氧化还原
阴极
法拉第效率
插层(化学)
容量损失
储能
电化学
锂(药物)
电池(电)
阳离子聚合
材料科学
离子
化学工程
化学
无机化学
电极
物理化学
热力学
有机化学
医学
功率(物理)
物理
高分子化学
工程类
内分泌学
作者
Bizhe Su,Shuilin Wu,Hanqin Liang,Wenchong Zhou,Junnan Liu,Damian Goonetilleke,Neeraj Sharma,Patrick H.‐L. Sit,Wenjun Zhang,Denis Y. W. Yu
标识
DOI:10.1021/acs.chemmater.0c02244
摘要
Sodium-ion batteries (NIBs) are a potential low-cost alternative to lithium-ion batteries for large-scale energy storage, but many high-capacity NIB cathode materials undergo irreversible structural changes during charge and discharge, leading to fast capacity fading. Herein, monoclinic NaVO3 exhibits good cycle performance with high capacity as a cathode material for NIBs. In situ synchrotron X-ray diffraction studies show that the material structure is virtually invariant during Na+ (de-)intercalation, with the a and b lattice parameters changing only by 0.13 and 0.19%, respectively. The material undergoes an oxygen redox reaction during initial charge while delivering a remarkable specific capacity of 245 mAh g–1 (1.2–4.7 V) with contributions from cationic (V4+/V5+) and anionic (O2–/O–) redox couples during discharge. The stable VO4 tetrahedral framework also enables the material to give superior rate and cycle capabilities, with a capacity of 164 mAh g–1 (67% utilization) at a current of 1000 mA g–1 (about 5C) and a capacity retention of 90% after 50 cycles. Density functional theory calculations further verify the stability of the material and the charge–discharge mechanism. This work can broaden the horizon for designing high-energy cathode materials with enhanced structural stability for sodium-ion batteries.
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