Materials Science and Engineering B · 2014 · 457 citations · 142 references
Overcharge of layered LiMO₂ cathodes induces a positive anode potential shift that drives lithium loss through interfacial side reactions, leading to oxygen loss, phase transformation, and dead regions due to electronic structure changes and defect formation. The review aims to elucidate atomistic degradation mechanisms of layered LiMO₂ cathode materials, focusing on active material interiors and interfaces. The authors synthesize recent in‑situ/in‑operando diffraction, modelling, and quasi‑in‑situ surface‑science studies of atomistic degradation, and discuss mitigation via solid‑state electrolytes and Li‑containing anodes.
This overview addresses the atomistic aspects of degradation of layered LiMO2 (M = Ni, Co, Mn) oxide Li-ion battery cathode materials, aiming to shed light on the fundamental degradation mechanisms especially inside active cathode materials and at their interfaces. It includes recent results obtained by novel in situ/in operando diffraction methods, modelling, and quasi in situ surface science analysis. Degradation of the active cathode material occurs upon overcharge, resulting from a positive potential shift of the anode. Oxygen loss and eventual phase transformation resulting in dead regions are ascribed to changes in electronic structure and defect formation. The anode potential shift results from loss of free lithium due to side reactions occurring at electrode/electrolyte interfaces. Such side reactions are caused by electron transfer, and depend on the electron energy level alignment at the interface. Side reactions at electrode/electrolyte interfaces and capacity fade may be overcome by the use of suitable solid-state electrolytes and Li-containing anodes.
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Projector augmented-wave method
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