Helium- and argon-broadening coefficients of phosphine lines in the ν2 and ν4 bands

Pressure broadening of phosphine lines by helium and argon at room temperature has been experimentally investigated by high-resolution diode-laser spectroscopy. The broadening coefficients are measured for 38 transitions of PH₃ in the ^QR branch of the ν₂ band and in the ^PP and ^RP branches of the ν₄ band. The recorded lines with J values ranging from 3 to 14 and K from 0 to 10 are located between 1062 and 1094 cm⁻¹. The retrieval of the collisional widths is carried out by fitting each spectral line with a Voigt profile, a Rautian profile and a speed-dependent Rautian profile. The latter model provides larger broadening coefficients than the Voigt model. They are also calculated on the basis of a semiclassical model involving the atom-atom Lennard-Jones potential. The theoretical results are in reasonable agreement with the experimental data and reproduce the J and K dependencies of the broadenings.     

Delocalized fermions in underdoped cuprate superconductors

Low-temperature heat transport was used to investigate the ground state of high-purity single crystals of the lightly doped cuprate YBa2Cu3O6.33. Samples were measured with doping concentrations on either side of the superconducting phase boundary. We report the observation of delocalized fermionic excitations at zero energy in the nonsuperconducting state, which shows that the ground state of underdoped cuprates is a thermal metal. Its low-energy spectrum appears to be similar to that of the d-wave superconductor, i.e., nodal. The insulating ground state observed in underdoped La2-xSrxCuO4 is attributed to the competing spin-density-wave order.     

The evolution of catalytic function

It is very likely that the main driving force of enzyme evolution is the requirement to improve catalytic and regulatory efficiency which results from the intrinsic performance as well as from the spatial and functional organization of enzymes in living cells.Kinetic co-operativity may occur in simple monomeric proteins if they display “slow” conformational transitions, at the cost of catalytic efficiency. Oligomeric enzymes on the other hand can be both efficient and co-operative. We speculate that the main reason for the emergence of co-operative oligomeric enzymes is the need for catalysts that are both cooperative and efficient. As it is not useful for an enzyme to respond to a change of substrate concentration in a complex kinetic way, the emergence of symmetry has its probable origin in a requirement for “functional simplicity”.In a living cell, enzyme are associated with other macromolecules and membranes. The fine tuning of their activity may also be reached through mutations of the microenvironment. Our hypothesis is that these mutations are related to the vectorial transport of molecules, to achieve the hysteresis loops of enzyme reactions generated by the coupling of reaction and diffusion, through the co-operativity brought about by electric interactions between a charged substrate and a membrane, and last but not least, through oscillations. As the physical origins of these effects are very simple and do not require complex molecular devices, it is very likely that the functional advantage generated by the spatial and functional organization of enzyme molecules within the cell have appeared in prebiotic catalysis or very early during the primeval stages of biological evolution.We shall began this paper by presenting the nature of the probable earliest catalysts in the RNA world.     

Variable electron-phonon coupling in isolated metallic carbon nanotubes observed by Raman scattering

We report the existence of broad and weakly asymmetric features in the high-energy (G) Raman modes of freely suspended metallic carbon nanotubes of defined chiral index. A significant variation in peak width (from 12 cm(-1) to 110 cm(-1)) is observed as a function of the nanotube's chiral structure. When the nanotubes are electrostatically gated, the peak widths decrease. The broadness of the Raman features is understood as the consequence of coupling of the phonon to electron-hole pairs, the strength of which varies with the nanotube chiral index and the position of the Fermi energy.     

Probing Proteins in Solution by Xe NMR Spectroscopy

The interaction of xenon with different proteins in aqueous solution is investigated by ¹²⁹Xe NMR spectroscopy. Chemical shifts are measured in horse metmyoglobin, hen egg white lysozyme, and horse cytochrome c solutions as a function of xenon concentration. In these systems, xenon is in fast exchange between all possible environments. The results suggest that nonspecific interactions exist between xenon and the protein exteriors and the data are analyzed in term of parameters which characterize the protein surfaces. The experimental data for horse metmyoglobin are interpreted using a model in which xenon forms a 1:1 complex with the protein and the chemical shift of the complexed xenon is reported (Locci et al., Keystone Symposia “Frontiers of NMR in Molecular Biology VI”, Jan. 9–15, 1999, Breckenridge, CO, Abstract E216, p. 53; Locci et al., XeMAT 2000 “Optical Polarization and Xenon NMR of Materials”, June 28–30, 2000, Sestri Levante, Italy, p. 46).     

Ultrabroadband conical emission generated from the ultraviolet up to the far-infrared during the optical filamentation in air

Ultraviolet and infrared conical emissions were observed during the filamentation in air of powerful femtosecond laser pulses produced by a portable terawatt laser system. The broadband spectrum was measured from 200 nm up to 14 microm and covered the complete optical transmission window of the atmosphere. The angularly resolved spectrum showed some X-wave structure across the frequency range analyzed. However, we demonstrated that the strong conical emission observed in the mid- and far-infrared is mainly owing to the four-wave mixing between the pump pulse and its blueshifted conical emission.     

Electrospinning of complex oxide nanofibers

Electrospinning is a versatile process for drawing fibers of diverse materials including polymers, ceramics, and composites. We demonstrate here its application in the synthesis of complex ceramic oxide materials. The phase formation and morphology of BaTiO₃ nanofibers synthesized via electrospinning is investigated as a function of heat treatment conditions. Fully crystallized BaTiO₃ nanofibers with the perovskite structure are obtained after annealing at 750 °C and show an average grain size of about 30 nm. Tetragonal crystal structure of the fibers is indicated by XRD peak splitting (calculated c/a ratio=1.007), and confirmed by Raman spectroscopy. Furthermore, the advancement in heat treatment of the electrospun fibers yields single crystalline BaTiO₃ nanofibers with 50 nm in diameter and lengths up to 1 μm.     

Pinning and depinning process of an incommensurate CDW as revealed by coherent X-ray diffraction

Experiments on the coherent X-ray diffraction, and their modeling, have been performed on the Charge Density Wave (CDW) system NbSe₃. The 2k_F$2k_F$ satellite reflection associated with the CDW has been measured with respect to external dc currents. Below the threshold current, reflection displays several fringes in the transverse direction which disappear when the threshold current is exceeded. In the sliding state, the transverse satellite profile has a form of two nonsymmetric peaks, one of them being centered at the same position as below the threshold and another one being shifted. The shift of the longitudinal peak position below the threshold current and the nonsymmetric peak in the transverse direction above the threshold one is interpreted as the influence of strong linear defect like a crystal step present on the sample surface, combined with induced arrays of dislocations. Coherent X-rays provide a new access to processes in a CDW driven by an external force in a random pinning potential.