材料科学
电解质
电化学
阴极
溶解
涂层
兴奋剂
锰
离子电导率
化学工程
电导率
原子层沉积
氧化物
无机化学
电极
纳米技术
图层(电子)
冶金
工程类
物理化学
化学
光电子学
作者
Panawan Vanaphuti,Yangtao Liu,Xiaotu Ma,Jinzhao Fu,Yulin Lin,Jianguo Wen,Zhenzhen Yang,Yan Wang
标识
DOI:10.1021/acsami.1c04718
摘要
While lithium, manganese-rich (LMR) layered oxide cathode materials offer high energy density (>900 Wh kg–1) and low cost, LMR is susceptible to continuous capacity and voltage decay from the oxygen migration and side reaction with aqueous electrolyte at high voltage. Herein, the integration of Na/F co-doping (CD) and AlF3 coating on LMR is achieved without the need of complex atomic layer deposition. Akin to pristine and CD samples, CD with 1 wt % AlF3 (CD-1.0 wt %) shows excellent electrochemical performance with the capacity and voltage retentions of 93 and 91% after 150 cycles at 0.5C, respectively, and increased ionic conductivity. Spectroscopic analysis indicates that the coating mainly influences the Co distribution, where Co is enriched on the surface, and partial diffusion of Al3+ ions toward the bulk, leading to a slight change of transition-metal (TM) valence states at the nanometer scale and the formation of a stable Lix(CoAl)Oy phase. Post-cycling analysis reveals that CD-1.0 wt % can alleviate the formation of rock-salt structure and Mn dissolution. Besides, little to no metal segregation is detected for the cycled CD-1.0 wt % sample. This finding presents the first instance to apply co-doping and AlF3 coating as a new strategy to enhance the structural homogeneity and takes another step toward their commercial viability.
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