Surface tension and interface free energy

Definition of surface tension as free-energy cost per area of an interface between coexisting phases; Ising/lattice-gas viewpoint.
Surface tension and interface free energy

Extension: interface free energy and surface tension

In systems with phase coexistence, an interface separating two stable phases costs free energy proportional to its area. The proportionality constant (possibly direction-dependent) is the surface tension.

A canonical setting is the below its critical temperature, where distinct infinite-volume phases exist (see and ).

Definition via boundary conditions (Ising example)

Let ΛL\Lambda_L be a large box with linear size LL, and impose boundary conditions that force an interface with normal direction n\mathbf{n} (for example, “++” on one side of a plane and “-” on the other). Let ZL+(n)Z_L^{+-}(\mathbf{n}) be the finite-volume partition function with such mixed boundary conditions, and let ZL++Z_L^{++} be the partition function with uniform “++” boundary conditions.

If AL(n)A_L(\mathbf{n}) is the cross-sectional area of the imposed interface, the surface tension in direction n\mathbf{n} is defined (when the limit exists) by

τ(n)=limL1βAL(n)log(ZL+(n)ZL++). \tau(\mathbf{n}) =\lim_{L\to\infty}-\frac{1}{\beta\,A_L(\mathbf{n})}\, \log\left(\frac{Z_L^{+-}(\mathbf{n})}{Z_L^{++}}\right).

Interpretation: the ratio of partition functions isolates the excess free energy due to creating the interface, normalized by area.

Key consequences and context

  • Coexistence and order: A positive τ(n)\tau(\mathbf{n}) is tied to coexistence of distinct phases and nonzero (an ).
  • Geometry: Directional dependence of τ(n)\tau(\mathbf{n}) leads to equilibrium crystal shapes via Wulff-type constructions (a geometric “dual” of interface costs).
  • Large deviations of profiles: Interface free energies govern probabilities of atypical magnetization profiles and droplet formation; this connects to and to the thermodynamic potential viewpoint via .