Bifunctional Oxygen-Defect Bismuth Catalyst toward Concerted Production of H2O2 with over 150% Cell Faradaic Efficiency in Continuously Flowing Paired-Electrosynthesis System

© 2024 Wiley‐VCH GmbH.

Bibliographische Detailangaben
Veröffentlicht in:Advanced materials (Deerfield Beach, Fla.). - 1998. - 36(2024), 39 vom: 03. Sept., Seite e2408341
1. Verfasser: Zhang, Qiqi (VerfasserIn)
Weitere Verfasser: Cao, Changsheng, Zhou, Shenghua, Wei, Wenbo, Chen, Xin, Xu, Rongjie, Wu, Xin-Tao, Zhu, Qi-Long
Format: Online-Aufsatz
Sprache:English
Veröffentlicht: 2024
Zugriff auf das übergeordnete Werk:Advanced materials (Deerfield Beach, Fla.)
Schlagworte:Journal Article hydrogen peroxide oxygen reduction reaction oxygen vacancy paired‐electrosynthesis water oxidation reaction
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520 |a The electrosynthesis of hydrogen peroxide (H2O2) from O2 or H2O via the two-electron (2e-) oxygen reduction (2e- ORR) or water oxidation (2e- WOR) reaction provides a green and sustainable alternative to the traditional anthraquinone process. Herein, a paired-electrosynthesis tactic is reported for concerted H2O2 production at a high rate by coupling the 2e- ORR and 2e- WOR, in which the bifunctional oxygen-vacancy-enriched Bi2O3 nanorods (Ov-Bi2O3-EO), obtained through electrochemically oxidative reconstruction of Bi-based metal-organic framework (Bi-MOF) nanorod precursor, are used as both efficient anodic and cathodic electrocatalysts, achieving concurrent H2O2 production at both electrodes with high Faradaic efficiencies. Specifically, the coupled 2e- ORR//2e- WOR electrolysis system based on such distinctive oxygen-defect Bi catalyst displays excellent performance for the paired-electrosynthesis of H2O2, delivering a remarkable cell Faradaic efficiency of 154.8% and an ultrahigh H2O2 production rate of 4.3 mmol h-1 cm-2. Experiments combined with theoretical analysis reveal the crucial role of oxygen vacancies in optimizing the adsorption of intermediates associated with the selective two-electron reaction pathways, thereby improving the activity and selectivity of the 2e- reaction processes at both electrodes. This work establishes a new paradigm for developing advanced electrocatalysts and designing novel paired-electrolysis systems for scalable and sustainable H2O2 electrosynthesis 
650 4 |a Journal Article 
650 4 |a hydrogen peroxide 
650 4 |a oxygen reduction reaction 
650 4 |a oxygen vacancy 
650 4 |a paired‐electrosynthesis 
650 4 |a water oxidation reaction 
700 1 |a Cao, Changsheng  |e verfasserin  |4 aut 
700 1 |a Zhou, Shenghua  |e verfasserin  |4 aut 
700 1 |a Wei, Wenbo  |e verfasserin  |4 aut 
700 1 |a Chen, Xin  |e verfasserin  |4 aut 
700 1 |a Xu, Rongjie  |e verfasserin  |4 aut 
700 1 |a Wu, Xin-Tao  |e verfasserin  |4 aut 
700 1 |a Zhu, Qi-Long  |e verfasserin  |4 aut 
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773 1 8 |g volume:36  |g year:2024  |g number:39  |g day:03  |g month:09  |g pages:e2408341 
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