Unconventional Magnetism and Band Gap Formation in LiFePO4: Consequence of Polyanion Induced Non-planarity
Ajit Jena, B. R. K. Nanda

TL;DR
This study reveals that in LiFePO4, polyanion-induced non-planarity causes asymmetric crystal fields, leading to atomic localization of Fe-d states and resulting in antiferromagnetic insulating behavior, challenging traditional mechanisms.
Contribution
It demonstrates that polyanion-induced symmetry lowering creates non-degenerate d states, explaining AFI in LiFePO4 beyond conventional models.
Findings
Polyanion effects induce non-degenerate Fe-d states.
Atomic localization of d states explains insulating behavior.
Weakly coupled Mott insulator characteristics confirmed.
Abstract
Oxygen plays a critical role in strongly correlated transition metal oxides as crystal field effect is one of the key factors that determine the degree of localization of the valence d/f states. Based on the localization, a set of conventional mechanisms such as Mott-Hubbard, Charge-transfer and Slater were formulated to explain the antiferromagnetic and insulating (AFI) phenomena in many of these correlated systems. From the case study on LiFePO4, through density-functional calculations, we demonstrate that none of these mechanisms are strictly applicable to explain the AFI behavior when the transition metal oxides have polyanions such as (PO4)3-. The symmetry-lowering of the metal-oxygen complex, to stabilize the polyanion, creates an asymmetric crystal field for d/f states. In LiFePO4 this field creates completely non-degenerate Fe-d states which, with negligible p-d and d-d covalent…
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