阳离子聚合
材料科学
氧化还原
电化学
密度泛函理论
组合化学
无机化学
电极
计算化学
物理化学
高分子化学
化学
冶金
作者
Thomas Marchandier,Sathiya Mariyappan,Maria A. Kirsanova,Artem M. Abakumov,Gwenaëlle Rousse,Dominique Foix,Moulay Tahar Sougrati,Marie Liesse Doublet,Jean‐Marie Tarascon
标识
DOI:10.1002/aenm.202201417
摘要
Abstract Extensive utilization of Li‐ion batteries for varieties of applications necessitates ceaseless improvements of electrode materials for achieving higher energy density. Towards this goal, Li‐rich layered oxides exhibiting high capacity due to cumulated cationic and anionic redox activities are under study for nearly a decade. Still, several unanswered questions remain with respect to these Li‐driven anionic redox reactions in terms of the activation process and long‐term consequences upon cycling. Here, the Li‐rich Li 3 NbS 4 phase is focused, and synthesized as two different polymorphs, namely ordered and disordered phases. From analyses of their chemical and electrochemical properties, a crystal‐electronic structure relationship is unraveled that triggers the anionic redox activity in these compounds. Moreover, through complementary theoretical calculations, the capability of cationic disorder to trigger anionic redox activity via the hybridization of cationic and non‐bonding anionic energy levels is shown. This finding is further supported by the appearance of anionic redox activity by introducing the disorder through cationic substitution. Altogether, the insights derived can help in designing new anionic redox materials with optimum performances for practical applications.
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