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Spinodal decomposition information


Microstructural evolution under the Cahn–Hilliard equation, demonstrating distinctive coarsening and phase separation.

Spinodal decomposition is a mechanism by which a single thermodynamic phase spontaneously separates into two phases (without nucleation).[1] Decomposition occurs when there is no thermodynamic barrier to phase separation. As a result, phase separation via decomposition does not require the nucleation events resulting from thermodynamic fluctuations, which normally trigger phase separation.

Spinodal decomposition is observed when mixtures of metals or polymers separate into two co-existing phases, each rich in one species and poor in the other.[2] When the two phases emerge in approximately equal proportion (each occupying about the same volume or area), characteristic intertwined structures are formed that gradually coarsen (see animation). The dynamics of spinodal decomposition is commonly modeled using the Cahn–Hilliard equation.

Spinodal decomposition is fundamentally different from nucleation and growth. When there is a nucleation barrier to the formation of a second phase, time is taken by the system to overcome that barrier. As there is no barrier (by definition) to spinodal decomposition, some fluctuations (in the order parameter that characterizes the phase) start growing instantly. Furthermore, in spinodal decomposition, the two distinct phases start growing in any location uniformly throughout the volume, whereas a nucleated phase change begins at a discrete number of points.

Spinodal decomposition occurs when a homogenous phase becomes thermodynamically unstable. An unstable phase lies at a maximum in free energy. In contrast, nucleation and growth occur when a homogenous phase becomes metastable. That is, another biphasic system becomes lower in free energy, but the homogenous phase remains at a local minimum in free energy, and so is resistant to small fluctuations. J. Willard Gibbs described two criteria for a metastable phase: that it must remain stable against a small change over a large area.[3]

  1. ^ Binder, K (1987-07-01). "Theory of first-order phase transitions". Reports on Progress in Physics. 50 (7): 783–859. doi:10.1088/0034-4885/50/7/001. ISSN 0034-4885. S2CID 250879624.
  2. ^ Gennes, Pierre-Gilles de. (1979). Scaling concepts in polymer physics. Ithaca, N.Y.: Cornell University Press. ISBN 0-8014-1203-X. OCLC 4494721.
  3. ^ Gibbs, J.W., Scientific Papers of J Willard Gibbs, 2 vols. Bumstead, H. A., and Van Name, R. G., eds. (Dover, New York, 1961) ISBN 0-918024-77-3

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