Dynamic Transformations of Layered Compounds at Full Delithiation Due to Surface Triggered Reactions

Abstract

Modern lithium-ion batteries using layered R-3m intercalation positive electrodes have insufficient practical capacity and energy density to meet the future demands of portable electronics, and electric vehicles. If the complete, reversible, theoretical capacity upon full delithiation of these materials could be accessed while retaining high voltages and a narrow voltage swing, a significant advancement in energy density could be achieved. Although, full delithiation of most layered compounds has been known for decades, the failure modes that prevent practical cycle life are still in question. This paper focuses on a model R-3m layered compound of Li[Ni0.8Co0.15Al0.05]O2 (NCA) and explores the failure modes at the surface and subsurface utilizing a unique combination of operando microcalorimetry / electrochemical impedance spectroscopy , high resolution transmission electron microscopy, electron energy loss spectroscopy, x-ray photo electron microscopy, x-ray absorption spectroscopy, hard x-ray photoelectron spectroscopy, and x-ray diffraction. The development of operando microcalorimetry (isothermal and DSC mode) enables simultaneous measurement of the heat flux, current, and impedance, while controlling the environmental temperature and the electrochemical testing parameters. Although surface changes are known in NCA, we explore the evolution of the surface and subsurface at extreme levels of delithiation and take efforts to isolate the failure modes induced by cycling vs. static transitions. The progression of the surface and subsurface structure and chemistry is found to be much more complex than previously identified and has direct implications to impedance development throughout the electrochemical cell. Specific attention was given to surface catalyzed triggers of the surface and subsurface failure modes, evolution of surface and subsurface phase transformations, and comments on the broad applicability of our findings to other layered compounds.