Density of states, and integral of the Sommerfeld type

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SUMMARY

The discussion focuses on deriving the density of states for a free electron gas using the Sommerfeld expansion. Key equations include the energy expression at zero temperature, ##E=2 \sum_{k\leq k_f} \frac{\hbar^2}{2m}k^2##, and the transition from summation to integration in the limit of large volume, leading to ##\lim \frac{E}{V}=u=\frac{1}{4\pi} \int \epsilon(k)f(\epsilon(k))d^3k##. The density of states is defined as ##g(\epsilon)=\frac{dn}{d\epsilon}##, where ##n=\frac{N}{V}##. The discussion clarifies the change of variables from wave vector k to energy ε, which is essential for deriving the density of states rigorously.

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  • Understanding of quantum mechanics, specifically electron behavior in solids.
  • Familiarity with the Fermi-Dirac distribution and its implications in statistical mechanics.
  • Knowledge of integrals in spherical coordinates and their applications in physics.
  • Basic concepts of solid state physics as outlined in "Solid State Physics" by Ashcroft and Mermin.
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  • Study the derivation of the Sommerfeld expansion and its applications in solid state physics.
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  • Investigate the implications of density of states on electronic properties of materials.
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Telemachus
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It is easy to show that when you have a quantum system, let's think for example in electrons in a metal, then there appears summation over electron states of the form, e.g. for the energy for a free electron gas at T=0K:

##E=2 \sum_{k\leq k_f} \frac{\hbar^2}{2m}k^2##

Where ##k_f## denotes the Fermi wave vector.

In general one has sums of the form:

##\sum_{k} F(\vec{k})##

Now, for a free electorn gas one has that the volume in k space per allowed k value is ##\Delta \vec{k}=\frac{8\pi^3}{V}## where V is the volume of the solid (I'm following Aschroft and Mermin, solid state physics, page 37). So that in the limit of large V, one has:

##\displaystyle \lim_{V\rightarrow \infty} \frac{1}{V} \sum_{k} F(\vec{k}) \Delta k= \int \frac{d^3k}{8\pi^3} F(k).##

For the energy at non zero temperature one has

##E=2 \sum_k \epsilon(k) f(\epsilon_k)##

With:
##\epsilon_k=\frac{\hbar^2}{2m}k^2##

In general one has a dependence on energy ##\epsilon## per electron on the wave vector k, and f denotes the Fermi-Dirac distribution.

In the limit of large V, one then has:

##\lim \frac{E}{V}=u=\frac{1}{4\pi} \int \epsilon(k)f(\epsilon(k))d^3k##

Now, for the arbitrary function ##F(k)##, one can solve the integral in spherical coordinates:
##\int \frac{d^3k}{8\pi^3} F(k)=\frac{1}{\pi^2}\int dk k^2 F(\epsilon_k)##

So, that's ok, now the next step the book does is the one that is not clear to me how to get. In this step, this integral is taken to the one that is commonly used to evaluate the internal energy, or the number of electrons, etc. its the integral which I call as the "Sommerfeld type" because is that Sommerfeld used to make the "Sommerfeld expansion"

In this step, it is introduced the density of states

##\frac{1}{\pi^2}\int dk k^2 f(\epsilon_k)=\int_{-\infty}^{\infty} d\epsilon g(\epsilon) F(\epsilon)##

Where is used the fact that the integrand depends on ##\vec k## only through the electronic energy ##\epsilon =\frac{\hbar^2}{2m}k^2##

I hoped to derive this result just by calculation of the differentials, to get something like ##d\epsilon g(\epsilon)=\frac{k^2 dk}{\pi^2}##

The density of states is defined as ##g(\epsilon)=\frac{dn}{d\epsilon}##

Where ##n=\frac{N}{V}## is the number of electrons per unit volume, the electronic density.
 
Hi Telemachus! I don't quite understand the question here - is it the change of variable from k to \epsilon that's causing confusion?
 
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Yes, that's it.
 
Yes, that's it, I don't understand how to get the density of states in that step. I know the integral makes perfect sense, I have used it, but I don't know how to derive the result rigorously.

PS: sorry for the double post.

PS2: I saw a mistake in the formula I've posted, it is obvious, but anyway it should read:

##\frac{1}{\pi^2}\int dk k^2 F(\epsilon_k)=\int_{-\infty}^{\infty} d\epsilon g(\epsilon) F(\epsilon)##
 
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The change of variables in the integral should be straightforward:
\epsilon = \frac{\hbar^2 k^2}{2m}\\<br /> <br /> k = \sqrt{\frac{2m}{\hbar^2}} \; \epsilon^{1/2}\\<br /> <br /> dk = \frac{1}{2} \sqrt{\frac{2m}{\hbar^2}} \; \epsilon^{-1/2} \; d\epsilon<br />
 
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Great, thanks! that's exactly what I wanted, I don't know why I couldn't see that the density of states emerged naturally from there!
 
No problem!

Btw your integrals should go from 0 to \infty, not from -\infty to \infty, since k and \epsilon are both positive.
 
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