Co3O4/Co nano-heterostructures embedded in N-doped carbon for lithium-O2 batteries

•Co3O4/Co nano-heterostructures embedded in the N-doped graphitized carbon matrix was prepared.•The Co3O4/Co nano-heterostructure interface and N-doped porous carbon matrix enhance the electrochemical performance synergetically.•The catalyst-based battery delivers a high discharge capacity and long...

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Veröffentlicht in:Electrochimica acta 2022-08, Vol.423, p.140577, Article 140577
Hauptverfasser: Ding, Lei, Huang, Tianyue, Zhang, Dawei, Qi, Pan, Zhang, Lihao, Lin, Cong, Luo, Hao
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Sprache:eng
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Zusammenfassung:•Co3O4/Co nano-heterostructures embedded in the N-doped graphitized carbon matrix was prepared.•The Co3O4/Co nano-heterostructure interface and N-doped porous carbon matrix enhance the electrochemical performance synergetically.•The catalyst-based battery delivers a high discharge capacity and long cycle life. Rational design and synthesis of high-performance bifunctional oxygen electrocatalysts with increased effective active sites and facilitated mass/electron transfer are in demand for the lithium-oxygen batteries (LOBs) to overcome the sluggish oxygen reduction/evolution kinetics. Herein, a simple yet effective strategy is proposed by annealing the Prussian blue analog (PBA) precursor under altered calcination conditions to achieve the efficient nano-heterojunction catalysts with optimized active sites. As a result, the obtained porous Co3O4/Co nano-heterostructures embedded in N-doped graphitized carbon matrix (Co3O4/Co@NC) exhibit outstanding electrochemical performance with a high specific capacity of 22,156 mA h g−1 at the current density of 100 mA g−1 and excellent stability, obviously superior to the LOBs based on the other single-component catalysts. Systematic investigations suggest that the enhanced electrochemical performance is ascribed to the Co3O4/Co nano-heterostructure interface and the N-doped porous carbon matrix. This study presents a simple and effective approach for boosting the PBA-derived catalysts with efficient reactivity for various catalytic applications. [Display omitted]
ISSN:0013-4686
1873-3859
DOI:10.1016/j.electacta.2022.140577