D O I
10.1016/j.ijhydene.2022.06.052
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The development of proton exchange membrane water electrolysis (PEMWE) offers an updating potential for electrolytic hydrogen isotope separation. However, it has a significantly lower separation factor than the traditional alkaline water electrolysis. In this study, we propose gold as a promising cathodic catalyst for efficient hydrogen isotope separation in PEMWE. Au/C has a protium-to-deuterium (H/D) separation factor of 7.47 in PEMWE, about twice that of Pt/C. In addition, the full cell's electrochemical performance is comparable to that of its Pt/C counterpart. The separation mechanism in PEMWE is explained by the transitional hydrogen evolution reaction mechanism from Heyrovsky to Tafel for Pt and the unchangeable Volmer mechanism for Au. The high separation factor for Au is also calculated by the H/D zero-point vibrational energy difference between transition state and reaction state through a simple density functional theory calculation. This work offers an effective strategy to improve hydrogen isotope separation efficiency in PEMWE. (c) 2022 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:26842 / 26849
页数:8
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