Screening Spinel Oxide Supports for RuO 2 to Boost Bifunctional Electrocatalysts for Advanced Zn–Air Batteries

The compositing strategy offers great potential in designing bifunctional oxygen electrocatalysts for Zn–air batteries. Recent reports reveal that the couple of RuO 2 , serving as a benchmark oxygen evolution reaction (OER) catalyst, with other oxygen reduction reaction (ORR) catalysts is a wise cho...

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Veröffentlicht in:Advanced functional materials 2024-09, Vol.34 (36)
Hauptverfasser: Zou, Xiaohong, Lu, Qian, Wu, Jie, Zhang, Kouer, Tang, Mingcong, Wu, Baoxin, She, Sixuan, Zhang, Xiao, Shao, Zongping, An, Liang
Format: Artikel
Sprache:eng
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Zusammenfassung:The compositing strategy offers great potential in designing bifunctional oxygen electrocatalysts for Zn–air batteries. Recent reports reveal that the couple of RuO 2 , serving as a benchmark oxygen evolution reaction (OER) catalyst, with other oxygen reduction reaction (ORR) catalysts is a wise choice to build highly efficient bifunctional electrocatalysts. However, the design criteria for ORR and OER activities of RuO 2 ‐based composite catalysts are still unclear. Herein, a series of transition metal (Fe, Co, Mn, and Ni)‐doped spinel oxides are designed to support RuO 2 nanorods for exploring the reaction mechanism. Through advanced technology, it is considered that increasing the content and binding energy of Co 3+ and enhancing the oxidation state of Ru 4+ is an efficient strategy to promote ORR and OER activities for RuO 2 /Co‐based spinel oxide composite catalysts. It is found that coupling Mn‐doping Co 3 O 4 (CMO) supports with RuO 2 can induce the highest catalytic activities in ORR/OER and excellent performance in rechargeable Zn–air batteries. Operando electrochemical impedance spectroscopy and theoretical calculation further prove the synergistic effect between RuO 2 and CMO supports originated from the oxygen overflow to overcome the large barrier for oxygen desorption on RuO 2 during OER and oxygen adsorption on CMO supports during ORR.
ISSN:1616-301X
1616-3028
DOI:10.1002/adfm.202401134