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On the microscopic mechanism for the stabilization of structural and ferroic states in displacive multiferroics
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10.1063/1.4795766
/content/aip/journal/jap/113/11/10.1063/1.4795766
http://aip.metastore.ingenta.com/content/aip/journal/jap/113/11/10.1063/1.4795766

Figures

Image of FIG. 1.
FIG. 1.

Differential scanning calorimetry curves (heating) for (1−x)BiFeO3-(x)PbTiO3 samples. Inset: Zoom of the low temperature region (lower than 450 °C) evidencing the step-like changes in the DSC baseline.

Image of FIG. 2.
FIG. 2.

(a) X-ray diffraction patterns at different temperatures, and (b) Rietveld refined lattice parameters and angles as a function of temperature, for the (0.75)BiFeO3-(0.25)PbTiO3 compound.

Image of FIG. 3.
FIG. 3.

Differential scanning calorimetry signal and temperature dependence of the dielectric constant, ε′, for the (0.75)BiFeO3-(0.25)PbTiO3 compound.

Image of FIG. 4.
FIG. 4.

Heating and cooling differential scanning calorimetric curves, and temperature dependent magnetization curves, for the (0.9)BiFeO3-(0.1)PbTiO3 compound. Inset: zoom of the differential scanning calorimetric curve around the Néel temperature.

Image of FIG. 5.
FIG. 5.

High resolution image obtained by transmission electron microscopy in the tetragonal symmetry (P4mm space group) of the (0.6)BiFeO3-(0.4)PbTiO3 compound oriented in [111] direction. (i) electron diffraction patterns, and (ii) high-resolution simulated image obtained in [111] zone axis.

Image of FIG. 6.
FIG. 6.

Schematic illustration showing different symmetries of the perovskite structure. (a) cubic (Pm-3m) nonpolar unit cell, (b) tetragonal (P4mm) ([001] direction) polar unit cell, and (c) rhombohedral (R3m) ([111] direction) polar unit cell.

Image of FIG. 7.
FIG. 7.

Schematic illustration of the weak ferromagnetic arrangement in BiFeO3-based solid solutions. (a) Illustrative cycloidal magnetic structure for the BiFeO3 compound. (b) illustrative breaking of the cycloidal magnetic structure for (1−x)BiFeO3-(x)PbTiO3 solid solutions reached by replacing Fe3+ for Ti4+ ions. MA—magnetic moment of the antiferromagnetic arrangement. MR—resultant magnetic moment of the weak ferromagnetic arrangement.

Image of FIG. 8.
FIG. 8.

Schematic illustration showing the behavior of the polarization vector under oscillating electric fields and thermal agitation. (a) When the maximum electric field is applied, there is a positive electric polarization in the sample. (b) When the maximum electric field is applied in the opposite direction, a negative electric polarization emerges. (c) By increasing temperature, the modulus of the electric polarization vector increases until TC. At TC, the thermal agitation contributes to increase the modulus of the electric polarization vector and the average off-center position of the Ti/Fe ion. Above TC, the cubic structure is stabilized and the geometric center of the negative and positive charges is the same.

Tables

Generic image for table
Table I.

Rietveld refined structural parameters, at different temperatures, for the (0.75)BiFeO3-(0.25)PbTiO3 compound.

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/content/aip/journal/jap/113/11/10.1063/1.4795766
2013-03-19
2014-04-21
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752b84549af89a08dbdd7fdb8b9568b5 journal.articlezxybnytfddd
Scitation: On the microscopic mechanism for the stabilization of structural and ferroic states in displacive multiferroics
http://aip.metastore.ingenta.com/content/aip/journal/jap/113/11/10.1063/1.4795766
10.1063/1.4795766
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