\(p-n\) junction (PHC504)

p-n junction

Semiconductors are the materials at the heart of many electronic devices. The elemental semiconductors are few, the only ones of any practical use being germanium (\(Ge\)) and silicon (\(Si\)) and only silicon is widely used nowadays. However, there are some compound semiconductors which find applications in light-emitting diodes, semiconductor lasers, microwave devices and other specialised areas. Most of these are based on elements from groups \(III\) and \(V\) of the periodic table and occasionally from groups \(II\) and \(VI\). These are known respectively as \(III-Y\) and \(II-VI\) compounds, examples being gallium arsenide (\(GaAs\)), gallium phosphide (\(GaP\)) and cadmium sulphide (\(CdS\)). The Semincondcting elements available in the Periodic Table are \(B\), \(C\), \(Si\), \(Ge\), \(As\), \(Se\), and \(Te\).

Electrons and holes in semiconductors

Semiconductors are only different from insulators because of conduction brought about by thermally generated charge carriers (intrinsic conduction) or by the addition of controlled amounts of impurities (extrinsic conduction), called dopants. In semiconductor devices only extrinsic conduction is desirable. The charge carriers are electrons and holes, which act just like positively-charged electrons. By adding the right kind of dopants it is possible to make semiconductor material which conducts either with electrons alone (\(n\)-type material) or with holes alone (\(p\)-type material). But first we must consider the ordinary processes of electrical conduction.

Electrical conductivity

The resistance, \(R\), of a bar of material of length, \(l\), and uniform cross-sectional area, \(A\), is

\[R = 1/\sigma A\]

where \(\sigma\) is the electrical conductivity of the material. If \(l\) is in \(m\), \(A\) in \(m^{2}\) and \(R\) in \(\Omega\), then \(\sigma\) is in \(S/m\). The reciprocal of the conductivity is the resistivity, \(\rho\), which has units of \(\Omega m\).

The electrical conductivity of materials is found to vary over a very wide range - wider than any other material property. Materials came to be classified according to the behaviour and magnitude of their conductivities. Some, mainly metals and alloys, were found to be good conductors at room temperature (\(\rho\) ranging from about \(10^{-8}\) for silver to \(10^{-6}\) \(\Omega m\) for nichrome resistance wire), with a conductivity which decreased with increasing temperature and did not change much when the metal was impure. Other materials, mainly non-metals such as sulphur, polystyrene and silica, were found to have a very low conductivity at room temperature (\(p = 10^{10}\) to \(10^{16}\) \(\Omega m\)) which increased rather rapidly with temperature.

Again it was found that the purity of the material had relatively little effect on the conductivity or its temperature coefficient. Then there was another class of materials, such as germanium, silicon and silicon carbide, which had very variable conductivities (\(p = 10^{-6}\) to \(10^{2}\) \(\Omega m\)) and temperature coefficients that could be positive or negative and depended, it was eventually discovered, on the kind of impurities present, sometimes only in tiny amounts. Though these materials came to be called semiconductors, there is no fundamental difference between insulators and semiconductors: diamond is widely considered to be an insulator, and mostly it is, but semiconducting diamonds are known. Finally a fourth type of material was discovered (by Kammerlingh Onnes in 1911) that had no resistance at all below a critical temperature: it was a superconductor.

Intrinsic conduction

Generally speaking the conductivity of metals is due to free electrons in them and these are largely absent from semiconductors. There does, however, appear to be a characteristic energy associated with the conduction process. If sufficiently energetic photons (quanta of e.m. radiation) are incident on a semiconductor its conductivity rises enormously. The photon's energy can be equated with the energy needed to transfer an electron from a bound state (the electron is said to be in the valence band) to a free or conducting state (then it is said to be in the conduction band). This characteristic energy is known as the band-gap energy or just the band gap.

Measurements in magnetic fields (Hall-effect measurements) show that there are two types of charge carrier: a negatively charged one identified with the electron and a positively charged one called a hole. When a photon causes an electron to transfer from valence band to conduction band it leaves behind a hole in the valence band. This hole can move under the influence of an electric field, that is it is a charge carrier that acts like a positively charged electron.

