4.8 Article

Self-sacrificed synthesis of three-dimensional Na3V2(PO4)3 nanofiber network for high-rate sodium ion full batteries

期刊

NANO ENERGY
卷 25, 期 -, 页码 145-153

出版社

ELSEVIER
DOI: 10.1016/j.nanoen.2016.03.018

关键词

Self-sacrificed; Na3V2(PO4)(3); Nanofiber network; Sodium-ion; Full batteries

资金

  1. National Basic Research Program of China [2013CB934103, 2012CB933003]
  2. International Science & Technology Cooperation Program of China [2013DFA50840]
  3. National Natural Science Foundation of China [51302203, 51272197, 51521001]
  4. Hubei Province Natural Science Fund for Distinguished Young Scholars [2014CFA035]
  5. National Natural Science Fund for Distinguished Young Scholars [51425204]
  6. Fundamental Research Funds for the Central Universities [WUT: 2015-III-021, 2015-III-032, 2015-III-052, 2015-PY-2]

向作者/读者索取更多资源

The morphological optimization of Na3V2(PO4)(3) (NVP) material has a great significance for improving the electrochemical performance since NVP suffers from intrinsic low electronic conductivity. For this purpose, a novel 3D NVP nanofiber network is controllably constructed via a facile self-sacrificed template method. Based on time-dependent experiments, an outside-in morphological evolution mechanism from microsphere to 3D nanofiber network is proposed. The as-synthesized material exhibits excellent cyclability (95.9% capacity retention over 1000 cycles at 10 C) and enhanced high-rate performance (94 mA h g(-1) at 100 C) for sodium half cell. Notably, when evaluated as full battery (NaTi2(PO4)(3) as anode) cathode, it also shows outstanding cycling stability (96.9% capacity retention over 300 cycles at 5 C) and superior rate capability (80 mA h g(-1) at 50 C). Such remarkable performance is attributed to the 3D nanofiber network structure, which provides multi-channel ionic diffusion pathway, continuous electronic conduction, and improved structural integrity. This self-sacrificed template strategy presented here can inspire new thought in constructing novel nanofiber/nanowire structures and accelerate the development of high-power sodium-ion batteries. (C) 2016 Elsevier Ltd. All rights reserved.

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