材料科学
电化学
阴极
法拉第效率
化学工程
锂(药物)
结构稳定性
扩散
粒子(生态学)
容量损失
金属
钴
纳米技术
粒径
结构变化
纳米晶
锂电池
电极
电池(电)
锂离子电池
表面扩散
纳米结构
作者
Hanisha Ponnuru,Sagar Jadhav,Michael W. Jones,Konstantin L. Firestein,Benedicta D. Arhatari,Ishara Wijesinghe,Sen Wang,Anthony P. O’Mullane,Cheng Yan
出处
期刊:Small
[Wiley]
日期:2025-11-02
卷期号:21 (48): e06548-e06548
被引量:2
标识
DOI:10.1002/smll.202506548
摘要
Abstract Single crystalline (SC) Ni‐rich layered lithium metal oxides are promising cathode materials for lithium‐ion batteries due to their high theoretical capacity (> 200 mAh g −1 ) and reduced cobalt composition. However, electrochemical behavior of Ni‐rich materials is underexplored and requires a better understanding to address existing challenges such as elongated Li‐ion diffusion pathways and unstable cycling performance. In this study, SC cathode materials with 83% and 90% Ni content are electrochemically cycled at 1 C from 3 to 4.5 V for up to 300 charge/discharge cycles to investigate changes in impedance, non‐faradaic and faradaic electrochemical active surface areas, and structural evolution. Non‐faradaic electrochemical active surface area (ECSA) measurement increases from 1.81 to 3.30 m 2 g −1 for smaller particles sized NCM 90 (3.12 µm) and 3.14 to 3.52 m 2 g −1 for larger particles sized NCM 83 (6.18 µm) after 300 cycles. Faradaic ECSA for NCM 83 increased by 34.4% at the reduction stage, whereas NCM 90 reduced by 61.46% contributing to recurring surface reconstruction and microcracking. Micro‐computed tomography reveals greater material loss in NCM 83 (≈4.5%) compared to NCM 90 (≈2%), attributed to larger particle size. These insights shed new light on surface and structural changes in SC high‐Ni cathodes and their effects on electrochemical performance.
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