(Invited) Switching on Electrocatalytic Activity for Synthetic Fuel Production

Abstract

The greatest challenge facing Solid oxide cells (SOC), in both fuel and electrolysis cell modes (i.e SOFCs and SOECs) is to deliver high, long-lasting electrocatalytic activity while ensuring cost and time-efficient electrode manufacture. Ultimately, this can best be achieved by growing appropriate nanoarchitectures under operationally relevant conditions, rather than through intricate ex situ procedures. In our approach, metal particles are grown directly from the oxide support though in situ redox exsolution. We demonstrated that by understanding and manipulating the surface chemistry of an oxide support with adequately designed bulk (non)stoichiometry, one can control the size, distribution and surface coverage of produced particles. We also revealed that the emergent particles are generally epitaxially socketed in the parent perovskite which appears to be the underlying origin of their remarkable stability, including unique resistance of metal particles to agglomeration and to hydrocarbon coking, whilst retaining catalytic activit. Operando redox treatments yield emergent nanomaterials at potentials in excess of 2V. Here we apply this technique to drive steam, CO2 and coelectrolysis processes at emergent metals and alloy particles.