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Dual-phase nanostructuring of layered metal oxides for high-performance aqueous rechargeable potassium ion microbatteries

Aqueous rechargeable microbatteries are promising on-chip micropower sources for a wide variety of miniaturized electronics. However, their development is plagued by state-of-the-art electrode materials due to low capacity and poor rate capability. Here we show that layered potassium vanadium oxides...

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Detalles Bibliográficos
Autores principales: Li, Ying-Qi, Shi, Hang, Wang, Sheng-Bo, Zhou, Yi-Tong, Wen, Zi, Lang, Xing-You, Jiang, Qing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6754412/
https://www.ncbi.nlm.nih.gov/pubmed/31541111
http://dx.doi.org/10.1038/s41467-019-12274-7
Descripción
Sumario:Aqueous rechargeable microbatteries are promising on-chip micropower sources for a wide variety of miniaturized electronics. However, their development is plagued by state-of-the-art electrode materials due to low capacity and poor rate capability. Here we show that layered potassium vanadium oxides, K(x)V(2)O(5)·nH(2)O, have an amorphous/crystalline dual-phase nanostructure to show genuine potential as high-performance anode materials of aqueous rechargeable potassium-ion microbatteries. The dual-phase nanostructured K(x)V(2)O(5)·nH(2)O keeps large interlayer spacing while removing secondary-bound interlayer water to create sufficient channels and accommodation sites for hydrated potassium cations. This unique nanostructure facilitates accessibility/transport of guest hydrated potassium cations to significantly improve practical capacity and rate performance of the constituent K(x)V(2)O(5)·nH(2)O. The potassium-ion microbatteries with K(x)V(2)O(5)·nH(2)O anode and K(x)MnO(2)·nH(2)O cathode constructed on interdigital-patterned nanoporous metal current microcollectors exhibit ultrahigh energy density of 103 mWh cm(−3) at electrical power comparable to carbon-based microsupercapacitors.