Structural and magnetic properties of the single-layer manganese oxide La1-xSr1+xMnO4
Creators
- 1. Department of Physics, Stanford University, Stanford, California 94305 (United States)
- 2. Stanford Synchrotron Radiation Laboratory, Stanford Linear Accelerator Center, Stanford, California 94309 (United States)
- 3. Department of Applied Physics, Stanford University, Stanford, California 94305 (United States)
- 4. NIST Center for Neutron Research, National Institute of Standards and Technology, Gaithersburg, Maryland 20899 (United States)
Description
Using x-ray and neutron scattering, we have studied the structural and magnetic properties of the single-layer manganite La1-xSr1+xMnO4(0≤x<0.7). Single crystals were grown by the floating-zone method at 18 La/Sr concentrations. The low-temperature phase diagram can be understood by considering the strong coupling of the magnetic and orbital degrees of freedom, and it can be divided into three distinct regions: low (x<0.12), intermediate (0.12≤x<0.45), and high (x≥0.45) doping. LaSrMnO4(x=0) is an antiferromagnetic Mott insulator, and its spin-wave spectrum is well described by linear spin-wave theory for the spin-2 square-lattice Heisenberg Hamiltonian with Ising anisotropy. Upon doping, as the eg electron concentration (1-x) decreases, both the two-dimensional antiferromagnetic spin correlations in the paramagnetic phase and the low-temperature ordered moment decrease due to an increase of frustrating interactions, and Neel order disappears above xc=0.115(10). The magnetic frustration is closely related to changes in the eg orbital occupancies and the associated Jahn-Teller distortions. In the intermediate region, there exists neither long-range magnetic nor superstructural order. Short-range-correlated structural 'nanopatches' begin to form above x∼0.25. At high doping (x≥0.45), the ground state of La1-xSr1+xMnO4 exhibits long-range superstructural order and a complex antiferromagnetic order, which differs from that at low doping. The superstructural order is thought to arise from charge and orbital ordering on the Mn sites, and for x=0.50 we conclude that it is of B2mm symmetry. For x>0.50, the superstructural order becomes incommensurate with the lattice, with a modulation wave vector ε that depends linearly on the eg electron concentration: ε=2(1-x). On the other hand, the magnetic order remains commensurate, but loses its long-range coherence upon doping beyond x=0.50
Additional details
Identifiers
- DOI
- 10.1103/PhysRevB.71.024435;
- arXiv
- arXiv:cond-mat/0405424v1;
Publishing Information
- Journal Title
- Physical Review. B, Condensed Matter and Materials Physics
- Journal Volume
- 71
- Journal Issue
- 2
- Journal Page Range
- p. 024435-024435.18
- ISSN
- 1098-0121
INIS
- Country of Publication
- United States
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 36102950
- Subject category
- S75: CONDENSED MATTER PHYSICS, SUPERCONDUCTIVITY AND SUPERFLUIDITY; S36: MATERIALS SCIENCE;
- Descriptors DEI
- ANTIFERROMAGNETIC MATERIALS; ANTIFERROMAGNETISM; HAMILTONIANS; HEISENBERG MODEL; ISING MODEL; JAHN-TELLER EFFECT; LANTHANUM COMPOUNDS; LAYERS; MAGNETIC PROPERTIES; MANGANESE OXIDES; NEUTRON DIFFRACTION; PHASE DIAGRAMS; SPIN WAVES; STRONG-COUPLING MODEL; STRONTIUM COMPOUNDS; X-RAY DIFFRACTION; ZONE MELTING
- Descriptors DEC
- ALKALINE EARTH METAL COMPOUNDS; CHALCOGENIDES; COHERENT SCATTERING; CRYSTAL GROWTH METHODS; CRYSTAL MODELS; DIAGRAMS; DIFFRACTION; INFORMATION; MAGNETIC MATERIALS; MAGNETISM; MANGANESE COMPOUNDS; MATERIALS; MATHEMATICAL MODELS; MATHEMATICAL OPERATORS; MELTING; OXIDES; OXYGEN COMPOUNDS; PARTICLE MODELS; PHASE TRANSFORMATIONS; PHYSICAL PROPERTIES; QUANTUM OPERATORS; RARE EARTH COMPOUNDS; SCATTERING; TRANSITION ELEMENT COMPOUNDS
Optional Information
- Notes
- (c) 2005 The American Physical Society