材料科学
降水
电极
烧结
化学工程
电化学
Crystal(编程语言)
氢氧化物
同步加速器
杂质
粒子(生态学)
过渡金属
粒径
冶金
化学
催化作用
生物化学
物理
海洋学
有机化学
物理化学
气象学
计算机科学
核物理学
工程类
程序设计语言
地质学
作者
Ning Zhang,Haifeng Yu,Aidan Fagan-Murphy,Matthew D. L. Garayt,Svena Yu,Divya Rathore,Adam F. G. Leontowich,Toby Bond,Chang‐Yong Kim,J. R. Dahn
标识
DOI:10.1149/1945-7111/ace4f7
摘要
Nickel-rich layered positive electrode materials are normally made by a “co-precipitation-sintering” method. Mixed transition metal hydroxides called “precursors” are prepared by co-precipitation to ensure homogeneous cation mixing at the atomic level and to create spherical particles which ensure high-performance poly-crystalline materials. Single crystal materials, which show better capacity retention in long-term cycling can be made from the same mixed transition metal hydroxide precursors by sintering at a higher temperature which inevitably destroys the spherical morphology present in the initial precursors. Here we describe a method for single crystal positive electrode material production which we call “all-dry synthesis” since it does not require the use of any liquid and creates no waste unlike the co-precipitation method. The exemplary reaction between Ni, MnCO 3, and LiOH·H 2 O was studied in situ by synchrotron XRD in order to define a proper heating scheme for the all-dry process. The crystal structure, particle morphology, surface residual impurities, and electrochemical performance of materials prepared by the “all-dry synthesis” method are equivalent to or even better than those of materials made using a conventional co-precipitation method.
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