RESUMO
We have studied the Ce valence as a function of pressure in CeRhIn5 at 300 K and at 22 K using x-ray absorption spectroscopy in partial fluorescent yield mode. At room temperature, we found no detectable change in Ce valence greater than 0.01 up to a pressure of 5.5 GPa. At 22 K, the valence remains robust against pressure below 6 GPa, in contrast to the predicted valence crossover at P = 2.35 GPa. This work yields an upper limit for the change in Ce-valence and suggests that the critical valence fluctuation scenario, in its current form, is unlikely.
RESUMO
The behavior of the f-electrons in the lanthanides and actinides governs important macroscopic properties but their pressure and temperature dependence is not fully explored. Cerium with nominally just one 4f electron offers a case study with its iso-structural volume collapse from the γ-phase to the α-phase ending in a critical point (p C, V C, T C), unique among the elements, whose mechanism remains controversial. Here, we present longitudinal (c L) and transverse sound speeds (c T) versus pressure from higher than room temperature to T C for the first time. While c L experiences a non-linear dip at the volume collapse, c T shows a step-like change. This produces very peculiar macroscopic properties: the minimum in the bulk modulus becomes more pronounced, the step-like increase of the shear modulus diminishes and the Poisson's ratio becomes negative-meaning that cerium becomes auxetic. At the critical point itself cerium lacks any compressive strength but offers resistance to shear.
RESUMO
An approach using polychromatic x-ray Laue diffraction is described for studying pressure induced microstructural changes of materials under pressure. The advantages of this approach with respect to application of monochromatic x-ray diffraction and other techniques are discussed. Experiments to demonstrate the applications of the method have been performed on the α â ß phase transition in Si at high pressures using a diamond anvil cell. We present the characterization of microstructures across the α-ß phase transition, such as morphology of both the parent and product phases, relative orientation of single-crystals, and deviatoric strains. Subtle inhomogeneous strain of the single-crystal sample caused by lattice rotations becomes detectable with the approach.
RESUMO
The 16 ID-D (Insertion Device - D station) beamline of the High Pressure Collaborative Access Team at the Advanced Photon Source is dedicated to high pressure research using X-ray spectroscopy techniques typically integrated with diamond anvil cells. The beamline provides X-rays of 4.5-37 keV, and current available techniques include X-ray emission spectroscopy, inelastic X-ray scattering, and nuclear resonant scattering. The recent developments include a canted undulator upgrade, 17-element analyzer array for inelastic X-ray scattering, and an emission spectrometer using a polycapillary half-lens. Recent development projects and future prospects are also discussed.
RESUMO
The longitudinal and transverse sound speeds, cL and cT, of polycrystalline cerium were measured under pressure across the iso-structural γ-α phase transition at 0.75 GPa to beyond 3 GPa. In contrast to previous methods all quantities were directly obtained and no assumptions were made about the size of the volume collapse. Up to the transition our values for cL are in excellent agreement with previous ones, while our values for cT are significantly lower. We deduce values for the adiabatic bulk modulus BS, the shear modulus [Formula: see text], and the pressure dependent Debye temperature, ΘD(p). ΘD(p) is in good agreement with recent results derived from phonon dispersion measurements on single crystals. The ratio of the Debye temperature values bracketing the transition indicates a lattice contribution to the entropy change across the volume collapse, ΔSvib(γ â α) ≈ (0.68 ± 0.06)kB, consistent with previous results obtained by neutron scattering, but significantly larger than other previously determined values.