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Lecture 18 Rev

This document summarizes carrier transport phenomena such as drift, diffusion, and mobility in semiconductors. It discusses diffusion current density and how diffusion occurs from high concentration to low concentration regions. The total current density takes into account electron and hole drift and diffusion currents. The Einstein relation links mobility and diffusion coefficients. The Hall effect is explained for determining semiconductor type. Excess carrier generation and recombination rates are also summarized.

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0% found this document useful (0 votes)
15 views

Lecture 18 Rev

This document summarizes carrier transport phenomena such as drift, diffusion, and mobility in semiconductors. It discusses diffusion current density and how diffusion occurs from high concentration to low concentration regions. The total current density takes into account electron and hole drift and diffusion currents. The Einstein relation links mobility and diffusion coefficients. The Hall effect is explained for determining semiconductor type. Excess carrier generation and recombination rates are also summarized.

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최윤서
Copyright
© © All Rights Reserved
We take content rights seriously. If you suspect this is your content, claim it here.
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Lecture 18

Last lecture we learned


• Carrier transport phenomena

• Drift, drift current density, and mobility

• Factors affecting the mobility


• Phonon scattering
• Ionized impurity atom

• Conductivity & resistivity


Carrier diffusion
• Diffusion is the process whereby particles flow from a region of high
concentration toward a region of low concentration

t=0 t>0

• If the molecules are electrically charged, the net flow of charge would result in
a diffusion current
Diffusion current density
• Assume that an e- concentration varies in one dimension (here, the
temperature is uniform so that the average thermal velocity of e- is independent
of x)

x
• Let 𝑙 be a distance less than the mean free path of an e-. In other words, it is
the average distance that an e- travels between collisions (𝑙 < 𝑣𝑡ℎ 𝜏𝑐𝑛 )
Average thermal velocity
Time before collision

• Then, e- moving to the right at 𝑥 = −𝑙 and e- moving to the left at 𝑥 = +𝑙 will


cross the 𝑥 = 0 plane.

𝑙 𝑙
𝑥 = −𝑙 𝑥=0 𝑥 = +𝑙

• 1/2 of the e- at 𝑥 = −𝑙 will be traveling to the right


• 1/2 of the e- at 𝑥 = +𝑙 will be traveling to the left
• The net rate of e- flow, 𝐹𝑛 , in the +x direction at x = 0 is then
1 1 1
𝐹𝑛 = 𝑛|−𝑙 𝑣𝑡ℎ − 𝑛|+𝑙 𝑣𝑡ℎ = 𝑣𝑡ℎ 𝑛|−𝑙 − 𝑛|+𝑙
2 2 2

• We can expand the e- concentration in a Taylor series about x = 0, we get:


1 𝑑𝑛 𝑑𝑛 𝑑𝑛
𝐹𝑛 = 𝑣𝑡ℎ 𝑛|0 − 𝑙 − 𝑛|0 + 𝑙 = −𝑣𝑡ℎ 𝑙
2 𝑑𝑥 𝑑𝑥 𝑑𝑥

• Each electron has a charge (-e), so the current is:


𝑑𝑛
𝐽 = −𝑒𝐹𝑛 = +𝑒𝑣𝑡ℎ 𝑙
𝑑𝑥

• This current is the electron diffusion current, and it is proportional to the density
gradient of the electron concentration.
• The diffusion of e- from a region of high concentration to a region of low
concentration produces a flux of e- flow in the negative x direction
• Since e- have a negative charge, the conventional current direction is in the
positive x direction
• We may write the e- diffusion current density for the 1D case as

𝑑𝑛
𝐽𝑛𝑥|𝑑𝑖𝑓𝑓 = 𝑒𝐷𝑛 • 𝐷𝑛 = electron diffusion coefficient [=] cm2/s (> 0)
𝑑𝑥

• The diffusion of holes, from a region of high concentration to a region of low


concentration, produces a flux of holes in the negative x direction. Since holes
are positively charged, the conventional diffusion current density is also in the
negative x direction.
𝑑𝑝
𝐽𝑛𝑥|𝑑𝑖𝑓𝑓 = −𝑒𝐷𝑝 • 𝐷𝑝 = hole diffusion coefficient [=] cm2/s (> 0)
𝑑𝑥
Total current density
• We now have 4 possible independent current mechanisms:
• Electron drift current
• Electron diffusion current
• Hole drift current
• Hole diffusion current

