ABSTRACT
The thermophysical properties of liquid germanium were recently measured both in parabolic flight experiments and on the ISS in the ISS-EML facility. The viscosity measurements differed between the reduced gravity experiments and the literature values. Since the oscillating drop method has been widely used in EML, further exploration into this phenomenon was of interest. Models of the magnetohydrodynamic flow indicated that turbulence was present during the measurement in the ISS-EML facility, which accounts for the observed difference.
ABSTRACT
A long-standing issue in the physics of the colossal magnetoresistance is the role of electron-phonon coupling, which manifests itself as Jahn-Teller polarons. The origin and architecture of polarons makes it possible to study their behavior by Raman spectroscopy, which allows to analyze the polaronic behavior in an applied magnetic field. We performed magnetic-field-dependent Raman spectroscopy on thin films of (La0.6Pr0.4)0.7Ca0.3MnO3 in a range of H = 0-50 kOe and compared the obtained Raman spectra with the magnetic field behavior of the electrical resistivity. In the vicinity of the Curie temperature, TC = 197 K, the intensity of the Jahn-Teller stretching mode at 614 cm-1 and of the bending mode at 443 cm-1 was found to be suppressed and enhanced, respectively. This observed behavior has a remarkable similarity with the field and temperature dependence of the colossal magnetoresistance in (La0.6Pr0.4)0.7Ca0.3MnO3. Our work provides direct evidence that the reduction of the amount of Jahn-Teller polarons at the phase transition is the main mechanism underlying the colossal magnetoresistance.
ABSTRACT
The precise nature of complex structural relaxation as well as an explanation for the precipitous growth of relaxation time in cooling glass-forming liquids are essential to the understanding of vitrification of liquids. The dramatic increase of relaxation time is believed to be caused by the growth of one or more correlation lengths, which has received much attention recently. Here, we report a direct link between the growth of a specific local-geometrical-order and an increase of dynamic-length-scale as the atomic dynamics in metallic glass-forming liquids slow down. Although several types of local geometrical-orders are present in these metallic liquids, the growth of icosahedral ordering is found to be directly related to the increase of the dynamic-length-scale. This finding suggests an intriguing scenario that the transient icosahedral connectivity could be the origin of the dynamic-length-scale in metallic glass-forming liquids.
ABSTRACT
We report photoinduced effects in nonlinear third harmonic ac electric transport-which is a measure for the density of correlated polarons-in thin films of [Formula: see text] (LBMO) and [Formula: see text] (LPCMO) manganites. Both materials show an enhancement of third harmonic voltage in the vicinity of the metal-to-insulator transition, indicating strong electron-lattice correlations within a phase-separated state. Relatively low laser excitation with a pulse fluence of [Formula: see text] leads to an increase (decrease) in nonlinearity in LBMO (LPCMO). With a high pulse fluence of 8mJ cm-2, we were also able to suppress the correlations in LBMO, which is accompanied by a decrease of third harmonic voltage by [Formula: see text] in our time-averaging measurement technique.
ABSTRACT
In a model metallic glass, we study the relaxation dynamics in both the linear and the nonlinear response regimes by numerical simulations of dynamical mechanical spectroscopy and analyze the atomic displacement statistics. We find that the primary (α) relaxation always takes place when the most probable atomic displacement reaches a critical fraction (~20%) of the average interatomic distance, irrespective of whether the relaxation is induced by temperature (linear response) or by mechanical strain (nonlinear response). Such a unified scenario, analogous to the well-known Lindemann criterion for crystal melting, provides insight into the structural origin of the strain-induced glass-liquid transition.
ABSTRACT
The origin of the martensitic transition in the magnetic shape memory alloy Ni-Mn-Ga has been widely discussed. While several studies suggest it is electronically driven, the adaptive martensite model reproduced the peculiar nonharmonic lattice modulation. We used femtosecond spectroscopy to probe the temperature and doping dependence of collective modes, and scanning tunneling microscopy revealed the corresponding static modulations. We show that the martensitic phase can be described by a complex charge-density wave tuned by magnetic ordering and strong electron-lattice coupling.
ABSTRACT
In multicomponent metallic glasses, we demonstrate that diffusion and secondary (ß) relaxation are closely related. The diffusion motion of the smallest constituting atoms takes place within the temperature and time regimes where the ß relaxations are activated, and, in particular, the two processes have similar activation energies. We suggest cooperative stringlike atomic motion plays an important role in both processes. This finding provides additional insights into the structural origin of the ß relaxations as well as the mechanisms of diffusions in metallic glasses.
ABSTRACT
In this work we analyzed the mechanical damping behavior of amorphous Pd(77.5)Cu(6.0)Si(16.5) below the glass transition temperature (T(g)) with creep/recovery measurements. Here a correlation between temperature stimulation and external stress is found in an exponential, multiplicative way. This demonstrates that not only is the yield stress of the material influenced by temperature variation (mechanical melting) but also the secondary relaxation is modified under stress and temperature.
