Electron heat capacity
In solid state physics the electron heat capacity or electronic specific heat describes the contribution of electrons to the heat capacity.
Heat is transported by phonons and by free electrons in solids. For pure metals, however, the electronic contributions dominate in the thermal conductivity. In impure metals, the electron mean free path is reduced by collisions with impurities, and the phonon contribution may be comparable with the electronic contribution.
Introduction
Although the Drude model was fairly successful in describing the electron motion within metals, it has some erroneous aspects: it predicts the Hall coefficient with the wrong sign compared to experimental measurements, the assumed additional electronic heat capacity to the lattice heat capacity, namely per electron at elevated temperatures, is also inconsistent with experimental values, since measurements of metals show no deviation from the Dulong–Petit law. The observed electronic contribution of electrons to the heat capacity is usually less than one percent of. This problem seemed insoluble prior to the development of quantum mechanics. This paradox was solved by Arnold Sommerfeld after the discovery of the Pauli exclusion principle, who recognised that the replacement of the Boltzmann distribution with the Fermi–Dirac distribution was required and incorporated it in the free electron model.Derivation within the free electron model
Internal energy
When a metallic system is heated from absolute zero, not every electron gains an energy as equipartition dictates. Only those electrons in atomic orbitals within an energy range of of the Fermi level are thermally excited. Electrons, in contrast to a classical gas, can only move into free states in their energetic neighbourhood.The one-electron energy levels are specified by the wave vector through the relation with the electron mass. This relation separates the occupied energy states from the unoccupied ones and corresponds to the spherical surface in k-space. As the ground state distribution becomes:
where
- is the Fermi–Dirac distribution
- is the energy of the energy level corresponding to the ground state
- is the ground state energy in the limit, which thus still deviates from the true ground state energy.
where the factor of 2 accounts for the spin up and spin down states of the electron.
Reduced internal energy and electron density
Using the approximation that for a sum over a smooth function over all allowed values of for finite large system is given by:where
- is the volume of the system
and the expression for the electron density can be written as:
The integrals above can be evaluated using the fact that the dependence of the integrals on can be changed to dependence on through the relation for the electronic energy when described as free particles,, which yields for an arbitrary function :
with
which is known as the density of levels or density of states per unit volume such that is the total number of states between and . Using the expressions above the integrals can be rewritten as:
These integrals can be evaluated for temperatures that are small compared to the Fermi temperature by applying the Sommerfeld expansion and using the approximation that differs from for by terms of order. The expressions become:
For the ground state configuration the first terms of the expressions above yield the internal energy and electron density of the ground state. The expression for the electron density reduces to. Substituting this into the expression for the internal energy, one finds the following expression:
Final expression
The contributions of electrons within the free electron model is given by:Compared to the classical result, it can be concluded that this result is depressed by a factor of which is at room temperature of order of magnitude. This explains the absence of an electronic contribution to the heat capacity as measured experimentally.
Note that in this derivation is often denoted by which is known as the Fermi energy. In this notation, the electron heat capacity becomes:
Comparison with experimental results for the heat capacity of metals
For temperatures below both the Debye temperature and the Fermi temperature the heat capacity of metals can be written as a sum of electron and phonon contributions that are linear and cubic respectively:. The coefficient can be calculated and determined experimentally. Some values are tabulated below:Species | Free electron value for in | Experimental value for in |
Li | 0.749 | 1.63 |
Be | 0.500 | 0.17 |
Na | 1.094 | 1.38 |
Mg | 0.992 | 1.3 |
Al | 0.912 | 1.35 |
K | 1.668 | 2.08 |
Ca | 1.511 | 2.9 |
Mn | 170 | 5.2 |
Fe | 4.98 | 10 |
Co | 4.98 | 10.3 |
Cu | 0.505 | 0.695 |
Zn | 0.753 | 0.64 |
Ga | 1.025 | 0.596 |
Rb | 1.911 | 2.41 |
Sr | 1.790 | 3.6 |
Ag | 0.645 | 0.646 |
Cd | 0.948 | 0.688 |
In | 1.233 | 1.69 |
Sn | 1.410 | 1.78 |
Cs | 2.238 | 3.20 |
Ba | 1.937 | 2.7 |
Au | 0.642 | 0.729 |
Hg | 0.952 | 1.79 |
Ti | 1.29 | 1.47 |
Pb | 1.509 | 2.98 |
The free electrons in a metal do not usually lead to a strong deviation from the Dulong–Petit law at high temperatures. Since is linear in and is linear in, at low temperatures the lattice contribution vanishes faster than the electronic contribution and the latter can be measured. The deviation of the approximated and experimentally determined electronic contribution to the heat capacity of a metal is not too large. A few metals deviate significantly from this approximated prediction. Measurements indicate that these errors are associated with the electron mass being somehow changed in the metal, for the calculation of the electron heat capacity the effective mass of an electron should be considered instead. For Fe and Co the large deviations are attributed to the partially filled d-shells of these transition metals, whose d-bands lie at the Fermi energy.
The alkali metals are expected to have the best agreement with the free electron model since these metals only one s-electron outside a closed shell. However even sodium, which is considered to be the closest to a free electron metal, is determined to have a more than 25 per cent higher than expected from the theory.
Certain effects influence the deviation from the approximation:
- The interaction of the conduction electrons with the periodic potential of the rigid crystal lattice is neglected.
- The interaction of the conduction electrons with phonons is also neglected. This interaction causes changes in the effective mass of the electron and therefore it affects the electron energy.
- The interaction of the conduction electrons with themselves is also ignored. A moving electron causes an inertial reaction in the surrounding electron gas.
Heat capacity of superconductors
Calculation for a superconductor
The calculation of the electron heat capacity for super conductors can be done in the BCS theory. The entropy of a system of fermionic quasiparticles, in this case Cooper pairs, is:where is the Fermi–Dirac distribution with
and
- is the particle energy with respect to the Fermi energy
- the energy gap parameter where and represents the probability that a Cooper pair is occupied or unoccupied respectively.
The last two terms can be calculated:
Substituting this in the expression for the heat capacity and again applying that the sum over in the reciprocal space can be replaced by an integral in multiplied by the density of states this yields:
Characteristic behaviour for superconductors
To examine the typical behaviour of the electron heat capacity for species that can transition to the superconducting state, three regions must be defined:- Above the critical temperature
- At the critical temperature
- Below the critical temperature
Superconductors at
This is just the result for a normal metal derived in the section above, as expected since a superconductor behaves as a normal conductor above the critical temperature.