• We can generalize this equation in 3D as:


• The electron mobility (𝜇𝑛 ) gives an indication of how well an e- moves in a
semiconductor as a result of the force of an electric field. The electron diffusion
coefficient (𝐷𝑛 ) gives an indication of how well an e- moves in a semiconductor
as a result of density gradient.

• The 𝜇𝑛 and 𝐷𝑛 are not independent parameters. Also 𝜇𝑝 and 𝐷𝑝 are not
independent parameters.
• In fact, their relation is summarized by the Einstein relation

𝐷𝑛 𝐷𝑝 𝑘𝐵 𝑇
= =
𝜇𝑛 𝜇𝑝 𝑒

𝜇 = cm2 Τ 𝑉 ∙ 𝑠

𝐷 = cm2 Τ𝑠
Hall effect
• Consider a charged particle moving in the positive x direction with a velocity 𝑣
as shown below:
• If a magnetic field is applied in the positive y direction, then a force is
developed on the particle that moves the particle in the positive z
direction (perpendicular to both the velocity and magnetic fields)
𝑣Ԧ
z
y 𝐹Ԧ = 𝑞 𝑣Ԧ × 𝐵
𝐵
x

• We can apply this effect to a semiconductor device to determine if the


semiconductor is n-type or p-type.
(Assuming the semiconductor is extrinsic with the conc. of majority carrier >> conc. of
minority carrier)
• Consider we have a semiconductor shown below:
𝐵

𝑑
𝐸 𝐼𝑥 𝑊
z
y
x
• Top view:
• In a p-type semiconductor (𝑝 > 𝑛), the • In a n-type semiconductor (𝑛 > 𝑝), the e-
holes accumulate at the bottom wall (y=0) accumulate at the top wall (y=W)

𝐵 𝐵

y y=0 y y=0

x 𝐹Ԧ x 𝐹Ԧ
• Due to accumulation of charge on one side, there is a net charge which
induces an electric field in the y direction

• p-type • n-type
- - - - - - - - - - - +++++++++++
𝐵
𝐵
++++++ + + ++ - - - - - - - - - - -
y y

𝐸𝐻 𝐸𝐻
x x

• The induced electric field is called the Hall field, and this produces a voltage
across the semiconductor which is called the Hall voltage

𝑉𝐻 = 𝐸𝐻 𝑊 • NOTE: here 𝐸𝐻 is the amount of electric field


and is a scalar quantity. Therefore, we assume
𝐸𝐻 to be positive in the +y direction
• At steady-state, the force due to magnetic field will be balanced by the force
due to induced electric field
𝐹 = 𝑞 𝐸𝐻 + 𝑣Ԧ × 𝐵 = 0
𝐵
which in scalar form, we can write:
𝑞𝐸𝐻 = 𝑞𝑣𝑥 𝐵𝑧 𝐸𝐻 = 𝑣𝑥 𝐵𝑧

Using the definition of Hall voltage, we obtain:

𝑉𝐻 = 𝑣𝑥 𝐵𝑧 𝑊
• For p-type semiconductor, the drift velocity of holes can be written as

(Using 𝑉𝐻 = 𝐸𝐻 𝑊)
• For n-type semiconductor, the Hall voltage and the e- concentration are given
by
NOTE: the Hall voltage is negative for n-type
semiconductor; therefore, the e-
concentration is actually a positive value

• Now, with the majority carrier concentration known, we can determine the
majority carrier mobility

• For p-type:

• For n-type:
• We can also define a Hall coefficient, for a material, as:
𝐸𝐻 𝑉𝐻 Τ𝑊 𝑉𝐻 𝑑
𝑅𝐻 = = =
𝐽𝑥 𝐵𝑧 𝐼𝑥 Τ𝑊𝑑 𝐵𝑧 𝐼𝑥 𝐵𝑧

