4.6 Article

Flexible self-supporting Ni2P@N-doped carbon anode for superior rate and durable sodium-ion storage

期刊

ELECTROCHIMICA ACTA
卷 321, 期 -, 页码 -

出版社

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.electacta.2019.134624

关键词

Ni2P polyhedrons; Microporous structure; Carbon fiber; Flexible; Sodium-ion batteries

资金

  1. National Natural Science Foundation of China [U1710256, 51572184]

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Transition-metal phosphides are considered as candidates for sodium-ion batteries (SIBs) due to the high theoretical specific capacity. However, serious volume variation and agglomeration during sodiation-desodiation hamper their development. Hence, a microporous structure of Ni2P@C-N polyhedrons embedding in highly rough carbon fiber (Ni2P@C-N subset of CF) is designed as self-supporting anode material. The synergistic effect of ultrasmall Ni2P particles (similar to 5 nm), graphitic carbon shell and adequate free space of carbon fibers buffer the volume change, the uniform distribution of Ni2P particles shorten Na+ diffusion path, the microporous structure endow adequate electrolyte penetration, the graphitic carbon shell and carbon fibers provide high conductive channel, and thus boosting a remarkable sodium storage performance. The Ni2P@C-N subset of CF delivers long cycling stability (196.8 mAh g(-1) at 1000 mA g(-1) over 1000 cycles with a capacity dropping of 0.04% cycle(-1)), superior rate capability (197.1 mAh g(-1) at 2000 mA g(-1), and returned to 752.5 mAh g(-1) at 100 mA g(-1)). Moreover, the flexible half-cell based on the Ni2P@C-N subset of CF electrode still maintains 81.7% capacity retention after repeated bending states. The full cell based on Ni2P@C-N subset of CF and Na3V2(PO4)(3) manifests a capacity of 185.9 mAh g(-1) over 100 cycles and energy density of similar to 217.4 Wh kg(-1) for SIBs. Furthermore, the hybrid energy storage mechanism can also contribute to the outstanding electrochemical performance. The Ni2P@C-N subset of CF shows a potential in flexible electrode materials for Na-storage device. (C) 2019 Published by Elsevier Ltd.

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