Abstract:We studied the two-dimensional freezing transitions in monolayers of microgel colloidal spheres with shortranged repulsions in video-microscopy experiments, and monolayers of hard disks, and Yukawa particles in simulations. These systems share two common features at the freezing points: (1) the bimodal distribution profile of the local orientational order parameter; (2) the two-body excess entropy, s 2 , reaches −4.5 ± 0.5 k B . Both features are robust and sensitive to the freezing points, so that they can po… Show more
“…Around φ = 0.65-0.69, however, there is a marked change in slope, which coincides with the start of the liquid-hexatic coexistence region. In [42] it was reported that at the melting transition −S 2 /k B takes the value of 4.5, which is indicated by the dashed horizontal line in figure 4(b). Our data reach this value at an area fraction of just over φ = 0.69, i.e.…”
Recently, the full phase behaviour of 2D colloidal hard spheres was experimentally established, and found to involve a first order liquid to hexatic transition and a continuous hexatic to crystal transition (Thorneywork et al 2017 Phys. Rev. Lett. 118 158001). Here, we expand upon this work by considering the behaviour of the bond-orientational correlation time and Frank's constant in the region of these phase transitions. We also consider the excess entropy, as calculated from the radial distribution functions, for a wide range of area fractions covering the liquid, hexatic and crystal phases. In all cases, the behaviour of these quantities further corroborates the previously reported melting scenario of 2D colloidal hard spheres.
“…Around φ = 0.65-0.69, however, there is a marked change in slope, which coincides with the start of the liquid-hexatic coexistence region. In [42] it was reported that at the melting transition −S 2 /k B takes the value of 4.5, which is indicated by the dashed horizontal line in figure 4(b). Our data reach this value at an area fraction of just over φ = 0.69, i.e.…”
Recently, the full phase behaviour of 2D colloidal hard spheres was experimentally established, and found to involve a first order liquid to hexatic transition and a continuous hexatic to crystal transition (Thorneywork et al 2017 Phys. Rev. Lett. 118 158001). Here, we expand upon this work by considering the behaviour of the bond-orientational correlation time and Frank's constant in the region of these phase transitions. We also consider the excess entropy, as calculated from the radial distribution functions, for a wide range of area fractions covering the liquid, hexatic and crystal phases. In all cases, the behaviour of these quantities further corroborates the previously reported melting scenario of 2D colloidal hard spheres.
“…However, the first-order nature of the liquid-hexatic transition is very weak, and the transition roughly obeys the KTHNY scenario. This basic behavior is common to other systems including particles interacting with soft repulsive potentials [13][14][15][16] and those with attractive potentials such as the Lennard-Jones potential [17], although it has recently be shown that the nature of the transitions depends on the softness of the potential in a delicate manner [16]. Monolayer granular matter has provided a model experimental system to study this fundamental problem.…”
Self-organization of active matter as well as driven granular matter in nonequilibrium dynamical states has attracted considerable attention not only from the fundamental and application viewpoints but also as a model to understand the occurrence of such phenomena in nature. These systems share common features originating from their intrinsically out-of-equilibrium nature, and how energy dissipation affects the state selection in such nonequilibrium states remains elusive. As a simple model system, we consider a nonequilibrium stationary state maintained by continuous energy input, relevant to industrial processing of granular materials by vibration and/or flow. More specifically, we experimentally study roles of dissipation in self-organization of a driven granular particle monolayer. We find that the introduction of strong inelasticity entirely changes the nature of the liquid-solid transition from two-step (nearly) continuous transitions (liquid-hexatic-solid) to a strongly discontinuous first-order-like one (liquid-solid), where the two phases with different effective temperatures can coexist, unlike thermal systems, under a balance between energy input and dissipation. Our finding indicates a pivotal role of energy dissipation and suggests a novel principle in the self-organization of systems far from equilibrium. A similar principle may apply to active matter, which is another important class of out-of-equilibrium systems. On noting that interaction forces in active matter, and particularly in living systems, are often nonconservative and dissipative, our finding may also shed new light on the state selection in these systems.
“…The fluid becomes unstable when the average centre-to-centre distance between alternating nearest neighbors becomes shorter than two disk diameters and the resulting gap between them is shorter than hard-core diameter and does not allow for the central disk to wander. Such a caging concept allows for both the quantitative and qualitative description of the thermodynamics of freezing transition in monodisperse hard-disk fluid and has been already utilized to discuss percolation [8].…”
The freezing mechanism, recently suggested for a monodisperse hard-disk fluid [Huerta et al, Phys. Rev. E, 2006, 74, 061106] is extended here to an equimolar binary hard-disk mixtures. We are showing that for diameter ratios, smaller than 1.15 the global orientational order parameter of the binary mixture behaves like in the case of a monodisperse fluid. Namely, by increasing the disk number density there is a tendency to form a crystallinelike phase. However, for diameter ratios larger than 1.15 the binary mixtures behave like a disordered fluid. We use some of the structural and thermodynamic properties to compare and discuss the behavior as a function of diameter ratio and packing fraction.
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