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Anchoring NiO Nanosheet on the Surface of CNT to Enhance the Performance of a Li-O(2) Battery

Li(2)O(2), as the cathodic discharge product of aprotic Li-O(2) batteries, is difficult to electrochemically decompose. Transition-metal oxides (TMOs) have been proven to play a critical role in promoting the formation and decomposition of Li(2)O(2). Herein, a NiO/CNT catalyst was prepared by anchor...

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Detalles Bibliográficos
Autores principales: Chen, Shuang, Wang, Shukun, Dong, Yunyun, Du, Hongmei, Zhao, Jinsheng, Zhang, Pengfang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9320305/
https://www.ncbi.nlm.nih.gov/pubmed/35889610
http://dx.doi.org/10.3390/nano12142386
Descripción
Sumario:Li(2)O(2), as the cathodic discharge product of aprotic Li-O(2) batteries, is difficult to electrochemically decompose. Transition-metal oxides (TMOs) have been proven to play a critical role in promoting the formation and decomposition of Li(2)O(2). Herein, a NiO/CNT catalyst was prepared by anchoring a NiO nanosheet on the surface of CNT. When using the NiO/CNT as a cathode catalyst, the Li-O(2) battery had a lower overpotential of 1.2 V and could operate 81 cycles with a limited specific capacity of 1000 mA h g(−1) at a current density of 100 mA g(−1). In comparison, with CNT as a cathodic catalyst, the battery could achieve an overpotential of 1.64 V and a cycling stability of 66 cycles. The introduction of NiO effectively accelerated the generation and decomposition rate of Li(2)O(2), further improving the battery performance. SEM and XRD characterizations confirmed that a Li(2)O(2) film formed during the discharge process and could be fully electrochemical decomposed in the charge process. The internal network and nanoporous structure of the NiO/CNT catalyst could provide more oxygen diffusion channels and accelerate the decomposition rate of Li(2)O(2). These merits led to the Li-O(2) battery’s better performance.