| Literature DB >> 32543824 |
Moxiang Ling1,2, Zhiqiang Lv1,2, Fan Li2,3, Junmei Zhao4, Huamin Zhang1, Guangjin Hou3, Qiong Zheng1, Xianfeng Li1.
Abstract
Tetragonal NaVPO4F has been regarded as an ideal cathode for sodium-ion batteries because of its high average plateau (3.8 V) and theoretical specific capacity (143 mA h g-1). However, the Na-storage performance is still hindered by unsatisfying thermal stability and poor conductivity. Herein, a stable tetragonal NaVPO4F has been synthesized by a novel solvent thermal method using a carbon coating precursor. The as-prepared NaVPO4F@C nanocomposite delivers a capacity of 133 mA h g-1 at 0.2 C, corresponding to an excellent energy density of 509 W h kg-1; when coupled with an HC anode, the full cell still displays an outstanding performance of 124 mA h g-1 at 0.05 C. Fast Na+ diffusion kinetics (DNa+ = 10-12 to 10-10 cm2 s-1) and small volume change (4.4%) are exploited, which ensures good rate trait and cycling stability of tetragonal NaVPO4F. Further, the Na+ extraction-insertion mechanism has been explored by analyzing the crystal structure change during in situ X-ray powder diffraction cycles.Entities:
Keywords: cathodes; crystal structure; high energy density; sodium ion batteries; tetragonal NaVPO4F
Year: 2020 PMID: 32543824 DOI: 10.1021/acsami.0c08846
Source DB: PubMed Journal: ACS Appl Mater Interfaces ISSN: 1944-8244 Impact factor: 9.229