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使用先进技术重新审视钴酸锂。

Revisiting LiCoO Using a State-of-the-Art Technique.

作者信息

Mukai Kazuhiko, Uyama Takeshi, Nonaka Takamasa

机构信息

Toyota Central Research and Development Laboratories, Inc., 41-1 Yokomichi, Nagakute, Aichi 480-1192, Japan.

出版信息

Inorg Chem. 2020 Aug 3;59(15):11113-11121. doi: 10.1021/acs.inorgchem.0c01598. Epub 2020 Jul 22.

Abstract

Lithium overstoichiometric cobalt oxide, Li(LiCo)O, still occupies a privileged position as a positive electrode material for lithium-ion batteries. However, despite its widespread applications in commercial lithium-ion batteries, little is known about its reaction mechanisms and the effects of δ on cyclability at deep charge. We herein revisited this material through a recently developed technique, i.e., rapid, alternating measurements of X-ray diffraction and X-ray absorption spectroscopy. The cyclability degraded when the charge cutoff voltage was >4.4 V versus Li/Li, which corresponds to the Li composition exhibiting a minimum (maximum) lattice parameter along the () axis. Differences in the structural parameters such as lattice parameters and bond distances clearly appeared between the charge and discharge reactions at a capacity below ∼220 mAh g. These changes occurred because deep charge and/or increasing the amount of δ induced a local distortion in the CoO octahedra. We found a critical Li extraction content that satisfied the need for both high capacity and cyclability for Li(LiCo)O, which can be applied to other layered materials.

摘要

锂过量化学计量比的钴氧化物Li(LiCo)O,作为锂离子电池的正极材料仍占据着特殊地位。然而,尽管它在商用锂离子电池中得到了广泛应用,但对于其反应机理以及δ对深度充电时循环性能的影响却知之甚少。我们在此通过一种最近开发的技术,即快速交替测量X射线衍射和X射线吸收光谱,重新研究了这种材料。当相对于Li/Li的充电截止电压>4.4 V时,循环性能会下降,这对应于Li组成沿()轴呈现最小(最大)晶格参数。在容量低于约220 mAh g时,充电和放电反应之间的结构参数(如晶格参数和键距)差异明显出现。这些变化的发生是因为深度充电和/或δ含量增加会导致CoO八面体发生局部畸变。我们发现了一个关键的锂提取含量,它满足了Li(LiCo)O高容量和循环性能的需求,这可应用于其他层状材料。

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