Highlights on the reversible nonpolar-to-polar P3121-P31 phase transition at low temperature in NaLa(SO4)2·H2O: mechanism and piezoelectric properties.

We report the existence in NaLa(SO4)2·H2O of a displacive phase transition under 200 K from the nonpolar P3121 to the polar P31 space group. This phase transition was predicted by density functional theory based calculations and experimentally confirmed from infrared spectroscopy and X-ray diffraction. The A2 polar irreducible representation is the primary order parameter. The structural water and hydrogen bonding are the mechanism driving the phase transition. The piezoelectric properties of this new P31 phase have been investigated by first principles based calculations. The highest piezoelectric-strain constants in the zero Kelvin limit are predicted for the d12 and d41 elements with values about 3.4 pC N-1. This compound could be interesting as piezoelectric actuator for cryogenic applications.

Nonresonant Polarized Raman Spectra Calculations of Nitrogen-Doped Single-Walled Carbon Nanotubes: Diameter, Chirality, and Doping Concentration Effects.

Raman spectra of nitrogen-doped single-walled carbon nanotubes are calculated using the spectral moment's method combined with the bond polarizability model. The influence of the nanotube diameter and chirality is investigated. We also address the important question of the effect of the N-doping concentration, and we propose an equation to estimate the doping concentration from the knowledge of the tube diameter and the frequency of the radial breathing mode.

Thermodynamic properties of the α-quartz-type and rutile-type GeO2 from first-principles calculations.

Phonon density-of-states and related thermodynamic properties of the α-quartz-type and rutile-type germanium dioxide (GeO2) are investigated from density functional perturbation theory. The significant density-of-states at the low frequencies in the α-quartz-type GeO2 are at the origin of (i) its lower internal energy below 250 K, (ii) its smaller free energy, (iii) its higher entropy, (iv) its lower Debye temperature and (v) its larger positive linear thermal expansion, with respect to the rutile-type GeO2.

Direct Aspiration versus Combined Technique for Distal Medium-Vessel Occlusions: Comparison on a Human Placenta Model.

BACKGROUND AND PURPOSE: Mechanical thrombectomy appears to be a promising option for distal medium-vessel occlusions, for which intravenous thrombolysis is effective but may be insufficient when used alone. This study aimed to determine the optimal technique for these distal mechanical thrombectomies using the human placenta model. MATERIALS AND METHODS: Twenty-four procedures were performed, allowing comparison of direct aspiration (n = 12) versus the combined technique (n = 12). Two positions of the aspiration catheter were tested for each of these techniques: in direct contact with the clot and at a distance from it (5-10 mm). Two types of clots were tested: red blood cell-rich clots and fibrin-rich clots. First-pass recanalization and induced arterial collapse and traction were assessed. RESULTS: The first-pass recanalization was less frequent for direct aspiration than for the combined technique, without reaching statistical significance (41.7% versus 75.0%, P = .098). Full collapse (P < .001) and extended arterial traction (P = .001) were significantly less frequent for direct aspiration. For direct aspiration with the aspiration catheter not in direct contact with the clot, there was not a single first-pass recanalization and there was systematic arterial collapse, resulting in a no-flow in the aspiration syringe. CONCLUSIONS: The combined technique appears to be more harmful, and although direct aspiration has a lower rate of first-pass recanalization, it seems appropriate to try direct aspiration as a first-line procedure. However, if the aspiration catheter cannot reach the clot, it is not useful or even risky to try aspiration alone. These results need to be confirmed by clinical studies.

Vibrational origin of the thermal stability in the high-performance piezoelectric material GaAsO4.

Theoretical calculations and experiments show the absence of libration modes of the tetrahedra in GaAsO(4), the most α-quartz-type distorted material. In consequence, the degree of dynamic disorder at high temperature is very low, making GaAsO(4) of high interest for high-temperature applications. This paper shows the importance of the theoretical calculations of vibration in oxide materials. In this way, it could be possible to extend this result to other materials and predict the thermal stability of the materials and their potential applications at high temperature.

First-principles study of the dynamical and nonlinear optical properties of urea single crystals.

Raman and infrared spectra of urea single crystals have been calculated using the density functional theory. This allowed us to assign the remaining experimental low-frequency phonon modes. Then, we have determined the sign of the second-harmonic nonlinear optical susceptibility coefficient in urea to be negative, clarifying a long debate in the literature. Finally, we computed for the first time the electro-optic coefficients of urea. We found that the electronic and ionic contributions have a similar order of magnitude and an opposite sign, yielding a smaller value than that expected, and necessitating further experimental clarifications.

Lattice dynamics of oligo(phenylenethienylene)s: a far-infrared and inelastic neutron scattering study.

New promising oligo(phenylenethienylene)s have been synthesized to realize suitable materials for improving electronic transport properties, particularly in organic field effect transistors (OFETs). Far-infrared and incoherent neutron scattering measurements have been performed to assign their phonon modes. The assignment of the main low-frequency phonon modes of these materials has been performed experimentally by using a filiation procedure. Assuming a small frequency dispersion of the high-frequency modes, the main intramolecular phonon modes of a model oligomer have been assigned by using first-principles calculations on its isolated molecule. These assignments constitute the preliminary work for a better understanding of these new promising materials in electronic and opto-electronics applications.