Silicon has a band gap of about \(1.1 ~eV\) (electron volts, \(1 ~eV = 1.6 \times 10^{-19} J\)), meaning that an electron (charge, \(-q = -1.6 \times 10^{-19} C\)) changes its potential by \(1.1 V\) on crossing the band gap. Germanium has a band gap of \(0.7 ~eV\) and diamond has one of \(5.4 ~eV\). Thermal energy can also cause the creation of electron-hole pairs that causes conduction. In a pure semiconductor kept in the dark, thermally generated charge carriers are the sole means of conduction. The numbers of them per unit volume (the intrinsic carrier concentration, \(n_{i}\) are given by

\[n_i = N~exp\left(\frac{-E_g}{2k_BT}\right)~~~~~~~~~~~~~~~~~~~~~~~~(1)\]

where \(N\) is a constant for a given semiconductor, \(E_{g}\) is the band gap energy in Joules, \(k_{B}\) is Boltzmann's constant (\(1.38 \times 10^{-23}~J/K\)) and \(T\) is the temperature in \(K\). The factor of \(2\) in the denominator of the exponent means that in classical terms, the electron starts off in the middle of the band gap. This is because electrons are not classical particles. Be that as it may, no matter how carefully prepared the material is, there will always be thermal carrier generation and associated conductivity.

The conductivity in any material is given by \(\sigma = nq \mu\), where \(\mu\) is the mobility of the charge carrier. The mobility is the speed (\(v\)) that a charge carrier acquires per unit electric field (\(E\)), that is \(\mu = v/E\). \(q\) is the magnitude of the electronic charge and n the number of charge carriers per unit volume. For an intrinsic semiconductor

\[\sigma =nq(\mu_{e} +\mu_{h})~~~~~~~~~~~~~~~~~~~~~~~~(2)\]

where \(n\) is the number of electron-hole pairs and \(\mu_{e}\) and \(\mu_{h}\) are the respective electron and hole mobilities. It is worthwhile putting some numbers into equations 1 and 2. The material constants for silicon are \(N = 3 \times 10^{25}/m3\), \(E_{g} = 1.1~~eV\) = \(1.76 \times 10^{-19}~J\), \(\mu_{e} = 0.14 m^{2}V^{-1}~s^{-1}\) and \(\mu_{h} = 0.05~m^{2}V^{-1}s^{-1}\), so at \(300~K\), equation \(2\) yields \(n_i= 2 \times 10^{16}~m^{-3}\) and equation \(3\) gives \(\sigma= 6 \times 10^{-4}~S/m\) or \(p = 1/\sigma = 1650~\Omega m\). A bar of intrinsic silicon \(100~mm\) long and of square cross-section, \(10\) mm by \(10\) mm, would then have, by equation 1, a resistance of \(1.7 M\Omega\). Compare this with a copper bar of the same size, which would have a resistance of \(17 \mu\Omega\). Equation 2 also shows that the carrier density and hence a will rapidly increase with temperature (by \(7 \%/K\)).

Extrinsic conduction

At 300 K the intrinsic carrier concentration is not very high in silicon and the numbers of electrons and holes are equal. Silicon is a covalently-bonded element with the same structure as diamond and germanium. Each silicon atom has four outer, bonding electrons and with them it forms four covalent bonds by which it is joined to four other silicon atoms arranged at the comers of a regular tetrahedron as in figure.

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Bonding electrons in Si around (a) a Si atom, (b) a P atom and (c) a B atom

If an atom of silicon is replaced by one of phosphorus, which has five electrons available for bonding, then it can form four bonds with neighbouring silicon atoms, using up four electrons and having one left over. This spare electron is readily detached from its parent atom (the ionisation energy is of the order of \(10 m~eV\)) to move into the nearby conduction band; at \(300 K\) practically all the phosphorus atoms are ionised. The concentration of phosphorus atoms, \(N_{D}= n\), the conduction-electron concentration. Phosphorus is known as a donor atom because it donates electrons to the conduction band. Arsenic and antimony behave as donors in silicon too.

