Does trapped O2 form in the bulk of LiNiO2 during charging?

• Published in: Energy & environmental science 2024-04, Vol.17 (7), p.2530-2540
• Main Authors: Juelsholt, Mikkel, Chen, Jun, Pérez-Osorio, Miguel A, Rees, Gregory J, De Sousa Coutinho, Sofia, Maynard-Casely, Helen E, Liu, Jue, Everett, Michelle, Agrestini, Stefano, Garcia-Fernandez, Mirian, Ke-Jin, Zhou, House, Robert A, Bruce, Peter G
• Format: Article
• Language: English
• Subjects: Batteries; Cathodes; Charging; Composition; Fluorescence; Heavy metals; Lithium-ion batteries; Oxidation; Oxygen; Plateaus; Rechargeable batteries; Transition metals; Valence
• ISSN: 1754-5692; 1754-5706
• DOI: 10.1039/d3ee04354a

LiNiO2 remains a critical archetypal material for high energy density Li-ion batteries, forming the basis of Ni-rich cathodes in use today. Nevertheless, there are still uncertainties surrounding the charging mechanism at high states of charge and the potential role of oxygen redox. We show that oxidation of O2− across the 4.2 V vs. Li+/Li plateau forms O2 trapped in the particles and is accompanied by the formation of 8% Ni vacancies on the transition metal sites of previously fully dense transition metal layers. Such Ni vacancy formation on charging activates O-redox by generating non-bonding O 2p orbitals and is necessary to form vacancy clusters to accommodate O2 in the particles. Ni accumulates at and near the surface of the particles on charging, forming a Ni-rich shell approximately 5 nm thick; enhanced by loss of O2 from the surface, the resulting shell composition is Ni2.3+1.75O2. The overall Ni oxidation state of the particles measured by XAS in fluorescence yield mode after charging across the plateau to 4.3 V vs. Li+/Li is approximately +3.8; however, taking account of the shell thickness and the shell Ni oxidation state of +2.3, this indicates a Ni oxidation state in the core closer to +4 for compositions beyond the plateau.