The Structural Characterization of Tin- and Titanium-Dopedα-Fe2O3Prepared by Hydrothermal Synthesis

The structural characteristics of tin- and titanium-dopedα-Fe₂O₃prepared by hydrothermal methods have been investigated by Rietveld structure refinement of the X-ray powder diffraction data. The analysis reveals that the dopant ions adopt two distinct sites: in addition to partially substituting at the octahedral Fe sites, they also occupy the interstitial octahedral sites which are vacant in theα-Fe₂O₃structure. The structural model deduced involves clusters of three substituted cations and is rational in that it represents microstructural regions of the rutile structure within a matrix ofα-Fe₂O₃.     

Optical lattice induced light shifts in an yb atomic clock

We present an experimental study of the lattice-induced light shifts on the (1)S(0) --> (3)P(0) optical clock transition (nu(clock) approximately 518 THz) in neutral ytterbium. The "magic" frequency nu(magic) for the 174Yb isotope was determined to be 394 799 475(35) MHz, which leads to a first order light shift uncertainty of 0.38 Hz. We also investigated the hyperpolarizability shifts due to the nearby 6s6p(3)P(0) --> 6s8p(3)P(0), 6s8p(3)P(2), and 6s5f(3)F(2) two-photon resonances at 759.708, 754.23, and 764.95 nm, respectively. By measuring the corresponding clock transition shifts near these two-photon resonances, the hyperpolarizability shift was estimated to be 170(33) mHz for a linear polarized, 50 microK deep, lattice at the magic wavelength. These results indicate that the differential polarizability and hyperpolarizability frequency shift uncertainties in a Yb lattice clock could be held to well below 10(-17).     

Ca(2.5)Sr(0.5)GaMn2O8: diamagnetic Ga in control of the structural and electronic properties of a bilayered manganate

The temperature dependence of the crystal structure and electronic properties of brownmillerite-like Ca(2.5)Sr(0.5)GaMn(2)O(8) has been studied by neutron powder diffraction and muSR spectroscopy. The results show that short-range 2D magnetic order begins to develop within the perovskite-like bilayers of MnO(6) octahedra approximately 50 K above the 3D Néel temperature of approximately 150 K. The bilayers show a structural response to the onset of magnetism throughout this temperature range whereas the GaO(4) layers that separate the bilayers only respond below the 3D ordering temperature. XANES spectroscopy shows that the sample contains Mn(3+) and Mn(4+) cations in a 1:1 ratio, and the behavior in the region of the Néel transition is interpreted as a local charge ordering. Electron diffraction and high-resolution electron microscopy have been used to show that the local microstructure is more complex than the average structure revealed by neutron diffraction, and that microdomains exist in which the GaO(4) tetrahedra show different orientations. It is argued that the bonding requirements of diamagnetic gallium control the electronic behavior within the perovskite-like bilayers.     

Thermodynamic properties of ternary alloys from Monte Carlo simulations

Methods are presented for obtaining both the integral and partial molar energies, entropies and free energies of the components in rigid ternary substitutional alloy systems from the one Monte Carlo simulation. Tests of the methods for some model systems are presented and discussed.     

Molecular beam maser measurements of relaxation cross sections in NH3

Direct measurements of scattering cross sections for NH₃ in well-defined quantum states are made using a molecular beam maser spectrometer. Cross sections are compared for a pure inversion state with those for a coherent superposition state for scattering gases He, Ar, N₂, N₂O, NH₃, CH₃H and CH₃CN. The cross sections are significantly larger for scattering of the pure inversion state by NH₃, CF₃H and CH₃CN than for scattering of the superposition state. The scattering is the same for both states on non-polar gases. These cross sections are related to relaxation parameters describing transitions between rotation and inversion states.     

Excluded volume effects and fractional viscoelasticity in polymers

Meccanica - The excluded volume effect is added to a fractional viscoelastic model for modeling fractal polymers. This reveals a physical connection between the fractional time derivative, fractal...