Régis Guégan

Structure of liquid and glassy methanol confined in cylindrical pores

We present a neutron scattering analysis of the density and the static structure factor of confined methanol at various temperatures. Confinement is performed in the cylindrical pores of MCM-41 silicates with pore diameters D=24 and 35 A. A change of the thermal expansivity of confined methanol at low temperature is the signature of a glass transition, which occurs at higher temperature for the smallest pore. This is evidence of a surface induced slowing down of the dynamics of the fluid. The structure factor presents a systematic evolution with the pore diameter, which has been analyzed in terms of excluded volume effects and fluid-matrix cross correlation. Conversely to the case of Van der Waals fluids, it shows that stronger fluid-matrix correlations must be invoked most probably in relation with the H-bonding character of both methanol and silicate surface.

Evidence of anisotropic quenched disorder effects on a smectic liquid crystal confined in porous silicon.

We present a neutron scattering analysis of the structure of the smectic liquid crystal octylcyanobiphenyl (8CB) confined in one-dimensional nanopores of porous silicon films (PS). The smectic transition is completely suppressed, leading to the extension of a short-range ordered smectic phase aligned along the pore axis. It evolves reversibly over an extended temperature range, down to 50 K below the N-SmA transition in pure 8CB. This behavior strongly differs from previous observations of smectics in different one-dimensional porous materials. A coherent picture of this striking behavior requires that quenched disorder effects are invoked. The strongly disordered nature of the inner surface of PS acts as random fields coupling to the smectic order. The one-dimensionality of PS nanochannels offers perspectives on quenched disorder effects, of which observation has been restricted to homogeneous random porous materials so far.

Rich polymorphism of a rod-like liquid crystal (8CB) confined in two types of unidirectional nanopores.

Abstract.We present a neutron and X-rays scattering study of the phase transitions of 4-n-octyl-4 -cyanobiphenyl (8CB) confined in unidirectional nanopores of porous alumina and porous silicon (PSi) membranes with an average diameter of 30nm. Spatial confinement reveals a rich polymorphism, with at least four different low temperature phases in addition to the smectic A phase. The structural study as a function of thermal treatments and conditions of spatial confinement allows us to get insights into the formation of these phases and their relative stability. It gives the first description of the complete phase behavior of 8CB confined in PSi and provides a direct comparison with results obtained in bulk conditions and in similar geometric conditions of confinement but with reduced quenched disorder effects using alumina anopore membranes.

Molecular dynamics of a short-range ordered smectic phase nanoconfined in porous silicon

4-n-octyl-4-cyanobiphenyl has been recently shown to display an unusual sequence of phases when confined into porous silicon (PSi). The gradual increase of oriented short-range smectic (SRS) correlations in place of a phase transition has been interpreted as a consequence of the anisotropic quenched disorder induced by confinement in PSi. Combining two quasielastic neutron scattering experiments with complementary energy resolutions, the authors present the first investigation of the individual molecular dynamics of this system. A large reduction of the molecular dynamics is observed in the confined liquid phase, as a direct consequence of the boundary conditions imposed by the confinement. Temperature fixed window scans reveal a continuous glasslike reduction of the molecular dynamics of the confined liquid and SRS phases on cooling down to 250 K, where a solidlike behavior is finally reached by a two-step crystallization process.

Relation between static short-range order and dynamic heterogeneities in a nanoconfined liquid crystal.

We analyze the molecular dynamics heterogeneity of the liquid crystal 4-n-octyl-4-cyanobiphenyl nanoconfined in porous silicon. We show that the temperature dependence of the dynamic correlation length xi_(wall) , which measures the distance over which a memory of the interfacial slowing down of the molecular dynamics persists, is closely related to the growth of the short-range static order arising from quenched random fields. More generally, this result may also shed some light on the connection between static and dynamic heterogeneities in a wide class of condensed and soft matter systems.

Incoherent Quasielastic Neutron Scattering Study of Molecular dynamics of 4-n-cyano-4'-octylbiphenyl.

We report incoherent quasielastic neutron scattering experiments on the thermotropic liquid crystal 4-n-octyl-4-cyanobiphenyl. The combination of time-of-flight and backscattering data allows analysis of the intermediate scattering function over about three decades of relaxation times. Translational diffusion and uniaxial molecular rotations are clearly identified as the major relaxation processes in, respectively, the nanosecond and picosecond time scales.

Structure and relaxation processes of an anisotropic molecular fluid confined into 1D nanochannels

Structural order parameters of a smectic liquid crystal confined into the columnar form of porous silicon are studied using neutron scattering and optical spectroscopic techniques. It is shown that both the translational and orientational anisotropic properties of the confined phase strongly couple to the one-dimensional character of the porous silicon matrix. The influence of this confinement induced anisotropic local structure on the molecular reorientations occurring in the picosecond timescale is discussed.

Sliding and translational diffusion of molecular phases confined into nanotubes

The remaining dynamical degrees of freedom of molecular fluids confined into capillaries of nano to sub-nanometre diameter are of fundamental relevance for future developments in the field of nanofluidics. These properties cannot be simply deduced from the bulk one since the derivation of macroscopic hydrodynamics most usually breaks down in nanoporous channels and additional effects have to be considered. In the present contribution, we review some general phenomena, which are expected to occur when manipulating fluids under confinement and ultraconfinement conditions.

Dynamics of 8CB confined into porous silicon probed by incoherent neutron backscattering experiments

Abstract.Confinement in the nanochannels of porous silicon stronglynaffects the phase behavior of the archetype liquid-crystaln4-n-octyl-4-cyanobiphenyl (8CB). Axa0very striking phenomenon is thendevelopment of a short-range smectic order, which occurs on a verynbroad temperature range. It suggests in this case that quenchedndisorder effects add to usual finite size and surface interactionneffects. We have monitored the temperature variation of thenmolecular dynamics of the confined fluid by incoherent quasielasticnneutron scattering. A strongly reduced mobility is observed at thenhighest temperatures in the liquid phase, which suggests that theninterfacial molecular dynamics is strongly hindered. A continuouslynincreasing slowdown appears on cooling together with a progressivengrowth of the static correlation length.

Bioprotectant glassforming solutions confined in porous silicon nanocapillaries

Glycerol and trehalose-glycerol binary solutions are glass-forming liquids with remarkable bioprotectant properties. In this paper, we address the effects of confining of these solutions in straight channels of diameter D=8 nm formed by porous silicon. Neutron diffraction and incoherent quasielastic neutron scattering are used to reveal the different effects of nanoconfinement and addition of trehalose on the intermolecular structure and molecular dynamics of the liquid and glassy phases, on a nanosecond timescale.