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Structural water engaged disordered vanadium oxide nanosheets for high capacity aqueous potassium-ion storage

Aqueous electrochemical energy storage devices using potassium-ions as charge carriers are attractive due to their superior safety, lower cost and excellent transport properties compared to other alkali ions. However, the accommodation of potassium-ions with satisfactory capacity and cyclability is...

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Detalles Bibliográficos
Autores principales: Charles, Daniel Scott, Feygenson, Mikhail, Page, Katharine, Neuefeind, Joerg, Xu, Wenqian, Teng, Xiaowei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5457508/
https://www.ncbi.nlm.nih.gov/pubmed/28534481
http://dx.doi.org/10.1038/ncomms15520
Descripción
Sumario:Aqueous electrochemical energy storage devices using potassium-ions as charge carriers are attractive due to their superior safety, lower cost and excellent transport properties compared to other alkali ions. However, the accommodation of potassium-ions with satisfactory capacity and cyclability is difficult because the large ionic radius of potassium-ions causes structural distortion and instabilities even in layered electrodes. Here we report that water induces structural rearrangements of the vanadium-oxygen octahedra and enhances stability of the highly disordered potassium-intercalated vanadium oxide nanosheets. The vanadium oxide nanosheets engaged by structural water achieves high capacity (183 mAh g(−1) in half-cells at a scan rate of 5 mV s(−1), corresponding to 0.89 charge per vanadium) and excellent cyclability (62.5 mAh g(−1) in full cells after 5,000 cycles at 10 C). The promotional effects of structural water on the disordered vanadium oxide nanosheets will contribute to the exploration of disordered structures from earth-abundant elements for electrochemical energy storage.