Stable heteroepitaxial interface of Li-rich layered oxide cathodes with enhanced lithium storage

Lithium and oxygen activities can have substantial influences on the kinetics of ion and electron transport and the structural integrity of Li-rich layered oxide (LLO) cathodes, since reversible oxygen redox is ascribed to the extra capacity beyond the theoretical capacity from transition metal redox at high voltages. Herein, we demonstrate a liquid-solid interfacial reaction to generate a heteroepitaxial interface with tunable Li/O activities on LLOs using molten boric acid. The experimental and theoretical analyses indicate that the atomic scale interface is comprised of a disordered rock salt structure containing substantial Li/O vacancies along the layered structure, associated with a segregation tendency of Ni and Co. The formation of this heteroepitaxial interface with Li/O vacancies improves the ionic/electronic conduction and electrochemical/structural stability, leading to a high discharge capacity of 283mAh g(-1) with initial Coulombic efficiency of 91.7% (0.1 C, 2.0-4.7 V vs. Li+/Li), excellent rate performance (246 and 159.7mAh g(-1) at 1 C and 10 C, respectively) and enhanced cyclic performance with a capacity retention of 92% after 100 cycles. The findings highlight the importance of a well-engineered interface for the design of high performance layered cathode materials for Li storage.