阳极
材料科学
锂(药物)
电化学
钙钛矿(结构)
电极
自行车
离子
化学工程
氧化物
结构稳定性
钛酸锂
纳米技术
锂离子电池
电池(电)
冶金
物理化学
化学
医学
功率(物理)
物理
考古
有机化学
结构工程
量子力学
工程类
历史
内分泌学
作者
Huaibing Liu,Jingchao Xiao,Haiyan He,Kuo Cao,Yixuan Li,Bicai Pan,Chunhua Chen
出处
期刊:Nano Energy
[Elsevier BV]
日期:2023-11-04
卷期号:119: 109065-109065
被引量:4
标识
DOI:10.1016/j.nanoen.2023.109065
摘要
Due to the advantages in rate capability, cycling performance, and structural stability, oxide perovskites have received increasing attention in the field of fast-charging lithium-ion batteries (LIBs). Here, cation-deficient perovskite Li0.35Nd0.55TiO3 (LNTO) is synthesized and reported as a novel high-performance anode material without further modification. With an average operating potential of 0.73 V vs. Li+/Li, the anode possesses a reversible specific capacity of 202 mAh g−1 at 0.1 C (1 C = 200 mA g−1). Owing to the intrinsically fast Li+ migration channels and three-dimensional skeleton structure, LNTO exhibits excellent rate performance (58 % capacity retention at 40 C) as well as impressive cycling stability (93.5 % capacity retention after 1600 cycles at 10 C). Structural evolution characterization demonstrates a simple solid-solution reaction with the volume change of only 5.51 %. The LiFePO4//LNTO full cell displays outstanding cycling stability (82.8 % capacity retention after 1000 cycles at 5 C) in practical application. Relating the A-site structure to the electrochemical performance, we further provide some insights for the rational design of next-generation fast-charging electrode materials.
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