Effects of Shock Pressure on Transition Pressure in Zr

Measurements of free surface velocity profiles of high-purity Zr samples under shock-wave loading are performed to study the dynamic strength and phase transition parameters. The peak pressure of the compression waves is within the range from 9 to 14 GPa, and the Hugoniot elastic limit is 0.5 GPa. An anomalous structure of shock waves is observed due to the α - ω phase transition in Zr. Shock pressure has effects on transition pressure which increases with increasing compression strength, and the stronger shocks have a lower transit time.     

Structural phase transformation of GaN under high-pressure: an exact exchange study

The phase transformation of GaN under high pressure is theoretically studied in the KS-DFT framework using the EXX method. Both KLI and LDA pseudopotentials were tried. The LDA-PP result for the transition pressure is 41.7 GPa while that of the KLI-PP is 41.5 GPa. Both results are in a very good agreement with the latest experimental value of 42 GPa. The effect of the nonlinear core correction is found to be small but not negligible.     

Pressure-induced phase transition in tysonite LaF3

We have studied the high-pressure phase stability of LaF₃ using full-potential linear augmented plane wave method. We have shown that experimentally observed orthorhombic phase is less stable compared to the theoretically predicted tetragonal structure above 25 GPa pressure. The structural transition is mainly due to the steric repulsion of ions and electrons to higher pressures.     

Laser ablation of gadolinium targets in liquids for nanoparticle preparation

Tight focusing of a sub-picosecond laser pulse in a transparent dielectric provides a mean for localized deposition and plasma formation. A micro-explosion in a confined geometry results in a sub-micron cavity formation. Our numerical simulations show the cavity size is strongly dependent on the parameters of the equation of state such as the Grüneisen coefficient or the latent heat of sublimation. A comparison of numerical simulations with experimental data should allow a tuning of equations of state in the domain of extreme parameters     

Energy balance of optical breakdown in water at nanosecond to femtosecond time scales

Received: 3 August 1998/Revised version: 20 October 1998     

A high pressure distorted α-uranium (Pnma) structure in plutonium

Under pressure many rare earths and actinide metals transform to α-U type structure or its lower symmetry distorted forms. We have reinterpreted the diffraction data of Dabos et al. for Pu [S. Dabos et al. J. Alloys Compd. 190 (1993) 237] and find that an Am IV type distorted α-U structure in Pnma space group can explain its high pressure phase. The structures of both the high pressure Am IV type phase and α-Pu, the 0.1 MPa phase, are shown to have a distorted hcp topology. The upturn in the atomic volume of Pu at 0.1 MPa can also be rationalized on the basis of this proposal.     

Pressure Effects on Solid State Phase Transformation of Aluminium Bronze in Cooling Process

Effects of high pressure （6 CPa） on the solid state phase transformation kinetic parameters of aluminum bronze during the cooling process axe investigated, based on the measurement and calculation of its solid state phase transformation temperature, duration and activation energy and the observation of its microstructures. The results show that high pressure treatment can reduce the solid phase transformation temperature and activation energy in the cooling process and can shorten the phase transformation duration, which is favorable when forming fine-grained aluminum bronze.     

Properties of C60 polymerized under high pressure and temperature

60 polymers. Pure and mixed phase polymeric samples were synthesized by simultaneously subjecting microcrystalline C₆₀ powder or pellets to various pressures () and temperatures (). The optical spectra of the orthorhombic, tetragonal, and rhombohedral C₆₀ polymer phases are observed to be quite distinct and rich. These spectra exhibit numerous lines and an overall downshift in frequency relative to C₆₀ is observed, consistent with a loss of double bonds from the fullerene cage. The LDMS spectra of a sample synthesized at under hydrostatic conditions and , exhibited a succession of clear peaks at mass numbers corresponding to , similar to the LDMS data on the C₆₀ photopolymer. This is taken as further evidence for interfullerene bonds in these high-pressure polymers. The XRD pattern of this sample indicates the presence of a strong texture in the sample. Received: 14 November 1996/Accepted: 8 January 1997     

Temperature dependence of terahertz radiation from n-type InSb and n-type InAs surfaces

