Tuning Both Anionic and Cationic Redox Chemistry of Li-Rich Li1.2Mn0.6Ni0.2O2 via a “Three-in-One” Strategy

阳离子聚合 氧化还原 溶解 阴极 锂(药物) 化学 无机化学 涂层 氧气 电化学 化学工程 电极 物理化学 高分子化学 有机化学 内分泌学 工程类 医学
作者
Qingyuan Li,De Ning,Dong Zhou,Ke An,Götz Schuck,Deniz Wong,Weijin Kong,Christian Schulz,G. Schumacher,Xiangfeng Liu
出处
期刊:Chemistry of Materials [American Chemical Society]
卷期号:32 (21): 9404-9414 被引量:44
标识
DOI:10.1021/acs.chemmater.0c03460
摘要

Anionic redox chemistry endows Li-rich layered oxide cathode with high specific capacity, but it also causes some critical issues such as voltage decay, structure degradation, and irreversible oxygen release. Herein, we propose to tune both the anionic and cationic redox chemistry of Li1.2Mn0.6Ni0.2O2 via a “three-in-one” strategy integrating Na doping for the Li site and Si substitution for the Mn and Na2SiO3 coating layer, which is achieved by the facile coating of Na+-conductive Na2SiO3. In comparison with the pristine or Li2SiO3-coating sample, the concerns of voltage fading, poor rate capability, structure degradation, and oxygen release have all been largely alleviated due to the “three-in-one” effect. First, the coating layer impedes the side reaction and the dissolution of transition metals (TMs). Second, Na+ is confirmed to be doped into the Li layers to facilitate the transport kinetics of lithium ions while Si4+ is doped into the TM site, which enhances the stability of the layered structure during cycling due to the strong Si–O bond and reduces the migration of TMs. Third, the integrated strategy also decreases the covalency of TM–O bonds, which is verified to improve the reversibility of anion redox chemistry and suppress oxygen evolution. The synergetic strategy sheds some light on exploring high-performance cathode materials by tuning both anionic and cationic redox chemistry.
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