阳极
材料科学
石墨
锂(药物)
电化学
纳米颗粒
化学工程
纳米技术
离子
电导率
电极
化学
复合材料
物理化学
有机化学
内分泌学
工程类
医学
作者
Wenhao Liu,Xuanpeng Wang,Jinshuai Liu,Changyuan Guo,Qiao Fan,Xiaoling Ding,Xiaobin Liao,Chunhua Han
出处
期刊:Chemsuschem
[Wiley]
日期:2023-02-17
卷期号:16 (10): e202300067-e202300067
被引量:7
标识
DOI:10.1002/cssc.202300067
摘要
Abstract To better satisfy the increasing demands for electric vehicles, it is crucial to develop fast‐charging lithium‐ion batteries (LIBs). However, the fast‐charging capability of commercial graphite anodes is limited by the sluggish Li + insertion kinetics. Herein, we report a synergistic engineering of uniform nano‐sized T‐Nb 2 O 5 particles on graphite (Gr@Nb 2 O 5 ) with C−O−Nb heterointerfaces, which prevents the growth and aggregation of T‐Nb 2 O 5 nanoparticles. Through detailed theoretical calculations and pair distribution function analysis, the stable existence of the heterointerfaces is proved, which can accelerate the electron/ion transport. These heterointerfaces endow Gr@Nb 2 O 5 anodes with high ionic conductivity and excellent structural stability. Consequently, Gr@10‐Nb 2 O 5 anode, where the mass ratio of T‐Nb 2 O 5 /graphite=10/100, exhibits excellent cyclic stability and incredible rate capabilities, with 100.5 mAh g −1 after 10000 stable cycles at an ultrahigh rate of 20 C. In addition, the synergistic Li + storage mechanism is revealed by systematic electrochemical characterizations and in situ X‐ray diffraction. This work offers new insights to the reasonable design of fast‐charging graphite‐based anodes for the next generation of LIBs.
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