Real-space determination of orbital states driving successive phase transitions in FeV2O4

TL;DR

This study combines advanced x-ray diffraction and density-functional theory to directly determine orbital states in FeV2O4, revealing their role in structural and magnetic phase transitions.

Contribution

It introduces a novel real-space approach using valence electron density analysis to resolve orbital states in strongly correlated materials.

Findings

Orbital rearrangements drive successive structural transitions.

Orbital anisotropy correlates with spin order.

VED analysis constrains theoretical solutions effectively.

Abstract

Direct experimental access to orbital states in strongly correlated materials remains a major challenge, despite their central role in driving coupled structural and magnetic phase transitions. In systems where electronic correlations, electron-lattice coupling, and relativistic spin-orbit interactions compete on comparable energy scales, even first-principles calculations often yield multiple metastable solutions, hindering the unambiguous identification of the ground state. Here, we demonstrate that the orbital states of the spinel oxide FeV2O4, which possesses active orbital degrees of freedom on both Fe and V ions, are uniquely resolved by combining valence electron density (VED) analysis based on state-of-the-art synchrotron x-ray diffraction with spin-polarized density-functional-theory calculations. Our results reveal that temperature-dependent rearrangements of orbital occupations drive successive structural transitions that accompany collinear and noncoplanar ferrimagnetic orders, establishing a direct correspondence between orbital anisotropy and spin structure. More broadly, this work shows that experimentally determined VED provides a decisive real-space constraint on competing theoretical solutions, offering a powerful and broadly applicable framework for elucidating the microscopic mechanisms of complex phase transitions in strongly correlated electron systems.