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Imaging Long-range Orientational Order In Monolayers Of Amphiphilic Molecules With Scanning Probe Force Microscope And Liquid Crystal Optical AmplificationLiang, Wenlang 01 January 2011 (has links)
Monolayers of amphiphilic molecules at interface provide a unique system for understanding the thermodynamic and rheological properties of quasi two-dimensional systems. They are also an excellent model accessible for studying cell membranes. The feature of longrange organization of molecular tilt azimuth in monolayers at the air/water interface is one of the most interesting findings over the past two decades, which leads to the formation rich and defined textures. By observing the changes in these textures, the transitions between tilted monolayer phases can be detected. We study the boojum and stripe textures formed in the liquid-condensed phase of pentadecanoic acid (PDA) monolayers at the air/water interface and find that they can be preserved after being transferred to glass substrates at low dipping speeds at a temperature lower than the room temperature. Frictional force microscopy confirms the long-range tilt order in the transferred boojums and stripes of PDA, implying the interaction of the PDA molecules with the glass surface does not change the tilt order. Polymerized stripe textures of pentacosadiynoic acid (PCA) monolayers can also be transferred onto solid substrates. Atomic force microscopy shows that the PCA stripe textures represent the regular variations of molecular packing densities in PCA monolayers. Furthermore, we find that the molecular orientation and packing density changes in monolayers can induce the local order of nematic liquid crystals. Due to the longrange orientation correlation of nematic liquid crystals, the boojum and stripe textures in monolayers can be observed by an optical microscope after liquid crystal optical amplification.
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Influence of mesoscopic structures on single molecule dynamics in thin smectic liquid crystal filmsSchulz, Benjamin, Täuber, Daniela, Schuster, Jörg, Baumgärtel, Thomas, von Borczyskowski, Christian 12 September 2013 (has links) (PDF)
Mesoscopic structures in liquids have an impact on the diffusion dynamics of the constituting molecules. Smectic 8CB liquid crystals on silicon wafers show the formation of mesoscopic structures on the μm scale at a film thickness of 200 nm. Depending on the kind of substrate (thermally grown or native SiOx), we observed the formation of focal conic domains (FCDs) and a new type of terraced holes, respectively. Dynamics are described via single perylene diimide tracer molecule tracking of translational diffusion and in the case of FCDs by a combination of translation and rotation detected via fluorescence correlation spectroscopy. Tailoring perylene diimide molecules such that the optical transition dipole moment follows the liquid crystal director allows mapping out FCDs and investigating the dynamics within a single FCD.
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Line Tension and Entropy for Molecularly Thin Liquid Crystal Films at Temperatures Corresponding to Less-Ordered Bulk PhasesYarzebinski, Joseph Santiago 04 August 2016 (has links)
No description available.
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Influence of mesoscopic structures on single molecule dynamics in thin smectic liquid crystal filmsSchulz, Benjamin, Täuber, Daniela, Schuster, Jörg, Baumgärtel, Thomas, von Borczyskowski, Christian January 2011 (has links)
Mesoscopic structures in liquids have an impact on the diffusion dynamics of the constituting molecules. Smectic 8CB liquid crystals on silicon wafers show the formation of mesoscopic structures on the μm scale at a film thickness of 200 nm. Depending on the kind of substrate (thermally grown or native SiOx), we observed the formation of focal conic domains (FCDs) and a new type of terraced holes, respectively. Dynamics are described via single perylene diimide tracer molecule tracking of translational diffusion and in the case of FCDs by a combination of translation and rotation detected via fluorescence correlation spectroscopy. Tailoring perylene diimide molecules such that the optical transition dipole moment follows the liquid crystal director allows mapping out FCDs and investigating the dynamics within a single FCD.
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HYDRODYNAMICS AND LINE TENSION OF LANGMUIR FILMS AT THE AIR-WATER INTERFACEZOU, LU 21 November 2007 (has links)
No description available.
