Journal Article

FZJ-2017-06257

http://join2-wiki.gsi.de/foswiki/pub/Main/Artwork/join2_logo100x88.png Structural water engaged disordered vanadium oxide nanosheets for high capacity aqueous potassium-ion storage

Charles, D. S. ; Feygenson, M.FZJ* ; Page, K. ; Neuefeind, J. ; Xu, W. ; Teng, X. (Corresponding author)

2017
Nature Publishing Group London

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Please use a persistent id in citations: http://hdl.handle.net/2128/15228  doi:10.1038/ncomms15520

Abstract: 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.

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Contributing Institute(s):

1. Neutronenstreuung (ICS-1)
2. Neutronenstreuung (Neutronenstreuung ; JCNS-1)

Research Program(s):

1. 551 - Functional Macromolecules and Complexes (POF3-551) (POF3-551)
2. 6G4 - Jülich Centre for Neutron Research (JCNS) (POF3-623) (POF3-623)
3. 6215 - Soft Matter, Health and Life Sciences (POF3-621) (POF3-621)

Appears in the scientific report 2017

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