Entropy-stabilized materials as a platform to explore terbium-based pyrochlore frustrated magnets
Two decades of work have shown that the physics of Tb-based pyrochlores is controlled by a subtle equilibrium between quadrupole-quadrupole and dipolar-dipolar magnetic interactions, as exemplified by the ordered spin ice Tb 2 Sn 2 O 7 and the quantum spin liquid candidate Tb 2 Ti 2 O 7 . The high-e...
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Veröffentlicht in: | Communications materials 2024-08, Vol.5 (1), p.162-10, Article 162 |
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Sprache: | eng |
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Zusammenfassung: | Two decades of work have shown that the physics of Tb-based pyrochlores is controlled by a subtle equilibrium between quadrupole-quadrupole and dipolar-dipolar magnetic interactions, as exemplified by the ordered spin ice Tb
2
Sn
2
O
7
and the quantum spin liquid candidate Tb
2
Ti
2
O
7
. The high-entropy approach is thus quite promising, as it offers the possibility of a delicate tuning of chemical disorder. In this work, we investigate the entropy-stabilized pyrochlore compound Tb
2
(TiZrHfGeSn)
2
O
7
. We report the lack of long range magnetic order, yet the observed magnetic diffuse scattering is characteristic of antiferromagnetic first-neighbor correlations. The crystal field excitation spectrum, with broaden levels, visibly reflects the smooth environmental disorder of the Tb environment. The low energy dynamics are characterized by a narrow mode at about 0.4 meV, consistent with specific heat. Remarkably, as illustrated by a model of random isotropic shifts of oxygen atoms around Tb ions, the spectral weight of this mode is a direct consequence of deviations from the D
3d
symmetry at Tb sites. In the light of these results, quadrupolar interactions are also discussed.
Frustrated magnetic systems such as pyrochlores are interesting for the complexity of their competing low-temperature phases. Here, the intrinsic disorder of the entropy-stabilized compound Tb
2
(TiZrHfGeSn)
2
O
7
is utilized to investigate the elusive ground state of Tb-based pyrochlore magnets. |
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ISSN: | 2662-4443 2662-4443 |
DOI: | 10.1038/s43246-024-00589-y |