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Geometric frustration on the trillium lattice in a magnetic metal-organic framework

Abstract:
In the dense metal-organic framework Na[Mn(HCOO)3], Mn2+ ions (S=5/2) occupy the nodes of a “trillium” net. We show that the system is strongly magnetically frustrated: the Néel transition is suppressed well below the characteristic magnetic interaction strength; short-range magnetic order persists far above the Néel temperature; and the magnetic susceptibility exhibits a pseudo-plateau at 1/3-saturation magnetization. A simple model of nearest-neighbor Heisenberg antiferromagnetic and dipolar interactions accounts quantitatively for all observations, including an unusual 2-k magnetic ground state. We show that the relative strength of dipolar interactions is crucial to selecting this particular ground state. Geometric frustration within the classical spin liquid regime gives rise to a large magnetocaloric response at low applied fields that is degraded in powder samples as a consequence of the anisotropy of dipolar interactions.
Publication status:
Published
Peer review status:
Peer reviewed

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Publisher copy:
10.1103/physrevlett.128.177201

Authors


More by this author
Institution:
University of Oxford
Division:
MPLS
Department:
Chemistry
Sub department:
Inorganic Chemistry
Role:
Author
More by this author
Institution:
University of Oxford
Division:
MPLS
Department:
Chemistry
Sub department:
Inorganic Chemistry
Oxford college:
St Hilda's College
Role:
Author
ORCID:
0000-0002-4297-1425


Publisher:
American Physical Society
Journal:
Physical Review Letters More from this journal
Volume:
128
Issue:
17
Article number:
177201
Place of publication:
United States
Publication date:
2022-04-26
Acceptance date:
2022-03-17
DOI:
EISSN:
1079-7114
ISSN:
0031-9007
Pmid:
35570439


Language:
English
Keywords:
Pubs id:
1246801
Local pid:
pubs:1246801
Deposit date:
2022-12-08

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