尖晶石
再分配(选举)
锂(药物)
离子
材料科学
相变
背景(考古学)
相(物质)
化学物理
粒子(生态学)
衍射
化学
热力学
物理
冶金
医学
古生物学
海洋学
有机化学
光学
政治
生物
政治学
地质学
法学
内分泌学
作者
Muhammad Mominur Rahman,Kangxuan Xia,Xiao‐Qing Yang,Kingo Ariyoshi,Enyuan Hu
出处
期刊:Nano Letters
[American Chemical Society]
日期:2023-07-18
卷期号:23 (15): 7135-7142
被引量:1
标识
DOI:10.1021/acs.nanolett.3c02042
摘要
Spinel-structured ordered-LiNi0.5Mn1.5O4 (o-LNMO) has experienced a resurgence of interest in the context of reducing scarce elements such as cobalt from the lithium-ion batteries. O-LNMO undergoes two two-phase reactions at slow rates. However, it is not known if such phenomenon also applies at fast rates. Herein, we investigate the rate-dependent phase transition behavior of o-LNMO through in operando time-resolved X-ray diffraction. The results indicate that a narrow region of the solid solution reaction exists for charge and discharge at both slow and fast rates. The overall phase transition is highly asymmetric at fast rates. During fast charge, it is a particle-by-particle mechanism resulting from an asynchronized reaction among the particles. During fast discharge, it is likely a core–shell mechanism involving transition from Li0+xNi0.5Mn1.5O4 to Li1+xNi0.5Mn1.5O4 in the outer layer of particles. The Li0.5Ni0.5Mn1.5O4 phase is suppressed during fast discharge and appears only through Li redistribution upon relaxation.
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