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Dynamique des dislocations coin et dissipation dans les films librement suspendus de cristal liquide smectiqueCaillier, François 18 November 2005 (has links) (PDF)
Les films librement suspendus de cristal liquide 8CB en phase smectique A sont très stables du fait de leur structure lamellaire. En effet, l'élasticité des couches compense la pression capillaire imposée par le ménisque qui le borde et qui joue le rôle de réservoir de matière. Lors de ce travail, nous nous sommes intéressés à la dynamique de ces films. Nous avons mis en évidence que le ménisque se comporte<br />comme un réservoir dissipatif.<br /><br />En régime quasi-statique, lorsque les échanges de matière entre le film et le ménisque sont lents, les écoulements de perméation autour des dislocations coin qui le composent sont à l'origine de sa perméabilité finie. Un modèle hydrodynamique montre que la dissipation est localisée à son entrée, dans la zone bien orientée et qu'elle dépend fortement de l'épaisseur du film. Dans les films fins, le ralentissement des boucles de dislocation et dans les films épais, la dynamique de relaxation de deux ménisques reliés par un même film ont permis de confirmer expérimentalement ce modèle.<br /><br />La dynamique d'effondrement d'une bulle a permis de caractériser la dissipation dans des régimes d'écoulements plus rapides en mettant en évidence un écart à la loi de Laplace (statique). Les expériences montrent qu'après une étape conduisant à la déstructuration du ménisque, ce qui le rend plus perméable, la bulle peut s'effondrer, la matière s'engouffrant dans le ménisque avec un comportement rhéofluidifiant. De plus, la nucléation et la croissance d'îlots peut rendre le processus moins dissipatif, ce qui est essentiellement observé dans les films fins.
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A Study of the Structure and Dynamics of Smectic 8CB Under Mesoscale ConfinementBenson, James January 2012 (has links)
The structure and dynamics of the smectic-A liquid crystal 8CB (4 cyano-4 octylbiphenyl) when sheared and confined to mesoscale gaps (with crossed cylindrical geometry and mica confining surfaces) were studied using a Surface Forces Apparatus (SFA). Triangular shear patterns with frequencies of 0.01, 0.1, 1.0 and 10 Hz, and amplitudes of 62.5 nm, 625 nm and 6.25 m were applied to samples at gap sizes of 0.5 and 5.0 m. The study was performed at room temperature (20.5C) and at two higher temperatures (22C and 27C). In order to minimize the thermal fluctuations within the test chamber and hence to allow for the rapid re-initialization of test runs, the SFA was modified to allow for quick, precise and remote control of the confining surfaces. The procedure maximized the number of tests that could be undertaken with a single pair of surfaces so that a single gap geometry could be maintained for the duration of the test run. In order to run the SFA remotely, scripts written with a commercial software package, LabVIEW, were used to control of the SFA components, its FECO-monitoring camera and all its peripheral electronic equipment as well. Samples were agitated to disrupt any shear-induced liquid crystal domain alignment from previous testing following each shear test, and methodologies were developed to ascertain the extent of confinement quickly and remotely following agitation. Separate methods were developed for gap sizes at each extreme of the mesoscale regime, where the transition from bulklike structure and dynamics to nano-confinement occurs (between 1 and 10 microns for smectic-A 8CB).
The results revealed that the greater amplitude-gap aspect ratio and surface-to-domain contact associated with smaller gaps facilitated reorientation of the domains in the shear direction. Evidence was also presented of domains at the higher end or outside of the mesoscale regime that, while straining and accreting, were unable to reorient and thereby led to an overall increase of viscoelastic response. The effective viscosity was found to obey a simple power law with respect to shear rate, , and the flow behaviour indices, n, slightly in excess of unity indicate shear thickening occurs with large enough shear amplitude, and that the viscosity reached a plateau near unity over shear rates of 0.005 to 500 s-1 within the mesoscale regime. Different K and n values were observed depending on the shear amplitude used.
Unlike bulk smectic 8CB, whose domains do not align well in the shear direction with large shear-strain amplitude, at mesoscale levels of confinement large amplitude shearing (up to 12.5 shear strain amplitude) was found to be very effective at aligning domains. In general domain reorientation is found to be much more rapid within the mesoscale regime than has been reported in bulk. Aggressive shearing was found to result in a complete drop in viscoelastic response within seconds, while gentler shearing is found to produce a very gradual increase that persists for more than six hours, with individual shear periods exhibiting frequent and significant deviations from the expected smooth shear path that may be a product of discrete domain reorientations.
