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A Stable Rechargeable Aqueous Zn–Air Battery Enabled by Heterogeneous MoS(2) Cathode Catalysts

Aqueous rechargeable zinc (Zn)–air batteries have recently attracted extensive research interest due to their low cost, environmental benignity, safety, and high energy density. However, the sluggish kinetics of oxygen (O(2)) evolution reaction (OER) and the oxygen reduction reaction (ORR) of cathod...

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Detalles Bibliográficos
Autores principales: Wang, Min, Huang, Xiaoxiao, Yu, Zhiqian, Zhang, Pei, Zhai, Chunyang, Song, Hucheng, Xu, Jun, Chen, Kunji
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9698408/
https://www.ncbi.nlm.nih.gov/pubmed/36432355
http://dx.doi.org/10.3390/nano12224069
Descripción
Sumario:Aqueous rechargeable zinc (Zn)–air batteries have recently attracted extensive research interest due to their low cost, environmental benignity, safety, and high energy density. However, the sluggish kinetics of oxygen (O(2)) evolution reaction (OER) and the oxygen reduction reaction (ORR) of cathode catalysts in the batteries result in the high over-potential that impedes the practical application of Zn–air batteries. Here, we report a stable rechargeable aqueous Zn–air battery by use of a heterogeneous two-dimensional molybdenum sulfide (2D MoS(2)) cathode catalyst that consists of a heterogeneous interface and defects-embedded active edge sites. Compared to commercial Pt/C-RuO(2), the low cost MoS(2) cathode catalyst shows decent oxygen evolution and acceptable oxygen reduction catalytic activity. The assembled aqueous Zn–air battery using hybrid MoS(2) catalysts demonstrates a specific capacity of 330 mAh g(−1) and a durability of 500 cycles (~180 h) at 0.5 mA cm(−2). In particular, the hybrid MoS(2) catalysts outperform commercial Pt/C in the practically meaningful high-current region (>5 mA cm(−2)). This work paves the way for research on improving the performance of aqueous Zn–air batteries by constructing their own heterogeneous surfaces or interfaces instead of constructing bifunctional catalysts by compounding other materials.