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Phase Transitions And Magnetic Order In Multiferroic And Ferromagnetic Rare Earth Manganites

Electronic Theses of Indian Institute of Science

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Title Phase Transitions And Magnetic Order In Multiferroic And Ferromagnetic Rare Earth Manganites
 
Creator Harikrishnan, S
 
Subject Ferromagnetic Manganites
Phase Transition
Crystal Growth
DyMnO3 Single Crystals
Manganites - Magnetism
Multiferroic Manganites
Manganites - Spin-glass State
Manganites - Electron Paramagnetic Resonance
Manganites - Magnetic Properties
Manganites - Thermal Properties
Rare Earth Manganites
Manganites - Phase Transition
Dy0.5Sr0.5MnO3
Rare Earth Magnetism
Pr0.60Sr0.40MnO3 Single Crystals
Mineralogy
 
Description Recent findings of multiferroicity and magnetoelectric effects in rare earth manganites have fuelled research in this class of materials. These multiferroics can be structurally divided into two classes – orthorhombic and hexagonal. Especially attractive are TbMnO3, HoMnO3 and DyMnO3. Since the ionic radius of Dy is at the boundary that separates the orthorhombic and hexagonal RMnO3, DyMnO3 can be synthesized in both the structures using different synthesis conditions. In this thesis, DyMnO3 single crystals (both hexagonal and orthorhombic) prepared using optical floating zone furnace are studied through structural, magnetic and thermal properties. The influence of rare earth ion on the magnetic phase transitions is revealed in magnetisation, ac susceptibility and specific heat studies. Moreover, doping RMnO3 (small R) with alkaline earth ions creates an arena to test the interesting physics of spin-glass-like phenomena in manganites that arises due to quenched disorder. In this regard, 50% strontium diluted DyMnO3 could be an ideal system to study the effects of quenched disorder and structural/magnetic inhomogeneities that govern the magnetic phases in manganites. Structural phase-coexistence and ensuing anomalous magnetism in Pr–based manganite Pr0.6Sr0.4MnO3 are also presented in this thesis.
Details of how the thesis is organized into eight chapters and a brief summary of each chapter follows:
Chapter 1 is an introduction to the physics of manganites which progresses into multiferroics and eventually discusses the spin-glass-like effects arising due to size mismatch. A discussion on the phase-coexistence and its effect on physical properties are also presented. Eventually, the scope of the thesis is outlined in the last section.
Chapter 2 outlines the basic experimental methods employed in this thesis work.
Chapter 3 describes the details of crystal growth by optical floating zone method. DyMnO3 crystals in both hexagonal and orthorhombic structures are grown by employing the ambience of argon and air respectively. The crystals in the two crystallographic variants are characterized by X ray diffraction, Energy dispersive X ray analysis and Inductively coupled plasma atomic emission spectroscopy. The crystal structures are refined using Rietveld method with FULLPROF code and found to be P63cm for hexagonal and Pnma for orthorhombic DyMnO3. Details of crystal growth of Dy1−xSrxMnO3 are also presented. The change in ambience has no effect in the crystal structure of this doped manganite. A comparison of the growth of undoped and doped systems is given. In a later section, the crystal growth and structure refinement of Pr0.6Sr0.4MnO3 are discussed and the optimized growth parameters are tabulated for various manganite systems grown in the present work.
Chapter 4 deals with the magnetic and thermal characterization of hexagonal and orthorhombic DyMnO3 single crystals. Magnetic measurements reveal the importance of rare earth magnetism in these compounds. The antiferromagnetic transition to a stacked triangular antiferromagnet is discernible from the specific heat studies of hexagonal DyMnO3, which is masked in the bulk magnetisation measurements. Various magnetic transitions pertaining to the antiferromagnetic sinusoidal – spiral – incommensurate magnet, are evident in the magnetisation and specific heat of orthorhombic DyMnO3 which belongs to the class of non-collinear magnets.
Chapter 5 deals with basic investigations on the spin-glass-like state in Dy0.5Sr0.5MnO3. Preliminary dc magnetisation shows indication of spin-glass state as a split in field-cooled and zero-field-cooled magnetisation cycles. Further, the failure of scaling of M(T) with H/T indicates the absence of superparamagnetism in Dy0.5Sr0.5MnO3. The dynamic susceptibility and its analysis using the theory of critical slowing down yield exponents pertaining to the spin-glasses. However, a four-order magnitude change is observed in the characteristic spin-flip time. This leads to the assumption that in Dy0.5Sr0.5MnO3 the spin entities are not atomic spins as in canonical spin-glasses but clusters of spins. The specific heat is analysed for signatures of spin-glass state and is found that a linear term in temperature is essential in fitting the observed data. The crystalline electric fields of Dy ion is also analysed attempting multiple Schottky-levels instead of two.
Chapter 6 concerns with the aging experiments performed in the spin-glass-like state in Dy0.5Sr0.5MnO3. Striking aging and chaos effects are observed through these measurements. However, owing to the clusters of spins present, deviations from the typical time-dependent behavior seen in canonical spin-glass materials are anticipated in Dy0.5Sr0.5MnO3. In fact, the relaxation measurements indicate that the glassy magnetic properties are due to a cooperative and frustrated dynamics in a heterogeneous or clustered magnetic state. In particular, the microscopic spin flip time obtained from dynamical scaling near the spin-glass transition temperature is four orders of magnitude larger than microscopic times found in atomic spin-glasses. Magnetic viscosity, deduced from the waiting time dependence of the zero field cooled magnetisation, exhibits a peak at a temperature T
 
Contributor Elizabeth, Suja
Bhat, H L
 
Date 2011-03-29T04:43:29Z
2011-03-29T04:43:29Z
2011-03-29
2009-04
 
Type Thesis
 
Identifier http://etd.iisc.ernet.in/handle/2005/1101
 
Language en_US
 
Relation G23458