Catalyst in a Stable Matrix: Engineering Robust Water Splitting Anodes for Long Term Operation at High Temperature in Acidic Media
Sibimol Luke a b, Manjuanth Chatti c, Asha Yadav d, Jiban Kangsabanik d, Akshat Tanksale b, Aftab Alam d, Aswani Yella a, Alexandr N Simonov c
a ME&MS, IITBombay, Powai,Mumbai, Mumbai, 400076, India
b Monash University, Department of Chemical Engineering, Australia
c School of Chemistry, Monash University, Victoria 3800, Australia
d IIT Indian Institute of Technology Bombay, Department Physics, India
Materials for Sustainable Development Conference (MATSUS)
Proceedings of Online nanoGe Fall Meeting 20 (OnlineNFM20)
#SolFuel20. Solar Fuels
Online, Spain, 2020 October 20th - 23rd
Organizer: Víctor A. de la Peña O'Shea
Contributed talk, Sibimol Luke, presentation 167
Publication date: 4th October 2020

Currently, water electrolysers (WE) based on acidic electrolytes, viz. proton-exchange membranes (PEM), are becoming a preferred technology for the electrolytic generation of green hydrogen fuel. One key limitation of PEM-WE is the low stability of anode catalysts, which are nowadays exclusively based on one of the rarest and most expensive metals – iridium. The less expensive transition metal oxide catalysts are most commonly less active and even more unstable. The instability problem can be overcome via integration of the catalytically active component, transition metal oxide, into a highly-conductive matrix that is thermodynamically stable under the conditions of the operating PEM-WE anode, i.e. at low pH and high temperature. The present report demonstrates the effectiveness of this approach with the antimony oxide matrix that is used to stabilise non-noble third row transition metal catalysts and ruthenium. Significantly improved stability as compared to that reported in the literature is demonstrated, in particular on a week timescale at industrially relevant temperature of 80oC at pH 0.3. Factors affecting the activity and stability as well as possible strategies for further improvements will be also presented and discussed.

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