Correlating Electrochemical Kinetic Parameters of Single LiNi1/3Mn1/3Co1/3O2 Particles with the Performance of Corresponding Porous Electrodes

Characterizing microscale single particles directly is requested for dissecting the performance-limiting factors at the electrode scale. In this work, we build a single-particle electrochemical setup and develop a physics-based model for extracting the solid-phase diffusion coefficient (D-s) and exchange current density (i(0)) from electrochemical impedance measurements. We find that the carbon coating on the LiNi1/3Mn1/3Co1/3O2 surface enhances i(0). In addition, D-s and i(0) decay irreversibly by approximate to 25% and approximate to 10%, respectively, when the cutoff charge voltage increases from 4.3 V to 4.4 V. Moreover, we correlate intrinsic parameters of single particles with the performance of porous electrodes. Porous electrodes assembled with active particles with higher i(0) values deliver a greater capacity and faster capacity fade. The methods developed in this combined experimental and theoretical work can be useful in correlating the single-particle scale and porous-electrode scale for other similar systems.