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A vanadium-based oxide-phosphate-pyrophosphate framework as a 4 V electrode material for K-ion batteries

K-ion batteries (KIBs) are promising for large-scale electrical energy storage owing to the abundant resources and the electrochemical specificity of potassium. Among the positive electrode materials for KIBs, vanadium-based polyanionic materials are interesting because of their high working voltage...

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Detalles Bibliográficos
Autores principales: Ohara, Mirai, Hameed, A. Shahul, Kubota, Kei, Katogi, Akihiro, Chihara, Kuniko, Hosaka, Tomooki, Komaba, Shinichi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8480335/
https://www.ncbi.nlm.nih.gov/pubmed/34603668
http://dx.doi.org/10.1039/d1sc03725k
Descripción
Sumario:K-ion batteries (KIBs) are promising for large-scale electrical energy storage owing to the abundant resources and the electrochemical specificity of potassium. Among the positive electrode materials for KIBs, vanadium-based polyanionic materials are interesting because of their high working voltage and good structural stability which dictates the cycle life. In this study, a potassium vanadium oxide phosphate, K(6)(VO)(2)(V(2)O(3))(2)(PO(4))(4)(P(2)O(7)), has been investigated as a 4 V class positive electrode material for non-aqueous KIBs. The material is synthesized through pyrolysis of a single metal–organic molecular precursor, K(2)[(VOHPO(4))(2)(C(2)O(4))] at 500 °C in air. The material demonstrates a reversible extraction/insertion of 2.7 mol of potassium from/into the structure at a discharge voltage of ∼4.03 V vs. K. Operando and ex situ powder X-ray diffraction analyses reveal that the material undergoes reversible K extraction/insertion during charge/discharge via a two-phase reaction mechanism. Despite the extraction/insertion of large potassium ions, the material demonstrates an insignificant volume change of ∼1.2% during charge/discharge resulting in excellent cycling stability without capacity degradation over 100 cycles in a highly concentrated electrolyte cell. Robustness of the polyanionic framework is proved from identical XRD patterns of the pristine and cycled electrodes (after 100 cycles).