When an atom of boron is substituted for one of silicon the position is different, as boron has only three electrons available for bonding, as a result, when it forms four bonds with a neighbouring silicon atom as in figure, there is a deficiency of an electron -a hole - in one of the bonds. This hole can also move about freely in the valence band and acts as a mobile positive charge carrier, though really the electrons move the other way. The boron atoms are also effectively \(100 \%\) ionised in silicon (though negatively, not positively like phosphorus), so the concentration of boron atoms, \(N_{A}= p\), the hole concentration. Boron is termed an acceptor because it accepts an electron from a silicon atom. In semiconductor devices, the dopant atom concentration far exceeds the intrinsic carrier density; conduction is thus said to be extrinsic. Figure shows the energy levels in extrinsic silicon. The higher up an electron is in figure , the higher is its energy. However, for holes, the lower it is, the higher is its energy.

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Energy levels in silicon. The donor and acceptor energy levels would be much closer to the band edges than in this diagram

The law of mass action applies to the charge carrier concentration in a semiconductor, that is the product of electron and hole concentration, \(p-n\), is constant at constant temperature. If electrons predominate, the material is said to be \(n\)-type and the electrons are the majority carriers, holes the minority carriers. If holes predominate, the material is \(p\)-type, holes are the majority and electrons the minority carriers.

Majority and Minority Carriers

In the intrinsic state, the number of free electrons in Ge or Si is due only to those few electrons in the valence band that have acquired sufficient energy from thermal or light sources to break the covalent bond or to the few impurities that could not be removed. The vacancies left behind in the covalent bonding structure represent our very limited supply of holes. In an n-type material, the number of holes has not changed significantly from this intrinsic level. The net result, therefore, is that the number of electrons far outweighs the number of holes. For the p-type material, the number of holes far outweighs the number of electrons. For this reason:

When the fifth electron of a donor atom leaves the parent atom, the atom remaining acquires a net positive charge, hence the plus sign in the donor-ion representation. For similar reasons, the minus sign appears in the acceptor ion. The n - and p-type materials represent the basic building blocks of semiconductor devices.

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The region around an \(p\)- and \(n\)- type with minority carriers and majority carriers.

The p-n junction

Whether a particular piece of semiconductor is \(p\)-type, \(n\)-type or intrinsic makes no difference to the direction of (conventional) current flow when a voltage is applied to its ends, though the current's magnitude will depend on the doping level. But when \(p\)- and \(n\)-type materials are joined, or a \(p-n\) junction is formed, matters undergo a great transform-ation: current is now found to flow much more easily in one direction than in the other. The junction is a rectifier, or diode. \(p-n\) junctions, singly or in combinations of two or more, are essential for the operation of many semiconductor devices.

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The region around an unbiased \(p-n\) junction. The ionised atoms in the depletion zone are immobile. The p-type region is more lightly doped than the \(n\)-type, so the depletion zone is wider there as the sum of the fixed charges is zero

Figure 3 shows a cross-section of a \(p-n\) junction, with no externally applied potential.

Before the junction is formed the n-type material consists of fixed, positively-charged donor ions and an equal number of conduction electrons, while the \(p\)-type material consists of fixed, negatively-charged acceptor ions and an equal number of holes. When the junction is formed, electrons from the \(n\)-type region diffuse into the p-type region (leaving a fixed positive charge behind) and combine with holes. Simultaneously, holes from the \(p\)-type region diffuse into the n-type region (leaving a fixed negative charge behind) and combine with free electrons, thus causing an absence of mobile charge carriers in the junction region. In the depletion region (or zone) in the vicinity of the junction a voltage called the built-in potential, \(V_{bi}\) is thus set up which opposes the diffusion of charge carriers across the junction. \(V_{bi}\) is about \(0.6 V\) in silicon, about \(1.2 V\) in \(GaAs\) and about \(0.3 V\) in germanium. Thus with no bias applied, the diffusion current for the electrons (from then-region), \(I_{er}\) is exactly equal to the current (due to thermally generated electrons in the p-region), \(I_{eg}\) produced by \(V_{bi}\)· The same is true for the hole currents, \(I_{hg}\) and \(I_{hr}\). The holes and electrons move in opposite directions, though the conventional currents are in the same direction because of the negative electronic charge: thus \(I_{ g} = I_{eg} + I_{hg}\).

