69 research outputs found

    Re-entrant ferroelectricity in liquid crystals

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    The ferroelectric (Sm C^*) -- antiferroelectric (Sm CA^*_A) -- reentrant ferroelectric (re Sm C^*) phase temperature sequence was observed for system with competing synclinic - anticlinic interactions. The basic properties of this system are as follows (1) the Sm C^* phase is metastable in temperature range of the Sm CA^*_A stability (2) the double inversions of the helix handedness at Sm C^* -- Sm CA^*_A and Sm CA^*_A% -- re-Sm C^* phase transitions were found (3) the threshold electric field that is necessary to induce synclinic ordering in the Sm CA^*_A phase decreases near both Sm CA^*_A -- Sm C^* and Sm CA^*_A -- re-Sm C^* phase boundaries, and it has maximum in the middle of the Sm CA^*_A stability region. All these properties are properly described by simple Landau model that accounts for nearest neighboring layer steric interactions and quadrupolar ordering only.Comment: 10 pages, 5 figures, submitted to PR

    Flexoelectricity and piezoelectricity - reason for rich variety of phases in antiferroelectric liquid crystals

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    The free energy of antiferroelectric liquid crystal which takes into account polar order explicitly is presented. Steric, van der Waals, piezoelectric and flexoelectric interactions to the nearest layers and dipolar electrostatic interactions to the nearest and to the next nearest layers induce indirect tilt interactions with chiral and achiral properties, which extend to the third and to the fourth nearest layers. Chiral indirect interactions between tilts can be large and induce helicoidal modulations even in systems with negligible chiral van der Waals interactions. If indirect chiral interactions compete with chiral van der Waals interactions, the helix unwinding is possible. Although strength of microscopic interactions change monotonically with decreasing temperature, effective interlayer interactions change nonmonotonically and give rise to nonmonotouous change of modulation period through various phases. Increased enatiomeric excess i.e. increased chirality changes the phase sequence.Comment: 4 pages, 1 figur

    Liquid Crystal-Solid Interface Structure at the Antiferroelectric-Ferroelectric Phase Transition

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    Total Internal Reflection (TIR) is used to probe the molecular organization at the surface of a tilted chiral smectic liquid crystal at temperatures in the vicinity of the bulk antiferroelectric-ferroelectric phase transition. Data are interpreted using an exact analytical solution of a real model for ferroelectric order at the surface. In the mixture T3, ferroelectric surface order is expelled with the bulk ferroelectric-antiferroelectric transition. The conditions for ferroelectric order at the surface of an antiferroelectric bulk are presented

    Unexpected electric-field-induced antiferroelectric liquid crystal phase in the Sm C*α temperature range and the discrete flexoelectric effect

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    The unique nanometer-sized helical structure in SmCα∗ may sometimes evolve continuously to the micrometer-sized one in SmC∗; conceivably ferroelectric SmCα∗ is to be unwound by an applied electric field. By drawing electric-field-induced birefringence contours in the field-temperature phase diagram and by studying the superlattice structure of the field-induced subphase with resonant x-ray scattering, we established that an applied field unexpectedly stabilizes the well-known antiferroelectric four-layer biaxial subphase as well as the other prototypal ferrielectric three-layer one in the SmCα∗ temperature range; the effective long-range interlayer interaction due to the discrete flexoelectric effect actually plays an important role in stabilizing not only the biaxial subphases but also the optically uniaxial SmCα∗ subphase, contrary to the notion that the competition between the direct interactions of the nearest-neighbor layers and those of the next-nearest-neighbor layers should be required for the nanometer-sized helical structure

    Evidence for the Role of Proton Shell Closure in Quasifission Reactions from X-Ray Fluorescence of Mass-Identified Fragments

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    The atomic numbers and the masses of fragments formed in quasifission reactions are simultaneously measured at scission in Ti48+U238 reactions at a laboratory energy of 286 MeV. The atomic numbers are determined from measured characteristic fluorescence x rays, whereas the masses are obtained from the emission angles and times of flight of the two emerging fragments. For the first time, thanks to this full identification of the quasifission fragments on a broad angular range, the important role of the proton shell closure at Z=82 is evidenced by the associated maximum production yield, a maximum predicted by time-dependent Hartree-Fock calculations. This new experimental approach gives now access to precise studies of the time dependence of the N/Z (neutron over proton ratios of the fragments) evolution in quasifission reactions.The authors acknowledge support from the Australian Research Council through Discovery Grants No. FL110100098, No. FT120100760, No. DP130101569, No. DE140100784, No. DP160 101254, and No. DP170102318. Support for accelerator operations through the NCRIS program is acknowledged. Two of us (C. S. and M. A.) acknowledge support from the Scientific Mobility Program of the Embassy of France in Australia. This research was undertaken with the assistance of resources from the National Computational Infrastructure (NCI), which is supported by the Australian Government

    Bone turnover in elderly men: relationships to change in bone mineral density

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    BACKGROUND: It is not clear whether bone turnover markers can be used to make inference regarding changes in bone mineral density (BMD) in untreated healthy elderly men. The present study was designed to address three specific questions: (i) is there a relationship between bone turnover markers and femoral neck BMD within an individual; (ii) is there a relationship between baseline measurements of bone turnover markers and subsequent change in BMD; and (iii) is there a relationship between changes in bone turnover markers and changes in femoral neck BMD? METHODS: The present study was part of the on-going Dubbo Osteoporosis Epidemiology Study, which was designed as a prospective investigation. Men who had had at least 3 sequential visits with serum samples available during follow-up were selected from the study population. Serum C-terminal telopeptide of type I collagen (sICTP), N-terminal propeptide of type I collagen (sPINP) and femoral neck BMD were measured by competitive radioimmunoassays. Femoral neck bone mineral density (BMD) was measured by a densitometer (GE Lunar Corp, Madison, WI). Various mixed-effects models were used to assess the association between the markers and changes in BMD. RESULTS: One hundred and one men aged 70 ± 4.1 years (mean ± SD) met the criteria of selection for analysis. On average, sPINP decreased by 0.7% per year (p = 0.026), sICTP increased by 1.7% per year (p = 0.0002), and femoral neck BMD decreased by 0.4% per year (p < 0.01). Within-subject analysis indicated that changes in BMD were significantly associated with changes in sPINP (p = 0.022), but not with changes in sICTP (p = 0.84). However, neither baseline sPINP (p = 0.50) nor baseline sICTP (p = 0.63) was associated with subsequent changes in BMD. Moreover, changes in BMD were not significantly associated with previous changes in sPINP (p = 0.13) or sICTP (p = 0.95). CONCLUSION: These results suggest that in elderly men of Caucasian background, changes in sPINP were inversely related to changes in BMD within an individual. However, neither sPINP nor sICTP was sufficiently sensitive to predict the rate of change in BMD for a group of individuals or for an individual

    Control of Helical Structure in Ferroelectric Liquid Crystals utilizing Polymer Stabilization

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    Polymer-Stabilized Ferroelectric Liquid Crystals and their Spontaneous Polarization

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