材料科学
镍
钴
溶解
电化学
阴极
储能
过渡金属
化学工程
高熵合金
容量损失
纳米技术
冶金
电极
微观结构
热力学
物理化学
物理
工程类
催化作用
功率(物理)
化学
生物化学
作者
Boyang Zhao,Xia Sun,Hongwei Bi,Tingzhou Yang,Haipeng Li,Dan Luo,Yongguang Zhang,Zhongwei Chen
标识
DOI:10.1002/adfm.202423717
摘要
Abstract The structural instability of lithium‐based transition metal layered oxides during electrochemical cycling‐exacerbated by phenomena such as metal dissolution and phase transitions‐induces rapid capacity degradation, thus constraining their applicability in high‐energy‐density lithium batteries. While coating these materials can bolster stability, the employment of electrochemically inactive coatings may inadvertently undermine energy storage performance, presenting a significant trade‐off. In response to this challenge, an innovative core‐shell cathode architecture is presented, wherein high entropy doped LiNi 1/6 Mn 1/6 Al 1/6 Ti 1/6 Mo 1/6 Ta 1/6 O 2 serves as the shell and nickel‐rich cobalt‐free LiNi 0.89 Mn 0.11 O 2 constitutes the core, synthesized through a simple two‐step co‐precipitation methodology (designated as LHECNM). This high‐entropy shell preserves the core's electrochemical performance while effectively mitigating phase transformations and transition metal ion dissolution, thereby enhancing structural robustness. Moreover, the core‐shell configuration significantly diminishes the energy barrier for Li + diffusion, facilitating superior ion transport dynamics. Consequently, LHECNM demonstrates remarkable electrochemical performance, achieving a discharge capacity of 201.57 mAh g −1 , a commendable rate capability up to 5C, and an impressive 92% capacity retention over prolonged cycling. This investigation elucidates a promising paradigm for the design of high‐entropy cathode materials, offering profound insights for the advancement of future energy storage technologies.
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