Electrooptical Kerr constant and third-order susceptibility measurements in nematic liquid crystals and their mixtures

We report for the first time the determination of the real part of the third order nonlinear susceptibilities ⁽³⁾ (–, , 0, 0) in the isotropic phase of two nematic liquid crystalsp-(ethoxybenzylidine)-p-butylaniline (EBBA) andp-(methoxybenzylidene)-p-butylaniline (MBBA) from electrooptic Kerr effect experiments. The highest value of ⁽³⁾ observed near nematic-to-isotropic transition temperature, at 632.8 nm is found to be 1.067×10^–20 m²V^–2 for EBBA and 6.602×10^–20 m²V^–2 for MBBA.     

Temperature dependence of the critical magnetic field of the structural transition in MBBA-based ferronematics

We studied the structural transitions in ferronematics based on the thermotropic nematic liquid crystal MBBA (4^′ -methoxybenzylidene-4-n-butylaniline) having a nematic-to-isotropic transition temperature T _N–I?=?48.0^○C and in MBBA-based ferronematics doped with a magnetic suspension consisting of Fe₃O₄ particles (10?nm in diameter) coated with oleic acid as a surfactant. The ferronematic samples were prepared with different volume concentrations of magnetic particles φ?=,1× 10^?4, 2× 10^?4 and 5×10^?4. The temperature dependences of the critical magnetic fields in a bias electric field under strong applied magnetic fields are presented. We calculated the surface density of anchoring energy W at the nematic–magnetic particle boundary. Scaling of the structural transition in the MBBA and MBBA-based ferronematics with the temperature of the nematic-to-isotropic transition was observed.     

Self-trapping of the <Emphasis Type="Italic">d</Emphasis>-<Emphasis Type="Italic">d</Emphasis> charge transfer exciton in bulk NiO evidenced by X-ray excited luminescence

Soft X-ray (XUV) excitation did make it possible to avoid the predominant role of the surface effects in luminescence of NiO and revealed a bulk luminescence with a puzzling well isolated doublet of very narrow lines with close energies near 3.3 eV which is assigned to recombination transitions in self-trapped d-d charge transfer (CT) excitons formed by coupled Jahn-Teller Ni⁺ and Ni³⁺ centers. The conclusion is supported both by a comparative analysis of the CT luminescence spectra for NiO and solid solutions Ni _x Zn_{1 − x} O, and by a comprehensive cluster model assignment of different p-d and d-d CT transitions, their relaxation channels. To the best of our knowledge, it is the first observation of the luminescence due to self-trapped d-d CT excitons.     

Terahertz dichroism of MBBA liquid crystal on rubbed substrate

Terahertz (THz) dichroism of a nematic liquid N-(p-methoxybenzylidene)-p-butylaniline (MBBA) was measured using a GaP Raman THz spectrometer. MBBA on a rubbed plastic substrate generates a band at around 4.0 THz: its liquid crystal phase shows strong dichroism, which well corresponds to that of the IR absorption caused by π(CH) of MBBA molecule reported in the literature. Based on inferences drawn from the present THz and the published IR dichroic results, the 4.0 THz band probably stems from lateral intermolecular or intramolecular interactions of MBBA molecules aligned to the rubbing direction. The results clearly demonstrate that THz spectroscopy is powerful for discussing of phase transition and dichroism of liquid crystals.     

Temperature dependence of the effective anchoring energy for a nematic-ferroelectric interface

Specific features of the anisotropic interaction between a nematic mixture and a polar surface of a ferroelectric triglycine sulfate crystal have been studied over a wide temperature range including the substrate's Curie point T_c. The mixture was composed of two nematic liquid crystals, 60% of p-methoxybenzylidene-p-n-butylaniline (MBBA) and 40% of p-ethoxybenzylidene-p-n-butylaniline (EBBA), and doped with a small amount of a dichroic dye. The temperature dependence of the polarized components of optical density D_j of the dye absorption band for the nematic and isotropic phases of the MBBA+EBBA mixture has been obtained using polarization optic techniques. The temperature-induced structural changes in the nematic layer near T_c were found to be related to the changes in the orientational part of the tensor order parameter Q_ik. The experimental data have been interpreted using the model, in which the dispersive van der Waals forces of the substrate stabilize the planar orientation of the nematic in the bulk competing with the short-range anchoring forces in the vicinity of T_c. At the same time, the anisotropic part of the surface energy has two terms with the orthogonal easy axes. The nature of the surface electric field and its effect on the director alignment at the interface have been clarified. Taking into account the known relation between anchoring strength and the nematic order parameter, the effective anchoring energy w_eff for the studied system has been determined as a function of temperature.     