When reverse bias is applied to the junction, that is the \(p\)-type side is made more negative than the \(n\)-type, the depletion region becomes larger as the bias voltage adds to \(V_{bi}\). The diffusion current, \(I_{r}\) that flows across the junction is very small, since only carriers with enough energy can surmount the potential barrier. But the current, \(I_{g}\), due to thermally generated minority carriers, remains unaffected by the bias field, resulting in a net reverse current, \(I_{g} - I_{r}\). When the junction is fotward biased (\(p\)-type side positive with respect to the \(n\)-type) the depletion zone is narrower than under zero bias and \(I_{r}\) is now very much greater than \(I_{g}\). Figure 4 shows the effect of bias polarity on the depletion zone widths and the forward current.

Reverse current is often called leakage current and its magnitude depends on the material and the size of the diode. Germanium diodes have high leakage currents - about \(1,000\) times that of silicon diodes (a silicon signal diode at room temperature typically has a leakage of around \(1 nA\)). Light causes the generation of additional electron-hole pairs in semiconductors thereby increasing the leakage current. The so-called dark current is the leakage current when no light falls on the semiconductor material.

The semiconductor diode, with applications too numerous to mention, is created by simply joining an n-type and a p-type material together, nothing more, just the joining of one material with a majority carrier of electrons to one with a majority carrier of holes.

No Applied Bias ( \(V = 0 V\))

When the two materials are “joined” the electrons and the holes in the region of the junction will combine, resulting in a lack of free carriers in the region near the junction.

The only particles displayed in this region are the positive and the negative ions remaining once the free carriers have been absorbed.

*This region of uncovered positive and negative ions is called the depletion region due to the “depletion” of free carriers in the region. *

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Currents and depletion zones in p-n junctions under different unbias conditions
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The region around an unbiased \(p-n\) junction.

If leads are connected to the ends of each material, a two-terminal device results. Three options then become available: no bias, forward bias, and reverse bias. The term bias refers to applying an external voltage across the two terminals of the device to extract a response. The condition is the no-bias situation if no external voltage is applied.

The absence of a voltage across a resistor results in zero current through it.

Under no-bias conditions, any minority carriers (holes) in the n-type material that find themselves within the depletion region for any reason whatsoever will pass quickly into the p-type material. The closer the minority carrier is to the junction, the greater the attraction for the layer of negative ions and the less the opposition offered by the positive ions in the depletion region of the n-type material. The majority of carriers (electrons) of the n-type material must overcome the attractive forces of the layer of positive ions in the n-type material and the shield of negative ions in the p-type material to migrate into the area beyond the depletion region of the p-type material. However, the number of majority carriers is so large in the n-type material that there will invariably be a small number of majority carriers with sufficient kinetic energy to pass through the depletion region into the p-type material. Again, the same type of discussion can be applied to the majority carriers (holes) of the p-type material.

In the absence of an applied bias across a semiconductor diode, the net flow of charge in one direction is zero.

Reverse-Bias Condition (\( V_{D} \lt 0~V\))

If an external potential of V volts is applied across the p - n junction such that the positive terminal is connected to the n-type material and the negative terminal is connected to the p-type material, as shown in the figure, the number of uncovered positive ions in the depletion region of the n-type material will increase due to the large number of free electrons drawn to the positive potential of the applied voltage. For similar reasons, the number of uncovered negative ions will increase in the p-type material. The net effect, therefore, is a widening of the depletion region. This widening of the depletion region will establish too great a barrier for the majority of carriers to overcome, effectively reducing the majority carrier flow to zero.

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Currents and depletion zones in p-n junctions under different bias conditions
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The region around an reversed biased \(p-n\) junction.

The number of minority carriers, however, entering the depletion region will not change, resulting in minority-carrier flow vectors of the same magnitude indicated in Fig. with no applied voltage.

The current that exists under reverse-bias conditions is called the reverse saturation current and is represented by \(I_{s}\).

