6533b873fe1ef96bd12d4488
RESEARCH PRODUCT
Classical nucleation theory for the crystallization kinetics in sheared liquids
David RichardThomas Specksubject
Materials scienceStatistical Mechanics (cond-mat.stat-mech)NucleationFOS: Physical sciencesThermodynamicsHard spheresStatistical mechanicsComputational Physics (physics.comp-ph)law.inventionPhysics::Fluid DynamicsShear modulusSurface tensionSimple shearlawClassical nucleation theoryCrystallizationPhysics - Computational PhysicsCondensed Matter - Statistical Mechanicsdescription
While statistical mechanics provides a comprehensive framework for the understanding of equilibrium phase behavior, predicting the kinetics of phase transformations remains a challenge. Classical nucleation theory (CNT) provides a thermodynamic framework to relate the nucleation rate to thermodynamic quantities such as pressure difference and interfacial tension through the nucleation work necessary to spawn critical nuclei. However, it remains unclear whether such an approach can be extended to the crystallization of driven melts that are subjected to mechanical stresses and flows. Here, we demonstrate numerically for hard spheres that the impact of simple shear on the crystallization rate can be rationalized within the CNT framework by an additional elastic work proportional to the droplet volume. We extract the local stress and strain inside solid droplets, which yield size-dependent values for the shear modulus that are about half of the bulk value. Finally, we show that for a complete description one also has to take into account the change of interfacial work between the strained droplet and the sheared liquid. From scaling reasons, we expect this extra contribution to dominate the work formation of small nuclei but become negligible compared to the elastic work for droplets composed of a few hundreds of particles.
year | journal | country | edition | language |
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2019-04-01 | Physical Review E |