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Synchrotron high-pressure high/low temperature techniques ID27 team: J.P. Perrillat, G. Garbarino, W. Crichton, P. Bouvier, S. Bauchau
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Outline Introduction – XRD Beamlines - Research examples AND Limitations Conclusion
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Near RP,RT3.5 Mbar T<6000 K Biology Geophysics HP synchrotron beamlines are multidisciplinary instruments ID27: Fully dedicated to HP XRD experiments In operation since 2006 in replacement of ID30
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Detectors Sample environment MirrorsMonochromator X-ray Source ESRF 6 GeV Beamline ID27-ESRF
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Diamond anvil cell Pressures up to 3 Mbar High temperatures Resistive heating up to 1000 K Laser heating T>4000 K Low temperature down to 5 K (Helium cryostat) Main X-ray techniques X-Ray single X-tal and powder diffraction in monochromatic mode
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The Paris-Edinburgh large volume cell: The only monochromatic LVC Pressure up to 17 GPa on 5 mm 3 sample volume Resistive heating up to 2300 K Main X-ray technique: X-ray diffraction on powders/liquids/amorphous materials
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Structure determination at very HP (P>1.2 Mbar) requires a very intense and very small X-ray beam. ID30 One remark:
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2 m -- 12 m -- ID30 ID27 Very intense micro-focused beam (2 microns) using two KB multi-layer mirrors at short wavelengths: 0.15< <0.4 Å
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Kirkpatrick-Baez focusing mirrors
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35 µ m P gauge (ruby ball) Micro-grains of iron and tungsten in helium pressure Medium High precision at ultra-high pressures: case of iron Interest: Geophysics: Main constituent of Earth’s core Physics: Magnetism
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High precision at ultra-high pressures: case of iron Fe W W 22 Ref: A. Dewaele, P. Loubeyre, F. Occelli, M. Mezouar, Phys. Rev. Lett. 97, 215504 (2006) Fe + W in He at 199 GPa
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Diamond breakage Max. P at ID30 Limitation: The diamond anvil cell not the X-ray beam!
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5 micron single crystal of oxygen in a 20 micron gasket hole (helium pressure medium) Structure of metallic oxygen? (insulator) (metal) transition at P~100 GPa
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ID30 O2O2 G. Weck,S. Desgreniers,P. Loubeyre, M. Mezouar ID30, 139 GPa Poor data quality, high background from the DAC
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G. Weck,S. Desgreniers,P. Loubeyre, M. Mezouar ID27, 139 GPa ID27 Data of much higher quality/ID30 BUT not enough to solve the structure… transition degrades the single X-tal quality (large rocking curves >1 ) Structure of metallic oxygen?
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+ Raman C2/c allows only 6 active Raman modes phase has the C2/m symmetry More single X-tal data of the phase (different orientations) Two possible monoclinic space groups: C2/c and C2/m G. Weck,S. Desgreniers,P. Loubeyre, M. Mezouar, PRL, in press
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Limitation: Single crystal quality! (not the X-ray beam) Solution: (In situ) HP/HT single X-tal growth
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P-T Phase diagram of sodium It is possible to grow a single x-tal of Na at ~120 GPa near RT and perform a full structural determination. Ref: Gregoryanz E, Degtyareva O, Somayazulu M, Hemley RJ, Mao HK, PRL, 94,185502 (2005)
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Ref: E. Gregoryanz, L. Lundegaard, M.I. McMahon,C. Guillaume, R.J. Nelmes, M.Mezouar, Science, 320,1054 (2008) Examples of high quality single x-tal diffraction patterns of Na collected at ID27 Beamsize~ 3 m; =0.3738 Å Sample volume~ 10x10x5 m 3 Phase diagram around the melting curve minimum at P=117 GPa Many new and unpredicted structures of very high complexity
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At atmospheric conditions Hydrogen is a fundamental element for biology, chemistry and physics At high pressure Hydrogen is of high interest for physics and geophysics -Principal constituent of giant planets such as Jupiter (90%) -Prediction of the existence of a metallic form of hydrogen by Eugene Wigner in 1935 Hydrogen at high very high pressure
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Ref. : R. Hemley, M. Hanfland, et al. (Geophysical Lab., Washington) Phase diagrams of H 2 and D 2 from spectroscopic measurements up to 200 GPa (1994) 3 phases identified but no structural determination of phase II and III. Phase I hcp lattice of freely-rotating molecules Phase II and III ??
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Equation of state of hydrogen I up to 120 GPa at ESRF ID09 (1996) BUT using the EDX technique no structural determination Single crystal of H 2 in helium pressure medium Ref.: P. Loubeyre et al., Nature, 383, 702 (1996)
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For almost 10 years, all attempts to solve the structure of phase II failed Too many experimental difficulties High pressure - Low Z material - Extremely reactive – Hydrogen is certainly the most difficult sample to study with X-rays at very HP.
