Symmetry and strain analysis of structural phase transitions in Pr_{0.48}Ca_{0.52}MnO_{3}

Carpenter, Michael A. and McKnight, Ruth E. A. and Howard, Christopher J. and Knight, Kevin S. (2010) Symmetry and strain analysis of structural phase transitions in Pr_{0.48}Ca_{0.52}MnO_{3}. Physical Review B, 82 (9). 094101. DOI 10.1103/PhysRevB.82.014113

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Abstract

Structural evolution as a function of temperature through the Pnma↔incommensurate (IC) phase transition in Pr0.48Ca0.52MnO3 perovskite has been analyzed from the perspectives of symmetry and strain. The structure and stability of both phases are shown to depend on combinations of order parameters which have symmetries associated with irreducible representations M3+, R4+, M2+, Γ3+ and Σ2 of space group Pm3̅ m. The physical origin of these can be understood in terms of octahedral tilting, cooperative Jahn-Teller distortions and charge order/Zener polaron ordering. The M2+ order parameter describes the Jahn-Teller ordering scheme which develops in LaMnO3 while the Γ3+ order parameter relates to an ordering scheme in which the unique axes of the distorted octahedra are all aligned in the same direction. Irrep Σ2 contains two components with gradient coupling and provides the symmetry-breaking mechanism by which the IC transition can occur. Each order parameter couples with macroscopic spontaneous strains in a manner that depends strictly on symmetry and this leads to specific interactions between the order parameters through their coupling with common strains. In order to establish the extent and importance of this coupling, symmetry-adapted strains have been extracted from a new set of lattice parameters obtained by high-resolution powder neutron diffraction in the temperature interval 10–1373 K. It is found that the predominant strain of the incommensurate structure (up to ∼2.5%) is a tetragonal shear strain which arises by bilinear coupling with the Γ3+ order parameter. This combination is probably responsible for most of the energy reduction accompanying the Pnma↔IC transition and also gives it some characteristics typical of a pseudoproper ferroelastic transition. Strain coupling promotes mean-field behavior and the evolution of the symmetry-breaking order parameter can be described by a standard Landau tricritical solution, q4∝(Tc−T) with Tc=237±2 K. Octahedral tilting at high temperatures is closely similar to tilting in the Pnma structure of other perovskites, such as SrZrO3. This is accompanied by a degree of Jahn-Teller ordering on the basis of the M2+ scheme below ∼775 K but is replaced by the Γ3+ scheme below Tc. In contrast with the tilting and Jahn-Teller effects, magnetic ordering at the Néel temperature (∼180 K) is accompanied by only the slightest volume strain and is not likely to influence the evolution of the other order parameters to any significant extent, therefore. An additional change in the volume strain below ∼85 K is perhaps related to changes in magnetic structure at lower temperatures. Line broadening in powder diffraction patterns collected in the temperature interval ∼150–260 K appears to be related to the presence of ferroelastic twins arising from octahedral tilting and draws attention to the fact that the Pnma↔IC transition takes place in a material which already contains heterogeneities. Finally, correlation of the repeat distance of the IC structure with Γ3+ distortions of MnO6 octahedra shows that the nature of the IC structure itself is also determined essentially by geometrical factors and strain.

Item Type: Article
Uncontrolled Keywords: 2010AREP; IA61;
Subjects: 03 - Mineral Sciences
Divisions: 03 - Mineral Sciences
Journal or Publication Title: Physical Review B
Volume: 82
Page Range: 094101
Identification Number: 10.1103/PhysRevB.82.014113
Depositing User: Sarah Humbert
Date Deposited: 09 Sep 2010 14:53
Last Modified: 23 Jul 2013 10:00
URI: http://eprints.esc.cam.ac.uk/id/eprint/1929

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