Lamellar-to-nematic phase transition in a lipid-surfactant mixture

A lyotropic system, consisting of a lecithin (DMPC) and a non-ionic surfactant (C₁₂E₅) in water was studied. The system exhibits a lamellar-to-nematic phase transition. The nematic phase appears as the temperature is decreased and only exists in a very limited temperature and concentration range, for specific lipid-to-surfactant ratios. While a lamellar phase is found at higher temperatures in both mixed and pure C₁₂E₅ systems, the transition to the nematic phase at lower temperatures coincides with a micellar phase in the pure C₁₂E₅ system. The transition appears to be driven by the strong temperature dependence of the surfactant film spontaneous curvature. The structural properties of the lamellar phase close to the lamellar-to-nematic boundary have been studied by polarised light microscopy and small-angle neutron and X-ray scattering experiments. The signature of a helical defect with Burgers vector of magnitude 2 is apparent in our data, close to the lamellar-to-nematic phase transition. The proliferation of screw dislocations in the lamellar phase might be a plausible mechanism for driving this transition. Received 6 July 1999 and Received in final form 17 April 2000     

Metallic behavior in dilute two-dimensional hole systems

We have studied the metallic behavior in low-density two-dimensional p-GaAs systems, close to the apparent metal-insulator transition. Two observations are made concerning the origins of the metallic-like behavior. Within a given sample the strength of the metallic behavior is almost independent of the asymmetry of the confining potential, and is predominantly determined by the low-temperature resistivity (i.e., by k(F)l). In all our samples we find that at low densities, close to the transition from insulating to metallic behavior, the fractional decrease in conductivity with increasing temperature scales as T/T(F).     

Mechanical properties of thin confined polymer films close to the glass transition in the linear regime of deformation: Theory and simulations

Over the past twenty years experiments performed on thin polymer films deposited on substrates have shown that the glass transition temperature T(g) can either decrease or increase depending on the strength of the interactions. Over the same period, experiments have also demonstrated that the dynamics in liquids close to the glass transition temperature is strongly heterogeneous, on the scale of a few nanometers. A model for the dynamics of non-polar polymers, based on percolation of slow subunits, has been proposed and developed over the past ten years. It proposes a unified mechanism regarding these two features. By extending this model, we have developed a 3D model, solved by numerical simulations, in order to describe and calculate the mechanical properties of polymers close to the glass transition in the linear regime of deformation, with a spatial resolution corresponding to the subunit size. We focus on the case of polymers confined between two substrates with non-negligible interactions between the polymer and the substrates, a situation which may be compared to filled elastomers. We calculate the evolution of the elastic modulus as a function of temperature, for different film thicknesses and polymer-substrate interactions. In particular, this allows to calculate the corresponding increase of glass transition temperature, up to 20 K in the considered situations. Moreover, between the bulk T(g) and T(g) + 50 K the modulus of the confined layers is found to decrease very slowly in some cases, with moduli more than ten times larger than that of the pure matrix at temperatures up to T(g) + 50 K. This is consistent with what is observed in reinforced elastomers. This slow decrease of the modulus is accompanied by huge fluctuations of the stress at the scale of a few tens of nanometers that may even be negative as compared to the solicitation, in a way that may be analogous to mechanical heterogeneities observed recently in molecular dynamics simulations. As a consequence, confinement may result not only in an increase of the glass transition temperature, but in a huge broadening of the glass transition.     

The liquid-vapour phase transition in fluid mercury

The paper discusses recent experimental results in the liquid-vapour critical region of metals which show that the existence of the metal-non-metal transition noticeably influences the electronic, thermodynamic, structural and interfacial features of the fluid. The main emphasis is on surface-induced phenomena. Reflectivity experiments on mercury against an optically transparent sapphire window close to the vapour-liquid coexistence curve reveal clearly the existence of a prewetting transition of mercury on the sapphire substrate. The transition line, which terminates at high temperatures at a prewetting critical temperature T _pwc lying below the bulk critical temperature T _c and at low temperatures at the wetting transition temperature T _w lies close to the bulk vapour-liquid coexistence curve.     

Effects of fluctuations in the orientational order parameter in the cyanobiphenyl (nCB) homologous series

Photopyroelectric measurements of the anisotropy in the thermal conductivity Deltak vs temperature in the nCB (n=5,ellipsis,9) series are reported. The data have been used to deduce the behavior of the orientational order parameter Q close to the nematic-isotropic (N-I) and smectic A-nematic (A-N) phase transitions, respectively. It has been shown that near the N-I transition the data for 5CB and 6CB are consistent with the so-called "tricritical hypothesis," which predicts beta=0.25. This is not true for 7CB and 8CB in which the order parameter exhibits a behavior that could be caused by the presence of fluctuations that become increasingly important when the transition temperature is approached. A very simple model, which takes into account the contribution of fluctuations to the orientational order, has been developed close to the A-N transition and it has been shown that it is in good agreement with the experimental results. A semiquantitative explanation for the observed behavior in compounds with different nematic range has been also given.     

