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Grzegorz Pająk

Publications and source records attributed to Grzegorz Pająk.

7 recordsLinked to original sources

Nematic twist--bend phase in an external field

Nematic twist--bend is the fifth nematic phase recognized in nature. This phase exhibits spiral orientational order, thus it is a chiral structure and it can be stabilized in systems composed of achiral molecules. The microscopic origin of this spontaneous chiral symmetry breaking is to a large extent unknown but phenomenologically it appears stabilized by assuming coupling between steric polar and orientational orderings. Understanding of how external fields affect the stability of this phase is of great intellectual interest and of relevance to potential applications. Within mesoscopic Landau--de Gennes theory we find that for compounds with positive anisotropy the helix unwinds to a polar uniaxial nematic, however negative material anisotropy gives rise to a rich sequence of new nematic phases obtained via mechanism of flattening the conical spiral.

cond-mat.soft↗

Twist-bend nematic phases of bent-shaped biaxial molecules

How change in molecular structure can affect relative stability and structural properties of the twist-bend nematic phase (N$_\text{TB}$)? Here we extend the mean-field model [C. Greco et al., Soft Matter, 2014, 10, 9318] for bent-shaped achiral molecules, to study the influence of arm molecular biaxiality and the value of molecule's bend angle on relative stability of N$_\text{TB}$. In particular we show that by controlling biaxiality of molecule's arms up to four ordered phases can become stable. They involve locally uniaxial and biaxial variants of N$_\text{TB}$, together with the uniaxial and the biaxial nematic phases. However, the V-shaped molecule show stronger ability to form stable N$_\text{TB}$ than a biaxial nematic phase, where the latter phase appears in the phase diagram only for bend angles greater than $140^\circ$ and for large biaxiality of the two arms.

cond-mat.soft↗

In a search for a shape maximizing packing fraction for two-dimensional random sequential adsorption

Random sequential adsorption (RSA) of various two dimensional objects is studied in order to find a shape which maximizes the saturated packing fraction. This investigation was begun in our previous paper [Cieśla et al., Phys. Chem. Chem. Phys. 17, 24376 (2015)], where the densest packing was studied for smoothed dimers. Here this shape is compared with a smoothed $n$-mers, spherocylinders and ellipses. It is found that the highest packing fraction out of the studied shapes is $0.58405 \pm 0.0001$ and is obtained for ellipses having long-to-short axis ratio of $1.85$, which is also the largest anisotropy among the investigated shapes.

cond-mat.mtrl-sci↗

Modulated nematic structures induced by chirality and steric polarization

What kind of one-dimensional modulated nematic structures (ODMNS) can form nonchiral and chiral bent-core and dimeric materials? Here, using Landau-deGennes theory of nematics, extended to account for molecular steric polarization, we study a possibility of formation of ODMNS, both in nonchiral and intrinsically chiral liquid crystalline materials. Besides nematic and cholesteric phases, we find four bulk ODMNS for nonchiral materials, two of which have not been reported so far. These new structures are longitudinal ($N_{LP}$) and transverse ($N_{TP}$) periodic waves where the polarization field being periodic in one dimension stays parallel and perpendicular, respectively, to the wave vector. The other two phases have all characteristic features of the twist-bend nematic phase ($N_{TB}$) and the splay-bend nematic phase ($N_{SB}$), but their fine structure appears more complex than that considered so far. The presence of molecular chirality converts nonchiral $N_{TP}$ and $N_{SB}$ into new $N_{TB}$ phases. Interestingly, the nonchiral $N_{LP}$ phase can stay stable even in the presence of intrinsic molecular chirality. Exemplary phase diagrams provide further insights into the relative stability of these new modulated nematic structures.

cond-mat.soft↗

Shapes for maximal coverage for two-dimensional random sequential adsorption

The random sequential adsorption of various particle shapes is studied in order to determine the influence of particle anisotropy on the saturated random packing. For all tested particles there is an optimal level of anisotropy which maximizes the saturated packing fraction. It is found that a concave shape derived from a dimer of disks gives a packing fraction of 0.5833, which is comparable to the maximum packing fraction of ellipsoids and spherocylinders and higher than any other studied shape. Discussion why this shape is so beneficial for random sequential adsorption is given.

cond-mat.mtrl-sci↗

Chiral Symmetry Breaking in Bent-Core Liquid Crystals

By molecular modeling we demonstrate that the nematic long-range order discovered in bent-core liquid crystal systems should reveal further spatially homogeneous phases. Two of them are identified as a tetrahedratic nematic ($N_T$) phase with $D_{2d}$ symmetry and a chiral tetrahedratic nematic ($N_T^*$) phase with $D_2$ symmetry. These new phases were found for a lattice model with quadrupolar and octupolar anisotropic interactions using Mean Field theory and Monte Carlo simulations. The phase diagrams exhibit tetrahedratic ($T$), $N_T$ and $N_T^*$ phases, in addition to ordinary isotropic ($I$), uniaxial nematic ($N_U$) and biaxial nematic ($N_B$) phases. To our knowledge, this is the first molecular model with spontaneous chiral symmetry breaking in non-layered systems.

cond-mat.soft↗

Stability of Biaxial Nematic Phase for Systems with Variable Molecular Shape Anisotropy

We study the influence of fluctuations in molecular shape on the stability of the biaxial nematic phase by generalizing the mean field model of Mulder and Ruijgrok [Physica A {\bf 113}, 145 (1982)]. We limit ourselves to the case when the molecular shape anisotropy, represented by the alignment tensor, is a random variable of an annealed type. A prototype of such behavior can be found in lyotropic systems - a mixture of potassium laurate, 1-decanol, and $D_2O$, where distribution of the micellar shape adjusts to actual equilibrium conditions. Further examples of materials with the biaxial nematic phase, where molecular shape is subject to fluctuations, are thermotropic materials composed of flexible trimeric- or tetrapod-like molecular units. Our calculations show that the Gaussian equilibrium distribution of the variables describing molecular shape (dispersion force) anisotropy gives rise to new classes of the phase diagrams, absent in the original model. Depending on properties of the shape fluctuations, the stability of the biaxial nematic phase can be either enhanced or depressed, relative to the uniaxial nematic phases. In the former case the splitting of the Landau point into two triple points with a direct phase transition line from isotropic to biaxial phase is observed.

cond-mat.soft↗