材料科学
兴奋剂
电化学
化学工程
涂层
结构稳定性
电极
动力学
格子(音乐)
不稳定性
电池(电)
光电子学
扩散
容量损失
降级(电信)
相变
相(物质)
图层(电子)
纳米技术
表层
化学稳定性
热传导
扩散阻挡层
电化学动力学
相变存储器
作者
Jiaming Miao,Sheng Zhou,Donghui Chen,Weiwu Yuan,Junwei Lin,Han Zhou,Liangwei Liu,Yibing Yang,Yi Xiao,Fushan Feng,Junhua Zhang,Zhou Yang,Xiang Ding,Lili Han
出处
期刊:Small
[Wiley]
日期:2026-06-09
卷期号:: e13120-e13120
标识
DOI:10.1002/smll.202513120
摘要
ABSTRACT High‐voltage LiCoO 2 (LCO) is considered as the solution to extend the battery life of smart electronic devices. However, it still suffers from severe interface instability and structural degradation above 4.7 V. Herein, we put forward a high‐entropy gradient‐like design via high‐entropy (TiO 2 , Al 2 O 3 , MgO, In 2 O 3 , and La 2 O 3 ) surface coating that combines an ultra‐thin high‐entropy coating layer of 1.35 nm thickness and subsurface gradient‐like doping of 1 nm depth. This surface structure can suppress side reactions and enhance Li + diffusion kinetics on the surface. Also, subsurface gradient‐like doping restrains lattice distortion from the irreversible O3‐H1‐3‐O1 phase transition so as to strengthen the electrochemical stability above 4.7 V. A series of in situ, ex situ characterizations and DFT calculations fundamentally clarify the optimized structure‐activity relationship and electronic/spatial effects. Hence, this high‐entropy lattice designed LCO displays a superior capacity of 197.24 mA h g −1 at 1C with 92.4% capacity retention during 400 cycles within 3.0–4.7 V in half‐cells. Moreover, when cycled in a full LCO//graphite pouch‐cell, it can show a competitive cycling capacity of 210.42 mA h g −1 at 0.5C and stability of 95.5% after 100 cycles during 3–4.6 V, manifesting strong practicality in high‐volumetric‐energy‐density and long‐lasting LCO materials.
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