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Register a new userImprinting magnetic information in manganites with X-rays
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The effect of x-rays on an orbital and charge ordered epitaxial film of a Pr$_{0.5}$Ca$_{0.5}$MnO$_{3}$ is presented. As the film is exposed to x-rays, the antiferromagnetic response increases and concomitantly the conductivity of the film improve. These results are discussed in terms of a persistent x-ray induced doping, leading to a modification of the magnetic structure. This effect allows writing electronic and magnetic domains in the film and represents a novel way of manipulating magnetism.
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We investigate a series of manganese oxides, the La0.225Pr0.4(Ca1-xSrx)0.375MnO3 system. The x = 0 sample is a prototype compound for the study of phase separation in manganites, where ferromagnetic and charge ordered antiferromagnetic phases coexist. Replacing Ca2+ by Sr2+ gradually turns the system into a homogeneous ferromagnet. Our results show that the material structure plays a major role in the observed magnetic properties. On cooling, at temperatures below 100 K, a strong contraction of the lattice is followed by an increase in the magnetization. This is observed both through thermal expansion and magnetostriction measurements, providing distinct evidence of magneto-elastic coupling in these phase separated compounds.
Using a two-orbital model and Monte Carlo simulations, we investigate the effect of nonmagnetic B-site substitution on half-doped CE-type manganites. The lattice defects induced by this substitution destabilize the CE phase, which transforms into (1) the ferromagnetic (FM) metallic competing state, or (2) a regime with short-range FM clusters, or (3) a spin-glass state, depending on couplings and on the valence of the B-site substitution. While a C-type antiferromagnetic state is usually associated with an average $e_{rm g}$ charge density less than 0.5, the nonmagnetic B-site substitution that lowers the $e_{rm g}$ charge density is still found to enhance the FM tendency in our simulations. The present calculations are in qualitative agreement with experiments and provide a rationalization for the complex role of nonmagnetic B-site substitution in modulating the phase transitions in manganites.
Recent progress in nanofabrication and additive manufacturing have facilitated the building of nanometer-scale three-dimensional structures, that promise to lead to an emergence of new functionalities within a number of fields, compared to state-of-the-art two dimensional systems. In magnetism, the move to three-dimensional systems offers the possibility for novel magnetic properties not available in planar systems, as well as enhanced performance, both of which are key for the development of new technological applications. In this review paper we will focus our attention on three-dimensional magnetic systems and how their magnetic configuration can be retrieved using X-ray magnetic nanotomography.
Magnetic properties of polycrystalline CaMn1-xRuxO3 (x = 0 - 0.5) samples were investigated in the temperature range 4.2 - 250 K, under external magnetic field up to 15 kOe and under hydrostatic pressure up to 12 kbar. Transport properties of the samples with x = 0.1, 0.2, 0.4, 0.5 were also investigated under pressure up to 10 kbar. For x up to 0.4, the pressure was found to suppress ferromagnetic correlations and to increase the resistivity, while for x = 0.5 to act in the opposite way. While long ferromagnetic order is completely suppressed, in small clusters ferromagnetic correlations probably survive under pressure, as was revealed for CaMn0.9Ru0.1O3. The pressure effect on the magnetic interactions and on the volume of ferromagnetic phase was found to depend strongly on the Ru-content, and absolute value of the pressure coefficient of spontaneous magnetization was found to decrease practically linearly with increasing x in the range 0.1 < x < 0.5. The experimental data are discussed in the frame of proposed energy-level diagram, which includes magneto-impurity states at low and moderate Ru-doping and mixed-valence states of Ru presented by a strongly-correlated t2g-like band at heavy Ru-doping. An impact of disorder introduced by Ru-doping on the energy diagram and on derived magnetic interactions is discussed. Predictions of the model regarding the pressure effects on conductivity and temperature scales characteristic for magnetic interactions are in reasonable agreement with experiment.
Multiferroic rare earth manganites attracted recent attention because of the coexistence of different types of magnetic and ferroelectric orders resulting in complex phase diagrams and a wealth of physical phenomena. The coupling and mutual interference of the different orders and the large magnetoelectric effect observed in several compounds are of fundamental interest and bear the potential for future applications in which the dielectric (magnetic) properties can be modified by the onset of a magnetic (dielectric) transition or the application of a magnetic (electric) field. The physical mechanisms of the magnetoelectric effect and the origin of ferroelectric order at magnetic transitions have yet to be explored. We discuss multiferroic phenomena in the hexagonal HoMnO3 and show that the strong magneto-dielectric coupling is intimately related to the lattice strain induced by unusually large spin-phonon correlations.
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