Investigation of three-terminal voltage-controlled switching devices prepared by molecular beam epitaxy

Three-terminal GaAs switching devices prepared by molecular beam epitaxy using p ⁺-n ^–-(p ⁺)-n ^–-n ⁺ structures are fabricated. The effects of the third-electrode position and the possible voltage-controlled operation on the device performance are discussed. Concepts are proposed to obtain new and improved voltage-controlled properties. The internal barrier of one proposed structure can be modulated directly and is found to be effective for the studied structures. The position of the third-electrode is found to affect the electrical properties profoundly due to different dominant mechanisms. Comparisions are made by defining a control efficiency. Due to the idea of varying the gate position, a conceptual understanding of such a set of results would enhance our understanding of the physics of bulk barrier devices in general.     

Effect of carbon nanotubes on the isotropic to nematic and the nematic to smectic- A phase transitions in liquid crystal and carbon nanotubes composites

A high-resolution ac-calorimetric study on the weakly first-order isotropic to nematic (I -N and the continuous nematic to smectic-A (N -SmA phase transitions of the liquid crystal octyl-cyanobiphenyl (8CB) doped with well-dispersed multiwall carbon nanotubes (CNTs) as a function of CNT concentrations is reported. Thermal scans were performed for all samples having CNT weight fraction from f_w \phi_{{w}}^{} = 0.0005 to 0.0060 over a wide temperature range well above and below the two transitions in pure 8CB. Both the I -N and the N -SmA transitions evolve in character and have their transition temperatures qualitatively offset by ∼ 1.10 K lower as compared to that in pure 8CB for all 8CB+CNTs samples. The enthalpy change associated with each phase transition is essentially the same as that of pure 8CB and remains unchanged with increasing f_w \phi_{{w}}^{} . However, there is an evidence that the thermal transport properties of the composites differ from the pure LC upon cooling below a f_w \phi_{{w}}^{} -dependent temperature within the nematic phase. In addition, a new C_p feature is resolved for intermediate f_w \phi_{{w}}^{} samples that appears to be correlated to this onset temperature.     

Pretransition and critical phenomena in the nematic phase of MBBA

The pretransition and critical phenomena in the nematic phase of p-methoxy-benzylidene p-n-butyl-anilline (MBBA) were studies by means of precision volume measurements. The relationship between the volume change and the order parameter of MBBA to yield the critical index ß is discussed.     

Electron energy-loss spectroscopy of UHV-cleaved NiO (100) surfaces

Electron energy-loss spectroscopy of ～ 200 eV electrons has been applied to the study of the electronic states of clean NiO (100) surfaces. Initial attempt has been made on the identification of observed peaks, and they are attributed to the one-electronic transitions (O^2-2p → Ni²⁺3d, 4s and 4p; Ni²⁺3d → 4p, 3p → 3d and 4s), and the collective excitations (bulk plasmons of O^2-2p, Ni²⁺3d electrons, and coupled 2p and 3d electrons).     

Kaon absorption from kaonic atoms and formation spectra of kaonic nuclei

We considered the kaon absorption from atomic states into the nucleus. We found that the nuclear density probed by the atomic kaon significantly depends on the kaon orbit. Then, we re-examined the meanings of the observed strengths of one-body and two-body kaon absorption, and investigated the effects to the formation spectra of kaon bound states by in-flight (K ^-, p) reactions. As a natural consequence, if the atomic kaon probes a smaller nuclear density, the ratio of the two-body absorption at nuclear center is larger than the observed value in kaonic atoms, and the depth of the imaginary potential is deeper even at smaller kaon energies as in kaonic nuclear states because of the large phase space for the two-body processes. This deeper imaginary potential makes the signals of kaonic nucleus formation more unclear in the (K ^-, p) spectra.     

Theoretical description of fluctuations in free-standing smectic-A films including spatial non-uniformity of their elastic characteristics

A theoretical study is reported of fluctuations in smectic layer displacements and of the correlations between them in free-standing smectic-A films formed of liquid-crystal compounds with smectic-A-isotropic liquid (Sm-A-I) and Sm-A-nematic (Sm-A-N) bulk phase transitions. The study took into account the dependence of the elastic constants for bending, K, and tension (compression), B, of smectic layers on distance to the free film surfaces. The calculations are compared with the results obtained within Hołyst’s model for spatially uniform, free-standing smectic-A films. It has been established that, below the temperature at which smectic order in the bulk of a liquid crystal disappears, taking into account the profiles of the elastic moduli K and B does not produce noticeable differences from this model. However, at temperatures considerably above the Sm-A-I and Sm-A-N phase transitions, their inclusion results in considerable discrepancies from the predictions of Hołyst’s model. Fiz. Tverd. Tela (St. Petersburg) 41, 1882–1889 (October 1999)     

