The efficiency of sunlight-driven reduction of carbon dioxide (CO), a process mimicking the photosynthesis in nature that integrates the light harvester and electrolysis cell to convert CO into valuable chemicals, is greatly limited by the sluggish kinetics of oxygen evolution in pH-neutral conditions. Current non-noble metal oxide catalysts developed to drive oxygen evolution in alkaline solution have poor performance in neutral solutions. Here we report a highly active and stable oxygen evolution catalyst in neutral pH, Brownmillerite SrGaCoO, with the specific activity about one order of magnitude higher than that of widely used iridium oxide catalyst.
View Article and Find Full Text PDF