Open-circuit dissolution of platinum from the cathode in polymer electrolyte membrane water electrolysers

被引:23
作者
Dodwell, J. [1 ]
Maier, M. [1 ]
Majasan, J. [1 ]
Jervis, R. [1 ]
Castanheira, L. [2 ]
Shearing, P. [1 ]
Hinds, G. [2 ]
Brett, D. J. L. [1 ]
机构
[1] UCL, Dept Chem Engn, Electrochem Innovat Lab, London WC1E 7JE, England
[2] Natl Phys Lab, Hampton Rd, Teddington TW11 0LW, Middx, England
基金
英国工程与自然科学研究理事会;
关键词
PEM water electrolyser; Differential pulse voltammetry; ICP-MS; Platinum dissolution; 3-Electrode cell; Accelerated stress test; OXYGEN EVOLUTION; PROTON ACTIVITY; PEM; ELECTROCATALYSTS; DEGRADATION; IRIDIUM; PERFORMANCE; HYDROGEN; CELLS; DURABILITY;
D O I
10.1016/j.jpowsour.2021.229937
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
Platinum is the state-of-the-art catalyst for hydrogen evolution in polymer electrolyte membrane (PEM) water electrolysers; however, its stability has only been characterized to a limited extent in situ. This study measures platinum dissolving from the cathode during intermittent operation of a 3-electrode PEM electrolyser cell, using a differential pulse voltammetry technique that provided detection limits for platinum of less than 2 ng L-1. Water samples were periodically taken during on-off current cycling, and during periods of open-circuit voltage (OCV) platinum dissolution was detected when the cathode potential rose above 0.85 V NHE due to diffusion of oxygen from the anode. This reached a maximum dissolution rate at the highest cathode potential of 1.02 V NHE, and gradually decayed over a 90 h period. The average total amount of platinum dissolved per 90 h OCV period was estimated to be 152 ng cm-2 or 0.005% of the initial electrode catalyst mass. The dissolution mechanism was predicted to be the same as that occurring in PEM fuel cell cathodes, although being kinetically hindered in PEM electrolysers by the slow diffusion of oxygen from the anode to the cathode.
引用
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页数:9
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