A Search for Low-Irreversible Capacity and High-Reversible Capacity Positive Electrode Materials in the Li–Ni–Mn–Co Pseudoquaternary System

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• 作者：Ramesh Shunmugasundaram ; Rajalakshmi Senthil Arumugam ; Kristopher J. Harris ; Gillian R. Goward ; J. R. Dahn
• 刊名：Chemistry of Materials
• 出版年：2016
• 出版时间：January 12, 2016
• 年：2016
• 卷：28
• 期：1
• 页码：55-66
• 全文大小：566K
• ISSN：1520-5002

文摘

A comprehensive search for Li-ion battery positive electrode materials that can simultaneously exhibit low irreversible capacity loss (IRC) (～10% or less) and high reversible capacity (>240 mAh/g) was performed in the Li–Ni–Mn–Co–O pseudoquaternary system. An array of high-capacity Li-rich layered oxides, most of which show an “oxygen release” plateau during the first charge, were synthesized with a wide range of Ni, Mn, and Co compositions, and their first-cycle electrochemical properties were investigated. Low-IRC materials could be synthesized at many Ni–Mn–Co combinations by synthesizing with an amount of lithium lower than that required by site occupation and oxidation state rules. Many of these “Li-deficient” low-IRC materials were found to be single-phase layered materials with inherent metal-site vacancies in their pristine state. For such single-phase materials, the amount of IRC depends on the concentration of metal-site vacancies in their pristine state. Increasing the Li deficiency eventually caused the appearance of the spinel phase, which, when it appears, lowers the IRC, irrespective of the Ni–Mn–Co precursor composition. The number of metal-site vacancies that can be incorporated into the single-phase layered materials depends on the overall metal composition, especially the Co concentration. Low-IRC behavior is correlated to the fraction of metal-site vacancies in the layered phase in both the single-phase and the two-phase materials. ⁷Li nuclear magnetic resonance (NMR) studies of low-IRC materials revealed the relative population of Li between the Li and TM layer. Formula unit calculation based on ⁷Li NMR results suggests that metal-site vacancies preferably occupy the sites in the Li layer, which could provide room for the intercalation of extra Li into the structure, hence reducing the irreversible capacity.