Magnetization reversal driven by electron localization-delocalization crossover in the inverse spinel Co2VO4

Thumbnail Image
Date
2022-03-07
Authors
Kademane, Abhijit Bhat
Bhandari, Churna
Paudyal, Durga
Cottrell, Stephen
Das, Pinaki
Liu, Yong
Yiu, Yuen
Kumar, C. M. Naveen
Siemensmeyer, Konrad
Hoser, Andreas
Major Professor
Advisor
Committee Member
Journal Title
Journal ISSN
Volume Title
Publisher
Iowa State University Digital Repository, Ames IA (United States)
Abstract
Neutron diffraction, magnetization, and muon spin relaxation measurements, supplemented by density functional theory (DFT) calculations are employed to unravel temperature-driven magnetization reversal in inverse spinel Co2VO4. All measurements show a second-order magnetic phase transition at T-C = 168 K to a collinear ferrimagnetic phase. Neutron diffraction measurements reveal two antiparallel ferromagnetic (FM) sublattices, belonging to magnetic ions on two distinct crystal lattice sites, where the relative balance between the two sublattices determine the net FM moment in the unit cell. As the evolution of the ordered moment with temperature differs between the two sublattices, the net magnetic moment reaches a maximum at T-NC = 138 K and reverses its sign at T-MR = 65 K. The DFT results suggest that the underlying microscopic mechanism for the reversal is a delocalization of the unfilled 3d-shell electrons on one sublattice just below T-C, followed by a gradual localization as the temperature is lowered. This delocalized-localized crossover is supported by muon spectroscopy results, as strong T-1 relaxation observed below T-C indicates fluctuating internal fields.
Series Number
Journal Issue
Is Version Of
Versions
Series
IS-J 10743
Type
article
Comments
This article is published as Kademane, Abhijit Bhat, Churna Bhandari, Durga Paudyal, Stephen Cottrell, Pinaki Das, Yong Liu, Yuen Yiu et al. "Magnetization reversal driven by electron localization-delocalization crossover in the inverse spinel Co 2 VO 4." Physical Review B 105, no. 9 (2022): 094408. DOI: 10.1103/PhysRevB.105.094408. Copyright 2022 American Physical Society. Posted with permission. DOE Contract Number(s): AC02-07CH11358.
Rights Statement
Copyright
Funding
Subject Categories
DOI
Supplemental Resources
Collections