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Fig. 1.1
No free electrons
Covalent bonded materials are poor conductors at normal temperature.
Have high melting and boiling temperature.
Fig. 1.3 Covalent atom
• EG of some semiconductors
– Silicon (Si): 1.1 eV
– Germanium (Ge): 0.7 eV
– Gallium arsenide (GaAs): 1.4 eV
– Zinc selenide (ZnSe): 2.7 eV
Fig. 1.6
Fig. 1.7
◦ For example, the bandgap energy Eg of the Carbon is about 6 eV. This large forbidden band separates the valance band
from the conduction band.
◦ Since the electron cannot acquire sufficient applied energy, conduction is impossible, and here Carbon is an insulator.
3. In semiconductors the width of the bandgap is relatively small ( ≈ 1 eV). Energies of these values normally
cannot be acquired from an applied field.
◦ Hence the valance band remains full, the conduction band empty and these materials are insulators at low temperature.
However, the conductivity increases with temperature so some valance electrons acquire thermal energy greater than Eg
and move to the conduction band.
Important terms
1. Coulomb’s law
The electrostatic force between two point electric charges q1 and q2 is directly proportional to the
product of the magnitudes of each charge and inversely proportional to the distance between the
charges:
𝑞1 𝑞2
𝐹=𝑘 (N) (1.1)
𝑟2
The electrons receive energy from both their position and motion.
The energy received by motion of electrons is called kinetic energy (K.E), while the energy gained from the
position is called potential energy (P.E).
1. The kinetic energy is defined as
1
K. E = mvd 2 (J) (1.5)
2
− m is the mass of electrons equals (9.11 x 10-31 Kg)
− vd is its drift velocity.
𝑞1 𝑞2
𝑃. 𝐸 = 𝑘 (J)
𝐿
For atoms the charges are equal and the distance between them equals to the radius of the orbit so the
potential energy is
𝑞2 (J) (1.6)
𝑃. 𝐸 = 𝑘
𝑟𝑛
− The constant k =1/ 4πɛ0 = 9x109,
− rn is the radius of n orbit.
To relate the current in a conductor to the drift velocity of the moving charges, consider
a wire of length L and a cross section area A in which a current I is flowing.
𝑞 𝑁𝐿 𝑞 𝑁 𝑣𝑑 (1.9)
𝐼= =
𝑡 𝐿 𝐿
The current density J (A/m2) in a conductor is defined as the current per unit area
Fig. 1.9
flowing in a particular direction.
𝐼
𝐽=𝐴 (A/m2) (1.10)
The current density J can be related to the drift velocity vd as follows:
qNvd
J= (A/m2) (1.11)
LA
So the current is proportional to both the electron concentration and the drift velocity.
Since the drift velocity is limited one can increase the current by increasing the carrier concentration.
Both are physical properties of materials. Using Eqs. (1.4) through (1.13), we can relate the current
density J to the electric field E in a metal as follows:
Since q and μ are constants, to increase the current density either we increase the applied voltage
(electric field) or the carrier concentration (n).
J=σE (A/m2 ) (1.15)
The conductivity σ ( Ω−1m−1) of the metal is given by
σ = nqμe (1.16)
Because n is independent of temperature in a metal, it follows that the decrease in electron mobility μ
with temperature causes the conductivity σ to decrease with temperature.
The resistivity is related to the resistance of the material as following, from (1.10)
𝐽 = 𝜎𝐸 (1.18)
• Replacing J as given in (1.11)
𝐼 = 𝜎𝐸𝐴
Solution
• First, the cross-sectional area of the bar:
Area= width x height
𝐴 = 4 𝑐𝑚 × 3 𝑐𝑚 = 12 𝑐𝑚2
• The resistance of aluminum is calculated using (1.14)
𝐿
𝑅=𝜌
𝐴
• From Table 1.1 the resistivity of the aluminum equals 2.65 x 10-8
125 𝑐𝑚
𝑅 = (2.65 × 10−8 )
12 𝑐𝑚2
𝑅 = 27.6 𝜇Ω