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An effective dual-modification strategy to enhance the performance of LiNi<sub>0.6</sub>Co<sub>0.2</sub>Mn<sub>0.2</sub>O<sub>2</sub> cathode for Li-ion batteries

Liang Wang, Jiashun Liang, Xiaoyu Zhang, Shenzhou Li, Tanyuan Wang, Feng Ma, Jiantao Han, Yunhui Huang, Qing Li

2021Nanoscale30 citationsDOI

Abstract

Ni-rich ternary layered oxides represent the most promising cathodes for lithium ion batteries (LIBs) due to their relatively large specific capacities and high energy/power densities. Unfortunately, their inherent chemical instability and surface side reactions during the charge/discharge processes lead to rapid capacity fading and poor cycling life, which seriously restrict their practical applications. Herein, we report a simple dual-modification strategy for preparing LiNi0.6Co0.2Mn0.2O2 (NCM622) cathode materials by Li2SnO3 surface coating and Sn4+ gradient doping. The gradient Sn doping stabilizes the layered structure due to the strong Sn-O covalent bond and relieves the Li+/Ni2+ cation disorder by the partial oxidation of Ni2+ to Ni3+. Besides, the ionic and electronic conductive Li2SnO3 coating serves as a protective layer to eliminate the side reactions with electrolyte/air. In LIB testing, the dual-modified NCM622 cathode with 2% Sn delivers an enhanced cycling performance with 88.31% capacity retention after 100 cycles from 3.0 to 4.5 V at 1C compared to the bare NCM622. Meanwhile, the dual-modified NCM622 shows an improved reversible capacity of 136.2 mA h g-1 at 5C and enhanced electrode kinetics. The dual-modification strategy may enable a new approach to simultaneously relieve the interfacial instability and bulk structure degradation of Ni-rich cathode materials for high energy density LIBs.

Topics & Concepts

CathodeMaterials scienceDual (grammatical number)Degradation (telecommunications)Chemical engineeringIonNanotechnologyPhysical chemistryChemistryComputer scienceOrganic chemistryTelecommunicationsArtEngineeringLiteratureAdvancements in Battery MaterialsAdvanced Battery Technologies ResearchExtraction and Separation Processes