The quasi-harmonic approximation is a phonon-based model of solid-state physics used to describe volume-dependent thermal effects, such as the thermal expansion. It is based on the assumption that the harmonic approximationholds for every value of the lattice constant, which is to be viewed as an adjustable parameter.
Overview
The quasi-harmonic approximation expands upon the harmonicphonon model of lattice dynamics. The harmonic phonon model states that all interatomic forces are purely harmonic, but such a model is inadequate to explain thermal expansion, as the equilibrium distance between atoms in such a model is independent of temperature. Thus in the quasi-harmonic model, from a phonon point of view, phonon frequencies become volume-dependent in the quasi-harmonic approximation, such that for each volume, the harmonic approximation holds.
Thermodynamics
For a lattice, the Helmholtz free energyF in the quasi-harmonic approximation is where Elat is the static internal lattice energy, Uvib is the internal vibrational energy of the lattice, or the energy of the phonon system, T is the absolute temperature, V is the volume and S is the entropy due to the vibrational degrees of freedom. The vibrational energy equals where N is the number of terms in the sum, is introduced as the characteristic temperature for a phonon with wave vectork in the i-th band at volume V and is shorthand for the number of -phonons at temperature T and volume V. As is conventional, is the reduced Planck constant and kB is the Boltzmann constant. The first term in Uvib is the zero-point energy of the phonon system and contributes to the thermal expansion as a zero-point thermal pressure. The Helmholtzfree energyF is given by and the entropy term equals from which F = U - TS is easily verified. The frequency ω as a function of k is the dispersion relation. Note that for a constant value of V, these equations corresponds to that of the harmonic approximation. By applying a Legendre transform, it is possible to obtain the Gibbs free energyG of the system as a function of temperature and pressure. Where P is the pressure. The minimal value for G is found at the equilibrium volume for a given T and P.
Derivable quantities
Once the Gibbs free energy is known, many thermodynamic quantities can be determined as first- or second-orderderivatives. Below are a few which cannot be determined through the harmonic approximation alone.
The Grüneisen parameter γ is defined for every phonon mode as where i indicates a phonon mode. The total Grüneisen parameter is the sum of all γis. It is a measure of the anharmonicity of the system and closely related to the thermal expansion.
