Donor and acceptor levels in band diagrams

In summary: I see. So the dispersion relation diagrams would show the shapes of the bands, while the generic band diagrams would just show the levels within the bands?I see. So the dispersion relation diagrams would show the shapes of the bands, while the generic band diagrams would just show the levels within the bands?That's correct.
  • #1
BeauGeste
49
0
1.in band diagrams, books usually show parabolic bands for the conduction band and the valence band. They will also make note of the acceptor and donor leves in the band gap.
However, they always draw straight horizontal lines for these levels.
Is that correct? The impurity levels are independent of k?

2. Another thing that really bothers me about band diagrams is when people draw them
filled. If I understand things, electrons can only exist in states on the actual curve of the band. For instance the conduction band at k=0 is parabolic and at energy 0. There cannot be an electron at k=0 at energy E above E=0 (unless it's on another band). I'm correct, right?
 
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  • #2
BeauGeste said:
1.in band diagrams, books usually show parabolic bands for the conduction band and the valence band. They will also make note of the acceptor and donor leves in the band gap.
However, they always draw straight horizontal lines for these levels.
Is that correct? The impurity levels are independent of k?

Not always. This is only a simplified description. But remember that even your "parabolic" bands are highly simplified. If you look at the actual band structure of many materials, you'll see spaghetti-like lines in various crystallographic directions. So in essence, if you already are using the simplified parabolic band, then drawing the donor/acceptor levels as being k-independent is acceptable.

2. Another thing that really bothers me about band diagrams is when people draw them
filled. If I understand things, electrons can only exist in states on the actual curve of the band. For instance the conduction band at k=0 is parabolic and at energy 0. There cannot be an electron at k=0 at energy E above E=0 (unless it's on another band). I'm correct, right?

You are right. The shading of those "occupied" part also annoys me because it causes confusion. What would be better is simply to draw the Fermi energy level and indicate that the band is occupied below that level.

Zz.
 
  • #3
Yeah, I was just thinking about the simplified description.
Why, though, are the impurity levels independent of k?
 
  • #4
Wait! So what are we assuming when we simplify that parabolic conduction and valance bands to a straight line?

edit: Really bad grammar. Let me rephrase, " Wait! So why is it OK to approximate these parabolic conduction and valance bands by straight lines?"
 
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  • #5
BeauGeste said:
Yeah, I was just thinking about the simplified description.
Why, though, are the impurity levels independent of k?

Because we approximate the dopant to be uniformly distributed and having a simple Rydberg-type energy state. That's why you get a distinct energy state.

Swapnil said:
Wait! So what are we assuming when we simplify that parabolic conduction and valance bands to a straight line?

We did not. It is the DOPANT acceptor or donor level that is approximated to be that.

Zz.
 
  • #6
ZapperZ said:
We did not. It is the DOPANT acceptor or donor level that is approximated to be that.
I'm sorry. I meant to ask you why was it OK to approximate the conduction and valence bands with straight lines to begin with (i.e when we are drawing energy-band diagrams)?
 
  • #7
Swapnil said:
I'm sorry. I meant to ask you why was it OK to approximate the conduction and valence bands with straight lines to begin with (i.e when we are drawing energy-band diagrams)?

This is a different question. The typical energy-band diagram has integrated out the k-dependence of the band dispersion. Thus, all you have is the energy bands, and the "straight line" doesn't mean anything other than to indicate where the band energy starts and stops.

Zz.
 
  • #8
ZapperZ said:
This is a different question. The typical energy-band diagram has integrated out the k-dependence of the band dispersion. Thus, all you have is the energy bands, and the "straight line" doesn't mean anything other than to indicate where the band energy starts and stops.

You you are saying that the energy E_c that we denote as a straight line in the Energy-band diagrams is actually the total energy which we got from summing up all the energies at all the different k values?
 
  • #9
Swapnil said:
You you are saying that the energy E_c that we denote as a straight line in the Energy-band diagrams is actually the total energy which we got from summing up all the energies at all the different k values?

Well, what do you think happened to the k-dependence, then?

Those "block" diagrams are more of an energy "density of states" sketch. This means that it is a "momentum averaged" band diagram. The FULL band diagram must include the band dispersion, which, by definition, includes E vs. k dependence.

Zz.
 
  • #10
My solid state prof distinguished between two types of band diagrams:

1. Dispersion relation diagrams. These show the dispersion curves E(k). These are often depicted as parabolic as you described. So here we're working in k-space.

2. Generic band diagrams, where straight horizontal lines denote certain energy boundaries (e.g. top of the valence band, bottom of the conduction band), and the vertical axis is still energy. Here, it is VAGUE what the x-axis means. All we know for sure is that this is not a k-space diagram. One interpretion you could choose is that this is a "real space" band diagram...(the energies mentioned are constant as a function of position in the specimen...and correspond to the maximum and minimum respectively of the two parabolas in the dispersion diagram). He asked us to do so on a test (in fact, he just said, "draw the real-space band diagram", and we were expected to know what he meant). Or...you could interpret the x-axis as being totally meaningless (i.e. this is not a plot, just a diagram, a pictorial representation of a band gap).

Or you could interpret it as...uh...what ZapperZ said. I'm not sure if I've contributed anything over and above what he said, but whatever...
 
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1. What are donor and acceptor levels in band diagrams?

Donor and acceptor levels refer to energy states within the band structure of a material that are caused by the presence of impurities or dopants. Donor levels are created by adding extra electrons to the material, while acceptor levels are created by removing electrons.

2. How do donor and acceptor levels affect the band structure?

Donor and acceptor levels introduce additional energy states within the band structure, which can shift the energy levels of the conduction and valence bands. This can impact the electrical and optical properties of the material, such as its conductivity and absorbance.

3. What is the difference between a donor and an acceptor level?

The main difference between donor and acceptor levels is the type of impurity or dopant responsible for their creation. Donor levels are caused by the addition of extra electrons, while acceptor levels are caused by the removal of electrons.

4. How do donor and acceptor levels affect the charge carrier concentration?

The presence of donor and acceptor levels can significantly impact the charge carrier concentration in a material. Donor levels can increase the concentration of electrons, while acceptor levels can decrease the concentration of electrons. This can affect the overall conductivity and electrical properties of the material.

5. Can donor and acceptor levels be controlled?

Yes, donor and acceptor levels can be controlled by intentionally introducing impurities or dopants into the material during the fabrication process. This allows for the manipulation of the band structure and the resulting properties of the material.

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