Self-Organized Integrated Electrocatalyst on Oxygen Conversion for Highly Durable Zinc-Air Batteries

被引:0
作者
Chang, Qian [1 ,2 ]
He, Feng [1 ,2 ]
Zhang, Zhihui [1 ,2 ]
Fu, Xinlong [1 ,2 ]
Wang, Yi [1 ,2 ]
Huang, Changshui [1 ,2 ]
Li, Yuliang [1 ,2 ]
机构
[1] Chinese Acad Sci, Inst Chem, CAS Key Lab Organ Solids, Beijing 100190, Peoples R China
[2] Univ Chinese Acad Sci, Sch Chem Sci, Beijing 100049, Peoples R China
基金
中国博士后科学基金; 中国国家自然科学基金;
关键词
bifunctional oxygen conversion; graphdiyne; integrated Janus nanoparticles; zinc-air batteries; REDUCTION; CATALYSTS;
D O I
10.1002/anie.202416664
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Efficient bifunctional electrocatalysts for oxygen reduction reaction (ORR) and oxygen evolution reaction (OER) are key for clean energy applications such as rechargeable metal-air batteries. Highly efficient bifunctional electrocatalysts have been the focus of great attention by scientists. Here, an innovative and continuous growth method is established to fabricate integrated Janus structure Co3O4/CoNGDY catalyst, which can work for bifunctional oxygen catalytic conversion, achieving highly durable zinc-air batteries. Embedded in the hydrangea-shaped N-doped graphdiyne (NGDY), the Co3O4/CoNGDY is self-organized by CoNGDY at the NGDY contact sites and Co3O4 at the upper part, in which Co3O4 works as OER catalyst and CoNGDY acts as ORR catalyst. Due to the incomplete charge transfer within integrated structure, NGDY reduces the d-band center of the Co sites, so the adsorption strength of intermediates is balanced, and the catalytic activity for ORR/OER is increased. The Co3O4/CoNGDY can serve as an efficient air electrode of rechargeable zinc-air batteries. The rechargeable Co3O4/CoNGDY-based aqueous zinc-air batteries demonstrate excellent performance with a high specific capacity of 746.8 mAh g-1 and an extremely long lifetime of more than 5000 hours. The recoverable modularized cylindrical Co3O4/CoNGDY-based solid-state zinc-air batteries with a power density of up to 167.6 mW cm-2 can be achieved.
引用
收藏
页数:9
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