八面体
电化学
离子
结晶学
化学
扩散
材料科学
四面体
电极
晶体结构
物理化学
物理
热力学
有机化学
作者
Patrick Rozier,Etsuro Iwama,Nagare Nishio,Kazuhisa BABA,Keisuke Matsumura,Kazuaki Kisu,Junichi Miyamoto,Wako Naoi,Yuki Orikasa,Patrice Simon,Katsuhiko Naoi
标识
DOI:10.1021/acs.chemmater.8b00721
摘要
The reversible lithiation/delithiation mechanism of the cation-disordered Li3VO4 material was elucidated, including the understanding of structural and electrochemical signature changes during cycling. The initial exchange of two Li induces a progressive and irreversible migration of Li and V ions from tetrahedral to octahedral sites, confirmed by the combination of in situ/operando X-ray diffraction and X-ray absorption fine structure analyses. The resulting cation-disordered Li3VO4 can smoothly and reversibly accommodate two Li and shows a Li+ diffusion coefficient larger by 2 orders of magnitude than the one of pristine Li3VO4, leading to improved electrochemical performance. This cation-disordered Li3VO4 negative electrode offers new opportunities for designing high-energy and high-power supercapacitors. Furthermore, it opens new paths for preparing disordered compounds with the general hexagonal close-packing structure, including most polyanionic compounds, whose electrochemical performance can be easily improved by simple cation mixing.
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