# Wulff construction

The Wulff construction is a method to determine the equilibrium shape of a droplet or crystal of fixed volume inside a separate phase (usually its saturated solution or vapor). Energy minimization arguments are used to show that certain crystal planes are preferred over others, giving the crystal its shape.

## Theory

In 1878 Josiah Willard Gibbs proposed[1] that a droplet or crystal will arrange itself such that its surface Gibbs free energy is minimized by assuming a shape of low surface energy. He defined the quantity

${\displaystyle \Delta G_{i}=\sum _{j}\gamma _{j}O_{j}~}$

Here ${\displaystyle \gamma _{j}}$ represents the surface (Gibbs free) energy per unit area of the ${\displaystyle j}$th crystal face and ${\displaystyle O_{j}}$ is the area of said face. ${\displaystyle \Delta G_{i}}$ represents the difference in energy between a real crystal composed of ${\displaystyle i}$ molecules with a surface and a similar configuration of ${\displaystyle i}$ molecules located inside an infinitely large crystal. This quantity is therefore the energy associated with the surface. The equilibrium shape of the crystal will then be that which minimizes the value of ${\displaystyle \Delta G_{i}}$.

In 1901 Russian scientist George Wulff stated[2] (without proof) that the length of a vector drawn normal to a crystal face ${\displaystyle h_{j}}$ will be proportional to its surface energy ${\displaystyle \gamma _{j}}$: ${\displaystyle h_{j}=\lambda \gamma _{j}}$. The vector ${\displaystyle h_{j}}$ is the "height" of the ${\displaystyle j}$th face, drawn from the center of the crystal to the face; for a spherical crystal this is simply the radius. This is known as the Gibbs-Wulff theorem.

In 1953 Herring gave a proof of the theorem and a method for determining the equilibrium shape of a crystal, consisting of two main exercises. To begin, a polar plot of surface energy as a function of orientation is made. This is known as the gamma plot and is usually denoted as ${\displaystyle \gamma ({\hat {n}})}$, where ${\displaystyle {\hat {n}}}$ denotes the surface normal, e.g., a particular crystal face. The second part is the Wulff construction itself in which the gamma plot is used to determine graphically which crystal faces will be present. It can be determined graphically by drawing lines from the origin to every point on the gamma plot. A plane perpendicular to the normal ${\displaystyle {\hat {n}}}$ is drawn at each point where it intersects the gamma plot. The inner envelope of these planes forms the equilibrium shape of the crystal.

## Proof

Various proofs of the theorem have been given by Hilton, Liebman, Laue,[3] Herring,[4] and a rather extensive treatment by Cerf.[5] The following is after the method of R. F. Strickland-Constable.[6] We begin with the surface energy for a crystal

${\displaystyle \Delta G_{i}=\sum _{j}\gamma _{j}O_{j}\,\!}$

which is the product of the surface energy per unit area times the area of each face, summed over all faces. This is minimized for a given volume when

${\displaystyle \delta \left(\sum _{j}\gamma _{j}O_{j}\right)_{V_{c}}=\sum _{j}\gamma _{j}\delta (O_{j})_{V_{c}}=0\,\!}$

Surface free energy, being an intensive property, does not vary with volume. We then consider a small change in shape for a constant volume. If a crystal were nucleated to a thermodynamically unstable state, then the change it would undergo afterward to approach an equilibrium shape would be under the condition of constant volume. By definition of holding a variable constant, the change must be zero, ${\displaystyle \delta (V_{c})_{V_{c}}=0}$. Then by expanding ${\displaystyle V_{c}}$ in terms of the surface areas ${\displaystyle O_{j}}$ and heights ${\displaystyle h_{j}}$ of the crystal faces, one obtains

${\displaystyle \delta (V_{c})_{V_{c}}={\frac {1}{3}}\delta \left(\sum _{j}h_{j}O_{j}\right)_{V_{c}}=0}$,

which can be written, by applying the product rule, as

${\displaystyle \sum _{j}h_{j}\delta (O_{j})_{V_{c}}+\sum _{j}O_{j}\delta (h_{j})_{V_{c}}=0\,\!}$.

The second term must be zero, that is,

${\displaystyle O_{1}\delta (h_{1})_{V_{c}}+O_{2}\delta (h_{2})_{V_{c}}+\ldots =0}$

This is because, if the volume is to remain constant, the changes in the heights of the various faces must be such that when multiplied by their surface areas the sum is zero. If there were only two surfaces with appreciable area, as in a pancake-like crystal, then ${\displaystyle O_{1}/O_{2}=-\delta (h_{1})_{V_{c}}/\delta (h_{2})_{V_{c}}}$. In the pancake instance, ${\displaystyle O_{1}=O_{2}}$ on premise. Then by the condition, ${\displaystyle \delta (h_{1})_{V_{c}}=-\delta (h_{2})_{V_{c}}}$. This is in agreement with a simple geometric argument considering the pancake to be a cylinder with very small aspect ratio. The general result is taken here without proof. This result imposes that the remaining sum also equal 0,

${\displaystyle \sum _{j}h_{j}\delta (O_{j})_{V_{c}}=0\,\!}$

Again, the surface energy minimization condition is that

${\displaystyle \sum _{j}\gamma _{j}\delta (O_{j})_{V_{c}}=0\,\!}$

These may be combined, employing a constant of proportionality ${\displaystyle \lambda }$ for generality, to yield

${\displaystyle \sum _{j}(h_{i}-\lambda \gamma _{j})\delta (O_{j})_{V_{c}}=0\,\!}$

The change in shape ${\displaystyle \delta (O_{j})_{V_{c}}}$ must be allowed to be arbitrary, which then requires that ${\displaystyle h_{j}=\lambda \gamma _{j}}$, which then proves the Gibbs-Wulff Theorem.

## References

1. ^ Josiah Willard Gibbs (1928) Collected Works
2. ^ G. Wulff (1901). "Zur Frage der Geschwindigkeit des Wachstums und der Auflösung der Krystallflagen". Zeitschrift für Krystallographie und Mineralogie. 34 (5/6): 449–530.
3. ^ Max von Laue (1943). "Der Wulffsche Satz für die Gleidigewichtsform von Kristallen". Zeitschrift für Kristallographie – Crystalline Materials. 105 (1–6): 124–133. doi:10.1524/zkri.1943.105.1.124. S2CID 101287509.
4. ^ C. Herring (1953). "Konferenz über Struktur und Eigenschaften fester Oberflächen Lake. Geneva (Wisconsin) USA, 29. September bis 1. Oktober 1952". Angewandte Chemie. 65 (1): 34–35. Bibcode:1953AngCh..65...34.. doi:10.1002/ange.19530650106.
5. ^ R Cerf (2006) The Wulff Crystal in Ising and Percolation Models, Springer
6. ^ R. F. Strickland-Constable: Kinetics and Mechanism of Crystallization, page 77, Academic Press, 1968.