"'Citations missing|date=March 2008
A semiconductor is a
solidmaterial that has electrical conductivityin between a conductor and an insulator; it can vary over that wide range either permanently or dynamically. [. They are used in many applications like solar cells. GoldBookRef|title=semiconductor|file=S05591]
Semiconductors are important in electronic
technology. Semiconductor devices, electronic components made of semiconductor materials, are essential in modern consumer electronics, including computers, mobile phones, and digital audio players. Siliconis used to create most semiconductors commercially, but dozens of other materials are used as well.
_In_a_single_H-atom_an_electron_resides_in_well_known_orbits._Note_that_the_orbits_are_called_s,p,d_in_order_of_increasing_circular_current.Image:CovalentBond.png|_Putting_two_atoms_together_leads_to_delocalized orbits across two atoms, a so called
covalent bond. Due to Paulis principle in every state there is max one electron. photoemission, inverse photoemission
After the band structure is determined states can be combined to generate
wave packets. As this is analogous to wave packages in free space, the results are similar.
alternative description, which does not really appreciate the strong Coulomb interaction, shoots free electrons into the crystal and looks at the scattering.
alternative description uses strongly localized unpaired electrons in chemical bonds, which looks almost like a
Explaining semiconductor energy bands
There are three popular ways to describe the electronic structure of a crystal.
Energy level splitting due to electron energy level Pauli exclusion
The first starts from single atoms. An atom has discrete energy levels.When two atoms come close each energy level splits into an upper and a lower level, whereby they delocalize across the two atoms.With more atoms the number of levels increases, and groups of levels form bands.Semiconductors contain many bands. If there is a large distance between the highest occupied state and the lowest unoccupied space, then a gap will likely remain between occupied and unoccupied bands even after band formation.
Bragg reflection in a diffuse lattice
A second way starts with free electrons
waves. When fading in an electrostatic potential due to the cores,due to Bragg reflectionsome waves are reflected and cannot penetrate the bulk, that is a band gap opens.In this description it is not clear, while the number of electrons fills up exactly all states below the gap.
Energy level splitting due to spin state Pauli exclusion
A third description starts with two atoms. The split states form a
covalent bondwhere two electrons with spin up and spin down are mostly in between the two atoms. Adding more atoms now is supposed not to lead to splitting, but to more bonds.This is the way silicon is typically drawn. The band gap is now formed by lifting one electron from the lower electron levelinto the upper level. This level is known to be anti-bonding, but bulk silicon has not been seen to lose atoms as easy as electrons arewandering through it. Also this model is most unsuitable to explain how in graded hetero-junction the band gap can vary smoothly.
Energy bands and electrical conduction
Like in other solids, the electrons in semiconductors can have energies only within certain bands (ie. ranges of levels of energy) between the energy of the ground state, corresponding to electrons tightly bound to the atomic nuclei of the material, and the free electron energy, which is the energy required for an electron to escape entirely from the material. The energy bands each correspond to a large number of discrete
quantum states of the electrons, and most of the states with low energy (closer to the nucleus) are full, up to a particular band called the " valence band". Semiconductors and insulators are distinguished from metalsbecause the valence band in the semiconductor materials is very nearly full under usual operating conditions, thus causing more electrons to be available in the conduction band.
The ease with which electrons in a semiconductor can be excited from the valence band to the conduction band depends on the
band gapbetween the bands, and it is the size of this energy bandgap that serves as an arbitrary dividing line (roughly 4 eV) between semiconductors and insulators.
