钝化
材料科学
溶解
阴极
过渡金属
化学工程
图层(电子)
多孔性
锂(药物)
电极
纳米技术
复合材料
物理化学
催化作用
化学
有机化学
内分泌学
工程类
医学
作者
Licheng Ju,Guanzhi Wang,Kun Liang,Maoyu Wang,George E. Sterbinsky,Zhenxing Feng,Yang� Yang
标识
DOI:10.1002/aenm.201903333
摘要
Abstract Electrode stabilization by surface passivation has been explored as the most crucial step to develop long‐cycle lithium‐ion batteries (LIBs). In this work, functionally graded materials consisting of “conversion‐type” iron‐doped nickel oxyfluoride (NiFeOF) cathode covered with a homologous passivation layer (HPL) are rationally designed for long‐cycle LIBs. The compact and fluorine‐rich HPL plays dual roles in suppressing the volume change of NiFeOF porous cathode and minimizing the dissolution of transition metals during LIBs cycling by forming a structure/composition gradient. The structure and composition of HPL reconstructs during lithiation/delithiation, buffering the volume change and trapping the dissolved transition metals. As a result, a high capacity of 175 mAh g −1 (equal to an outstanding volumetric capacity of 936 Ah L −1 ) with a greatly reduced capacity decay rate of 0.012% per cycle for 1000 cycles is achieved, which is superior to the NiFeOF porous film without HPL and commercially available NiF 2 ‐FeF 3 powders. The proposed chemical and structure reconstruction mechanism of HPL opens a new avenue for the novel materials development for long‐cycle LIBs.
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