Lattice Diffusion Coefficient

Lattice diffusion (also called bulk or volume diffusion) refers to atomic diffusion within a crystalline lattice.P. Heitjans, J. Karger, Ed, “Diffusion in condensed matter: Methods, Materials, Models,” 2nd edition, Birkhauser, 2005, pp. 1-965. Diffusion within the crystal lattice occurs by either interstitial or substitutional mechanisms and is referred to as lattice diffusion. In interstitial lattice diffusion, a diffusant (such as C in an iron alloy), will diffuse in between the lattice structure of another crystalline element. In substitutional lattice diffusion (self-diffusion for example), the atom can only move by substituting place with another atom. Substitutional lattice diffusion is often contingent upon the availability of point vacancies throughout the crystal lattice. Diffusing particles migrate from point vacancy to point vacancy by the rapid, essentially random jumping about (jump diffusion). Since the prevalence of point vacancies increases in accordance with the Arrhenius equation, the rate of crystal solid state diffusion increases with temperature. For a single atom in a defect-free crystal, the movement can be described by the "random walk" model.

Diffusion Coefficient for Interstitial Diffusion

An atom diffuses in the interstitial mechanism by passing from one interstitial site to one of its nearest neighboring interstitial sites. The movement of atoms can be described as jumps, and the interstitial diffusion coefficient depends on the jump frequency. The jump frequency, $\Gamma$, is given by:

$\Gamma=zv \exp\left ( \frac \right )$

where

* $z$ is the number of nearest neighboring interstitial sites.
* $v$ is vibration frequency of the interstitial atom due to thermal energy.
* $\Delta G_m$ is the activation energy for the migration of the interstitial atom between sites.

$\Delta G_m$ can be expressed as the sum of activation enthalpy term $\Delta H_m$ and the activation entropy term $-T\Delta S_m$, which gives the diffusion coefficient as:

D = \left \frac \alpha^2 zv \exp\frac \right exp\frac

where

* $\alpha$ is the jump distance.

The diffusion coefficient can be simplified to an Arrhenius equation form:

$D = D_0 \exp\frac$

where

* $D_0$ is a temperature-independent material constant. $D_0 = \frac \alpha^2 zv \exp\frac$
* $Q_I$ is the activation enthalpy. $Q_I = \Delta H_m$

In the case of interstitial diffusion, the activation enthalpy $Q_I$ is only dependent on the activation energy barrier to the movement of interstitial atoms from one site to another. The diffusion coefficient increases exponentially with temperature at a rate determined by the activation enthalpy $Q_I$.

Diffusion Coefficient for Substitution Diffusion

Self-Diffusion

The rate of self-diffusion can be measured experimentally by introducing radioactive A atoms (A*) into pure A and measuring the rate at which penetration occurs at various temperatures. A* and A atoms have approximately identical jump frequencies since they are chemically identical. The diffusion coefficient of A* and A can be related to the jump frequency and expressed as:

$D_A^* = D_A = \frac \alpha^2 \Gamma$

where

* $D_A^*$ is the diffusion coefficient of radioactive A atoms in pure A.
* $D_A$ is the diffusion coefficient of A atoms in pure A.
* $\Gamma$ is the jump frequency for both the A* and A atoms.
* $\alpha$ is the jump distance.

An atom can make a successful jump when there are vacancies nearby and when it has enough thermal energy to overcome the energy barrier to migration. The number of successful jumps an atom will make in one second, or the jump frequency, can be expressed as:

$\Gamma = zv X_v \exp\frac$

where

* $z$ is the number of nearest neighbors.
* $v$ is the frequency of temperature-independent atomic vibration.
* $X_v$ is the vacancy fraction of the lattice.
* $\Delta G_m$ is the activation energy barrier to atomic migration.

In thermodynamic equilibrium,

$X_v = X_v^e = \exp\frac$

where $\Delta G_v$ is the free energy of vacancy formation for a single vacancy.

The diffusion coefficient in thermodynamic equilibrium can be expressed with $\Delta G_m$ and $\Delta G_v$, giving:

$D_A = \frac \alpha^2 zv \exp\frac$

Substituting ΔG = ΔH – TΔS gives:

$D_A = \frac \alpha^2 zv \exp\frac \exp\frac$

The diffusion coefficient can be simplified to an Arrhenius equation form:

$D_A = D_0 \exp\frac$

where

* $D_0$ is approximately a constant. $D_0 = \frac \alpha^2 zv \exp\frac$
* $Q_S$ is the activation enthalpy. $Q_S = \Delta H_m + \Delta H_v$

Compared to that of interstitial diffusion, the activation energy for self-diffusion has an extra term (ΔH_v). Since self-diffusion requires the presence of vacancies whose concentration depends on ΔH_v.

Vacancy Diffusion

Diffusion of a vacancy can be viewed as the jumping of a vacancy onto an atom site. It is the same process as the jumping of an atom into a vacant site but without the need to consider the probability of vacancy presence, since a vacancy is usually always surrounded by atom sites to which it can jump. A vacancy can have its own diffusion coefficient that is expressed as:

$D_v = \frac \alpha^2 \Gamma _v$

where $\Gamma_v$ is the jump frequency of a vacancy.

The diffusion coefficient can also be expressed in terms of enthalpy of migration ($\Delta H_m$) and entropy of migration ($\Delta S_m$) of a vacancy, which are the same as for the migration of a substitutional atom:

$D_v = \frac \alpha^2 zv \exp\frac \exp\frac$

Comparing the diffusion coefficient between self-diffusion and vacancy diffusion gives:

$D_v = \frac$

where the equilibrium vacancy fraction $X_v^e = \exp\frac$

Diffusion in a Binary System

In a system with multiple components (e.g. a binary alloy), the solvent (A) and the solute atoms (B) will not move in an equal rate. Each atomic species can be given its own intrinsic diffusion coefficient $\tilde_A$ and $\tilde_B$, expressing the diffusion of a certain species in the whole system. The interdiffusion coefficient $\tilde$ is defined by the Darken's equation as:

$\tilde = \tilde_A X_B + \tilde_B X_A$

where $X_A$ and $X_B$ are the amount fractions of species A and B, respectively.

See also

* Kirkendall effect
* Phase transformations in solids
* Mass diffusivity

References

{{reflist

External links

Classical and nanoscale diffusion (with figures and animations)

Diffusion