Elucidating Lithium Alloying-Induced Degradation Evolution in High-Capacity Electrodes

Alloy electrode materials offer high capacity in lithium-ion batteries; however, they exhibit rapid degradation resulting in particle disintegration and electrochemical performance decay. In this study, the evolution of lithium alloying-induced degradation due to electrochemomechanical interactions is examined based on a multipronged electrochemical and microstructural analysis. Copper–tin (Cu6Sn5) is chosen as an exemplary alloy electrode material. Electrodes with compositional variations were fabricated, and electrochemical performance was examined under varying conditions including voltage window, C-rate, and short- and long-term cycling. Morphology and composition analyses of pristine and cycled electrodes were conducted using micrography and spectroscopy techniques. Alloying-induced electrode microstructural evolution was probed using X-ray microtomography. The rapid capacity fading was found to be caused by mechanical degradation of the electrode. Driving the electrode to a lower potential (E ≈ 0.2 V vs Li/Li+) induced Li–Sn alloy formation and provided the characteristic large capacity; however, this led to a large volume expansion and active particle cracking and disintegration. Copper expulsion was found to be a consequence of the alloy formation; however, it was not the primary contributor to the dramatic electrochemical performance decay.