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Structure solved in 2005 by a combination of mononochromatic XRD from ID30/ID09 and neutron data from LLB (Igor Goncharenko) Phase II has an hcp incommensurate structure with a local orientational order (Pa3 local symmetry). More details in:
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ID30 Phase III of hydrogen not reachable at ID30 because of the too large beam size ID27
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10 µm single crystal of H 2 in helium pressure medium P>150 GPa Very weak diffraction peak of H 2 at P=150 GPa 100 Limitations: Control of crystal orientations Compton scattering from diamonds
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Only result so far: Evolution of the 100 d-spacing of hydrogen up to phase III Structure of phase III is still an open question…
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Experimental method - Double-sided laser heating system at ID27 Dedicated experimental hutch – The system is mounted on a high stability 5 tons marble
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Double-sided laser heating system at ID27 Accessible PT domain for in situ powder XRD: P>2 Mbar; T>4000 K
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Laser beam X-ray beam Sample Imaging and T measurement
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The accurate determination of melting curves is of fundamental interest in different research areas such as physics and geophysics. 2 classical experimental methods -Optical measurements in the laser heated diamond anvil cell -Melting induced by shock compression Ab-initio calculations Large temperature discrepancies between these 3 methods T>1500 K at 2 megabar for iron. Melting at HP
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Lead is a good candidate for melting studies using XRD : good YAG laser absorber high Z material melting curve determined by optical DAC technique, shock compression and calculated using ab-initio methods in a wide pressure domain Theory (Cricchio et al. MD) ---- Large discrepancy in melting temperatures T>1000 K at P=80 GPa Melting curve of lead
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New approach developed at beamline ID27 : Fast in situ X-ray diffraction in the double-sided laser heated diamond anvil cell. Advantages: It is sensitive to the bulk of the sample (#surface) The XRD measurements are performed at thermodynamic equilibrium (#shock) It uses well established pyrometric methods Also important: X-ray diffraction in the laser heated DAC provides an unambiguous signature of the melt at thermodynamic equilibrium and identifies chemical reactions if any.
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Laser beam X-ray beam Double sided laser heating of iron in argon at 1.2 Mbar in a 60 m gasket hole Collaboration: R. Boehler, MPI Mainz D. Errandonea, Univ. of Valencia The sample is heated on both sides by 2 focused YAG laser providing a maximum power of 80 Watts. The 2 lasers are slightly defocused in order to create a large and homogenous heated area of about 30 microns. The temperature is measured at the center of the hot spot by analyzing the pyrometric signal emitted by a 2x2 µm 2 area The X-ray beam is highly focused on a 3x3 µm 2 area which is 10 times smaller than the heated area The X-ray beam is perfectly aligned at the center of the laser hot spot (within 1 µm precision) by a direct visualization of the fluorescence signal created by the X-ray beam on a CCD camera Experimental method
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The temperature is gradually increased by tuning the laser power For each increment of the laser power, the temperature is measured by pyrometry and a diffraction pattern is automatically collected -The temperature increment is ~30 K -The typical cycle time is ~2 seconds The pressure is measured in situ using NaCl as pressure marker More than 5000 XRD patterns have been collected! Experimental method
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P=61 GPa Experimental method
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Melting at P=61 GPa NaCl pressure medium E=33 keV Focused X-ray beam of 3x3 m2 Mar CCD detector 1 frame/2 sec.
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Melting curve in good agreement with theory but in contradiction with previous experimental data (Shock, or optically in DAC) Ref: A. Dewaele, M. Mezouar, N. Guignot, P. Loubeyre, Phys. Rev. B 76, 144106 (2007)
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Limitations: Detector: commercial CCD detectors are too slow for sub-second time resolved experiments. the photon flux is not the problem Sample containers: major problems in laser heated DACs liquid confinement and chemical reactions Possible solution: optimized containers: Ref.: R. Benedetti et al., Appl. Phys. Lett., 92, 141903 (2008) Al2O3 O2 Au
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Conclusion: HP Beamlines with outstanding performance in terms of photon flux and focusing capabilities are in operation Limitations are mostly coming from “external” factors: Max. P: Limited by the DAC Background from the DAC for light elements studies Sample preparation: single X-tal growth at megabar pressures, Solutions: Use of complementary techniques: Neutrons (for low P), Raman, Brillouin, IXS,… micro-assemblies for laser heated DAC Improved sample environment laboratories on site: HPSynch at APS, PECS (partnership for science at extreme conditions) at the ESRF
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