Combining high pressure and coherent diffraction: a first feasibility test

We present a first experiment combining high pression and coherent X-ray diffraction. By using a dedicated diamond anvil cell, we show that the degree of coherence of the X-ray beam is preserved when the X-ray beam passes through the diamond cell. This observation opens the possibility of studying the dynamics of slow fluctuations under high pressure.Comment: 3 pages, 2 figures, GHPR 2009 conferenc

A combined XAS and XRD Study of the High-Pressure Behaviour of GaAsO4 Berlinite

Combined X-ray absorption spectroscopy (XAS) and X-ray diffraction (XRD) experiments have been carried out on GaAsO4 (berlinite structure) at high pressure and room temperature. XAS measurements indicate four-fold to six-fold coordination changes for both cations. The two local coordination transformations occur at different rates but appear to be coupled. A reversible transition to a high pressure crystalline form occurs around 8 GPa. At a pressure of about 12 GPa, the system mainly consists of octahedral gallium atoms and a mixture of arsenic in four-fold and six-fold coordinations. A second transition to a highly disordered material with both cations in six-fold coordination occurs at higher pressures and is irreversible.Comment: 8 pages, 5 figures, LaTeX2

High Pressure X-Ray Diffraction Study of UMn2Ge2

Uranium manganese germanide, UMn2Ge2, crystallizes in body-centered tetragonal ThCr2Si2 structure with space group I4/mmm, a = 3.993A and c = 10.809A under ambient conditions. Energy dispersive X-ray diffraction was used to study the compression behaviour of UMn2Ge2 in a diamond anvil cell. The sample was studied up to static pressure of 26 GPa and a reversible structural phase transition was observed at a pressure of ~ 16.1 GPa. Unit cell parameters were determined up to 12.4 GPa and the calculated cell volumes were found to be well reproduced by a Murnaghan equation of state with K0 = 73.5 GPa and K' = 11.4. The structure of the high pressure phase above 16.0 GPa is quite complicated with very broad lines and could not be unambiguously determined with the available instrument resolution

Dynamics of the magnetic and structural a -> e phase transition in Iron

We have studied the high-pressure iron bcc to hcp phase transition by simultaneous X-ray Magnetic Circular Dichroism (XMCD) and X-ray Absorption Spectroscopy (XAS) with an X-ray dispersive spectrometer. The combination of the two techniques allows us to obtain simultaneously information on both the structure and the magnetic state of Iron under pressure. The magnetic and structural transitions simultaneously observed are sharp. Both are of first order in agreement with theoretical prediction. The pressure domain of the transition observed (2.4 $\pm$ 0.2 GPa) is narrower than that usually cited in the literature (8 GPa). Our data indicate that the magnetic transition slightly precedes the structural one, suggesting that the origin of the instability of the bcc phase in iron with increasing pressure is to be attributed to the effect of pressure on magnetism as predicted by spin-polarized full potential total energy calculations

Mesures de spectrométrie et de dosimétrie neutron aux postes de travail pour l'étalonnage de dosimètres individuels PGP-DIN

International audience(ManuAcrit r e p le 3 juillet 2002, accepté le 29 septembre 2002) Dans le cadre de la mise en application des recommandations décrites dans la publication 60 de la CIPR, des mesures de spectrométrie neutron ont été réalisées à plusieurs postes de travail au CEA de Valduc. Le but de ces mesures était la détermination de nouveaux coefficients d'étalonnage h affecter aux dosimètres individuels neutron PGP-DIN afin de restituer correctement les doses reçues par les opérateurs séjournant h ces postes. Ces mesures ont été effectuées au cours de deux campagnes successives. La tluence neutronique et le débit d'équivalent de dose amhiantH*(IO) ont été mesurés en fonction de l'énergie avec le spectromètre ROSPEC et un système de sphères de BONNER. Les champs de radiations étant toutefois mixtes, c'est-à-dire présentant une composante neutronique et photonique, des mesures de débits d'équivalent de dose ambiant photon aux postes de travail considérés ont également été réalisées à l'aide de débitmètres d'ambiance. Les dosimètres individuels PGP-DIN ont été positionnés sur un fantôme (ISO) d'eau. Des calculs effectués h l'aide du code MCNP ont été comparés aux résultats expérimentaux. Neutron spectrometry and dosimetry measurement at workplaces for calibration of individual PGP-DIN dosimeters. Measurements to determine new coefficients for individual neutron dosimeters PGP-DIN complying with the ICRP 60 recommendations were performed at two workplaces at the CEA of Valduc: a storage r w m and a plutonium reprocessing plant. Two spectrometry campaigns were performed allowing a better assessment of doses received by operators worki.ng at these workplaces. Neutron energy fluence and ambient dose equivalent rate H*(10) distributions were measured as function of neutron energy by using the ROSPEC device and BONNER spheres spectrometer. The radiation field being mixed neutron and gamma, the gamma component was also evaluated: neutron and photon dose-rate meters were nsed to evaluate the ambient dose rate equivalent. Individual dosemeters were positioned on an ISO water slab phantom. In addition, calculations were performed using the MCNP simulation code for different configurations. ' Insiitui de radioprotection ct de sûre16 nucléaire, DPHD, B.P. 17. 92262 Fontcnay-aux-Roses Cedcx, France

