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Paul D Beale

Publications and source records attributed to Paul D Beale.

3 recordsLinked to original sources

Grain-boundary free energy via thermodynamic integration.

In a previous publication by Lusk and Beale [Phys. Rev. E 69, 026117 (2004)], fluctuating cell (FC) theory was used to estimate the free energy of symmetric tilt grain boundaries in an assembly of nearly hard disks. The FC method is much faster than the more traditional thermodynamic integration, but the accuracy of the algorithm has not been assessed in association with persistent defect structures. This motivated the present work wherein the FC free energies are compared directly with the data obtained via thermodynamic integration from an Einstein crystal to an assembly of hard disks. This comparison is made over the range of possible misorientations for symmetric tilt boundaries and indicates that the FC method gives quantitatively accurate estimates for grain-boundary free energy. We also demsonstrate that the FC approximation is quantitatively accurate at determining the free-energy contribution of each particle whether in the bulk or the grain boundary. The FC calculation is about two orders of magnitude faster than a full thermodynamic integration. This approach may offer a numerically efficient means of estimating the free energy of persistent defect structures to greater accuracy than is afforded by the quasiharmonic and local harmonic approximations.

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Grain-boundary free energy in an assembly of elastic disks.

Grain-boundary free energy is estimated as a function of misoriention for symmetric tilt boundaries in an assembly of nearly hard disks. Fluctuating cell theory is used to accomplish this since the most common techniques for calculating interfacial free energy cannot be applied to such assemblies. The results are analogous to those obtained using a Leonard-Jones potential, but in this case the interfacial energy is dominated by an entropic contribution. Disk assemblies colorized with free and specific volume elucidate differences between these two characteristics of boundary structure. Profiles are also provided of the Helmholtz and Gibbs free energies as a function of distance from the grain boundaries. Low angle grain boundaries are shown to follow the classical relationship between dislocation orientation/spacing and misorientation angle.

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Acoustic crystal thermodynamic integration method.

The acoustic crystal thermodynamic integration method is a generalization of the Einstein crystal method developed by Frenkel and Ladd. The name is derived from the acoustic branches of the phonon spectrum of the reference system. The method is designed to calculate the Helmholtz free energy of classical solid phases using Monte Carlo or molecular dynamics simulations. It has several advantages over the Einstein crystal method. For large systems, the Einstein crystal method suffers from very long correlation times near the zero coupling limit because the reference system breaks the overall translational symmetry of model systems. The acoustic crystal method does not break translational symmetry, so correlation times for the acoustic crystal are small. This makes the acoustic crystal method superior to the Einstein crystal method for large system sizes. Also the acoustic crystal method does not artificially introduce long-range order in low-dimensional systems.

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