材料科学
阴极
化学工程
锂(药物)
电化学
涂层
同步加速器
表面改性
图层(电子)
电极
阳极
表面工程
吸收(声学)
镍
化学稳定性
X射线光电子能谱
分析化学(期刊)
磷酸铁锂
吸附
吸收光谱法
溶剂
扩散
扩散层
滴定法
复合材料
无机化学
单晶
作者
Shadab Ali Ahmed,Tripti Agnihotri,Ashok Ranjan,Chia‐Yu Chang,Rehbar Hasan,Elango Balaji Tamilarasan,Yosef Nikodimos,Kassie Nigus Shitaw,Tsung‐I Yeh,Bereket Woldegbreal Taklu,Weisheng Liao,Boligarla Vinay,She‐Huang Wu,Wei-Nien Joe Su,Bing‐Joe Hwang
出处
期刊:Small
[Wiley]
日期:2025-11-18
卷期号:22 (1): e06613-e06613
被引量:9
标识
DOI:10.1002/smll.202506613
摘要
Abstract Nickel‐rich layered oxides, such as LiNi 0.83 Mn 0.06 Co 0.11 O 2 (NMC), are among the most promising cathode materials for high‐energy‐density lithium‐ion batteries. However, their practical implementation is limited by surface instability and the presence of residual lithium compounds, which degrade performance and complicate scalability. In this study, a dual‐functional surface modification strategy using lithium dihydrogen phosphate (LiH 2 PO 4 ) is presented. A wet impregnation procedure is used to transform the residual surface contaminants (LiOH, Li 2 CO 3 ) into an advantageous surface coating (Li 3 PO 4 ) on single crystal nickel‐rich (SCNMC) cathode materials rather than directly eliminating them through solvent washing process., as confirmed by titration and in situ Gas Chromotography‐Mas (GC‐MS), while the resulting ≈4 nm Li 3 PO 4 layer enhances structural stability, suppresses nickel migration, and mitigates electrolyte‐induced side reactions. Electrochemical tests reveal significantly improved cycling stability (72.96% capacity retention after 100 cycles at 0.2C compared to 18.25% for pristine SCNMC) and enhanced rate capability, supported by improved Li + diffusion kinetics. Synchrotron X‐ray Absorption Spectroscopy (XAS) and post‐mortem analyses further confirm the preservation of Ni oxidation states and reduced cross‐talk effects.
科研通智能强力驱动
Strongly Powered by AbleSci AI