The in situ formation of defective CoOOH catalysts from semi-oxidized Co for alkaline oxygen evolution reaction

Electrochemical water splitting based on Co oxide electrocatalysts provides a promising means for renewable hydrogen production from water. Identifying the structure evolution and real-time active structure of Co-based electrocatalysts under operational conditions is crucial for understanding the OE...

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Veröffentlicht in:Journal of materials chemistry. A, Materials for energy and sustainability Materials for energy and sustainability, 2022-09, Vol.10 (37), p.20011-20017
Hauptverfasser: Wang, Lan, Pan, Ya, Wu, Dan, Liu, Xiaokang, Cao, Linlin, Zhang, Wei, Chen, Honglei, Liu, Tong, Liu, Dong, Chen, Tao, Ding, Tao, Wang, Yi, Ding, Chenglong, Kang, Caitao, Li, Changli, He, Jingfu, Yao, Tao
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container_issue 37
container_start_page 20011
container_title Journal of materials chemistry. A, Materials for energy and sustainability
container_volume 10
creator Wang, Lan
Pan, Ya
Wu, Dan
Liu, Xiaokang
Cao, Linlin
Zhang, Wei
Chen, Honglei
Liu, Tong
Liu, Dong
Chen, Tao
Ding, Tao
Wang, Yi
Ding, Chenglong
Kang, Caitao
Li, Changli
He, Jingfu
Yao, Tao
description Electrochemical water splitting based on Co oxide electrocatalysts provides a promising means for renewable hydrogen production from water. Identifying the structure evolution and real-time active structure of Co-based electrocatalysts under operational conditions is crucial for understanding the OER mechanism and rational design of efficient catalysts. Here, we systematically synthesized three types of Co-based precatalysts, including Co/graphene oxide (GO), Co–CoO/GO and Co 3 O 4 /GO, to clarify the critical effects of the precatalyst structure for OER. The electrochemical test results confirm that the Co–CoO/GO precatalyst shows a lower overpotential compared to Co/GO and Co 3 O 4 /GO precatalysts and commercial RuO 2 /C. A thorough in situ analysis by XAFS revealed that the Co–CoO/GO precatalysts are oxidized and self-assembled into CoOOH during water oxidation and possess a much higher O vacancy density compared with the CoOOH derived from Co/GO, while the Co 3 O 4 /GO precatalyst maintains its structure during operation. This strategy of in situ creation of defects in CoOOH provides a guideline for the rational design of future catalysis systems.
doi_str_mv 10.1039/D2TA02989H
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Identifying the structure evolution and real-time active structure of Co-based electrocatalysts under operational conditions is crucial for understanding the OER mechanism and rational design of efficient catalysts. Here, we systematically synthesized three types of Co-based precatalysts, including Co/graphene oxide (GO), Co–CoO/GO and Co 3 O 4 /GO, to clarify the critical effects of the precatalyst structure for OER. The electrochemical test results confirm that the Co–CoO/GO precatalyst shows a lower overpotential compared to Co/GO and Co 3 O 4 /GO precatalysts and commercial RuO 2 /C. A thorough in situ analysis by XAFS revealed that the Co–CoO/GO precatalysts are oxidized and self-assembled into CoOOH during water oxidation and possess a much higher O vacancy density compared with the CoOOH derived from Co/GO, while the Co 3 O 4 /GO precatalyst maintains its structure during operation. 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source Royal Society Of Chemistry Journals 2008-
subjects Catalysis
Catalysts
Chemical synthesis
Cobalt oxides
Design defects
Electrocatalysts
Electrochemistry
Graphene
Hydrogen production
Oxidation
Oxygen evolution reactions
Self-assembly
Water splitting
title The in situ formation of defective CoOOH catalysts from semi-oxidized Co for alkaline oxygen evolution reaction
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