From these findings, certain traits of the smectic 8CB domain structures under mesoscale confinement were deduced, including how they respond to shear depending on the level of confinement, and how their reorientation due to shear varies not only with shear rate but also independently with shear amplitude. An equation describing the viscosity change as a function of both shear rate and shear amplitude is proposed. The shear amplitude dependence introduces the notion of shearing beyond the proposed smectic 8CB “viscoelastic limit”, which was shown to exhibit behaviour in accordance with Large Amplitude Oscillatory Shear (LAOS) techniques developed for Fourier Transform rheology. The findings provided an understanding of the behavioural changes that occur as one reduces the level of confinement of smectic materials from bulk to nanoconfinement.
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A Study of the Structure and Dynamics of Smectic 8CB Under Mesoscale ConfinementBenson, James January 2012 (has links)
The structure and dynamics of the smectic-A liquid crystal 8CB (4 cyano-4 octylbiphenyl) when sheared and confined to mesoscale gaps (with crossed cylindrical geometry and mica confining surfaces) were studied using a Surface Forces Apparatus (SFA). Triangular shear patterns with frequencies of 0.01, 0.1, 1.0 and 10 Hz, and amplitudes of 62.5 nm, 625 nm and 6.25 m were applied to samples at gap sizes of 0.5 and 5.0 m. The study was performed at room temperature (20.5C) and at two higher temperatures (22C and 27C). In order to minimize the thermal fluctuations within the test chamber and hence to allow for the rapid re-initialization of test runs, the SFA was modified to allow for quick, precise and remote control of the confining surfaces. The procedure maximized the number of tests that could be undertaken with a single pair of surfaces so that a single gap geometry could be maintained for the duration of the test run. In order to run the SFA remotely, scripts written with a commercial software package, LabVIEW, were used to control of the SFA components, its FECO-monitoring camera and all its peripheral electronic equipment as well. Samples were agitated to disrupt any shear-induced liquid crystal domain alignment from previous testing following each shear test, and methodologies were developed to ascertain the extent of confinement quickly and remotely following agitation. Separate methods were developed for gap sizes at each extreme of the mesoscale regime, where the transition from bulklike structure and dynamics to nano-confinement occurs (between 1 and 10 microns for smectic-A 8CB).
The results revealed that the greater amplitude-gap aspect ratio and surface-to-domain contact associated with smaller gaps facilitated reorientation of the domains in the shear direction. Evidence was also presented of domains at the higher end or outside of the mesoscale regime that, while straining and accreting, were unable to reorient and thereby led to an overall increase of viscoelastic response. The effective viscosity was found to obey a simple power law with respect to shear rate, , and the flow behaviour indices, n, slightly in excess of unity indicate shear thickening occurs with large enough shear amplitude, and that the viscosity reached a plateau near unity over shear rates of 0.005 to 500 s-1 within the mesoscale regime. Different K and n values were observed depending on the shear amplitude used.
Unlike bulk smectic 8CB, whose domains do not align well in the shear direction with large shear-strain amplitude, at mesoscale levels of confinement large amplitude shearing (up to 12.5 shear strain amplitude) was found to be very effective at aligning domains. In general domain reorientation is found to be much more rapid within the mesoscale regime than has been reported in bulk. Aggressive shearing was found to result in a complete drop in viscoelastic response within seconds, while gentler shearing is found to produce a very gradual increase that persists for more than six hours, with individual shear periods exhibiting frequent and significant deviations from the expected smooth shear path that may be a product of discrete domain reorientations.
From these findings, certain traits of the smectic 8CB domain structures under mesoscale confinement were deduced, including how they respond to shear depending on the level of confinement, and how their reorientation due to shear varies not only with shear rate but also independently with shear amplitude. An equation describing the viscosity change as a function of both shear rate and shear amplitude is proposed. The shear amplitude dependence introduces the notion of shearing beyond the proposed smectic 8CB “viscoelastic limit”, which was shown to exhibit behaviour in accordance with Large Amplitude Oscillatory Shear (LAOS) techniques developed for Fourier Transform rheology. The findings provided an understanding of the behavioural changes that occur as one reduces the level of confinement of smectic materials from bulk to nanoconfinement.
