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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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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