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…………… (1) Integrating across the depletion region gives …………… (2) Under equilibrium conditions. …………… (3) Solving for ξ in equation (3) and making use of the Einstein relationship. We obtain …………… (4) Substituting Equation (4) into Equation (2), and completing the integration then yields
…………… (5) For the specific case of a non-degenerately doped step junction where ND and NA are the n- and p-side doping concentrations, one denies. …………… (6) …………… (7) and therefore …………… (8) It is useful to perform a sample computation to gauge the relative magnitude of the built in voltage. Choosing ND= NA = 1015/ cm3 and a Si diode maintained at 300 K, One computes Vbi= (0.0259) ln(1030/1020) 0.6 V. This is a typical result. In non-degenerately doped diodes Vbi < EG/q, or Vbi is less than the band gap energy converted into volts. Non-degenerately doped Ge, Si, and GaAs diodes maintained at room temperature exhibits a Vbi less than 0.66 V, 1.12 V. and 1.42 V respectively. From the energy band diagram, we observed …………… (9) …………… (10) …………… (11) Clearly, for a Non-degenerately doped diode bosh (Ei — EF) p-side, and (EF — Ei) n-side are less than EG/2, making Vbi < EG/q Moreover, in a Non-degenerately doped step junction under equilibrium conditions, …………… (12) …………… (13)
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Taking logarithms on both sides, we get ……………… (29)
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Ect = the bottom and top energy levels of conduction band n = ……….(2) can be written as n = = n = - ……….(3) we know that above Ect, there is no electrons. Hence, Equation (3) becomes n = - n = ……….(4) The Fermi-Dirac distribution function fe(E) can be represented as: (E) = ……….(5) Compared to the exponential value, so the ‘1’ in the denominator can be neglected. So >>1 Hence, (E) = = ……….(6) The density of electron states ge(E) in the energy space from E = 0 to E can be written as: (E) = [ ]3/2 (E - 0) ½ ……….(7) where me* is the effective mass of an electron and h is Planck’s constant. (E)dE = [ ]3/2 (E - 0) ½dE ……….(8) To evaluate n, the density of states is counted from Ec, since the minimum energy state in conduction band is Ec. so eq (8) can become (E)dE = [ ]3/2 (E - Ec) ½dE ……….(9) Substituting Equations (6) and (9) in (4) gives n = 3/2 (E-)1/2dE n = [ ]3/2 1/2dE ………… (10) The above equation can be simplified by the following substitution: Put ɛ = E − Ec ………… (11) So, dɛ = dE In Equation (11), Ec is constant, as we change the variable E to ε in Equation (10), the integral limits also change. In Equation (11), as E → Ec then ε → 0 and E → ∞, then ε also → ∞. the exponential term in Equation (10) becomes: = exp [] = exp [] ………… (12) Substituting Equations (11) and (12) in (10), we get: n = [ ]3/2 dE n = [ ]3/2 dE ………… (13) Above integral (I) can be simplified by substitution. Put ε = x2 so that dɛ = 2x dx I =2x dx =dx = =T)3/2 ………… (14) Substituting Equation (14) in (13) gives: n = [ ]3/2T)3/2 n = n = n = ………… (15) The term is almost a constant compared with the exponential term as the temperature changes. So, it is a pseudo constant and is given by the symbol NC. So, we have n =Nc ………… (16) Density of Holes in Valence Band The number of holes per unit volume of semiconductor in the energy range E and E + dE in valence band is represented as P(E) dE. Proceeding same way (as in case of electrons) we have Therefore, we have: P(E) dE = gh(E) dE fh(E) ………. (17) dE = width of Energy band gh(E) = The density of holes’ states per unit volume fh(E) = Fermi-Dirac distribution function i.e. probability that a hole occupies an electron state The number of electrons present in the conduction band per unit volume of material ‘n’ is obtained by integrating P(E) dE between the limits Evb and EV where EV = the bottom energy levels of valence band Evb = the bottom and top energy levels of valence band The total number of holes present in the valence band per unit volume of material ‘p’ is obtained by integrating P(E) dE ………. (18) Equation (18) can be represented as: ………. (19)
Now we know that below Evb no holes are present. Hence, Equation (19) becomes ………. (20) We know hole can also be defined as absence of an electron. presence of a hole = the absence of an electron Hence, the Fermi-Dirac function of holes fh(E) in the valence band is: Compared to exponential, the ‘1’ in the denominator is negligible,
Hence, ………. (21) The density of hole states between E and E + dE in valence band can be written similar to Equation (8.9) for electrons. ………. (22)
Where mh* is the effective mass of hole. Substituting Equations (21) and (22) in (20), ………. (23) The above equation can be simplified by the substitution: Put ɛ = EV − E ............. (24) so dɛ = − dE In Equation (24), EV is constant, as we change the variable E to ε in Equation (23), the integral limits also change. In Equation (24), as E → EV then ε → 0 and E→ −∞, then ε → ∞ the exponential term in Equation (23) becomes: ............. (25) Substituting Equations (24) and (25) in (23), we get: …………. (26) From Equation (14), we know the integral value T)3/2 put here and we get …………. (27) ….The term is almost constant compared with the exponential term as the temperature changes. So, it is a pseudo constant and is given by the symbol NV. So, we have …………… (28)
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………..(35) concentration of acceptor ions N−A = acceptor concentration x probability of finding an electron in acceptor level ………..(36) Similarly, the donor ions concentration is ………..(37)
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- For N-type, Hall coefficient RH= negative
- For P-type, Hall coefficient RH= Positive
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Sr.no | Parameter | CB | CE | CC |
1 | Common terminal betnI/p & o/p | Base | Emitter | collector |
2 | Input Current | IE | IB | IB |
3 | Output Current | IC | IC | IE |
4 | Current Gain | = | = | ɤ==1 |
5 | Input Vtg. | VEB | VBE | VBC |
6 | Output Vtg. | VCB | VCE | VCC |