How Do You Calculate Carrier Concentration in Doped Silicon?

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Homework Help Overview

The discussion revolves around calculating carrier concentration in silicon doped with phosphorus, specifically focusing on determining the electron concentration (n), hole concentration (p), and Fermi energy (E_F) at room temperature (300K). Participants explore the implications of full ionization and charge neutrality in the context of semiconductor physics.

Discussion Character

  • Exploratory, Conceptual clarification, Mathematical reasoning, Assumption checking

Approaches and Questions Raised

  • Participants discuss the assumption of full ionization and its implications for donor concentration. Questions arise regarding the relationship between n and Nd, as well as how to accurately calculate p given the absence of acceptor doping. There is also exploration of the Fermi level's behavior in doped versus intrinsic silicon.

Discussion Status

Participants are actively engaging with the problem, offering insights and corrections to each other's reasoning. Some have provided guidance on using the neutrality equation and the relationship between intrinsic and doped carrier concentrations. Multiple interpretations of the calculations and assumptions are being explored, with no explicit consensus reached yet.

Contextual Notes

Key assumptions include the full ionization of phosphorus dopants and the absence of acceptor doping. Participants reference known values for intrinsic carrier concentration and other semiconductor parameters, which are critical for the calculations being discussed.

Master J
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Hope you can give me a hand here guys.
I'm finding the whole carrier concentration thing a bit confusing!

Si doped with say 10^17 P (/cm3). At 300K, calculate n, p, E_F (Fermi energy).

Now I know the relations such as n=(N_c)exp[(E_c-E_F)/kT], N_c given

I just can't figure out where to start. If we assume full ionization, then should n just be the doner concentration?? But then how do I find p?

I know, from charge neutrality, that n + Nd = p + Na (assuming full ionization).
 
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"Si doped with say 10^17 P (/cm3)" , it is doped with what exactly?
 
Maybe it wasnt clear sorry. The P meant Phosphorous, ie. electron doner.
 
i thought p=per .. now it is clear ..

the first step when you assumed full ionization was a good one .. and the reason of that is , because the ionization energy of Phosphorous in Si is 45 mev, which is so low and for that reason we can say that we have full ionization situation ..

the statement "If we assume full ionization, then should n just be the doner concentration" is not correct , the full ionization just leads you to the fact that Nd+ = Nd (you get my point?) ..

another good step you did, is using the neutrality equation n + Nd = p + Na ..

I will give few things to start with ..


1) since Si is not doped with acceptor what does that tell you?
2)you can assume that n (approximately) = Nd in a case where Nd is much greater than ni (the intrinsic concentration of Si, i think this one is either given or you have the values Nc, Nv, and Eg) ..

3) following 1 & 2 you should get n, then get p ..

4)then Ef should be obtained easily ..
 
If its not doped with acceptors, then Na = 0

So we have: n + Nd = p

Yes I have Nc, Nv and Eg.

p is just the intrinsic value, since no acceptors were added??

If we assume full ionization, then is n just the intrinsic electron conc. PLUS the doner density(one electron per doner)??
 
Master J said:
If its not doped with acceptors, then Na = 0

So we have: n + Nd = p

Yes I have Nc, Nv and Eg.

p is just the intrinsic value, since no acceptors were added??

If we assume full ionization, then is n just the intrinsic electron conc. PLUS the doner density(one electron per doner)??

ok good Na = 0 since Si is not doped with any acceptor ..

well, to answer your last question .. let me ask you a question :)

is the Fermi level the same for both cases when Si is doped (with acceptor or donor or both) and when it is not doped at all ? >> ( answer this question while having a look at the expression used to find p) ..
 
Assuming my answer to find p is right?

ni^2 = Nc.Nv.exp[-Eg/kT] ... gives me intrinsic conc. squared...hence p, which is just the intrinsic conc?

Well, the Fermi level moves towards either the valence or conduction band, depending upon which is the amjority carrier, according to:

E_F = (Ec +Ev)/2 -(1/2).ln(p/n) + (3/4).ln(Mp/Mn)

...
 
Ok so here's an attempt! :-)


(ni)^2 = Nc.Nv.exp(-Eg/kT) = 2.66*10^19


n = ni + Nd = 10^17 ( so yea, ni doesn't really matter in comparison).

Therefore,

p = (ni)^2 / n = (ni)^2 / Nd = 266

Now 266 holes / cm^3 seems REALLY small! Is that right?
 
the neutrality equation is supposed to be n+Na=p+Nd (correct me if I am wrong) ...

When i suggested that in case Nd much greater than ni then Nd = n .. I didnt mean to push you to say n=ni+Nd?.. If that confused you .. Just plug p = ni^2/n in the neutrality equation and find n .. When you find n , then you can easily find p ..

>> i believe that your value for n and p is correct .. my comment was all about why u wrote n = ni + Nd ... You can repeat solving the question taking in consideration my last note and you will see that you will get the same answer..
 
  • #10
Master J said:
Assuming my answer to find p is right?

ni^2 = Nc.Nv.exp[-Eg/kT] ... gives me intrinsic conc. squared...hence p, which is just the intrinsic conc?

Well, the Fermi level moves towards either the valence or conduction band, depending upon which is the amjority carrier, according to:

E_F = (Ec +Ev)/2 -(1/2).ln(p/n) + (3/4).ln(Mp/Mn)

...

im so sorry i didnt pay attention to this post .. your answer was not right!

you can not assume that p is just intrinsic value ! .. you mentioned that the Fermi level would not be the same in case you don't have doping with a case where you have doping ..

I think that p = Nv exp[(E_F-E_v)/kT], so how it would be the same? if you have a second view please provide us with it ..
 
  • #11
But isn't the intrinsic conc. squared always equal to np??

And the intrinsic conc. squared does not depend on E_F:

(n_i)^2 = Nv.Nc.exp[-Eg/kT]

So with that I can get p = (n_i)^2 / n ...where n is approx. = N_d
 
  • #12
yes ni^2 is always equal n*p .. What i meant is that in the case of doping p won't be the same as p when you have no doping, you get my point?, so that's why you have to calculate it with the relation ni^2=np .. I am sorry in case if i misunderstood what you said ..
 

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