Homogeneous Nucleation in Inhomogeneous Media I: Nucleation in a Temperature Gradient

We introduce a general formalism to analyze nucleation phenomena in inhomogeneous media which considers the influence of the metastable phase, which is treated as a heat bath in which clusters are embedded, in the dynamics of the nucleation process. A kinetic equation for the evolution of the probability density of the clusters, taking into account possible inhomogeneities in the bath, is derived using mesoscopic nonequilibrium thermodynamics. From it, we obtain the nucleation rate and analyze the role played by the metastable phase in the process. We discuss in particular condensation and polymer crystallization in a temperature gradient.Comment: 18 pages, 3 figures, accepted for publication in J. Chem. Phy

Deviations from Arrhenius dynamics in high temperature liquids, a possible collapse, and a viscosity bound

Liquids realize a highly complex state of matter in which strong competing kinetic and interaction effects come to life. As such, liquids are, generally, more challenging to understand than either gases or solids. In weakly interacting gases, the kinetic effects dominate. By contrast, low temperature solids typically feature far smaller fluctuations about their ground state. Notwithstanding their complexity, with the exception of quantum fluids (e.g., superfluid helium) and supercooled liquids (including glasses), various aspects of common liquid dynamics such as their dynamic viscosity are often assumed to be given by rather simple, Arrhenius-type, activated forms with nearly constant (i.e., temperature independent) energy barriers. In this paper, we analyze experimentally measured viscosities of numerous liquids far above their equilibrium melting temperature to see how well this assumption fares. We find, for the investigated liquids, marked deviations from simple activated dynamics. Even far above their equilibrium melting temperatures, as the temperature drops, the viscosity of these liquids increases more strongly than predicted by activated dynamics dominated by a single uniform energy barrier. For metallic fluids, the scale of the prefactors of the best Arrhenius fits for the viscosity is typically consistent with that given by the product (nh) with n the number density and h Planck's constant. More generally, in various fluids (whether metallic or nonmetallic) that we examined, (nh) constitutes a lower bound scale on the viscosity. We find that a scaling of the temperature axis (complementing that of the viscosity) leads to a partial collapse of the temperature dependent viscosities of different fluids; such a scaling allows for a functional dependence of the viscosity on temperature that includes yet is far more general than activated Arrhenius form alone. We speculate on relations between non-Arrhenius dynamics and thermodynamic observables

Structure of the icosahedral Ti-Zr-Ni quasicrystal

The atomic structure of the icosahedral Ti-Zr-Ni quasicrystal is determined by invoking similarities to periodic crystalline phases, diffraction data and the results from ab initio calculations. The structure is modeled by decorations of the canonical cell tiling geometry. The initial decoration model is based on the structure of the Frank-Kasper phase W-TiZrNi, the 1/1 approximant structure of the quasicrystal. The decoration model is optimized using a new method of structural analysis combining a least-squares refinement of diffraction data with results from ab initio calculations. The resulting structural model of icosahedral Ti-Zr-Ni is interpreted as a simple decoration rule and structural details are discussed.Comment: 12 pages, 8 figure

Crystallization of a supercooled liquid and of a glass - Ising model approach

Using Monte Carlo simulations we study crystallization in the three-dimensional Ising model with four-spin interaction. We monitor the morphology of crystals which grow after placing crystallization seeds in a supercooled liquid. Defects in such crystals constitute an intricate and very stable network which separate various domains by tensionless domain walls. We also show that the crystallization which occurs during the continuous heating of the glassy phase takes place at a heating-rate dependent temperature.Comment: 7 page

An epitaxial model for heterogeneous nucleation on potent substrates

© The Minerals, Metals & Materials Society and ASM International 2012In this article, we present an epitaxial model for heterogeneous nucleation on potent substrates. It is proposed that heterogeneous nucleation of the solid phase (S) on a potent substrate (N) occurs by epitaxial growth of a pseudomorphic solid (PS) layer on the substrate surface under a critical undercooling (ΔT ). The PS layer with a coherent PS/N interface mimics the atomic arrangement of the substrate, giving rise to a linear increase of misfit strain energy with layer thickness. At a critical thickness (h ), elastic strain energy reaches a critical level, at which point, misfit dislocations are created to release the elastic strain energy in the PS layer. This converts the strained PS layer to a strainless solid (S), and changes the initial coherent PS/N interface into a semicoherent S/N interface. Beyond this critical thickness, further growth will be strainless, and solidification enters the growth stage. It is shown analytically that the lattice misfit (f) between the solid and the substrate has a strong influence on both h and ΔT ; h decreases; and ΔT increases with increasing lattice misfit. This epitaxial nucleation model will be used to explain qualitatively the generally accepted experimental findings on grain refinement in the literature and to analyze the general approaches to effective grain refinement.EPSRC Centre for Innovative Manufacturing in Liquid Metal Engineerin

Homogeneous nucleation of quark-gluon plasma, finite size effects and long-lived metastable objects

The general formalism of homogeneous nucleation theory is applied to study the hadronization pattern of the ultra-relativistic quark-gluon plasma (QGP) undergoing a first order phase transition. A coalescence model is proposed to describe the evolution dynamics of hadronic clusters produced in the nucleation process. The size distribution of the nucleated clusters is important for the description of the plasma conversion. The model is most sensitive to the initial conditions of the QGP thermalization, time evolution of the energy density, and the interfacial energy of the plasma-hadronic matter interface. The rapidly expanding QGP is first supercooled by about $\Delta T = T - T_c = 4-6$. Then it reheats again up to the critical temperature T_c. Finally it breaks up into hadronic clusters and small droplets of plasma. This fast dynamics occurs within the first $5-10 fm/c$. The finite size effects and fluctuations near the critical temperature are studied. It is shown that a drop of longitudinally expanding QGP of the transverse radius below 4.5 fm can display a long-lived metastability. However, both in the rapid and in the delayed hadronization scenario, the bulk pion yield is emitted by sources as large as 3-4.5 fm. This may be detected experimentally both by a HBT interferometry signal and by the analysis of the rapidity distributions of particles in narrow p_T-intervals at small p_T on an event-by-event basis.Comment: 29 pages, incl. 12 figures and 1 table; to be published in Phys. Rev.