Demystifying charge-compensation mechanisms and Oxygen dimerization in Li-rich Li2NiO3 cathodes

TY - JOUR

T1 - Demystifying charge-compensation mechanisms and Oxygen dimerization in Li-rich Li2NiO3 cathodes

AU - Banerjee, Hrishit

AU - Grey, Clare P.

AU - Morris, Andrew

N1 - Publisher Copyright: © 2025 The Royal Society of Chemistry.

PY - 2025/7/8

Y1 - 2025/7/8

N2 - Li-rich cathodes are gaining popularity for Li-ion batteries due to their higher capacity compared to standard layered cathodes. However, the redox mechanisms in these materials are still not clear, nor is the origin of the extra capacity observed experimentally. We investigate the elusive charge-compensation mechanisms and their impact on potential oxygen-dimer formation in a recently synthesized Li-rich cathode, Li2NiO3. Using state-of-the-art ab initio dynamical mean-field theory, we show that the excess capacity in Li2NiO3 comes from a combined Ni and O redox, unlike its layered counterpart LiNiO2, where O redox predominates. Moreover, we demonstrate O dimer formation via a plot of the electron localization function for the first time, and attribute this formation to the higher oxidation state of O, even in the pristine material. Finally, we show that Li migration to the interlayer tetrahedral sites at the end of charge is potentially unlikely due to the end configuration being higher in energy and the stabilization of the parent structure caused by O dimerization. Without this microscopic understanding, it is not possible to design better Li-rich high Ni-content cathodes with higher capacity and minimal degradation.

AB - Li-rich cathodes are gaining popularity for Li-ion batteries due to their higher capacity compared to standard layered cathodes. However, the redox mechanisms in these materials are still not clear, nor is the origin of the extra capacity observed experimentally. We investigate the elusive charge-compensation mechanisms and their impact on potential oxygen-dimer formation in a recently synthesized Li-rich cathode, Li2NiO3. Using state-of-the-art ab initio dynamical mean-field theory, we show that the excess capacity in Li2NiO3 comes from a combined Ni and O redox, unlike its layered counterpart LiNiO2, where O redox predominates. Moreover, we demonstrate O dimer formation via a plot of the electron localization function for the first time, and attribute this formation to the higher oxidation state of O, even in the pristine material. Finally, we show that Li migration to the interlayer tetrahedral sites at the end of charge is potentially unlikely due to the end configuration being higher in energy and the stabilization of the parent structure caused by O dimerization. Without this microscopic understanding, it is not possible to design better Li-rich high Ni-content cathodes with higher capacity and minimal degradation.

UR - https://www.scopus.com/pages/publications/105010918560

U2 - 10.1039/D5TA03794H

DO - 10.1039/D5TA03794H

M3 - Article

SN - 2050-7488

VL - 13

SP - 25375

EP - 25383

JO - Journal of Materials Chemistry A: Materials for Energy and Sustainability

JF - Journal of Materials Chemistry A: Materials for Energy and Sustainability

ER -