Novel multiferroic state and ME enhancement by breaking the AFM frustration in LuMn1−xO3
Author(s) -
F. Figueiras,
D. V. Karpinsky,
Pedro B. Tavares,
J. N. Gonçalves,
S. YáñezVilar,
António M. dos Santos,
Alexandra Franz,
Michael Tovar,
J. Agostinho Moreira,
V. S. Amaral
Publication year - 2016
Publication title -
physical chemistry chemical physics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.053
H-Index - 239
eISSN - 1463-9084
pISSN - 1463-9076
DOI - 10.1039/c6cp07682c
Subject(s) - frustration , multiferroics , condensed matter physics , materials science , atomic force microscopy , state (computer science) , physics , nanotechnology , ferroelectricity , quantum mechanics , mathematics , algorithm , dielectric
This study provides a comprehensive insight into the effects of controlled off-stoichiometry on the structural and multiferroic properties of the hexagonal manganite LuMn 1-x O 3+δ (x = 0.02; δ ∼ 0), supported by neutron powder diffraction measurements confirming single phase P6 3 cm symmetry and evidencing a relevant ferromagnetic component, below T N ∼ 90 K, which breaks the archetypal geometrically frustrated antiferromagnetic state typically ascribed to LuMnO 3 . The perturbations in the triangular disposition of spins prompt an additional electric polarization contribution and a clear enhancement of the magnetoelectric coupling which are in good agreement with the results of first principles calculations. In addition, Raman spectroscopy, dielectric permittivity, pyroelectric current and magnetic measurements as a function of temperature point out the precursor effects of the magnetic phase transitions involving a strong coupling between spins, lattice and electric order, even above the Néel temperature.
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