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A high-capacity cathode for rechargeable K-metal battery based on reversible superoxide-peroxide conversion
As a promising low-cost energy storage device, the development of a rechargeable potassium-ion battery (KIB) is severely hindered by the limited capacity of cathode candidates. Regarded as an attractive capacity-boosting strategy, triggering the O-related anionic redox activity has not been achieved...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8566171/ https://www.ncbi.nlm.nih.gov/pubmed/34858601 http://dx.doi.org/10.1093/nsr/nwaa287 |
Sumario: | As a promising low-cost energy storage device, the development of a rechargeable potassium-ion battery (KIB) is severely hindered by the limited capacity of cathode candidates. Regarded as an attractive capacity-boosting strategy, triggering the O-related anionic redox activity has not been achieved within a sealed KIB system. Herein, in contrast to the typical gaseous open K-O(2) battery (O(2)/KO(2) redox), we originally realize the reversible superoxide/peroxide (KO(2)/K(2)O(2)) interconversion on a KO(2)-based cathode. Controlled within a sealed cell environment, the irreversible O(2) evolution and electrolyte decomposition (induced by superoxide anion (O(2)(−)) formation) are effectively restrained. Rationally controlling the reversible depth-of-charge at 300 mAh/g (based on the mass of KO(2)), no obvious cell degradation can be observed during 900 cycles. Moreover, benefitting from electrolyte modification, the KO(2)-based cathode is coupled with a limited amount of K-metal anode (merely 2.5 times excess), harvesting a K-metal full-cell with high energy efficiency (∼90%) and long-term cycling stability (over 300 cycles). |
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