材料科学
掺杂剂
阴极
微观结构
锂(药物)
钴
镍
电化学
氧化钴
化学工程
溶解
氧化物
氧化锂
锂钴氧化物
锂离子电池
无机化学
兴奋剂
电池(电)
冶金
磷酸钒锂电池
电极
物理化学
光电子学
化学
物理
医学
工程类
量子力学
功率(物理)
内分泌学
作者
Hanseul Kim,Youngsun Kong,Won Mo Seong,Arumugam Manthiram
标识
DOI:10.1021/acsami.3c02009
摘要
Microstructural engineering is becoming notably important in the realization of cobalt-free, high-nickel layered oxide cathodes for lithium-ion batteries since it is one of the most effective ways to improve the overall performance by enhancing the mechanical and electrochemical properties of cathodes. In this regard, various dopants have been investigated to improve the structural and interfacial stabilities of cathodes with doping. Yet, there is a lack of a systematic understanding of the effects of dopants on microstructural engineering and cell performances. Herein, we show controlling the primary particle size by adopting dopants with different oxidation states and solubilities in the host structure as an effective way for tuning the cathode microstructure and performance. The reduction in the primary particle size of cobalt-free high-nickel layered oxide cathode materials, e.g., LiNi0.95Mn0.05O2 (NM955), with high-valent dopants, such as Mo6+ and W6+, gives a more homogeneous distribution of Li during cycling with suppressed microcracking, cell resistance, and transition-metal dissolution compared to lower-valent dopants, such as Sn4+ and Zr4+. Accordingly, this approach offers promising electrochemical performance with cobalt-free high-nickel layered oxide cathodes.
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