Inequivalent routes across the Mott transition in V2O3 explored by X-ray absorption

The changes in the electronic structure of V2O3 across the metal-insulator transition induced by temperature, doping and pressure are identified using high resolution x-ray absorption spectroscopy at the V pre K-edge. Contrary to what has been taken for granted so far, the metallic phase reached under pressure is shown to differ from the one obtained by changing doping or temperature. Using a novel computational scheme, we relate this effect to the role and occupancy of the a1g orbitals. This finding unveils the inequivalence of different routes across the Mott transition in V2O

Pressure evolution of electronic and crystal structure of non-centrosymmetric EuCoGe3_3

We report on the pressure evolution of the electronic and crystal structures of the noncentrosymmetric antiferromagnet EuCoGe3. Using a diamond anvil cell, we performed high pressure fluorescence detected near-edge x-ray absorption spectroscopy at the Eu L3, Co K, and Ge K edges and synchrotron powder x-ray diffraction. In the Eu L3 spectrum, both divalent and trivalent Eu peaks are observed from the lowest pressure measurement (~2 GPa). By increasing pressure, the relative intensity of the trivalent Eu peak increases, and an average Eu valence continuously increases from 2.2 at 2 GPa to 2.31 at~50 GPa. On the other hand, no discernible changes are observed in the Co K and Ge K spectra as a function of pressure. With the increase in pressure, lattice parameters continuously decrease without changing I4mm symmetry. Our study revealed a robust divalent Eu state and an unchanged crystal symmetry of EuCoGe3 against pressure.Comment: Accepted in PRB https://journals.aps.org/prb/accepted/b2073O6fL9e1ca40307905b1de5bf05de12d8fc1

K-edge x-ray dichroism investigation of Fe1-xCoxSi : experimental evidence for spin polarization crossover

Both Fe and Co K-edge x-ray magnetic circular dichroism (XMCD) have been employed as element-specific probes of the magnetic moments in the composition series of the disordered ferromagnet Fe1-xCoxSi (for x = 0.2, 0.3, 0.4, 0.5). A definitive single peaked XMCD profile occurs for all compositions at both Fe and Co K-edges. The Fe 4p orbital moment, deduced from the integral of the XMCD signal, has a steep dependence on x at low doping levels and evolves to a different (weaker ) dependence at x ≥ 0.3, similar to the behavior of the magnetization in the Co composition range studied here. It is systematically higher, by at least a factor of two, than the corresponding Co orbital moment for most of the composition series. Fine structure beyond the K-edge absorption (limited range EXAFS) suggests that the local order (atomic environment) is very similar across the series, from the perspective of both the Fe and Co absorbing atom. The variation in the XMCD integral across the Co composition range has two regimes, that which occurs below x=0.3 and then evolves to different behavior at higher doping levels. This is more conspicuously present in the Fe contribution. This is rationalized as the evolution from a half-metallic ferromagnet at low Co doping to that of a strong ferromagnet at x > 0.3 and as such, spin polarization crossover occurs. The Fermi level is tuned from the majority spin band for x < 0.3 where a strongly polarized majority spin electron gas prevails, to a regime where minority spin carriers dominate at higher doping. The evolution of the Fe-derived spin polarized (3d) bands, indirectly probed here via the 4p states, is the primary determinant of the doping dependence of the magnetism in this alloy series.NRF and URC-UJ.http://www.elsevier.com/locate/jmmmhb201