Electrode reconstruction strategy for oxygen evolution reaction: maintaining Fe-CoOOH phase with intermediate-spin state during electrolysis

Computational calculations and experimental studies reveal that the CoOOH phase and the intermediate-spin (IS) state are the key factors for realizing efficient Co-based electrocatalysts for the oxygen evolution reaction (OER). However, according to thermodynamics, general cobalt oxide converts to t...

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Veröffentlicht in:Nature communications 2022-02, Vol.13 (1), p.605-605, Article 605
Hauptverfasser: Lee, Woong Hee, Han, Man Ho, Ko, Young-Jin, Min, Byoung Koun, Chae, Keun Hwa, Oh, Hyung-Suk
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Sprache:eng
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Zusammenfassung:Computational calculations and experimental studies reveal that the CoOOH phase and the intermediate-spin (IS) state are the key factors for realizing efficient Co-based electrocatalysts for the oxygen evolution reaction (OER). However, according to thermodynamics, general cobalt oxide converts to the CoO 2 phase under OER condition, retarding the OER kinetics. Herein, we demonstrate a simple and scalable strategy to fabricate electrodes with maintaining Fe-CoOOH phase and an IS state under the OER. The changes of phase and spin states were uncovered by combining in-situ /operando X-ray based absorption spectroscopy and Raman spectroscopy. Electrochemical reconstruction of chalcogenide treated Co foam affords a highly enlarged active surface that conferred excellent catalytic activity and stability in a large-scale water electrolyzer. Our findings are meaningful in that the calculated results were experimentally verified through the operando analyses. It also proposes a new strategy for electrode fabrication and confirms the importance of real active phases and spin states under a particular reaction condition. The phase and spin state affect catalytic activity of Co-based catalysts for oxygen evolution reaction. Herein, the authors demonstrate a simple reconstruction strategy to fabricate electrodes maintaining a Fe-CoOOH phase and an intermediate-spin state during catalysis.
ISSN:2041-1723
2041-1723
DOI:10.1038/s41467-022-28260-5