Failure of mean field theory at large N

We study strongly coupled lattice QCD with N colors of staggered fermions in 3+1 dimensions. While mean field theory describes the low temperature behavior of this theory at large N, it fails in the scaling region close to the finite temperature second order chiral phase transition. The universal critical region close to the phase transition belongs to the 3D XY universality class even when N becomes large. This is in contrast to Gross-Neveu models where the critical region shrinks as N (the number of flavors) increases and mean field theory is expected to describe the phase transition exactly in the limit of infinite N. Our work demonstrates that infrared fluctuations can be important close to second order phase transitions even when N is strictly infinite.     

Heterogeneous dynamics at the glass transition in van der Waals liquids: Determination of the characteristic scale

Recent experiments have demonstrated that the dynamics in liquids close to the glass transition temperature is strongly heterogeneous. The characteristic size of these heterogeneities has been measured to be a few nanometers at T _g. We extend here a recent model for describing the heterogeneous nature of the dynamics which allows both to derive this length scale and the right orders of magnitude of the heterogeneities of the dynamics close to the glass transition. Our model allows then to interpret quantitatively small probes diffusion experiments. Received 29 March 2002 and Received in final form 11 November 2002 RID="a" ID="a"e-mail: long@lps.u-psud.fr     

Landau-Ginzburg treatment of nuclear matter at finite temperature

Based on recent studies of the temperature dependence of the energy and specific heat of liquid nuclear matter, a phase transition is suggested at a temperature ∼ 0.85 MeV. We apply the Landau-Ginzburg theory to this transition and determine the behaviour of the energy and specific heat close to the critical temperature in the condensed phase. Received: 29 July 2000 / Accepted: 20 October 2000     

Study of the superconducting transition in YBa2Cu3O7−δ single crystal by thermopower measurements

We have determined the superconducting transition in YBa₂Cu₃O_7−δ single crystal by measurements of thermopower. Two transitions were observed in both the ab-plane and the c-direction. The high temperature transition may have a close relation to the surface shell of the crystal.     

35Cl NQR and2H NMR analysis of the critical dynamics close to the displacive normal-incommensurate phase transition in an organic crystal

Nuclear magnetic resonance (NMR) experiments,³⁵C1 nuclear quadrupole resonance (NQR) and²H NMR, have been performed close to the displacive normal-incommensurate phase transition in the organic crystal of bis-(4-chlorophenyl)-sulfone. Calculations using coherent neutron scattering results show that the soft-mode contribution cannot explain the rapid increase of the spin-lattice relaxation rates close to the transition temperature. Calculations of the spectral densities taking into account the existence of a central-peak phenomenon describe both³⁵C1 NQR and²H NMR spin-lattice relaxation rates on approaching the phase transition. In this way, the width of the central peak can be estimated to be in the range of several gigahertz.     

Temperature dependence of the relaxation time of the superconducting order parameter

We have measured the temperature dependences of the relaxation time of the superconducting order parameter and of the equilibrium energy gap close to the transition temperature in very clean films of aluminum. The results are only consistent with the temperature and energy gap dependence predicted by Schmid and Schön. We also show that the magnitude and mean free path dependence of the electron inelastic collision time is in good agreement with calculations.     

Si(111)4×1-In表面上铟原子的粘着系数随温度的突变现象

用AES和RHEED研究铟原子在Si(111)4×1-In结构表面粘着系数与温度的关系。在110℃以下,几乎为零的铟原子的粘着系数是由于4×1-In结构的原子排列使表面呈现价键饱和状态所致;在110—120℃温区内发生的粘着系数的阶跃变化可以用表面熔化所导致的有序-无序的相变模型来解释;高于120℃,粘着系数始终接近于1。 关键词：     

On the two-parametric theory of superconductivity

The concept of spin fluctuations in the Hubbard model is used for deriving a closed system of equations for the superconducting order parameter Δ and spin susceptibility. The limiting cases of low temperatures and temperatures close to the superconducting transition temperature are considered. The temperature dependences of the parameter Δ and the Knight shift are obtained. The conditions under which the second-order phase transition turns to the first-order phase transition are established.     

Aging of thin polymer films cast from a near-theta solvent

We have examined the aging behavior of spin-cast thin polymer films as a function of their processing history. Films prepared from solutions close to the Θ?temperature were aged for varying times at room temperature, followed by a dewetting experiment above the glass transition temperature of the polymer. The characteristic aging time varied strongly with the quality of the solvent, which is attributed to distorted chain conformations in the as-cast films. This is an indication for the nonequilibrium nature of thin polymer films, possibly causing some of their unexplained properties.     