Raman scattering intensities in BaTiO(3) and PbTiO(3) prototypical ferroelectrics from density functional theory.

Nonlinear optical susceptibilities and Raman scattering spectra of the ferroelectric phases of BaTiO(3) and PbTiO(3) are computed using a first-principles approach based on density functional theory and taking advantage of a recent implementation based on the nonlinear response formalism and the 2n+1 theorem. These two prototypical ferroelectric compounds were chosen to demonstrate the accuracy of the Raman calculation based both on their complexity and their technological importance. The computation of the Raman scattering intensities has been performed not only for the transverse optical modes, but also for the longitudinal optical ones. The agreement between the measured and computed Raman spectra of these prototypical ferroelectrics is remarkable for both the frequency position and the intensity of Raman lines. This agreement presently demonstrates the state-of-the-art in the computation of Raman responses on one of the most complex systems, ferroelectrics, and constitutes a step forward in the reliable prediction of their electro-optical responses.

Correlations between structure and far-infrared active modes in polythiophenes.

We have investigated the experimental X-ray and far-infrared responses of three polythiophenes synthesized from a thiophene, alpha-bithiophene, and alpha-quaterthiophene monomer. The X-ray data show that the crystallinity of the different polythiophene samples depends on the synthesis conditions. An excellent correlation between the crystallinity of polythiophenes and their far-infrared signatures is demonstrated. In addition, the assignment of the far-infrared phonon modes in polythiophenes is given by using both an experimental filiation procedure and first-principles calculations. In particular, the ring libration inside the polymeric chain, directly involved in the electron-phonon coupling, is assigned.

Raman scattering in crystalline oligothiophenes: a comparison between density functional theory and bond polarizability model.

Raman intensity of intramolecular and lattice modes of crystalline alpha-bithiophene (alpha-2T) are investigated within density functional theory using a nonlinear response formalism. First, comparison between the calculated Raman spectrum and the experimental data allows the assignment of the main Raman lines over the whole frequency range. Then, a bond polarizability (BP) model, limited to first neighbors, is built. We show that, although the BP model cannot reproduce the changes of dielectric susceptibility under individual atomic displacements, it is accurate enough to reproduce the profile of the unpolarized nonresonant Raman spectrum of alpha-2T powder. Finally, the BP model, fitted on our first-principles results on alpha-2T, is applied with success to the alpha-quaterthiophene polymorph phases and alpha-sexithiophene, demonstrating on practical examples that first-principles and BP approaches are powerful complementary tools to calculate the nonresonant Raman spectrum of alpha-2T and make reasonable predictions on larger oligothiophenes.

Infrared spectroscopy of single-walled carbon nanotubes.

By using the spectral moments method, we calculate the infrared spectra of chiral and achiral single-walled carbon nanotubes (SWCNTs) of different diameters and lengths. We show that the number of the infrared modes, their frequencies, and intensities depend on the length and chirality of the nanotubes. Furthermore, the dependence of the infrared spectrum as a function of the size of the SWCNT bundle is analyzed. These predictions are useful to interpret the experimental infrared spectra of SWCNTs.

Far- and mid-infrared of crystalline 2,2'-bithiophene: ab initio analysis and comparison with infrared response.

Infrared intramolecular vibrations and lattice modes in the crystalline phase of 2,2'-bithiophene (2T) are investigated using the direct method combined with density functional theory (DFT)-based total energy calculations. For the first time, the far- and mid-infrared responses have been calculated from the Gamma-point modes and the Born effective charge tensors of the 2T crystalline phase. The relative good agreement between the calculated and experimental infrared spectra allows us to assign the origin of the main features of the experimental spectra, which is of particular interest in the far-infrared domain. These assignments are useful for understanding all the properties of the 2T crystalline phase in which phonon-phonon and electron-phonon interactions play an important role.

Polymorphism of crystalline alpha-quaterthiophene and alpha-sexithiophene: ab initio analysis and comparison with inelastic neutron scattering response.

Phonons in the alpha-quaterthiophene (4T) and alpha-sexithiophene (6T) polymorph phases are investigated using the direct method combined with density functional theory (DFT)-based total energy calculations. The simulation of inelastic neutron scattering spectra (INS) on the LT and HT polymorph phases of 4T and 6T enable the corresponding spectral signatures of these materials to be identified. In particular, there are two fingerprints: (i) the low-frequency vibrational modes (frequencies lower than 200 cm(-1)) and (ii) the vibrational modes in the 600-900 cm(-1) frequency range. The good agreement with the INS experimental data allows us to assign unambiguously the origin of all features (first-order and high-order processes) of these spectra and to predict that the LT phase is the phase measured experimentally both on the 4T and 6T materials. Moreover, the broad background in the 600-1400 cm(-1) frequency range and the well-defined features which appear around 940 cm(-1) in the calculated INS spectra of 4T/HT and 6T/HT are assigned to multiphonon contributions. This multiphonon contribution at 940 cm(-1), which is absent in the 4T/LT and 6T/LT INS spectra, also constitutes a fingerprint of the HT phases. Finally, the calculated dispersion curves of the two polymorph phases of 4T and 6T are given.

Design of a rangefinder for military purposes.

Design considerations for military pulse rangefinders are discussed. The practical aspects of modularity, cooling, optical design, and solid state receiver performance are reviewed. A measure of overal system performance is developed and compared for several military rangefinders.