Insight into the Redox Reaction Heterogeneity within Secondary Particles of Nickel-Rich Layered Cathode Materials

Nickel-rich LiNixCoyMn1–x–yO2 (nickel-rich NCM, 0.6 ≤ x < 1) cathode materials suffer from multiscale reaction heterogeneity within the electrode during the electrochemical energy storage process. However, owing to the lack of appropriate diagnostic tools, the systematic understanding and observation on the redox reaction heterogeneity at the individual secondary-particle level is still limited. Raman spectroscopy can not only reflect the depth of the redox reaction through probing the vibrational information on the metal–oxygen coordination structure but also sensitively detect the local structure changes of different regions within the secondary particle with suitable spatial resolution. Therefore, Raman spectroscopy is applied here to conveniently conduct the high-resolution and in-depth analysis of the rate-dependent reaction heterogeneity within nickel-rich NCM secondary particles. It is found that, under high-rate conditions, the oxidation/reduction reaction mainly occurs in the surface region of the particles and the cause of this particle-scale reaction heterogeneity is the limitation of the slow solid-phase Li+ diffusion and the transient charging/discharging processes. In addition, this reaction heterogeneity would aggravate the structural instability of the material continuously during the charging/discharging cycles, thus resulting in a slowdown in the kinetics of Li+ de/intercalation and the apparent capacity decay. This work can not only provide fundamental insight into the rational modification of high-power nickel-rich NCM materials but also guide the setting of electrochemical operating conditions for high-power lithium-ion batteries (LIBs).