Gyrotropic and piezoelectric coefficients and attenuation of elastic waves in BaTiO3

Using Landau theory of phase transition, expressions for gyrotropic coefficients and piezoelectric coefficients are obtained for barium titanate in the tetragonal phase. Both coefficients vanish at the ferroelectric phase transition temperature. The piezoelectric coefficients tallied with the literature values. The attenuation coefficients for elastic waves propagating along the principal directions in tetragonal, orthorhombic and rhombohedral phases are derived based on Landau theory. It is predicted that there will be slight amplification for both longitudinal and transverse modes in the rhombohedral phase at a temperature close to the rhombohedral phase transition temperature.     

Heterogeneous dynamics at the glass transition in van der Waals liquids, in the bulk and in thin films

It has been shown over the last few years that the dynamics close to the glass transition is strongly heterogeneous, both by measuring the diffusion coefficient of tagged particles or by NMR studies. Recent experiments have also demonstrated that the glass transition temperature of thin polymer films can be shifted as compared to the same polymer in the bulk. We propose here first a thermodynamical model for van der Waals liquids, which accounts for experimental results regarding the bulk modulus of polymer melts and the evolution of the density with temperature. This model allows us to describe the density fluctuations in such van der Waals liquids. Then, by considering the thermally induced density fluctuations in the bulk, we propose that the 3D glass transition is controlled by the percolation of small domains of slow dynamics, which allows to explain the heterogeneous dynamics close to T _g. We show then that these domains percolate at a lower temperature in the quasi-2D case of thin suspended polymer films and we calculate the corresponding glass transition temperature reduction, in quantitative agreement with experimental results of Jones and co-workers. In the case of strongly adsorbed films, we show that the strong adsorption amounts to enhance the slow domains percolation. This effect leads to 1) a broadening of the glass transition and 2) an increase of T _g in quantitative agreement with experimental results. For both strongly and weakly adsorbed films, the shift in T _g is given by a power law, the exponent being the inverse of that of the correlation length of 3D percolation. Received 21 March 2000 and Received in final form 4 December 2000     

Studies on Nematic Liquid Crystal Using Spin Wave Theory

A spin wave theory is proposed to study nematic liquid crystals. Since the orientation of the molecular long axis and the angular momentum of the molecule rotating around its long axis have the same direction, operators can be introduced to research the nematic liquid crystal. By transforming the intermolecular interaction potential,the Hamiltonian of the system has the same form as that of the ferromagnetic substance. The relation of the order parameters to the reduced temperature can be obtained. It is in good agreement with the experimental results in the low temperature region. In the high temperature region close to the transition point, by using the Hamiltonian, the transition point can be obtained, which is near to the Maier-Saupe‘s result.     

Zigzag instability of a χ disclination line in a cholesteric liquid crystal

We studied the formation of χ disclination lines in planar cholesteric samples placed in a temperature gradient near the cholesteric to smectic A phase transition. We observed that the first simple line which forms close to the smectic-cholesteric front zigzags when it is perpendicular to the direction of planar anchoring and is straight for other orientations. This instability is similar to Herring instability for crystalline surfaces. We show numerically that it originates from a strong increase of the elastic anisotropy close to the transition. In addition, we propose a new method to measure the pitch divergence at the smectic to cholesteric phase transition.     

Disordered surface sheets in solid matter near bulk instabilities

In this article, I review surface-sensitive X-ray scattering experiments using evanescent X-ray scattering and asymptotic Bragg scattering techniques which have been carried out in order to investigate the thermodynamic behaviour of the surface and the subsurface layers when the bulk of the system approaches a phase transition. I discuss the surface structures of the binary alloys Fe₃Al and Cu₃Au close to the order-disorder transition, the surface of the molecular crystal NH₄Br near the critical temperature and ice single-crystal surfaces close the bulk melting point. The observed surface phenomena range from surface disorder and surface-induced new universal critical behaviour to surface melting and surface segregation. They all have in common that they are not bound to the outermost layers, but rather occur within a surface sheet whose thickness can grow to a mesoscopic or even macroscopic size.     

Microscopic study of a pressure-induced ferromagnetic-spin-glass transition in the geometrically frustrated pyrochlore (Tb1-xLax)2Mo2O7

We have studied (Tb1-xLax)2Mo2O7 pyrochlores by neutron diffraction and muSR at ambient and under applied pressure. (Tb,La) substitution expands the lattice and induces a change from a spin-glass-like state (x=0) to a noncollinear ferromagnet (x=0.2). In the ferromagnetic structure, the Tb moments orient close to their local anisotropy axes as for an ordered spin ice, while the Mo ones orient close to the net moment. The temperature dependence of the muSR relaxation rates and static local fields suggests a second transition of dynamical nature below the Curie transition. Under pressure, the long range order breaks down and a spin-glass-like state is recovered. The whole set of data provides a microscopic picture of the spin correlations and fluctuations in the region of the ferromagnetic-spin-glass threshold.