An Amiable Design of Cobalt Single Atoms as the Active Sites for Oxygen Evolution Reaction in Desalinated Seawater

초록

Green fuel from water splitting is hardcore for future generations, and the limited source of fresh water (<1%) is a bottleneck. Seawater cannot be used directly as a feedstock in current electrolyzer techniques. Until now single atom catalysts were reported by many synthetic strategies using notorious chemicals and harsh conditions. A cobalt single-atom (CoSA) intruding cobalt oxide ultrasmall nanoparticle (Co<inf>3</inf>O<inf>4</inf> USNP)-intercalated porous carbon (PC) (CoSA-Co<inf>3</inf>O<inf>4</inf>@PC) electrocatalyst was synthesized from the waste orange peel as a single feedstock (solvent/template). The extended X-ray absorption fine structure spectroscopy (EXAFS) and theoretical fitting reveal a clear picture of the coordination environment of the CoSA sites (CoSA-Co<inf>3</inf>O<inf>4</inf> and CoSA-N<inf>4</inf> in PC). To impede the direct seawater corrosion and chlorine evolution the seawater has been desalinated (Dseawater) with minimal cost and the obtained PC is used as an adsorbent in this process. CoSA-Co<inf>3</inf>O<inf>4</inf>@PC shows high oxygen evolution reaction (OER) activity in transitional metal impurity-free (TMIF) 1 M KOH and alkaline Dseawater. CoSA-Co<inf>3</inf>O<inf>4</inf>@PC exhibits mass activity that is 15 times higher than the commercial RuO<inf>2</inf>. Theoretical interpretations suggest that the optimized CoSA sites in Co<inf>3</inf>O<inf>4</inf> USNPs reduce the energy barrier for alkaline water dissociation and simultaneously trigger an excellent OER followed by an adsorbate evolution mechanism (AEM). © 2023 Wiley-VCH GmbH.

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