Solution-based thermodynamic modeling, aided by first-principles calculations, is employed here to examine phase transformations in the Al-Sm binary system which may give rise to product phases that are metastable or have a composition that deviates substantially from equilibrium. In addition to describing the pure undercooled Al liquid with a two-state model that accounts for structural ordering, thermodynamic descriptions of the fcc phase, and intermediate compounds (Al4Sm-β, Al11Sm3-α, Al3Sm-δ, and Al2Sm-σ) are reanalyzed using special quasirandom structure and first-principles calculations. The possible phase compositions are presented over a range of temperatures using a "Baker-Cahn" analysis of the energetics of solidification and compared with reports of rapid solidification. The energetics associated with varying degrees of chemical partitioning are quantified and compared with experimental observations of the metastable Al11Sm3-α primary phase and reports of amorphous solids. Keywords Ames Laboratory Disciplines Condensed Matter Physics | Engineering Physics | Materials Science and Engineering CommentsThis article is from Physical Review B 78 (2008) Solution-based thermodynamic modeling, aided by first-principles calculations, is employed here to examine phase transformations in the Al-Sm binary system which may give rise to product phases that are metastable or have a composition that deviates substantially from equilibrium. In addition to describing the pure undercooled Al liquid with a two-state model that accounts for structural ordering, thermodynamic descriptions of the fcc phase, and intermediate compounds ͑Al 4 Sm-␤, Al 11 Sm 3 -␣, Al 3 Sm-␦, and Al 2 Sm-͒ are reanalyzed using special quasirandom structure and first-principles calculations. The possible phase compositions are presented over a range of temperatures using a "Baker-Cahn" analysis of the energetics of solidification and compared with reports of rapid solidification. The energetics associated with varying degrees of chemical partitioning are quantified and compared with experimental observations of the metastable Al 11 Sm 3 -␣ primary phase and reports of amorphous solids.

Soft materials with high thermal conductivity are critical for flexible electronics, energy storage and transfer, and human-interface devices and robotics. However, fundamental heat transport limitations in soft and deformable materials present significant challenges for achieving high thermal conductivity. Here, a systematic study of soft composites with solid, liquid, and solid-liquid multiphase metal fillers dispersed in elastomers reveals key strategies to tune the thermal-mechanical response of soft materials. Experiments supported by thermodynamic and kinetic modeling demonstrate that multiphase systems quickly form intermetallics that solidify and degrade mechanical response with modest gains in thermal conductivity. In contrast, liquid metal 1 This is the author manuscript accepted for publication and has undergone full peer review but has not been through the copyediting, typesetting, pagination and proofreading process, which may lead to differences between this version and the Version of Record. Please cite this article as

No abstract

No abstract

No abstract

No abstract

No abstract

CALPHAD assessment of the thermodynamic properties of a series of Pu-based alloys is briefly presented together with some results on the kinetics of phase formation and transformations in Pu-Ga alloys.