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An investigation of relaxor ferromagnets

Abstract:

Q–dependent diffuse scattering was observed at low angles in a neutron diffraction experiment performed on the relaxor ferromagnet La3Ni2SbO9 using a spin–polarised beam. The nuclear component could be modelled using direct Monte–Carlo methods if it was assumed that short (~5.5 Å) Sb–Sb contacts were energetically disfavoured. The magnetic component of the diffuse scattering at 110 K (TC = 108 K) was analysed using both direct and reverse Monte–Carlo techniques. When antiferromagnetic nearest–neighbour coupling was assumed to be dominant in this perovskite, second neighbour coupling was found to be weak but non–zero with third–neighbour coupling being negligible. The short–range structural and magnetic orderings were found to have correlation lengths of 15 and 9 Å, respectively.

The consequences of replacing d10 Sb5+ by d0 pentavalent cations were investigated; all the compounds reported are isostructural with La3Ni2SbO9. La3Ni2TaO9 was found to be a relaxor ferromagnet but La3Ni2NbO9 behaved as a spin glass below 35 K. Solid solutions La3Ni2SbxTayNb1–x–yO9 were synthesised and characterised. It was again shown that the relaxor behaviour is incompatible with the presence of Nb5+ in the system. In contrast, doping La3Ni2B’O9 (B’ = Sb, Ta or Nb) with Cu2+ cations was found to increase TC and the bulk magnetisation. For example, La3Ni1.75Cu0.25NbO9 exhibits ferrimagnetic behaviour below ~90 K with the development of long–range G–type magnetic ordering. It is proposed that relaxor regions and long–range ordered regions coexist in this system.

The sensitivity of cation ordering, and hence magnetic behaviour, to the charge difference between Ni2+ and the diamagnetic six–coordinate cation was studied by replacing Sb5+ by Te6+ or W6+. Electron microscopy revealed a significant level of cation disorder in a severely–twinned sample of SrLa2Ni2TeO9; spin–glass and antiferromagnetic phases coexist below 35 K. The Ni2+ cations in CaLn2Ni2WO9 (Ln = La, Pr or Nd) form a spin glass, although the behaviour of each composition reflects the magnetic properties of Ln3+.

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Division:
MPLS
Department:
Chemistry
Sub department:
Inorganic Chemistry
Oxford college:
St Catherine's College
Role:
Author

Contributors

Institution:
University of Oxford
Division:
MPLS
Department:
Chemistry
Department:
Inorganic Chemistry Laboratory
Role:
Supervisor


DOI:
Type of award:
DPhil
Level of award:
Doctoral
Awarding institution:
University of Oxford


Language:
English
Keywords:
Subjects:
UUID:
uuid:33289083-3b3f-46f8-89c0-b501e2a2650a
Deposit date:
2019-09-05

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