The term saturation comes from the fact that it reaches its maximum level quickly and does not change significantly with increases in the reverse bias potential

Forward-Bias Condition ( \(V_{D} \gt 0\) \(V\))

A forward bias or “on” condition is established by applying the positive potential to the p-type material and the negative potential to the n-type material, as shown in Fig. 1.14.

The application of a forward-bias potential V D will “pressure” electrons in the n-type material and holes in the p-type material to recombine with the ions near the boundary and reduce the width of the depletion region, as shown in Fig. The resulting minority-carrier flow of electrons from the p-type material to the n-type material (and of holes from the n-type material to the p-type material) has not changed in magnitude (since the conduction level is controlled primarily by the limited number of impurities in the material), but the reduction in the width of the depletion region has resulted in a heavy majority flow across the junction. An electron of the n-type material now “sees” a reduced barrier at the junction due to the reduced depletion region and a strong attraction for the positive potential applied to the p-type material. As the applied bias increases in magnitude, the depletion region will continue to decrease in width until a flood of electrons can pass through the junction, resulting in an exponential rise in current, as shown in the forward-bias region of the characteristics.

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The region around an forward biased \(p-n\) junction.
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The IV characteristics of \(p-n\) junction.

The general characteristics of a semiconductor diode can be defined by the following equation, referred to as Shockley’s equation, for the forward- and reverse-bias regions:

\[I_{D} = I_{s}(e^{V_{D}/\eta V_T} - 1)~(A)\]

where \(I\) s is the reverse saturation current \(V_{D}\) is the applied forward-bias voltage across the diode \(n\) is an ideality factor, which is a function of the operating conditions and physical construction; it has a range between \(1\) and \(2\) depending on a wide variety of factors (\( n=1\) will be assumed throughout this text unless otherwise noted).

The voltage \(V_T\) in Eq. is called the thermal voltage and is determined by

\[V_T = \frac{kT_{K}}{q}~(V)\]

where \(k\) is Boltzmann's constant \(1.38 \times 10^{-23}\) \(J/K\)

\(T_K\) is the absolute temperature in kelvins \(273\) \(K\) the temperature in \(°C\)

\(q\) is the magnitude of electronic charge \(1.6 \times 10^{-19}\) \(C\)

If we expand the equation of each region:

\[I_{D} = I_{s}e^{V_{D}/\eta V_T} - I_{s})~(A)\]

For positive values of \(V_{D}\), the first term of the above equation will grow very quickly and totally overpower the effect of the second term. The result is the following equation, which only has positive values and takes on the exponential format \(e^{x}\).

\[I_{D} = I_{s}(e^{V_{D}/\eta V_T})~(V_{D}~positive)\]

For negative values of \(V_D\), the exponential term drops very quickly below the level of \(I\), and the resulting equation for \(I_{D}\) is simply

\[I_{D} = -I_{s} (V_{D}~negative)\]

For negative values of \(V_{D}\), the current is essentially horizontal at the level of \(-I_{s}\).

The actual reverse saturation current of a commercially available diode will normally be measurably larger than that appearing as the reverse saturation current in Shockley’s equation.

This increase in level is due to a wide range of factors that include

Breakdown Region

Even though the scale of Fig. is in tens of volts in the negative region, there is a point where the application of too negative a voltage with the reverse polarity will result in a sharp change in the characteristics, as shown in Fig. The current increases at a very rapid rate in a direction opposite to that of the positive voltage region. The reverse bias potential that results in this dramatic change in characteristics is called the breakdown potential and is given the label \(V_{BV}\).

Avalanche breakdown

As the voltage across the diode increases in the reverse-bias region, the velocity of the minority carriers responsible for the reverse saturation current \(I_{s}\) will also increase. Eventually, their velocity and associated kinetic energy (WK= 12mv2) will be sufficient to release additional carriers through collisions with otherwise stable atomic structures. That is, an ionization process will result whereby valence electrons absorb sufficient energy to leave the parent atom. These additional carriers can then aid the ionization process to the point where a high avalanche current is established, and the avalanche breakdown region is determined.

