Electrolyte Additive Therapy Realizes Simultaneous Ni and Mn Redox for Spinel LiNi0.5Mn1.5O4 Cathode at 2.3–4.95 V

尖晶石 材料科学 阴极 氧化还原 电解质 电化学 无机化学 化学工程 分析化学(期刊) 电极 物理化学 冶金 化学 色谱法 工程类
作者
Feng Hai,Xin Gao,Wenting Chen,Weicheng Xue,Mingtao Li,Weibo Hua,Wei Tang
出处
期刊:Advanced Functional Materials [Wiley]
卷期号:35 (4) 被引量:4
标识
DOI:10.1002/adfm.202414337
摘要

Abstract The development of cobalt‐free, high‐energy‐density cathode materials is an important prerequisite for the commercialization of the next generation of high‐energy‐density, cost‐effective lithium batteries. Co‐free spinel LiNi 0.5 Mn 1.5 O 4 (LNMO) with simultaneous Ni and Mn multi‐cation redox reactions possesses a high theoretical specific capacity of 230 mAh g −1 and a theoretical energy density of 865 Wh kg −1 . Unfortunately, LNMO cycled at 2.3–4.95 V suffered from severe interfacial dynamic evolution and electrolyte decomposition, leading to uncontrollable transition metal dissolution and a rapid decrease of reversible specific capacity. Here, It is demonstrated that the addition of an appropriate amount of lithium difluorophosphate (LiDFP) to a common carbonate‐based electrolyte can achieve stable cycling of LNMO in the voltage range of 2.3–4.95 V. The LNMO‐Li cell retained 82.8% of its initial capacity (175.2 mAh g −1 ) after 300 cycles. The improved cycle performance is attributed to the robust interface formed by the decomposition of LiDFP, which inhibits the dissolution of transition metals and the continued decomposition of the electrolyte. This work provides important insights for the development of the next generation of high‐energy‐density cobalt‐free lithium batteries.
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