Physical upcycling of spent artificial diamond accelerant into bifunctional oxygen electrocatalyst with dual-metal active sites for durable rechargeable Zn-air batteries

被引:33
|
作者
Ding, Kuixing [1 ,4 ]
Hu, Jiugang [1 ]
Zhao, Liming [2 ]
Jin, Wei [3 ]
Yu, Huanan [4 ]
Liu, Yunpeng [5 ]
Wu, Zhonghua [5 ]
Cai, Shan [1 ]
Yang, Yi [1 ]
Zou, Guoqiang [1 ]
Hou, Hongshuai [1 ]
Ji, Xiaobo [1 ]
机构
[1] Cent South Univ, Coll Chem & Chem Engn, Changsha 410083, Peoples R China
[2] China Jiliang Univ, Coll Standardizat, Hangzhou 310018, Peoples R China
[3] Suzhou Univ Sci & Technol, Sch Environm Sci & Engn, Suzhou 215009, Peoples R China
[4] China Jiliang Univ, Coll Mat & Chem, Hangzhou 310018, Peoples R China
[5] Chinese Acad Sci, Beijing Synchrotron Radiat Facil BSRF, Inst High Energy Phys, Beijing 100049, Peoples R China
基金
中国国家自然科学基金;
关键词
Physical upcycling; Dual -metal active sites; In situ Raman; Bifunctional electrocatalysts; Rechargeable Zn -air batteries; N-DOPED CARBON; NANOPARTICLES; CATALYSTS; EFFICIENT; EVOLUTION; ALLOY;
D O I
10.1016/j.nanoen.2024.109270
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The low-cost and efficient bifunctional electrocatalysts for the oxygen reduction reaction (ORR) and oxygen evolution reaction (OER) is critical for advanced rechargeable Zn-air batteries (ZABs). Herein, we designed and fabricated a bifunctional m-Fe2.04Ni0.66 @GCFs catalyst using a sustainable physical upcycling strategy involving spent artificial diamond accelerants. Experiments and theoretical calculations verified that dual -metal active -site synergy between *Fe2.04Ni0.66 @GC and Fe2.04 *Ni0.66 @GC enhances the rapid adsorption/desorption of *OOH/ *OH species, thereby improving ORR/OER performance. In situ Raman technique confirmed that ORR/OER activities are dependent on the FeOOH, Fe(OH)2, and beta-NiOOH intermediates formed during the reaction. Impressively, the m-Fe2.04Ni0.66 @GCFs catalyst exhibited outstanding ORR/OER activities with a small potential difference of only 0.73 V in alkaline media. The assembled rechargeable ZAB exhibited high peak power density (115.2 mW cm -2), large specific capacity (786.9 mA h g-1), and long-term charge -discharge cycling stability of more than 1200 cycles. These results not only contribute to the design of efficient bifunctional catalysts, but also provide a new approach to the high -value utilisation of waste catalyst resources.
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页数:11
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