Zener breakdown

The avalanche region ( \(V_{BV}\) ) can be brought closer to the vertical axis by increasing the doping levels in the p- and n-type materials. However, as \(V_{BV}\) decreases to very low levels, such as \(5\) \(V\), another mechanism, called Zener breakdown, will contribute to the sharp change in the characteristic. It occurs because there is a strong electric field in the region of the junction that can disrupt the bonding forces within the atom and “generate” carriers. Although the Zener breakdown mechanism is a significant contributor only at lower levels of \(V_{BV}\), this sharp change in the characteristic at any level is called the Zener region, and diodes employing this unique portion of the characteristic of a \(p–n\) junction are called Zener diodes.

The breakdown region of the semiconductor diode described must be avoided if the response of a system is not to be completely altered by the sharp change in characteristics in this reverse-voltage region. The maximum reverse-bias potential that can be applied before entering the breakdown region is called the peak inverse voltage (referred to simply as the \(PIV\) rating) or the peak reverse voltage (denoted the \(PRV\) rating).

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The Zener region around an reversed biased \(p-n\) junction.

If an application requires a PIV rating more significant than that of a single unit, several diodes of the same characteristics can be connected in series. Diodes are also connected in parallel to increase the current-carrying capacity.

Temperature Effects

Temperature can have a marked effect on the characteristics of a semiconductor diode, as demonstrated by the characteristics of a silicon diode.

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The effect of temperature on the \(p-n\) junction characteristics.

A glossary of terms

Terms Details
Acceptor A dopant atom that has fewer valence electrons than the host semiconductor material, so that it can accept one or more electrons from the valence band of the host and gives rise to a corresponding number of holes in the valence band. Boron is an acceptor atom in silicon
Band gap The energy difference, \(E_{g}\), between the top of the valence band and the bottom of the conduction band, usually given in electron volts (\(~eV\)), where \(1 ~eV = 1.6 \times 10^{-19} J\). In silicon the band gap is about \(1.1 ~eV\).
Bias The potential applied to a \(p-n\) junction. Positive bias means that the \(p\)-type side of the junction is at a higher potential than the \(n\)-type side, negative bias means vice versa
Charge carrier compensation Either a negatively-charged electron or a positively charged hole The reduction in charge-carrier concentration in a semiconductor that is brought about by incorporating both donors and acceptors into the semiconductor material. Hence reduced conductivity
Conduction band A region of energy states lying above the valence band and separated from it by an energy gap in which electrons are not bound to their parent atoms and can move under the influence of applied fields
Conductivity Defined by \(\sigma= nq\mu\), where \(n\) = charge carriers/\(m_{3}\), \(q\), the electronic charge = \(1.6 \times 10^{-19} C\), \(\mu\) = mobility (\(q.v.\)) in \(m^{2}/V/s\). The reciprocal of the resistivity (\(q.v.\))
conductivity type Determined by the majority charge carriers. When these are electrons the material is \(n\)-type and when these are holes it is \(p\)-type
Depletion region A volume of material near a \(p-n\) junction in which oppositely charged carriers have combined so that the mobile charge carrier concentration is very small
Donor A dopant atom which has more valence electrons than its host semiconductor, so that it tends to give up electrons to the conduction band, so making the material \(n\)-type. Examples are phosphorus and arsenic in silicon
Dopant An element which is incorporated in controlled amounts into a semiconductor during crystal growth. At working temperatures the dopant is ionised and supplies electrons or holes to the host to produce a vast excess of one or the other, so making the material \(p\)-type or \(n\)-type
Extrinsic conduction Conduction brought about by charge carriers from ionised dopants
Hole The absence of an electron in the valence band, which acts like a positively charged electron
Intrinsic conduction Conduction by hole-electron pairs produced by ionisation of the semiconductor material. Ionisation means that electrons in the valence band must cross the band gap to reach the conduction band. At normal temperatures there are few carriers produced like this and conductivity is low
Majority carrier The more-numerous charge-carrier. Electrons in \(n\)-type material, holes in p-type
Minority carrier The less-numerous charge-carrier. Holes in n-type material, electrons in p-type
Mobility The speed acquired by a charge carrier in unit electric field, \(\mu = v/E= \sigma/nq\)
p-n junction The plane dividing \(p\)-type from \(n\)-type material, which lies within the depletion region resistivity valence band
Resistivity Given by \(\rho = RA/l\), where \(R\) = resistance in \(\Omega\) measured between the ends of a bar of material, cross-sectional area \(A m^{2}\) and length \(l~m\)
Valance band The region of energy states lying below the conduction band by \(E_{g}\), the gap energy. Holes are free to move in the valence band like electrons in the conduction band

