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Register a new userRearrangement of 2D aggregates of droplets under compression: signatures of the energy landscape from crystal to glass
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Added by
Kari Dalnoki-Veress
Publication date
2019
fields
Physics
and research's language is
English
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We study signatures of the energy landscapes evolution through the crystal-to-glass transition by compressing 2D finite aggregates of oil droplets. Droplets of two distinct sizes are used to compose small aggregates in an aqueous environment. Aggregates range from perfectly ordered monodisperse single crystals to disordered bidisperse glasses. The aggregates are compressed between two parallel boundaries, with one acting as a force sensor. The compression force provides a signature of the aggregate composition and gives insight into the energy landscape. In particular, crystals dissipate all the stored energy through single catastrophic fracture events whereas the glassy aggregates break step-by-step. Remarkably, the yielding properties of the 2D aggregates are strongly impacted by even a small amount of disorder.
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Using the potential energy landscape formalism we show that, in the temperature range in which the dynamics of a glass forming system is thermally activated, there exists a unique set of basis glass states each of which is confined to a single metabasin of the energy landscape of a glass forming system. These basis glass states tile the entire configuration space of the system, exhibit only secondary relaxation and are solid-like. Any macroscopic state of the system (whether liquid or glass) can be represented as a superposition of basis glass states and can be described by a probability distribution over these states. During cooling of a liquid from a high temperature, the probability distribution freezes at sufficiently low temperatures describing the process of liquid to glass transition. The time evolution of the probability distribution towards the equilibrium distribution during subsequent aging describes the primary relaxation of a glass.
We develop the elastically collective nonlinear Langevin equation theory of bulk relaxation of glass-forming liquids to investigate molecular mobility under compression conditions. The applied pressure restricts more molecular motion and therefore significantly slows-down the molecular dynamics when increasing the pressure. We quantitatively determine the temperature and pressure dependence of the structural relaxation time. To validate our model, dielectric spectroscopy experiments for three rigid and non-polymeric supramolecules are carried out at ambient and elevated pressures. The numerical results quantitatively agree with experimental data.
The nematic twist-bend (TB) phase, exhibited by certain achiral thermotropic liquid crystalline (LC) dimers, features a nanometer-scale, heliconical rotation of the average molecular long axis (director) with equally probable left- and right-handed domains. On meso to macroscopic scales, the TB phase may be considered as a stack of equivalent slabs or pseudo-layers, each one helical pitch in thickness. The long wavelength fluctuation modes should then be analogous to those of a smectic-A phase, and in particular the hydrodynamic mode combining layer compression and bending ought to be characterized by an effective layer compression elastic constant $B_{eff}$ and average director splay constant $K_1^{eff}$. The magnitude of $K_1^{eff}$ is expected to be similar to the splay constant of an ordinary nematic LC, but due to the absence of a true mass density wave, $B_{eff}$ could differ substantially from the typical value of $sim 10^6$ Pa in a conventional smectic-A. Here we report the results of a dynamic light scattering study, which confirms the pseudo-layer structure of the TB phase with $B_{eff}$ in the range $sim 10^3-10^4$ Pa. We show additionally that the temperature dependence of $B_{eff}$ at the TB to nematic transition is accurately described by a coarse-grained free energy density, which is based on a Landau-deGennes expansion in terms of a heli-polar order parameter that characterizes the TB state and is linearly coupled to bend distortion of the director.
Electrostatic interactions play an important role in numerous self-assembly phenomena, including colloidal aggregation. Although colloids typically have a dielectric constant that differs from the surrounding solvent, the effective interactions that arise from inhomogeneous polarization charge distributions are generally neglected in theoretical and computational studies. We introduce an efficient technique to resolve polarization charges in dynamical dielectric geometries, and demonstrate that dielectric effects emph{qualitatively} alter the predicted self-assembled structures, with surprising colloidal strings arising from many-body effects.
We numerically study the relaxation dynamics of several glass-forming models to their inherent structures, following quenches from equilibrium configurations sampled across a wide range of temperatures. In a mean-field Mari-Kurchan model, we find that relaxation changes from a power-law to an exponential decay below a well-defined temperature, consistent with recent findings in mean-field $p$-spin models. By contrast, for finite-dimensional systems, the relaxation is always algebraic, with a non-trivial universal exponent at high temperatures crossing over to a harmonic value at low temperatures. We demonstrate that this apparent evolution is controlled by a temperature-dependent population of localised excitations. Our work unifies several recent lines of studies aiming at a detailed characterization of the complex potential energy landscape of glass-formers.
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