The azimuthal angle dependence and the temperature dependence of terahertz (THz) radiation generated from n-type (111) InSb and n-type (111) InAs surfaces irradiated with ∼80 fs near-infrared laser pulses are investigated. The azimuthal angle dependence shows that the contribution of the difference-frequency mixing (DFM) is not dominant for both materials at the excitation density of ∼1 GW/cm². At an appropriate azimuthal angle, the radiation due to DFM is excluded from the total THz radiation and the temperature dependence of THz radiation due to the surge current is observed. The increase of THz radiation with decrease of the temperature is found to be much more pronounced for InSb than for InAs. The different temperature dependence can be attributed to the different radiation mechanisms dominant for both materials. Especially, the temperature dependence of the THz radiation from InSb is well explained by the photo-Dember effect. Received: 9 May 2000 / Revised version: 17 August 2000 / Published online: 5 October 2000     

More on shear modulus collapse of lattices at high pressure

In his recent paper, Shear modulus collapse of lattices at high pressure, J. Phys. Cond. Matt. 16 (2004) L125, V.V. Kechin claims that the zero temperature shear modulus of a metallic solid vanishes at a high critical pressure, and the critical pressures for this shear modulus collapse lie in the range 0-250 Mbar for elemental metals. Here we demonstrate that Kechin's arguments contain an erroneous assumption, and therefore, do not prove that all metals become mechanically unstable at high pressures. Ab initio calculations and experimental results on a number of solids are analyzed to confirm our conclusion.     

Structural Transition of Gd2O3：Eu Induced by High Pressure

The structural transition of bulk and uano-size Gd2O3：Eu are studied by high pressure energy disperse x-ray diffraction （XRD） and high pressure photoluminescence. Our results show that in spite of different size of Gd2O3 particles, the cubic structure turns into a possible hexagonal one above 13.4 GPa. When the pressure is released, the sample reverses to the monoclinic structure. No cubic structure presents in the released samples. That is to say, the compression and relaxation of the sample leads to the cubic Gd2O3：Eu then turns into the monoclinic one.     

Thermal conductivity of pressure polymerized C60

60 polymerization in the temperature interval at pressures below by measurements of the time dependence of the thermal conductivity. It has been found at that the polymerization process at is slower than the reverse transformation from “polymeric” to “monomeric” phase at . The thermal conductivity of polymerized C₆₀ was measured in the temperature range and found to increase with increasing temperature, which reflects strong phonon scattering. Both the presence of non-bonded C₆₀ molecules and a high degree of structural disorder in the crystalline lattice of the polymeric phase might be responsible for the behaviour of . The results for are qualitatively similar to those reported previously for C₆₀ polymerized at higher , but an order of magnitude smaller. Received: 20 September 1996/Accepted: 11 November 1996     

Pulsed holmium laser ablation of tissue phantoms: correlation between bubble formation and acoustic transients

5 Pa served as tissue phantoms to evaluate such effects. Holmium laser pulses (wavelength: 2.12 μm, duration: 180 μs FWHM), were delivered through 400 and 600 μm diameter optical fibers inserted into cubes of clear gel. Bubble effects were investigated using simultaneous flash micro-videography and pressure recording for radiant exposures of 20–382 J/cm². Bubble formation and bubble collapse induced pressure transients were observed regardless of phantom stiffness. Bubbles of up to 4.2 mm in length were observed in gels with a Young’s modulus of 2.9×10⁵ Pa at a pulse energy of 650 mJ. An increase of Young’s modulus (reduction in water content) led to a monotonic reduction of bubble size. In the softest gels, bubble dimensions exceeded those observed in water. Pressure amplitudes at 3 mm decreased from 100±14 bars to 17±6 bars with increasing Young’s modulus over the studied range. Theoretical analysis suggested a major influence on bubble dynamics of the mass and energy transfer through the bubble boundary. Received: 26 August 1996/Revised version: 10 February 1997     

