Origin of Structural Evolution in Capacity Degradation for Overcharged NMC622 via Operando Coupled Investigation

The nickel-rich layered oxide materials have been selected as promising cathode materials for the next generation lithium ion batteries because of their large capacity and comparably high operating voltage. However, at high voltage (beyond 4.30 V vs Li/Li + ), the members of this family are all suffering from a rapid capacity decay, which was commonly concerned with crystal lattice distortion and related cation disordering. In this work, the quasi-spherical Ni-rich layered LiNi 0.6 Co 0.2 Mn 0.2 O 2 (QS-NMC622) material was successfully synthesized through the carbonate co-precipitation method. A coupled measurement, which is a combination of potentiostatic intermittent titration technique (PITT) and in situ X-ray diffraction (XRD), was deployed to simultaneously capture the structural changes and lithium ion diffusion coefficient of QS-NMC622 material during the first cycle. With help of in situ XRD patterns and high-resolution transmission electron microscope (HR-TEM) images, a defective spinel framework of Fd 3̅ m space group was detected along with a rapid decreasing lattice-parameter c and lattice distortion at deep delithiated state, which causes poor kinetics related to lithium ion mobility. The new-born framework seems to transform and remain as full spinel structure in the parent phase to the end of charge/discharge with high voltage, which could deteriorate both the surface and body structure stability during the subsequent cycles. This established coupled in situ measurement could be applied to simultaneously investigate the structure transformation and kinetics of cathode materials during charge/discharge.