• For p-type, we have


1 𝐼𝑥 𝐵𝑧
𝑅𝐻 = 𝑉𝐻 = 𝑅𝐻
𝑒𝑝 𝑑

• For n-type, we have


1 𝐼𝑥 𝐵𝑧
𝑅𝐻 = − 𝑉𝐻 = 𝑅𝐻
𝑒𝑛 𝑑
Excess carrier generation and recombination
• At thermal equilibrium, the net carrier concentrations are independent of time

• Looking closely, at thermal equlibrium, e- are continually being excited from the
valence band into the conduction band. At the same time, e- moving randomly
through the crystal in the conduction band may come in close proximity to
holes and “fall” into the empty states in the valence band

• Therefore, the rate at which e- and


holes are generated and the rate at
which they recombine must be equal
• Using symbols, we can write this as:

Thermal- 𝐺𝑛0 = 𝐺𝑝0 = 𝑅𝑛0 = 𝑅𝑝0 *Unit = #/(cm3·s)


generation Recombination
rate of e- rate of hole
Thermal- Recombination
generation rate of e-
rate of hole

• e- and holes can also be generated by an external force, i.e. high-energy photons.
In this case, these e- and holes are called excess e- and excess holes
• These excess e- and excess holes are created in pairs, so their generation rates
are the equal
𝑔𝑛′ = 𝑔𝑝′ *Unit = #/(cm3·s)
Generation Generation
rate of rate of
excess e- excess hole
• When excess e- and holes are generated, the concentration of e- in the
conduction band and of holes in the valence band increase above their
thermal-equilibrium value:
𝑛 = 𝑛0 + 𝛿𝑛 𝑝 = 𝑝0 + 𝛿𝑝

e- concentration in • Similar definitions for hole


the conduction band (in the valence band)
Thermal equilibrium Excess e-
e- concentration in concentration in the
the conduction band conduction band
• As the external force perturbes the equilibrium condition,

𝑛𝑝 ≠ 𝑛0 𝑝0 = 𝑛𝑖2

• As in the case of thermal equilibrium, an excess e- may “fall down” into the
valence band, leading to recombination

• The excess e- and holes recombine in pairs,


so the recombination rates must be equal:

𝑅𝑛′ = 𝑅𝑝′
Recombination Recombination
rate of excess rate of excess
e- hole

*Unit = #/(cm3·s)
• In the direct band-to-band recombination, the recombination occurs
spontaneously; thus, the probability of an e- and hole recombining is constant
with time
• The net rate of change in the e- concentration can be written as

• With: • And, 𝛼𝑟 𝑛𝑖2 is the thermal-equilibrium


generation rate
• Since excess e- and holes are created and recombine in pairs, we have
𝛿𝑛 𝑡 = 𝛿𝑝(𝑡)

• NOTE: excess e- and hole concentrations are equal, so we can simply use
the term excess carriers to mean either

• We can solve the above equation by imposing the condition of low-level


injection , which puts limits on the magnitude of the excess carrier
concentration
• Consider a p-type material (𝑝0 ≫ 𝑛0 ) under low-level injection (𝛿𝑛 𝑡 ≪ 𝑝0 ),
then we have:

• We can solve the above equation and get:

−1
𝜏𝑛0 = 𝛼𝑟 𝑝0 = excess minority carrier lifetime

• The recombination rate – which is defined as a positive quantity – of excess


minority carrier e- can be written as:
• For the direct band-to-band recombination, the excess majority carrier holes
recombine at the same rate, so that for the p-type material:

• In the case of an n-type material (𝑛0 ≫ 𝑝0 ) under low-level injection (𝛿𝑛 𝑡 ≪


𝑛0 ), the decay of minority carrier holes occurs with a time constant

𝜏𝑝0 = 𝛼𝑟 𝑛0 −1 excess minority carrier lifetime

• The recombination rate of the majority carrier e- will be the same as that of the
minority carrier holes, so we have

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