Directed Surface Reconstruction of Fe Modified Co2VO4 Spinel Oxides for Water Oxidation Catalysts Experiencing Self-Terminating Surface Deterioration

© 2024 Wiley‐VCH GmbH.

Bibliographische Detailangaben
Veröffentlicht in:Advanced materials (Deerfield Beach, Fla.). - 1998. - 36(2024), 31 vom: 09. Aug., Seite e2401818
1. Verfasser: Li, Ang (VerfasserIn)
Weitere Verfasser: Tang, Xiaoxia, Cao, Runjie, Song, Dongcai, Wang, Fangzheng, Yan, Hua, Chen, Hongmei, Wei, Zidong
Format: Online-Aufsatz
Sprache:English
Veröffentlicht: 2024
Zugriff auf das übergeordnete Werk:Advanced materials (Deerfield Beach, Fla.)
Schlagworte:Journal Article CV activation cation leaching oxygen evolution reaction surface reconstruction
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520 |a Affordable highly efficient catalysts for electrochemical oxygen evolution reaction (OER) play pivotal roles in green hydrogen production via water electrolysis. Regarding the non-noble metal-based electrocatalysts, considerable efforts are made to decipher the cation leaching and surface reconstruction; yet, little attention is focused on correlating them with catalytical activity and stability. Herein, in situ reconstruction of Fe-modified Co2VO4 precursor catalyst to form a highly active (Fe,V)-doped CoOOH phase for OER is reported, during which partial leaching of V accelerates the surface reconstruction and the V reserved in the reconstructed CoOOH layer in the form of alkali-resistant V2O3 serves for dynamic charge compensation and prevention of excessive loss of lattice oxygen and Co dissolution. Fe substitution facilitates Co pre-oxidation and endows the catalysts with structural flexibility by elevating O 2p band level; hence, encouraging participation of lattice oxygen in OER. The optimized Co2Fe0.25V0.75O4 electrode can afford current densities of 10 and 500 mA cm-2 at low overpotentials of 205 and 320 mV, respectively, with satisfactory stability over 600 h. By coupling with Pt/C cathode, the assembled alkaline electrolyzer can deliver 500 mA cm-2 at a low cell voltage of 1.798 V, better than that of commercial RuO2 (+) || Pt/C (-) 
650 4 |a Journal Article 
650 4 |a CV activation 
650 4 |a cation leaching 
650 4 |a oxygen evolution reaction 
650 4 |a surface reconstruction 
700 1 |a Tang, Xiaoxia  |e verfasserin  |4 aut 
700 1 |a Cao, Runjie  |e verfasserin  |4 aut 
700 1 |a Song, Dongcai  |e verfasserin  |4 aut 
700 1 |a Wang, Fangzheng  |e verfasserin  |4 aut 
700 1 |a Yan, Hua  |e verfasserin  |4 aut 
700 1 |a Chen, Hongmei  |e verfasserin  |4 aut 
700 1 |a Wei, Zidong  |e verfasserin  |4 aut 
773 0 8 |i Enthalten in  |t Advanced materials (Deerfield Beach, Fla.)  |d 1998  |g 36(2024), 31 vom: 09. Aug., Seite e2401818  |w (DE-627)NLM098206397  |x 1521-4095  |7 nnns 
773 1 8 |g volume:36  |g year:2024  |g number:31  |g day:09  |g month:08  |g pages:e2401818 
856 4 0 |u http://dx.doi.org/10.1002/adma.202401818  |3 Volltext 
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