阴极
材料科学
透射电子显微镜
离子
堆积
容量损失
相(物质)
电池(电)
过渡金属
相变
兴奋剂
化学物理
纳米技术
化学
电极
电化学
凝聚态物理
物理化学
光电子学
热力学
功率(物理)
物理
有机化学
生物化学
催化作用
作者
Byung Cheol Lee,Jeon Kim,Hee‐Soo Kim,Geon‐Tae Park,Yang‐Kook Sun,Chong Seung Yoon
标识
DOI:10.1002/cssc.202401856
摘要
LiNi0.95Co0.04Al0.01O2 (NCA95) is charged up to 4.6 V to study its structural stability at a highly delithiated state using transmission electron microscopy (TEM). The TEM analysis shows that the localized depletion of Li ions near the surface triggers the transition from the H3 phase to the H4 phase with the H4 phase with the O1 stacking appearing as a series of stacking faults even at 4.4 V. The H3 → H4 transition appears to be irreversible and leads to the initial capacity loss. In addition, intraparticle cracks are observed when charged above 4.3 V. These intraparticle microcracks, unlike interparticle cracks that become sealed upon Li‐uptake, likely remain during deintercalation, compromising the mechanical stability of the cathode and lead to fast deterioration of the cycling stability. The TEM analysis of the overcharged NCA95 cathode suggests a clear limit above which the cathode can be cycled without significant capacity loss. The introduction of doping elements that promote the migration of Ni2+ ions into the Li layer would hinder the H3 → H4 transition and help suppress the intraparticle cracks.
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