Phase transitions of fluids confined in porous silicon: A differential calorimetry investigation

The phase transitions of non-polar organic fluids and of water, confined in the pores of porous silicon samples, were investigated by Differential Scanning Calorimetry (DSC). Two types of PS samples (p^- and p⁺ type) with different pore size and morphology were used (with spherical pores with a radius of about 1.5 nm and cylindrical shape with a radius of about 4 nm respectively). The DSC results clearly show that the smaller the pores are, the larger is the decrease in the transition temperature. Moreover, a larger hysteresis between melting and freezing is observed for p⁺ type than for p^- type samples. A critical review of the thermodynamical properties of small particles and confined fluids is presented and used to interpret and discuss our DSC results. The effects of the chemical dissolution as well as the influence of anodization time are presented, showing that thick p⁺ type porous silicon layers are non-homogeneous. The DSC technique which was used for the first time to investigate fluids confined in porous silicon, enables us to deduce original information, such as the pore size distribution, the decrease in the freezing temperature of confined water, and the thickness of non-freezing liquid layer at the pore wall surface. Received: 11 May 1998 / Revised and Accepted: 29 July 1998     

Distinct critical fluctuations and molecular motions manifest in a model biomembrane

Lattice dynamics in bis-(n-C₁₆H₃₇NH₃)₂SnCl₆, where the hydrocarbon part is analogous to lipid membrane, was investigated by means of 200 MHz ¹H nuclear magnetic resonance. As a result, critical fluctuations and molecular dynamics associated with the phase transitions, an order-disorder and a conformational phase transition, were distinguished in a wide temperature range. The dynamical origin of the critical fluctuations, observed in the long-chain compounds but not in the short-chain compounds, by the laboratory frame spin-lattice relaxation measurements, is revealed and discussed in this work.     

Fine structure and isotope shift of the 3s4d 3 D-3s3p 3 P, 3s5d 3 D-3s3p 3 P and 3p 2 3 P-3s3p 3 P Transitions of MgI

Summary We report the measurements of the³ D(3s4d)-³ P(3s3p)³ D(3s5d)-³ P(3s3p), and³ P(3p ²)-³ P(3s3p) transition frequency of MgI, the fine-structure separation and isotope shift between²⁴Mg and²⁶Mg. The measurements have been performed in a metastable atomic beam; a good agreement is found for data already existing in the literature. The accuracy of the measurements reported in this paper is mainly limited by the Doppler broadening of theI ₂ transitions used as a reference and by the precision in the knowledge of the related wavelengths.     

How to measure the pomeron phasein diffractive dipion photoproduction

The study of charge asymmetry of pions in the high-energy process ep → eπ⁺π^-p (γp → π⁺π^-p) at very small dipion momenta offers a method to measure the phase of the forward hadronic (quasi-) elastic amplitude γp → ρp. We estimate the potential of such measurements at HERA. Received: 19 February 2004, Revised: 1 August 2005, Published online: 3 November 2005     

Dynamical behavior of the phase transition of strained from atomistic simulations

Using an atomistic shell model we study the temperature dependence of the ferroelectric properties of BaTiO₃ under biaxial compressive strain applicable to growth on perovskites substrate. Molecular dynamics simulations show a “r→c→p” sequence of phase transitions when temperature is increased, and the absence of an “ac phase”. The first-order paraelectric-to-ferroelectric phase transition presents in bulk changes to a second-order one as a consequence of the in-plane constraint imposed by the mechanical boundary conditions. From the tetragonal ferroelectric c phase, the transition takes place in a finite range of temperature where the lattice parameter normal to the plane keeps approximately constant until T_c is reached. Analysis of the local polarization behavior reveals an order–disorder dynamics as the dominant mechanism of the transition.     

High resolution off-magic-angle spinning NMR for cholesteric liquid crystals

High resolution NMR of cholesteric liquid crystals is realized by off-magic-angle spinning (OMAS). Using the average potential theory, it is shown that the pitch axes of a cholesteric liquid crystal with a positive (negative) magnetic susceptibility anisotropy are aligned along the spinning axis with an OMAS angle larger (smaller) than the magic angle without any distortion of the helical structure, which is untwisted or distorted by the static magnetic field in some static samples. Hence, the line broadening due to the anisotropies of chemical shifts and/or quadrupole couplings is removed, while information of the anisotropies in cholesteric alignments can be obtained from the line positions. A detailed theoretical analysis of effects of spinning frequency and molecular diffusion along the pitch axis on the linewidth is given, predicting that the resolution is improved greatly at a spinning frequency much higher than the rotational diffusion coefficient. These theoretical results are verified by ¹³C OMAS experiments on a cholesteric liquid crystal of p-ethoxybenzyl-p-[(S)-2- methylbutyl]aniline (EBMBA) and cholesteric mixtures of p-methoxybenzylidene-p-n-butylaniline (MBBA) and cholesteryl chloride (CC).     

