Chandra Shekhar Pati Tripathi

Different modulated structures of topological defects stabilized by adaptive targeting nanoparticles

It is demonstrated that interactions between nanoparticles and topological defects induce a twist-grain boundary phase in a chiral liquid crystal. The occurrence of this phase, the analogue of the Shubnikov phase in type-II superconductors, is driven by direct interactions between surface-functionalized CdSe quantum dots and screw dislocations. It is shown that, within an adaptive-defect-core-targeting mechanism, nanoparticles of appropriate size and functionalization adapt to qualitatively different cores of topological defects such as disclination lines and screw dislocations. This mechanism enables the effective reduction of the energetically costly, singular defect core volume, while the surrounding phase ordering remains relatively weakly affected. The findings suggest new pathways towards the controlled assembly of superstructures in diverse, symmetry-broken, condensed-matter systems, ranging from nanoparticle-decorated liquid crystals to superconductors.

Blue phase III widening in CE6-dispersed surface-functionalised CdSe nanoparticles

The phase transition behaviour of the chiral liquid crystal CE6 doped with spherical surface-functionalised CdSe nanoparticles has been examined by means of high-resolution adiabatic scanning calorimetry and polarising microscopy. The addition of nanoparticles results in an essentially stabilised blue phase III. The phase diagram is displayed upon heating and cooling and the enthalpy changes involved in the conversion between the blue phases are determined. The dispersion of functionalised nanoparticles is prominent for the stabilisation of blue phase III, which is potentially useful for applications, especially if applied on liquid crystals that exhibit blue phases close to room temperature.

Electrical conductivity and glass formation in nitrile-functionalized pyrrolidinium bis(trifluoromethylsulfonyl)imide ionic liquids: chain length and odd–even effects of the alkyl spacer between the pyrrolidinium ring and the nitrile group

The electrical conductivity of a series of pyrrolidinium bis(trifluoromethylsulfonyl)imide ionic liquids, functionalized with a nitrile (cyano) group at the end of an alkyl chain attached to the cation, was studied in the temperature range between 173 K and 393 K. The glass formation of the ionic liquids is influenced by the length of the alkyl spacer separating the nitrile function from the pyrrolidinium ring. The electrical conductivity and the viscosity do not show a monotonic dependence on the alkyl spacer length, but rather an odd-even effect. An explanation for this behavior is given, including the potential energy landscape picture for the glass transition.

Large heat capacity anomaly near the consolute point of the binary mixture nitromethane and 3-pentanol

The large critical anomaly in the isobaric heat capacity C(p,x)(T) of the binary mixture nitromethane + 3-pentanol is measured using high-resolution adiabatic scanning calorimetry. The unique features of this technique provided an alternative approach to the study of the critical behavior of C(p,x)(T), providing further C(p,x)(T) related quantities from which valuable information could be extracted. Our data are in full agreement with the predictions of the Modern Theory of Critical Phenomena; specifically, 3D-Ising model values for the critical exponent α and the universal amplitude ratio values of the leading critical amplitudes, as well as for the first correction-to-scaling ones, provide the optimum fits to represent the experimental data. Evidence for the need of higher-order terms, i.e., first correction-to-scaling term, is given. The large value of the coefficient E for the linear temperature dependence of the background obtained is ascribed to a possible contribution of the regular linear background term, of a higher-order asymmetry term, and of the second correction-to-scaling term. Internal consistency of C(p,x)(T) and its related quantities is successfully checked.

Adiabatic scanning calorimetry study of ionic liquid crystals with highly ordered crystal smectic phases

Adiabatic scanning calorimetry was used to study four ionic liquid crystals whose phase sequences include highly ordered crystal smectic phases (crystal smectic E or T phases). The ionic liquids were based on piperidinium or morpholinium cations with long alkyl chains; the anions were tetrafluoroborate or hexafluorophosphate. High-resolution heat capacity and enthalpy data were obtained, from which the total transition heat and latent heat for the observed phase transitions were determined. All transitions displayed a non-zero latent heat and were thus found to be first order.

Evidence from adiabatic scanning calorimetry for the Halperin-Lubensky-Ma effect at the N-SmA phase transitions in mixtures of 7OCB+heptane with an injected SmA phase

The high-resolution adiabatic scanning calorimetric technique has been used to investigate the nematic-smectic A transition (N-SmA in binary mixtures of the non-smectogenic liquid crystal heptyloxycyanobiphenyl (7OCB) and heptane, exhibiting a so-called injected smectic A phase. With the exception of a mixture with the lowest heptane mole fraction for which only an upper limit of 0.2 ± 0.2 J kg−1 for a possible latent heat could be obtained, for all other mixtures finite latent heats were obtained. The mole fraction dependence of the latent heat could be well fitted with a crossover function consistent with a mean-field free energy expression with a non-zero cubic term arising from the Halperin-Lubensky-Ma (HLM) coupling between the SmA order parameter and the orientational director fluctuations. The mole fraction dependence of the heat capacity effective critical exponents is similar to that observed in mixtures of the two liquid crystals octyloxycyanobiphenyl (8OCB) and nonylcyanobiphenyl (9OCB). The thermal behavior observed along the N-SmA phase transition line yields further strong evidence for the HLM coupling effect.