Defect engineering is an important means of improving the electrochemical performance of the CoO electrocatalyst in the oxygen evolution reaction (OER). In this study, soft X-ray absorption spectroscopy (SXAS) is used to explore the electronic structure of CoO under OER for the first time. The defect-rich CoO (D-CoO) has a Co state with Co at both octahedral (O) and tetrahedral (T) sites and Co at O, whereas CoO has Co with Co and Co at T and O sites, respectively. SXAS reveals that upon increasing the voltage, the Co in D-CoO is converted to low-spin Co, some of which is further converted to low-spin Co; most Co in CoO is converted to Co but rarely to Co. When the voltage is switched off, Co intermediates quickly disappear. These findings reveal Co(O) in D-CoO can be rapidly converted to active low-spin Co under conditions, which cannot be observed by XAS.
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http://dx.doi.org/10.1021/acs.jpclett.2c01557 | DOI Listing |
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