材料科学
X射线光电子能谱
电解质
阴极
图层(电子)
降级(电信)
表层
氧化物
化学工程
傅里叶变换红外光谱
化学稳定性
水分
纳米技术
物理化学
复合材料
冶金
电极
化学
工程类
电信
计算机科学
作者
Junkai Zhao,Zhixing Wang,Jiexi Wang,Huajun Guo,Xinhai Li,Guochun Yan,Weihua Gui,Ning Chen
标识
DOI:10.1016/j.ceramint.2018.04.166
摘要
Abstract The severe degradation of Ni-rich cathode materials on exposure to air is a crucial restriction for their large-scale application. To overcome this issue, a MnO2 functional layer has been introduced to the surface of LiNi0.8Co0.15Al0.05O2 oxide via a wet-chemical method. Compared with pristine sample, the modified LiNi0.8Co0.15Al0.05O2 shows an enhanced chemical stability because of its low sensitivity to moisture and CO2. The formation of absorbed Li2CO3/LiOH species and spontaneous reduction of Ni3+ to Ni2+ on the surface of MnO2-modified sample have been delayed remarkably, which is confirmed by characterizations of SEM, TEM, XPS and FTIR. Benefit from these merits, the modified LiNi0.8Co0.15Al0.05O2 displays a specific capacity of 183 mAh g−1 at 0.1 C after air-storage for 40 days, while the pristine sample drops from 195 to 144 mAh g−1 promptly. Meanwhile, the MnO2 layer inhibits the generation of HF and protects the active material against the erosion of electrolyte in the working cell. Therefore, the MnO2 modified LiNi0.8Co0.15Al0.05O2 after storage shows a capacity retention of 87.1% at 1 C after 100 cycles, which is more stable than that of stored pristine sample (70.3%).
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