4.8 Article

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

Journal

JOURNAL OF POWER SOURCES
Volume 498, Issue -, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.jpowsour.2021.229937

Keywords

PEM water electrolyser; Differential pulse voltammetry; ICP-MS; Platinum dissolution; 3-Electrode cell; Accelerated stress test

Funding

  1. National Measurement System of the UK Department for Business, Energy & Industrial Strategy
  2. EPSRC [EP/L015277/1, EP/P009050/1, EP/M014371/1, EP/M009394/1, EP/M023508/1, EP/L015749/1, EP/N022971/1]

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Platinum is the state-of-the-art catalyst for hydrogen evolution in polymer electrolyte membrane (PEM) water electrolysers, but its stability in situ has only been characterized to a limited extent. This study measured platinum dissolution from the cathode during intermittent operation of a 3-electrode PEM electrolyser cell, finding that platinum dissolution was most pronounced during open-circuit voltage periods when the cathode potential exceeded 0.85 V NHE.
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.

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