煅烧
尖晶石
锂(药物)
共沉淀
材料科学
电化学
锰
分析化学(期刊)
氧化物
结构精修
过渡金属
无机化学
化学工程
电极
化学
冶金
催化作用
晶体结构
结晶学
物理化学
医学
工程类
内分泌学
生物化学
色谱法
作者
Mitsuharu Tabuchi,Mitsunori Kitta,Koji Yazawa,Kei Kubota
标识
DOI:10.1149/1945-7111/ac3526
摘要
High-capacity Li 1+x (Ni 0.3 Mn 0.7 ) 1-x O 2 , (0 < x < 1/3) samples were synthesized by the coprecipitation–calcination method. Both electrochemical cycle and high-rate performances were drastically improved by selecting an N 2 atmosphere as final calcination. Scanning transmission electron microscopy—energy dispersive X-ray spectroscopy analysis showed that the sample calcined in an N 2 atmosphere had a more homogeneous transition metal distribution into primary particles than that calcined in air. The solid-state 7 Li nuclear magnetic resonance data showed that electrochemically inactive domains were only diminished for the sample calcined in an N 2 atmosphere after electrochemical activation. X-ray Rietveld analysis revealed that the suitable transition metal distribution and content of the samples were different from those of typical layered rock-salt materials. Only that calcined in an N 2 atmosphere had no spinel formation during charging and no oxide ion insertion reaction during discharging. No positive Co substitution effect was observed under the optimized preparation conditions. At the 100th cycle, the discharge capacity was 216 mAh g −1 , which corresponds to 87% of the initial capacity (251 mAh g −1 ) at optimizing synthetic condition.
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