ABSTRACT
In the liquid state, glass-forming Ni59.5Nb40.5 and Ni60Nb34.8Sn5.2 alloys exhibit an extraordinarily high packing fraction. The self-correlation functions measured using quasielastic neutron scattering clearly show the slowing down of microscopic dynamics with an increase in packing fraction. The self-diffusivity in liquid Ni60Nb34.8Sn5.2 decreases by about 2 orders of magnitude within a temperature range of 360 K. For these highly fragile systems, the critical packing fraction obtained form the analysis of incoherent data is in excellent agreement with the prediction made by mode-coupling theory. Our results provide the first experimentally observed value for the critical packing fraction in glass-forming metallic liquids.
ABSTRACT
It is generally believed that nature does not provide materials with negative refraction. Here we demonstrate experimentally that such materials do exist at least at GHz frequencies: ferromagnetic metals reveal a negative refraction index close to the frequency of the ferromagnetic resonance. The experimental realization utilizes a colossal magnetoresistance manganite La(2/3)Ca(1/3)MnO(3) as an example. In this material the negative refractive index can be achieved even at room temperature using external magnetic fields.
ABSTRACT
Epitaxial La(3/4)Ca(1/4)MnO3/MgO(100) (LCMO) thin film shows an unusual rhombohedral (R-3c) structure with a new perovskite superstructure at room temperature due to the CE-type ordering of La and Ca with modulation vector q=1/4[011]. A-site ordered film was found to be electronically homogeneous down to the 1 nm scale as revealed by scanning tunnelling microscopy/spectroscopy. In contrast, orthorhombic and A-site disordered LCMO demonstrate a mesoscopic phase separation far below the Curie temperature (TC). Unique La/Ca ordering compensates the cation mismatch stress within one supercell, a(S) approximately 1.55 nm, and enhances the electronic homogeneity. The phase separation does not seem to be a unique mechanism for the colossal magnetoresistance (CMR) as very large CMR approximately 500% was also observed in A-site ordered films.
ABSTRACT
Room temperature (TR) elastic constants and compressive yield strengths of approximately 30 metallic glasses reveal an average shear limit gammaC=0.0267+/-0.0020, where tauY=gamma CG is the maximum resolved shear stress at yielding, and G the shear modulus. The gammaC values for individual glasses are correlated with t=TR/Tg , and gamma C for a single glass follows the same correlation (vs t=T/Tg). A cooperative shear model, inspired by Frenkel's analysis of the shear strength of solids, is proposed. Using a scaling analysis leads to a universal law tauCT/G=gammaC0-gammaC1(t)2/3 for the flow stress at finite T where gammaC0=(0.036+/-0.002) and gammaC1=(0.016+/-0.002).
ABSTRACT
'Colossal magnetoresistance' in perovskite manganites such as La0.7Ca0.3MnO3 (LCMO), is caused by the interplay of ferro-paramagnetic, metal-insulator and structural phase transitions. Moreover, different electronic phases can coexist on a very fine scale resulting in percolative electron transport. Here we report on (LCMO)1-x:(MgO)x (0 < x < or = 0.8) epitaxial nano-composite films in which the structure and magnetotransport properties of the manganite nanoclusters can be tuned by the tensile stress originating from the MgO second phase. With increasing x, the lattice of LCMO was found to expand, yielding a bulk tensile strain. The largest colossal magnetoresistance of 10(5)% was observed at the percolation threshold in the conductivity at xc 0.3, which is coupled to a structural phase transition from orthorhombic (0 < x < or 0.1) to rhombohedral R3c structure (0.33 < or = x < or = 0.8). An increase of the Curie temperature for the Rc phase was observed. These results may provide a general method for controlling the magnetotransport properties of manganite-based composite films by appropriate choice of the second phase.
Subject(s)
Crystallization/methods , Crystallography/methods , Ferric Compounds/chemistry , Magnesium Oxide/chemistry , Calcium Compounds/chemistry , Electric Conductivity , Electron Transport , Materials Testing , Microscopy, Electron, Scanning , Molecular Conformation , Oxides/chemistry , Sensitivity and Specificity , Temperature , Titanium/chemistryABSTRACT
Thin films of La0.7Sr0.3MnO3 on MgO show a metal insulator transition and colossal magnetoresistance. The shape of this transition can be explained by intrinsic spatial inhomogeneities, which give rise to a domain structure of conducting and insulating domains at the submicrometer scale. These domains then undergo a percolation transition. The tunneling conductance and tunneling gap measured by scanning tunneling spectroscopy were used to distinguish and visualize these domains.
ABSTRACT
Metallic amorphous thin films evaporated on a substrate can be characterized by different growth regimes in dependence of the film thickness concerning surface morphology and intrinsic film stresses, independent of the details of the applied material systems. Here, a model is presented to link the surface topography and characteristic surface measures with the observed film stresses. This allows quantitative prediction of stresses in dependence of film preparation parameters for a tailored film production.
