氢氧化物
粒径
碳酸盐
降水
电化学
化学工程
镍
碳酸锂
无机化学
钴
粒子(生态学)
材料科学
锂(药物)
氧化物
化学
电极
冶金
有机化学
地质学
离子
气象学
物理化学
内分泌学
工程类
物理
海洋学
医学
离子键合
作者
Jae-Sung Seo,Jae‐won Lee
标识
DOI:10.1016/j.jallcom.2016.10.062
摘要
We co-precipitated the precursor of a nickel-rich cathode material with high energy density—layered lithium nickel cobalt aluminum oxide (NCA, Li(NixCoyAl1−x−y)O2)—via a carbonate route, and we tested the cell performance of NCA synthesized from this precursor. The precursor for NCA had been previously co-precipitated via a hydroxide route, with a long residence time that caused low productivity. We obtained spherical precursor particles with uniform particle size distribution through the carbonate route. We found that the precursor has the form of (Ni0.8Co0.16Al0.04)(CO3)0.41(OH)1.18 and the precursor particles grow much faster than the hydroxide form with the same metal composition, (Ni0.8Co0.16Al0.04)(OH)2. The faster particle growth rate is attributed to the low solubility of the precursor in mild pH condition of co-precipitation (pH = 8.0). NCA from this precursor showed an initial discharge capacity of 183 mAh/g at 0.1C-rate, while retaining 91% of its capacity after 100 cycles representing improved performance over those of NCA from the hydroxide route with the same residence time. We believe faster particle growth, uniform particle size distribution, and morphology to be the reasons for the improved performance.
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