Density of States -- alternative derivation

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SUMMARY

The discussion centers on the derivation of the Density of States (DOS) in k-space, emphasizing its necessity in solid state physics. Participants clarify that k-space allows for a uniform distribution of states, making it easier to derive DOS compared to energy space. They also mention that for systems like the harmonic oscillator, DOS can be derived directly in energy-space due to uniform state distribution. The conversation highlights the importance of k-space in understanding band structures and their relation to physical properties of solids.

PREREQUISITES
  • Understanding of Density of States (DOS)
  • Familiarity with k-space and its significance in solid state physics
  • Basic knowledge of particle-in-a-box quantum states
  • Concept of energy-space and its relationship to DOS
NEXT STEPS
  • Study the derivation of DOS in k-space for various quantum systems
  • Explore the relationship between band structure and DOS in solid state physics
  • Learn about the harmonic oscillator and its DOS derivation in energy-space
  • Read R. Baierlein's "Thermal Physics" for alternative derivations in n-space
USEFUL FOR

Solid state physicists, condensed matter researchers, and students seeking to deepen their understanding of the Density of States and its derivation methods in k-space and energy-space.

Alex Cros
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I am trying to understand the derivation for the DOS, I get stuck when they introduce k-space. Why is it necessary to introduce k-space? Why is the DOS related to k-space? Perhaps if someone could come up to a slightly different derivation (any dimensions will do) that would help.
My doubt ELI5: If we have a region full of potatos and we want to find the density of potatos we count the potatos and we divide by the area/volume, we don't need to go into potato-space.
 
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Alex Cros said:
I am trying to understand the derivation for the DOS, I get stuck when they introduce k-space. Why is it necessary to introduce k-space? Why is the DOS related to k-space? Perhaps if someone could come up to a slightly different derivation (any dimensions will do) that would help.
My doubt ELI5: If we have a region full of potatos and we want to find the density of potatos we count the potatos and we divide by the area/volume, we don't need to go into potato-space.
The problem with that last approach is that this would give you the total density of potatoes, not the density of potatoes as a function of the distance from the middle of the field :smile:

The reason for going to k-space, part from the fact that k-space is very useful for solid state physics, is that it is easier to find the density of states in a space where the states are uniformly distributed. For particle-in-a-box states, this is the case for k-space. It would also be the case in n-space (with n the quantum number), and some authors use that instead. It would not be true for energy space, so this is why one finds the density of states first in k-space, and then converts it to energy.

If you want to find the density of states for the harmonic oscillator, then you can directly start in energy-space, since the states are uniformly distributed there (since ##E \propto n##).
 
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DrClaude said:
The problem with that last approach is that this would give you the total density of potatoes, not the density of potatoes as a function of the distance from the middle of the field :smile:

The reason for going to k-space, part from the fact that k-space is very useful for solid state physics, is that it is easier to find the density of states in a space where the states are uniformly distributed. For particle-in-a-box states, this is the case for k-space. It would also be the case in n-space (with n the quantum number), and some authors use that instead. It would not be true for energy space, so this is why one finds the density of states first in k-space, and then converts it to energy.

If you want to find the density of states for the harmonic oscillator, then you can directly start in energy-space, since the states are uniformly distributed there (since ##E \propto n##).
Thank you so much! Could you explain how this is done in n-space, (I can't really picture k-space) or perhaps refer to a book that does that, I am struggling to find any alternative derivation!

Thanks in advance! :)
 
Alex Cros said:
Thank you so much! Could you explain how this is done in n-space, (I can't really picture k-space) or perhaps refer to a book that does that, I am struggling to find any alternative derivation!
There is not much difference between doing it in k-space and n-space.

You can find it in the R. Baierlein, Thermal Physics (CUP).
 
Alex Cros said:
Thank you so much! Could you explain how this is done in n-space, (I can't really picture k-space) or perhaps refer to a book that does that, I am struggling to find any alternative derivation!

Thanks in advance! :)

I can use the question you posed in the first post and ask you the same thing: Why would you want to do this in real space?

For solid state/condensed matter physicists, k-space is more useful for many reasons. The diffraction pattern that we get from measurements directly map the k-space of the crystal structure. But more important than that, the band structure is a set of dispersion curves in E vs. k! This band structure practically determines a significant portion of the property of the solid. And BTW, the sum of the band structure over all k-space gives the DOS at a particular energy.

We do a lot of things in k-space because it is USEFUL, more useful than in real-space.

Zz.
 
"If we have a region full of potatos and we want to find the density of potatos we count the potatos and we divide by the area/volume, we don't need to go into potato-space."

Many years ago when I was studying the Dirac eqn. my beloved teacher, Professor Oreste Piccioni, handed back an exam paper and said to me: "Fred, the proton, she's not a little potato!"

Peace.
Fred
 
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