Model Questions

  1. (a) A length of round copper wire has a diameter of \(1~mm\), calculate what length of wire will have a resistance of \(1 k\Omega\) if \(\sigma = 60 MS/m\). (b) If a cylindrical piece of silicon, \(1 mm\) in diameter, is doped with \(10^{20} m^{-3}\) atoms of phosphorus, what length is required to give a resistance of \(1 k\Omega\), assuming the phosphorus is fully ionised and that the electronic mobility in silicon is \(0.1 m^{2} v^{-1} s^{-}1\) (c) If the free electron concentration in copper is \(8.5 \times 10^{28} m-3\), what is the electronic mobility in copper? What is the ratio of electronic mobilities in silicon and copper? [(a) \(47.1 km\) (b) \(1.26 mm\) (c) \(0.0047 m^{2}V^{-1} s^{-1}\), \(\mu_{Si}\mu_{Cu} = 21.3\) ]

  2. Find the relative rate of change of electrical conductivity with temperature in an intrinsic semiconductor from equation 2, assuming that the mobility of the charge carriers is not dependent on temperature. Given that the bandgaps of germanium, silicon and gallium arsenide are \(0.66\), \(1.1\) and \(1.42 ~eV\), what will be the percentage change in their intrinsic conductivity when the temperature is increased from \(300 K\) to \(302 K\)? [\(d\sigma/\sigma dT = E_{g}/2kT^{2}\), \(8.6 \%\), \(14.2 \%\) and \(18.2 \%\)]

  3. In an extrinsic semiconductor the carrier concentration is found to be constant above \(100 K\), but the carrier mobility goes as \(T^{-1.5}\); how will the relative conductivity change with temperature at \(300 K\)? What will the percentage change in conductivity be as the temperature increases from \(300 K\) to \(302 K\)? [ \(d\sigma/\sigma dT = = -1.5/T\), \(-1 \%\)]

  4. At a certain temperature, the carrier concentration in a semiconductor is proportional to \(exp(-E_{c}/2kT)\), where \(E_{c}\) is the carrier's ionisation energy. The mobility of the carriers is proportional to \(T^{-1.5}\). If \(E_{c}\) = \(0.05 ~eV\), at what temperature will the temperature coefficient of the conductivity (\(d\sigma/\sigma dT\)) be zero? [\(193 K\)]

  5. The mobility of electrons is five times the mobility of holes in a certain semiconductor. When doped with \(10^{22}\) atoms of phosphorus per \(m^{3}\) it is found to have a conductivity of \(10 S/m\). What are the carrier mobilities? What will the conductivity of a \(p\)-type sample be if the carrier density is \(10^{21} m^{-3}\)? (Assume full ionisation of dopants.) [\(6.25 \times 10^{-3}\) and \(1.25 \times 10^{-3}\) \(m^{2}/V/s\), \(0.2 S/m\)]

  6. In a sample of semiconducting material the electronic mobility is a times the hole mobility and the intrinsic hole concentration is \(p\) per unit volume. Derive an expression for the minimum conductivity. If \(\mu_{h} = 0.009~m^{2}V^{-1} s^{-1}\), \(\alpha= 3\) and \(p = 10^{16}\) \(m^{-3}\), what is the minimum conductivity and what are the corresponding electron and hole concentrations? [\(\sigma_{min} = 2pq\mu_{h}\sqrt{a}\) (\(q = 1.6 \times 10^{-19} C\)), \(5 \mu S/m\), \(5.8 \times 10^{15} m^{-3}\), \(1.73 \times 10^{16} m^{-3}\)]