电化学
兴奋剂
材料科学
钠
离子半径
阴极
晶体结构
X射线光电子能谱
化学工程
离子键合
离子
电极
化学
结晶学
冶金
光电子学
物理化学
有机化学
工程类
作者
Jiahao Li,Jun Cheng,Yanjun Chen,Chao Wang,Li Guo
出处
期刊:Ionics
[Springer Science+Business Media]
日期:2020-09-26
卷期号:27 (1): 181-190
被引量:40
标识
DOI:10.1007/s11581-020-03791-3
摘要
The Na3V2(PO4)3 (NVP) and its binary-doped Na2.96K0.04V2-xZr(3/4)x(PO4)3/C are prepared by a facile solid-phase method. The crystal structure, morphological characteristics, and electrochemical properties are analyzed by XRD, XPS, SEM, and electrochemical tests. The results reveal that K+ and Zr4+ have been successfully doped into NVP system without damaging the original structure. The co-doping strategy can broaden the channels of Na+ migration to facilitate the ionic conductivities. Meanwhile, it is beneficial to stabilizing the crystal structure effectively by introducing the K+ and Zr4+ with larger ionic radius. All the electrochemical properties of co-doped system are better than that of NVP, resulting from the lager channel for Na+ diffusion and enhanced intrinsic electrical conductivities by co-doping. Notably, Na2.96K0.04V1.93Zr0.0525(PO4)3/C exhibits the best electrochemical performance. It delivers a high discharge capacity of 107.3 mAh g−1 at 0.1 C; it remains 92.3 mAh g−1 after 400 cycles at 2 C, corresponding to the capacity retention of 92.02%; it still maintains 100.0 mAh g−1 even at 10 C rate.
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