Magnetic and structural properties of the solid solution CuAl2(1−x)Ga2xO4

Abstract CuAl2O4 is a ternary oxide spinel with Cu2+ ions ( $$s=1/2$$ s = 1 / 2 ) primarily populating the A-site diamond sublattice. The compound is reported to display evidence of spin glass behavior but possess a non-frozen magnetic ground state below the transition temperature. On the other hand...

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Main Authors: T. J. Bullard, M. A. Susner, K. M. Taddei, J. A. Brant, T. J. Haugan
Format: Article
Language:English
Published: Nature Publishing Group 2021-05-01
Series:Scientific Reports
Online Access:https://doi.org/10.1038/s41598-021-89197-1
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spelling doaj-a433b15ed7fa4c11ac234d90f3664f8c2021-06-06T11:40:07ZengNature Publishing GroupScientific Reports2045-23222021-05-0111111210.1038/s41598-021-89197-1Magnetic and structural properties of the solid solution CuAl2(1−x)Ga2xO4T. J. Bullard0M. A. Susner1K. M. Taddei2J. A. Brant3T. J. Haugan4UES, Inc.UES, Inc.Oak Ridge National LaboratoryAerospace Systems Directorate, Air Force Research Laboratory, Wright-Patterson AFBAerospace Systems Directorate, Air Force Research Laboratory, Wright-Patterson AFBAbstract CuAl2O4 is a ternary oxide spinel with Cu2+ ions ( $$s=1/2$$ s = 1 / 2 ) primarily populating the A-site diamond sublattice. The compound is reported to display evidence of spin glass behavior but possess a non-frozen magnetic ground state below the transition temperature. On the other hand, the spinel CuGa2O4 displays spin glass behavior at ~ 2.5 K with Cu2+ ions more readily tending to the B-site pyrochlore sublattice. Therefore, we investigate the magnetic and structural properties of the solid solution CuAl2(1-x)Ga2xO4 examining the evolution of the magnetic behavior as Al3+ is replaced with a much larger Ga3+ ion. Our results show that the Cu2+ ions tend to migrate from tetrahedral to octahedral sites as the Ga3+ ion concentration increases, resulting in a concomitant change in the glassy magnetic properties of the solution. Results indicate glassy behavior for much of the solution with a general trend towards decreasing magnetic frustration as the Cu2+ ion shifts to the B-site. However, the $$x=0.1$$ x = 0.1 and 0.2 members of the system do not show glassy behavior down to our measurement limit (1.9 K) suggesting a delayed spin glass transition. We suggest that these two members are additional candidates for investigation to access highly frustrated exotic quantum states.https://doi.org/10.1038/s41598-021-89197-1
collection DOAJ
language English
format Article
sources DOAJ
author T. J. Bullard
M. A. Susner
K. M. Taddei
J. A. Brant
T. J. Haugan
spellingShingle T. J. Bullard
M. A. Susner
K. M. Taddei
J. A. Brant
T. J. Haugan
Magnetic and structural properties of the solid solution CuAl2(1−x)Ga2xO4
Scientific Reports
author_facet T. J. Bullard
M. A. Susner
K. M. Taddei
J. A. Brant
T. J. Haugan
author_sort T. J. Bullard
title Magnetic and structural properties of the solid solution CuAl2(1−x)Ga2xO4
title_short Magnetic and structural properties of the solid solution CuAl2(1−x)Ga2xO4
title_full Magnetic and structural properties of the solid solution CuAl2(1−x)Ga2xO4
title_fullStr Magnetic and structural properties of the solid solution CuAl2(1−x)Ga2xO4
title_full_unstemmed Magnetic and structural properties of the solid solution CuAl2(1−x)Ga2xO4
title_sort magnetic and structural properties of the solid solution cual2(1−x)ga2xo4
publisher Nature Publishing Group
series Scientific Reports
issn 2045-2322
publishDate 2021-05-01
description Abstract CuAl2O4 is a ternary oxide spinel with Cu2+ ions ( $$s=1/2$$ s = 1 / 2 ) primarily populating the A-site diamond sublattice. The compound is reported to display evidence of spin glass behavior but possess a non-frozen magnetic ground state below the transition temperature. On the other hand, the spinel CuGa2O4 displays spin glass behavior at ~ 2.5 K with Cu2+ ions more readily tending to the B-site pyrochlore sublattice. Therefore, we investigate the magnetic and structural properties of the solid solution CuAl2(1-x)Ga2xO4 examining the evolution of the magnetic behavior as Al3+ is replaced with a much larger Ga3+ ion. Our results show that the Cu2+ ions tend to migrate from tetrahedral to octahedral sites as the Ga3+ ion concentration increases, resulting in a concomitant change in the glassy magnetic properties of the solution. Results indicate glassy behavior for much of the solution with a general trend towards decreasing magnetic frustration as the Cu2+ ion shifts to the B-site. However, the $$x=0.1$$ x = 0.1 and 0.2 members of the system do not show glassy behavior down to our measurement limit (1.9 K) suggesting a delayed spin glass transition. We suggest that these two members are additional candidates for investigation to access highly frustrated exotic quantum states.
url https://doi.org/10.1038/s41598-021-89197-1
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