Lee SMoysiadou AChu Y.-CHAO MING CHENHu X.2022-04-252022-04-25202217545692https://www.scopus.com/inward/record.uri?eid=2-s2.0-85124201163&doi=10.1039%2fd1ee02999a&partnerID=40&md5=6c448b52770afb966d9378ad5fdecb32https://scholars.lib.ntu.edu.tw/handle/123456789/606872The oxygen evolution reaction (OER) is the bottleneck reaction of water splitting, which can be used to generate green hydrogen from renewable electricity. Cobalt iron oxyhydroxides (CoFeOxHy) are among the most active OER catalysts in alkaline medium. However, the active sites of these catalysts remain unclear. Here we use operando ultraviolet-visible (UV-Vis), X-ray absorption, and Raman spectroscopy to reveal oxidations of both Fe and Co ions in CoFeOxHy during the OER. By analyzing samples with different Fe contents and thickness, we find that the concentration of Fe4+ species at the surface, but not the concentration of Co4+ in the bulk, scales with the catalytic activity. These results indicate an Fe4+-containing active site in CoFeOxHy. This journal is ? The Royal Society of Chemistry.Cobalt compoundsIron compoundsOxygenX ray absorptionActive oxygenActive siteAlkaline mediaFe and CoIron speciesOperandoOxyhydroxidesRenewable electricityWater splitting]+ catalystCatalyst activitychemical reactionconcentration (composition)detection methodhydroxideintertidal environmentiron[SDGs]SDG7journal article10.1039/d1ee02999a2-s2.0-85124201163