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

被引:166
作者
Charles, Daniel Scott [1 ]
Feygenson, Mikhail [2 ,3 ]
Page, Katharine [2 ]
Neuefeind, Joerg [2 ]
Xu, Wenqian [4 ]
Teng, Xiaowei [1 ]
机构
[1] Univ New Hampshire, Dept Chem Engn, Durham, NH 03824 USA
[2] Oak Ridge Natl Lab, Div Chem & Engn Mat, Oak Ridge, TN 37830 USA
[3] Forschungszentrum Julich, Juelich Ctr Neutron Sci, D-52425 Julich, Germany
[4] Argonne Natl Lab, Div Xray Sci, 9700 S Cass Ave, Argonne, IL 60439 USA
基金
美国国家科学基金会;
关键词
CATHODE MATERIAL; CHARGE STORAGE; BATTERIES; SODIUM; V2O5; ELECTRODES; INTERCALATION; MG; PSEUDOCAPACITORS; PERFORMANCE;
D O I
10.1038/ncomms15520
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
070301 [无机化学]; 070403 [天体物理学]; 070507 [自然资源与国土空间规划学]; 090105 [作物生产系统与生态工程];
摘要
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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页数:8
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