Density of States: Explanation & Applications

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The density of states (DOS) quantifies the number of orbitals per unit energy range, allowing one to determine how many states exist within a specific energy interval. By integrating the DOS over an energy range, one can find the total number of states between two energy levels. At low temperatures, the number of active electrons in a free Fermi gas can be approximated using the DOS, leading to insights about thermal energy and specific heat. The relationship between DOS and energy is crucial for understanding phenomena like specific heat in materials. This foundational concept has significant applications in condensed matter physics and materials science.
Repetit
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Density of states??

According to C. Kittel the density of states is the "number of orbitals per unit energy range". Alright, that's fine, but what exactly does this mean? I can understand the calculations, finding the totalt number of states by considering the fermi sphere and the volume of a single state in k-space, and then differentiating this expression with respect to the energy. But if the DOS is the number of orbitals (states) per unit energy, what would for example happen if i multiply this DOS by some energy? What would i get? Apparently some number of orbitals, but what would this number tell me?

Please enligthen me, I am sort of confused on this topic. It would certainly be nice if you could give me some examples of applications of DOS as well.

Thanks in advance!
 
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Hi Repetit,

It's really all in the definition. The question you would often like to answer is "how many states are there in a given energy range?" The answer to this question is given by the density of states which is literally just the derivative of the number of states with respect to energy. Therefore, if N(E) is the density of states, the answer to the question "how many states are there between E_1 and E_2 is simply \int^{E_2}_{E_1} N(E) dE. An important approximation to this formula obtains when the energy range \Delta E = E_2 - E_1 is small compared to the scale of variations in N(E). In such a situation the number of states is given simply by N(E^*) \Delta E where E^* something between E_1 and E_2. This is actually just the mean value theorem, but you don't usually know what E^* is, so you often just choose E^* = E_1 say, and the error in your approximation is second order in \Delta E.

Example: At low temperatures, meaning kT << E_F, the number of "active" electrons in a free Fermi gas is simply the number of electrons in a thin shell of thickness kT at the Fermi surface. This number is N(E_F) k T, per the approximation above. Each of these active electrons carries a thermal energy of order kT, thus the thermal energy of a free fermi gas at low temperatures is given by N(E_F) (kT)^2 up to numerical factors of order one. This predicts a specific heat C_V = \frac{\partial E}{\partial T} \sim T, a result which is observed in experiments.

Hope this helps. I can expound on the example if what I've said is too cryptic.
 
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Time reversal invariant Hamiltonians must satisfy ##[H,\Theta]=0## where ##\Theta## is time reversal operator. However, in some texts (for example see Many-body Quantum Theory in Condensed Matter Physics an introduction, HENRIK BRUUS and KARSTEN FLENSBERG, Corrected version: 14 January 2016, section 7.1.4) the time reversal invariant condition is introduced as ##H=H^*##. How these two conditions are identical?

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