Distinguishing bulk redox from near-surface degradation in lithium nickel oxide cathodes

区分锂镍氧化物正极中的本体氧化还原和近表面降解

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作者:Lijin An, Jack E N Swallow, Peixi Cong, Ruomu Zhang, Andrey D Poletayev, Erik Björklund, Pravin N Didwal, Michael W Fraser, Leanne A H Jones, Conor M E Phelan, Namrata Ramesh, Grant Harris, Christoph J Sahle, Pilar Ferrer, David C Grinter, Peter Bencok, Shusaku Hayama, M Saiful Islam, Robert House, 

Abstract

Ni-rich layered oxide cathodes can deliver higher energy density batteries, but uncertainties remain over their charge compensation mechanisms and the degradation processes that limit cycle life. Trapped molecular O2 has been identified within LiNiO2 at high states of charge, as seen for Li-rich cathodes where excess capacity is associated with reversible oxygen redox. Here we show that bulk redox in LiNiO2 occurs by Ni-O rehybridization, lowering the electron density on O sites, but importantly without the involvement of molecular O2. Instead, trapped O2 is related to degradation at surfaces in contact with the electrolyte, and is accompanied by Ni reduction. O2 is removed on discharge, but excess Ni2+ persists forming a reduced surface layer, associated with impeded Li transport. This implicates the instability of delithiated LiNiO2 in contact with the electrolyte in surface degradation through O2 formation and Ni reduction, highlighting the importance of surface stabilisation strategies in suppressing LiNiO2 degradation.

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