Prediction of the solid-liquid interface energy of a multicomponent metallic alloy via a solid-liquid interface sublattice model

Based on the theoretical consideration on the size-dependence of solid-liquid interface energy, a model for the intrinsic interface stress of metallic, ionic and semiconductor nanosolid has been developed, free from adjustable parameters. Modeling predictions agree well with experimental observations and other theoretical results.

Download Full-text

Size Range of Solid−Liquid Interface Energy of Organic Crystals

The Journal of Physical Chemistry B ◽

10.1021/jp0202439 ◽

2002 ◽

Vol 106 (16) ◽

pp. 4266-4268 ◽

Cited By ~ 12

Author(s):

Z. Wen ◽

M. Zhao ◽

Q. Jiang

Keyword(s):

Size Range ◽

Interface Energy ◽

Liquid Interface ◽

Organic Crystals ◽

Solid Liquid Interface ◽

Solid Liquid

Download Full-text

Phase-Field Microstructure Solidification of Al–2 wt% Si Alloys

Journal of Engineering Materials and Technology ◽

10.1115/1.4044280 ◽

2019 ◽

Vol 142 (1) ◽

Author(s):

J. B. Allen

Keyword(s):

Directional Solidification ◽

Phase Field ◽

Maximum Concentration ◽

Dendritic Growth ◽

Interface Energy ◽

Liquid Interface ◽

Two Dimensional ◽

Solid Liquid Interface ◽

Solid Liquid ◽

Dilute Alloy

In this work, we develop one- and two-dimensional phase-field simulations to approximate dendritic growth of a binary Al–2 wt% Si alloy. Simulations are performed for both isothermal as well as directional solidification. Anisotropic interface energies are included with fourfold symmetries, and the dilute alloy assumption is imposed. The isothermal results confirm the decrease in the maximum concentration for larger interface velocities as well as reveal the presence of parabolic, dendrite tips evolving along directions of maximum interface energy. The directional solidification results further confirm the formation of distinctive secondary dendritic arm structures that evolve at regular intervals along the unstable solid/liquid interface.

Download Full-text

Determination of the Solid-Liquid Interface Energy in the Al-Cu-Ag System

Metallurgical and Materials Transactions A ◽

10.1007/s11661-007-9275-6 ◽

2007 ◽

Vol 38 (9) ◽

pp. 1956-1964 ◽

Cited By ~ 38

Author(s):

A. Bulla ◽

C. Carreno-Bodensiek ◽

B. Pustal ◽

R. Berger ◽

A. Bührig-Polaczek ◽

...

Keyword(s):

Interface Energy ◽

Liquid Interface ◽

Solid Liquid Interface ◽

Solid Liquid

Download Full-text

The solid–liquid interface energy of organic crystals

Journal of Physical Organic Chemistry ◽

10.1002/poc.1136 ◽

2007 ◽

Vol 20 (4) ◽

pp. 236-240 ◽

Cited By ~ 13

Author(s):

H.M. Lu ◽

Z. Wen ◽

Q. Jiang

Keyword(s):

Interface Energy ◽

Liquid Interface ◽

Organic Crystals ◽

Solid Liquid Interface ◽

Solid Liquid

Download Full-text

MODELING OF SURFACE STRESS OF SEMICONDUCTORS

Surface Review and Letters ◽

10.1142/s0218625x03004597 ◽

2003 ◽

Vol 10 (01) ◽

pp. 49-53

Author(s):

Q. JIANG ◽

D. S. ZHAO ◽

M. ZHAO

Keyword(s):

Surface Stress ◽

Interface Energy ◽

Liquid Interface ◽

Thermodynamic Consideration ◽

Covalent Bonds ◽

Elastic Distortion ◽

Almost All ◽

Solid Liquid Interface ◽

Solid Liquid ◽

Surrounding Liquid

A general equation for surface stress is established based on a thermodynamic consideration of the size dependence of solid–liquid interface energy under an assumption that the solid–liquid interface of a particle immersed in surrounding liquid disappears when almost all atoms of the particle are located on its surface. The predicted surface stresses of semiconductors in terms of the model are in agreement with the first principles calculations and calculations based on forces associated with the elastic distortion of the covalent bonds.

Download Full-text