Dynamic NMR investigation of plastic crystals in bulk and confined in porous materials

In this work, the molecular dynamics of four organic compounds confined in silica pores of nominal diameter 6 and 20 nm are studied by high-field (9.4 T) nuclear magnetic resonance (NMR), and the results are discussed with reference to the bulk substances. By using organic compounds forming soft plastic crystals on freezing as adsorbates, damage to the pore structures can be avoided. NMR lineshapes, spin-lattice relaxation times (T ₁), spin-spin relaxation timesT ₂ and diffusivities are reported as a function of temperature. Since the porous grains are much greater than the distance travelled by the molecules during the experiment, intracrystalline NMR parameters were obtained. However, the shortT ₂ (∼1 ms) encountered in both the bulk and confined samples prohibited measurements ofT ₂ and the diffusivity in the low-temperature ordered phases. The confinement in the pores gives rise to substantial changes in the phase behavior and molecular dynamics. Thus, the¹H lineshape observations of the confined samples clearly reveal a narrow-line component superimposed on a broad resonance at temperatures well below the transition point of the bulk material. In the freezing region, the narrow-line component is attributed to the surface layer and the undercooled liquid in the smaller pores that remains unfrozen. In the two-component, low-temperature region, the narrow component corresponds to the surface layer, while the broad component originates from the crystalline phase at the center of the pores.     

Study of the structure of light,unstable nuclei and the mechanism of elastic proton scattering

The review presents calculations of elastic p ⁶He-, p ⁸Li-, p ⁹Li- and p ⁹C scattering in the framework of the Glauber theory of multiple diffraction scattering at intermediate energies of 70 and 700 MeV/nucleon. The most significant result of the calculations is that we have utilized realistic three-body wave functions obtained within modern nuclear models. The relation is found between differential cross sections and intercluster potentials, where the nuclear wave functions are calculated. Conclusions are made concerning the types of potentials which describe most realistically the available experimental data. The method for calculation of three-body wave functions in α-n-n-, α-t-n-, ⁷Be-p-p-, α-t-2n-, and ⁷Li-n-n models is described with discussion of inter-cluster potentials and the quantum-number configurations taken into consideration. It is revealed how the wave functions and the nuclear electromagnetic characteristics calculated using these wave functions depend on the choice of intercluster potentials. The derivation of matrix elements (amplitudes) of pA scattering in the framework of the Glauber approach with three-body wave functions is presented by an example of ⁶He nucleus. Discussing the results of calculation of differential cross sections and the analyzing power (A _y ), we established how the calculated characteristics depend on a wave-function structure and dynamics of the process determined by a Glauber operator of multiple scattering. The calculated differential cross sections and analyzing powers are compared with available experimental data and calculations by other authors performed for different formalisms, which allows us to make justified conclusions.     

NMR investigations of hexamethyldisilane confined in controlled pore glasses: Pore size distribution and molecular dynamics studies

In this work, the melting-point depression and molecular dynamics of hexamethyldisilane confined within five controlled pore glasses, with mean diameters ranging from 7.9 to 23.9 nm, are studied by high-field (9.4 T) nuclear magnetic resonance (NMR), and the results are discussed with reference to the bulk substance. The melting-point depression in pores with radiusR follows the simplified Gibbs-Thompson equation ΔT=k _p/(R−s) with ak _p value of 74 K · nm and ans value of 1 nm. To our knowledge, this is the first time thek _p value of hexamethyldisilane is reported. Proton spin-lattice relaxation times (T ₁), spin-spin relaxation times (T ₂), and diffusivities (D) are reported as a function of temperature. The confinement in the pores gives rise to substantial changes in the molecular dynamics and the phase behavior. The line-shape measurements reveal a two-phase system assigned to a relatively mobile component at the pore walls and a crystalline solid at the center of the pores. However, theT ₂ measurements show that the mobile phase also embraces a minor component attributed to nonfrozen liquid in pockets or micropores. The diffusivity of the major narrow-line component is approximately three orders of magnitude larger than that in the plastic bulk phase, reflecting fast diffusion of mobile molecules. Below the melting region,T ₁ of the narrow line is significantly shorter thanT ₁ of the broad line, suggesting that the molecular reorientation is more hindered close to the surface than at the center of the pore.