Picosecond X-ray diffraction studies of laser-excited acoustic phonons in InSb

We have employed time-resolved X-ray diffraction with picosecond temporal resolution to measure the time-dependent rocking curves of laser-irradiated asymmetrically cut single InSb crystals. Coherent acoustic phonons were excited in the crystals by irradiation with 800-nm, 100-fs laser pulses at irradiances between 0.25 and 12 mJ/cm². The induced time-dependent strain profiles (corresponding to the coherent phonons) were monitored by diffracting collimated, monochromatic pulses of X-rays from the irradiated crystals. Recording of the diffracted radiation with a fast low-jitter X-ray streak camera resulted in an overall temporal resolution of better than 2 ps. The strain associated with the coherent phonons modifies the rocking curve of the crystal in a time-dependent manner, and the rocking curve is recorded by keeping the angle of incidence of the X-rays upon the crystal fixed, but varying the energy of the incident X-rays around a central energy of 8.453 keV (corresponding to the peak of the rocking curve of the unperturbed crystal). The observed time-dependent diffraction from the irradiated crystals is in reasonable agreement with simulations over a wide range of energies from the unperturbed rocking-curve peak. Received: 22 March 2002 / Revised version: 25 March 2002 / Published online: 6 June 2002     

Electronic structure of the Co4Sn6Te6 ternary skutterudite phase

The electronic structure of Co₄Sn_6–x Te_6+x (x = 0, 1) ternary skutterudite systems has been investigated using ab ‐initio band structure computation. The x = 0 system is a semiconductor like the binary Co₄Sb₁₂, but with a lower band gap. The best dopant concentration for Co₄Sn₆Te₆ is estimated to be lower than that of Co₄Sb₁₂, with the highest electronic fig‐ ure‐of‐merit Z_eT for the n‐doped system. Finally, the increased charge transfer between the 8c Co and 24g Sn and Te atoms in Co₄Sn₆Te₆ compared to that of Co₄Sb₁₂ could be one reason for the observed decrease of thermal conductivity in ternary skutterudite systems. (© 2007 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim)     

Numerical Simulation of Wave Propagation and Phase Transition of Tin under Shock-Wave Loading

We undertake a nmnerical simulation of shock experiments on tin reported in the literature, by using a multiphase equation of state （MEOS） and a multiphase Steinberg Guinan （MSG） constitutive model for tin in theβ, γ and liquid phases. In the MSG model, the Bauschinger effect is considered to better describe the unloading behavior. The phase diagram and Hugoniot of tin are calculated by MEOS, and they agree well with the experimental data. Combined with the M130S and MSG models, hydrodynamic computer simulations are successful in reproducing the measured velocity profile of the shock wave experiment. Moreover, by analyzing the mass fraction contour as well as stress and temperature profiles of each phase for tin, we further discuss the complex behavior of tin under shock-wave loading.     

Raman spectroscopy study of REH3 under pressure

The Raman spectroscopic studies of two rare earth trihydrides: Y H₃, HoH₃, have been performed in the pressure range from ambient up to 16 GPa and 25 GPa respectively. For the first time samples of REH₃ in the form of powder have been studied by Raman spectroscopy using the Diamond Anvil Cell (DAC) technique. A rapid decrease of Raman activity has been observed for the hydrides under pressure values in the vicinity of structural phase transition. Metallization as a possible reason for the observed dramatic change of the REH₃ Raman activity has been discussed.     

Investigations of pressure induced structural phase transformations in pentaerythritol

We have investigated the pressure induced structural changes in pentaerythritol {2,2-bis-(hydroxymethyl)-1,3-propanediol} with the help of X-ray diffraction studies. Our results show that this compound undergoes transformations to a lower symmetry phase between 5.2-5.9 GPa. It further undergoes phase transformations at ∼8.5 and ∼11 GPa; eventually evolving to a disordered phase beyond 14-15 GPa in agreement with our earlier Raman studies. On release of pressure from 18.5 GPa, the compound transforms back to the initial tetragonal phase.     

Microscopic growth mechanisms for carbon and boron-nitride nanotubes

Received: 27 November 1998 / Accepted: 18 December 1998     

The optical properties of HgS under high pressures

The DOS (density of states) and the optical properties of HgS under high pressure are studied with the first-principle computations. The change of the imaginary part, ε₂(ω), of the dielectric function shows that HgS tends to metallization with increasing pressure, and this well agrees with the band gap calculations and the conductivities measurement results in the previous work. Under the pressures below 15 GPa, ε₂(ω) is relatively anisotropic and tends to be more anisotropic with increasing pressure; while under the pressures above 15 GPa, the anisotropy decreases and finally becomes almost absolutely isotropic after the phase transition. The behavior of ε₂(ω) is strongly related to the structure change in the cinnabar to rocksalt phase transition process under high pressure.