Ni-Rich LiNi0.8Co0.1Mn0.1O2 Oxide Coated by Dual-Conductive Layers as High Performance Cathode Material for Lithium-Ion Batteries

材料科学 阴极 涂层 锂(药物) X射线光电子能谱 化学工程 电导率 氧化物 离子电导率 介电谱 导电体 电化学 复合材料 电解质 电极 冶金 内分泌学 物理化学 工程类 化学 医学
作者
Shi Chen,Tao He,Yuefeng Su,Yun Lu,Liying Bao,Lai Chen,Qiyu Zhang,Jing Wang,Renjie Chen,Feng Wu
出处
期刊:ACS Applied Materials & Interfaces [American Chemical Society]
卷期号:9 (35): 29732-29743 被引量:337
标识
DOI:10.1021/acsami.7b08006
摘要

Ni-rich materials are appealing to replace LiCoO2 as cathodes in Li-ion batteries due to their low cost and high capacity. However, there are also some disadvantages for Ni-rich cathode materials such as poor cycling and rate performance, especially under high voltage. Here, we demonstrate the effect of dual-conductive layers composed of Li3PO4 and PPy for layered Ni-rich cathode material. Fourier transform infrared spectroscopy and X-ray photoelectron spectroscopy show that the coating layers are composed of Li3PO4 and PPy. (NH4)2HPO4 transformed to Li3PO4 after reacting with surface lithium residuals and formed an inhomogeneous coating layer which would remarkably improve the ionic conductivity of the cathode materials and reduce the generation of HF. The PPy layer could form a uniform film which can make up for the Li3PO4 coating defects and enhance the electronic conductivity. The stretchy PPy capsule shell can reduce the generation of internal cracks by resisting the internal pressure as well. Thus, ionic and electronic conductivity, as well as surface structure stability have been enhanced after the modification. The electrochemistry tests show that the modified cathodes exhibited much improved cycling stability and rate capability. The capacity retention of the modified cathode material is 95.1% at 0.1 C after 50 cycles, whereas the bare sample is only 86%, and performs 159.7 mAh/g at 10 C compared with 125.7 mAh/g for the bare. This effective design strategy can be utilized to enhance the cycle stability and rate performance of other layered cathode materials.
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