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Characterization of heterogeneous diffusion in confined soft matterTäuber, Daniela 26 October 2011 (has links) (PDF)
A new method, probability distribution of diffusivities (time scaled square displacements between succeeding video frames), was developed to analyze single molecule tracking (SMT) experiments. This method was then applied to SMT experiments on ultrathin liquid tetrakis(2-ethylhexoxy)silane (TEHOS) films on Si wafer with 100 nm thermally grown oxide, and on thin semectic liquid crystal films. Spatial maps of diffusivities from SMT experiments on 220 nm thick semectic liquid crystal films reveal structure related dynamics. The SMT experiments on ultrathin TEHOS films were complemented by fluorescence correlation spectroscopy (FCS). The observed strongly heterogeneous single molecule dynamics within those films can be explained by a three-layer model consisting of (i) dye molecules adsorbed to the substrate, (ii) slowly diffusing molecules in the laterally heterogeneous near-surface region of 1 - 2 molecular diameters, and (iii) freely diffusing dye molecules in the upper region of the film. FCS and SMT experiments reveal a strong influence of substrate heterogeneity on SM dynamics. Thereby chemisorption to substrate surface silanols plays an important role. Vertical mean first passage times (mfpt) in those films are below 1 µs. This appears as fast component in FCS autocorrelation curves, which further contain a contribution from lateral diffusion and from adsorption events. Therefore, the FCS curves are approximated by a tri-component function, which contains an exponential term related to the mfpt, the correlation function for translational diffusion and a stretched exponential term for the broad distribution of adsorption events. Lateral diffusion coefficients obtained by FCS on 10 nm thick TEHOS films, thereby, are effective diffusion coefficients from dye transients in the focal area. They strongly depend on the substrate heterogeneity. Variation of the frame times for the acquisition of SMT experiments in steps of 20 ms from 20 ms to 200 ms revealed a strong dependence of the corresponding probability distributions of diffusivities on time, in particular in the range between 20 ms and 100 ms. This points to average dwell times of the dye molecules in at least one type of the heterogeneous regions (e.g. on and above silanol clusters) in the range of few tens of milliseconds.
Furthermore, time series of SM spectra from Nile Red in 25 nm thick poly-n-alkyl-methacrylate (PnAMA) films were studied. In analogy to translational diffusion, spectral diffusion (shifts in energetic positions of SM spectra) can be studied by probability distributions of spectral diffusivities, i.e. time scaled square energetic displacements. Simulations were run and analyzed to study contributions from noise and fitting uncertainty to spectral diffusion. Furthermore the effect of spectral jumps during acquisition of a SM spectrum was investigated. Probability distributions of spectral diffusivites of Nile Red probing vitreous PnAMA films reveal a two-level system. In contrast, such probability distributions obtained from Nile Red within a 25 nm thick poly-n-butylmethacrylate film around glass transition and in the melt state, display larger spectral jumps. Moreover, for longer alkyl side chains a solvent shift to higher energies is observed, which supports the idea of nanophase separation within those polymers.
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A New AC-Radio Frequency Heating Calorimetry Technique for Complex FluidsBarjami, Saimir 28 April 2005 (has links)
We have developed a new modulation calorimetry technique using RF-Field heating. This technique eliminates temperature gradients across the sample leading to a higher precision in evaluating the heat capacity compared to the previous techniques. A frequency scan was carried out on a 8CB+aerosil sample showing a wide plateau indicating the region of frequency independent heat capacity. A temperature scan was then performed through the first-order nematic to isotropic and second order smectic-A to nematic transitions and was shown to be consistent with the previous work. The amplitude of the RF heating power applied to the sample depends on the permittivity and the loss factor of the sample. Since the permittivity of a dielectric material has a strong temperature dependence in liquid crystals, new information is obtained. The heat capacity measurements have a relative resolution of better than 0.06%, and the phase shift a resolution of 0.03%, were shown to be significant improvements over traditional heating methods. We then applied this new RF calorimetry on bulk and aerosil 8CB dispersions. For the bulk 8CB, the step-like character of smectic-A to nematic transition, and first order nematic to isotropic transitions indicated the strong dominance of the permittivity and the loss factor of the material. For the 8CB+aerosil samples at different silica density, our data were consistent with the previous work and provides clear evidence for the coupling between the smectic-A and nematic phases. We have undertaken a combined T-dependent optical and calorimetric investigation of CCN47+aerosil samples through the I-N transition over a range of silica densities displaying the double I-N transition peak. This work offers compelling evidence that the I-N transition with weak quenched random disorder proceeds via a two-step process in which random-dilution is followed by random-field interactions on cooling from the isotropic phase, a previously unrecognized phenomena.
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