ترغب بنشر مسار تعليمي؟ اضغط هنا

Demixing and orientational ordering in mixtures of rectangular particles

93   0   0.0 ( 0 )
 نشر من قبل Enrique Velasco Dr
 تاريخ النشر 2007
  مجال البحث فيزياء
والبحث باللغة English




اسأل ChatGPT حول البحث

Using scaled-particle theory for binary mixtures of two-dimensional hard particles with rotational freedom, we analyse the stability of nematic phases and the demixing phase behaviour of a variety of mixtures, focussing on cases where at least one of the components consists of hard rectangles or hard squares. A pure fluid of hard rectangles may exhibit, aside from the usual uniaxial nematic phase, an additional (tetratic) oriented phase, possessing two directors, which is the analogue of the biaxial or cubatic phases in three- dimensional fluids. There is computer simulation evidence that the tetratic phase might be stable with respect to phases with spatial order for rectangles with low aspect ratios. As hard rectangles are mixed with other particles not possessing stable tetratic order by themselves, the tetratic phase is destabilised, via a first- or second-order phase transition, to uniaxial nematic or isotropic phases; for hard rectangles of low aspect ratio tetratic order persists in a relatively large range of volume fractions. The order of these transitions depends on the particle geometry, dimensions and thermodynamic conditions of the mixture. The second component of the mixture has been chosen to be hard discs or disco-rectangles, the geometry of which is different from that of rectangles, leading to packing frustration and demixing behaviour, or simply rectangles of different aspect ratio. These mixtures may be good candidates for observing thermodynamically stable tetratic phases in monolayers of hard particles. Finally, demixing between fluid (isotropic--tetratic or tetratic--tetratic) phases is seen to occur in mixtures of hard squares of different sizes when the size ratio is sufficiently large.

قيم البحث

اقرأ أيضاً

239 - Bao-quan Ai , Zhi-gang Shao , 2018
We study a binary mixture of polar chiral (counterclockwise or clockwise) active particles in a two-dimensional box with periodic boundary conditions. Beside the excluded volume interactions between particles, particles are also subject to the polar velocity alignment. From the extensive Brownian dynamics simulations, it is found that the particle configuration (mixing or demixing) is determined by the competition between the chirality difference and the polar velocity alignment. When the chirality difference competes with the polar velocity alignment, the clockwise particles aggregate in one cluster and the counterclockwise particles aggregate in the other cluster, thus particles are demixed and can be separated. However, when the chirality difference or the polar velocity alignment is dominated, particles are mixed. Our findings could be used for the experimental pursuit of the separation of binary mixtures of chiral active particles.
The combinations of particle aspect ratio and enthalpic-barrier templates that lead to translational and orientational ordering of monolayers of rectangular particles are determined using Monte Carlo simulations and density functional theory. For suf ficiently high enthalpic barriers, we find that only specific combinations of particle sizes and template spacings lead to ordered arrays. The pattern multiplication factor provided by the template extends to approximately ten times the smallest dimension of the particle.
The concept of symmetry breaking has been a propelling force in understanding phases of matter. While rotational symmetry breaking is one of the most prevalent examples, the rich landscape of orientational orders breaking the rotational symmetries of isotropic space, i.e. $O(3)$, to a three-dimensional point group remain largely unexplored, apart from simple examples such as ferromagnetic or uniaxial nematic ordering. Here we provide an explicit construction, utilizing a recently introduced gauge theoretical framework, to address the three-dimensional point-group-symmetric orientational orders on a general footing. This unified approach allows us to enlist order parameter tensors for all three dimensional point groups. By construction, these tensor order parameters are the minimal set of simplest tensors allowed by the symmetries that uniquely characterize the orientational order. We explicitly give these for the point groups ${C_n, D_n, T, O, I} subset SO(3)$ and ${C_{nv}, S_n, C_{nh}, D_{nh}, D_{nd}, T_h, T_d, O_h, I_h}subset O(3)$ for $n={1,2,3,4,6, infty}$. This central result may be perceived as a roadmap for identifying exotic orientational orders that may become more and more in reach in view of rapid experimental progress in e.g. nano-colloidal systems and novel magnets.
We introduce the spatial correlation function $C_Q(r)$ and temporal autocorrelation function $C_Q(t)$ of the local tetrahedral order parameter $Qequiv Q(r,t)$. Using computer simulations of the TIP5P model of water, we investigate $C_Q(r)$ in a broad region of the phase diagram. First we show that $C_Q(r)$ displays anticorrelation at $rapprox 0.32$nm at high temperatures $T>T_Wapprox 250$ K, which changes to positive correlation below the Widom line $T_W$. Further we find that at low temperatures $C_Q(t)$ exhibits a two-step temporal decay similar to the self intermediate scattering function, and that the corresponding correlation time $tau_Q$ displays a dynamic crossover from non-Arrhenius behavior for $T>T_W$ to Arrhenius behavior for $T<T_W$. Finally, we define an orientational entropy $S_Q$ associated with the {it local} orientational order of water molecules, and show that $tau_Q$ can be extracted from $S_Q$ using an analog of the Adam-Gibbs relation.
We investigate the phase behavior and kinetics of a monodisperse mixture of active (textit{i.e.}, self-propelled) and passive isometric Brownian particles through Brownian dynamics simulations and theory. As in a purely active system, motility of the active component triggers phase separation into a dense and a dilute phase; in the dense phase we further find active-passive segregation, with rafts of passive particles in a sea of active particles. We find that phase separation from an initially disordered mixture can occur with as little as 15 percent of the particles being active. Finally, we show that a system prepared in a suitable fully segregated initial state reproducibly self-assembles an active corona which triggers crystallization of the passive core by initiating a compression wave. Our findings are relevant to the experimental pursuit of directed self-assembly using active particles.
التعليقات
جاري جلب التعليقات جاري جلب التعليقات
سجل دخول لتتمكن من متابعة معايير البحث التي قمت باختيارها
mircosoft-partner

هل ترغب بارسال اشعارات عن اخر التحديثات في شمرا-اكاديميا