The Interplay Between Electron Localization, Magnetic Order, and Jahn-Teller Distortion that Dictates LiMnO$_2$ Phase Stability

TL;DR

This study uses advanced computational methods to clarify the thermodynamic stability of LiMnO2 polymorphs, revealing the importance of magnetic order and Jahn-Teller distortions in phase stability relevant for battery cathodes.

Contribution

It demonstrates that hybrid-GGA and self-consistent Hubbard U calculations accurately reproduce experimental LiMnO2 phase stability, highlighting the role of magnetic order and Jahn-Teller effects.

Findings

Hybrid-GGA and U calculations match experimental phase stability.

Collinear Jahn-Teller order increases Mn-O covalency and stability.

Phases are strongly insulating with band gaps > 3 eV.

Abstract

The development of Mn-rich cathodes for Li-ion batteries promises to alleviate supply chain bottlenecks in battery manufacturing. Challenges in Mn-rich cathodes arise from Jahn-Teller (JT) distortions of Mn$^{3+}$, Mn migration, and phase transformations to spinel-like order, which can affect the electrochemical performance. These phenomena motivate an ab initio re-examination of the thermodynamics of the LiMnO2 polymorphs. It is found that the generalized gradient approximation (GGA - PBEsol) and meta-GGA (r2SCAN) density functionals with empirical on-site Hubbard U corrections yield spurious stable phases for LiMnO2, such as predicting a phase with gamma-LiFeO2-like order (g-LiMnO2) to be the ground state instead of the orthorhombic (Pmmn) phase, which is the experimentally known ground state. Accounting for the antiferromagnetic (AFM) order in each structure has a substantial effect on the total energies and resulting phase stability. By using hybrid-GGA (HSE06) and GGA with self-consistent Hubbard parameters (on-site U and inter-site V), the experimentally observed LiMnO2 phase stability trends are recovered. The calculated Hubbard U in the experimentally observed orthorhombic, layered, and spinel phases are significantly smaller than U in g-LiMnO2 and disordered layered structures. The smaller values of U are correlated with a collinear ordering of JT distortions, in which all $e_g$ orbitals are oriented in the same direction. This cooperative JT effect leads to increased Mn-O covalency, which contributes to the greater electronic stability compared to the phases with noncollinear JT arrangements, and also generate greater vibrational entropy, which helps stabilize these phases at high temperature. These phases are shown to be strongly insulating with large calculated band gaps > 3 eV, computed using HSE06 and $G_0W_0$.