Sn, S co-doped LiCoO2 with low lithium ion diffusion energy barrier and high passivation surface for fast charging lithium ion batteries.

[Display omitted] • A fully supported lattice network can be achieved by Sn and S co-doping LCO. • The desired LCO–Sn 0.6 cathode possesses very low Li+ diffusion energy barrier. • The self-passivating surface on LCO-Sn 0.6 promotes form effective CEI. • LCO–Sn 0.6 exhibits high capacity of 114 mAh g−1 under fast charging of 5.5A g−1. High-voltage lithium cobalt oxide (LCO) has been widely used in 5G smart electronics. However, maintaining the stability of high-voltage LCO structures under fast charging and discharging conditions is still a challenge that hinders its application in fast-charging lithium-ion batteries. Here, we propose a new idea of fully supported lattice network and self-passivating surface to construct a fast-charging cathode and realize high performance fast-charging lithium-ion battery. A fully supported lattice network can be achieved by one-step solid-phase sintering of Sn and S co-doped LCO, reducing the energy barrier of Li+ transport and allowing rapid Li+ solid-state diffusion. The self-passivating surface is formed on the surface of LCO-Sn 0.6 by de-solvation with solvent molecules, which significantly increases the adsorption energy of EC and LiPF 6 on LCO-Sn 0.6 , and greatly reduces the absorption ability of EC and LiPF 6 on LCO-Sn 0.6 to form effective CEI membranes. The superior performance with high capacity (114 mAh g−1) under extremely fast charging conditions (20 C, 1 C = 274 mA g−1) is achieved on Sn and S co-doped LCO cathode, that is, it can reach more than 60% SOC after only 2 min of fast charging. In situ Raman spectroscopy and in situ XRD further confirm the reversible transformation of Sn and S co-doped LCO microstructure during charge and discharge processes. These results provide a platform for the design of novel fast-charging cathode materials with fully supported lattice network and self-passivating surface, while stabilizing lattice structure and significantly enhancing ionic solid-state diffusion dynamics. [ABSTRACT FROM AUTHOR]