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Charge disproportionation and collinear magnetic order in the frustrated triangular antiferromagnet AgNiO2

Abstract:
We report a high-resolution neutron diffraction study of the crystal and magnetic structure of the orbitally-degenerate frustrated metallic magnet AgNiO2. At high temperatures the structure is hexagonal with a single crystallographic Ni site, low-spin Ni3+ with spin-1/2 and two-fold orbital degeneracy, arranged in an antiferromagnetic triangular lattice with frustrated spin and orbital order. A structural transition occurs upon cooling below 365 K to a tripled hexagonal unit cell containing three crystallographically-distinct Ni sites with expanded and contracted NiO6 octahedra, naturally explained by spontaneous charge order on the Ni triangular layers. No Jahn-Teller distortions occur, suggesting that charge order occurs in order to lift the orbital degeneracy. Symmetry analysis of the inferred Ni charge order pattern and the observed oxygen displacement pattern suggests that the transition could be mediated by charge fluctuations at the Ni sites coupled to a soft oxygen optical phonon breathing mode. At low temperatures the electron-rich Ni sublattice (assigned to a valence close to Ni2+ with S = 1) orders magnetically into a collinear stripe structure of ferromagnetic rows ordered antiferromagnetically in the triangular planes. We discuss the stability of this uncommon spin order pattern in the context of an easy-axis triangular antiferromagnet with additional weak second neighbor interactions and interlayer couplings.
Publication status:
Published

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Publisher copy:
10.1103/PhysRevB.77.094439

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Institution:
University of Oxford
Division:
MPLS
Department:
Physics
Sub department:
Condensed Matter Physics
Role:
Author


Journal:
Phys. Rev. B More from this journal
Volume:
77
Issue:
9
Pages:
094439
Publication date:
2007-10-15
DOI:
EISSN:
1550-235X
ISSN:
1098-0121


Language:
English
Keywords:
Pubs id:
pubs:66306
UUID:
uuid:1e3d8a90-e6b1-413d-a449-596ff6f85168
Local pid:
pubs:66306
Source identifiers:
66306
Deposit date:
2012-12-19

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