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D Schebarchov

Publications and source records attributed to D Schebarchov.

3 recordsLinked to original sources

Superheating and solid-liquid phase coexistence in nanoparticles with nonmelting surfaces.

We present a phenomenological model of melting in nanoparticles with facets that are only partially wet by their liquid phase. We show that in this model, as the solid nanoparticle seeks to avoid coexistence with the liquid, the microcanonical melting temperature can exceed the bulk melting point and that the onset of coexistence is a first-order transition. We show that these results are consistent with molecular dynamics simulations of aluminum nanoparticles which remain solid above the bulk melting temperature.

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Static, transient, and dynamic phase coexistence in metal nanoclusters.

Molecular dynamics simulations are used to examine static and dynamic coexistence between solid and liquid phases in nanoscale silver, copper, and nickel clusters. We find static coexistence in the 561-atom copper icosahedron, the 561-atom silver icosahedron, and the 923-atom nickel icosahedron, and in cluster sizes above these thresholds, but not in smaller clusters. Nonetheless, in smaller clusters we typically observe either dynamic coexistence between fully solid and liquid states or transient coexistence which is essentially dynamic coexistence between a fully solid state and a solid-liquid state.

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Transition from icosahedral to decahedral structure in a coexisting solid-liquid nickel cluster.

We have used molecular dynamics simulations to construct a microcanonical caloric curve for a 1415 atom Ni icosahedron. Prior to melting, the Ni cluster exhibits static solid-liquid phase coexistence. Initially, a partial icosahedral structure coexists with a partially wetting melt. However, at energies very close to the melting point the icosahedral structure is replaced by a truncated decahedral structure that is almost fully wet by the melt. This structure remains until the cluster fully melts. The transition appears to be driven by a preference for the melt to wet the decahedral structure.

Journal Article↗