电化学
电解质
锂(药物)
扫描电子显微镜
X射线光电子能谱
涂层
化学工程
扩散
分解
透射电子显微镜
材料科学
阴极
无机化学
分析化学(期刊)
化学
电极
复合材料
纳米技术
物理化学
医学
内分泌学
物理
有机化学
色谱法
工程类
热力学
作者
Dae‐Hyun Cho,Chang-Heum Jo,Woosuk Cho,Young‐Jun Kim,Hitoshi Yashiro,Yang‐Kook Sun,Seung‐Taek Myung
摘要
In order to confirm reasons that deteriorate cathode performances, Ni-rich Li[Ni0.7Mn0.3]O2 is modified by lithium isopropoxide to artificially provide lithium excess environment by forming Li2O on the surface of active materials. X-ray diffraction patterns indicate that the lithium oxide coating does not affect structural change comparing to the bare material. Scanning electron microscopy and transmission electron microscopy data show the presence of coating layers on the surface of Li[Ni0.7Mn0.3]O2. Electrochemical tests demonstrate that the Li2O-coated Li[Ni0.7Mn0.3]O2 exhibits a greater irreversible capacity with a small capacity because of the presence of insulating layers composed of lithium compounds on the active materials since these layers delay facile Li+ diffusion. Also, the Li2O layer forms byproducts such as Li2CO3, LiOH, and LiF, as are proved by X-ray photoelectron spectroscopy and time-of-flight secondary ion mass spectrometry. The presence of residual lithium tends to bond with hydrocarbons induced from decomposition of electrolytic salt during electrochemical reactions. And the reaction, accelerated by the decomposition of electrolytic salt that produces the byproducts, causes the formation of passive layers on the surface of active material. As a result, the new layers consequently impede diffusion of lithium ions that deteriorate electrochemical properties.
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