In the picture of covalent bonds, an electron moves by hopping to a neighboring bond. Because of the
Pauli exclusion principleit has to be lifted into the higher anti-bonding state of that bond. In the picture of delocalized states, for example in one dimension that is in a wire, for every energy there is a state with electrons flowing in one direction and one state for the electrons flowing in the other. For a net current to flow some more states for one direction than for the other direction have to be occupied and for this energy is needed. For a metal this can be a very small energy in the semiconductor the next higher states lie above the band gap. Often this is stated as: full bands do not contribute to the electrical conductivity. However, as the temperature of a semiconductor rises above absolute zero, there is more energy in the semiconductor to spend on lattice vibration and — more importantly for us — on lifting some electrons into an energy states of the "conduction band", which is the band immediately above the valence band. The current-carrying electrons in the conduction band are known as "free electrons", although they are often simply called "electrons" if context allows this usage to be clear.
Electrons excited to the conduction band also leave behind
electron holes, or unoccupied states in the valence band. Both the conduction band electrons and the valence band holes contribute to electrical conductivity. The holes themselves don't actually move, but a neighboring electron can move to fill the hole, leaving a hole at the place it has just come from, and in this way the holes appear to move, and the holes behave as if they were actual positively charged particles.
covalent bondbetween neighboring atoms in the solid is ten times stronger than the binding of the single electron to the atom, so freeing the electron does not imply destruction of the crystal structure.
Holes: electron absence as a charge carrier
The notion of holes, which was introduced for semiconductors, can also be applied to
metals, where the Fermi levellies "within" the conduction band. With most metals the Hall effectreveals electrons to be the charge carriers, but some metals have a mostly filled conduction band, and the Hall effectreveals positive charge carriers, which are not the ion-cores, but holes. Contrast this to some conductors like solutions of salts, or plasma. In the case of a metal, only a small amount of energy is needed for the electrons to find other unoccupied states to move into, and hence for current to flow. Sometimes even in this case it may be said that a hole was left behind, to explain why the electron does not fall back to lower energies: It cannot find a hole. In the end in both materials electron-phonon scattering and defects are the dominant causes for resistance.
" or "Fermi level". Under absolute zero conditions the Fermi energy can be thought of as the energy up to which available electron states are occupied. At higher temperatures, the Fermi energy is the energy at which the probability of a state being occupied has fallen to 0.5.
The dependence of the electron energy distribution on temperature also explains why the conductivity of a semiconductor has a strong temperature dependency, as a semiconductor operating at lower temperatures will have fewer available free electrons and holes able to do the work.
In the preceding description an important fact is ignored for the sake of simplicity: the "dispersion" of the energy. The reason that the energies of the states are broadened into a band is that the energy depends on the value of the
wave vector, or "k-vector", of the electron. The k-vector, in quantum mechanics, is the representation of the momentumof a particle.
The dispersion relationship determines the
effective mass, , of electrons or holes in the semiconductor, according to the formula:
The effective mass is important as it affects many of the electrical properties of the semiconductor, such as the electron or hole mobility, which in turn influences the "diffusivity" of the charge carriers and the
electrical conductivityof the semiconductor.
Typically the effective mass of electrons and holes are different. This affects the relative performance of "p-channel" and "n-channel"
IGFETs, for example (Muller & Kamins 1986:427).
The top of the valence band and the bottom of the conduction band might not occur at that same value of k. Materials with this situation, such as
siliconand germanium, are known as " indirect bandgap" materials. Materials in which the band extrema are aligned in k, for example gallium arsenide, are called " direct bandgap" semiconductors. Direct gap semiconductors are particularly important in optoelectronicsbecause they are much more efficient as light emitters than indirect gap materials.
Carrier generation and recombination
ionizing radiationstrikes a semiconductor, it may excite an electron out of its energy level and consequently leave a hole. This process is known as "electron–hole pair generation". Electron-hole pairs are constantly generated from thermal energyas well, in the absence of any external energy source.
Electron-hole pairs are also apt to recombine.
Conservation of energydemands that these recombination events, in which an electron loses an amount of energylarger than the band gap, be accompanied by the emission of thermal energy (in the form of phonons) or radiation (in the form of photons).
In some states, the generation and recombination of electron–hole pairs are in equipoise. The number of electron-hole pairs in the
steady stateat a given temperature is determined by quantum statistical mechanics. The precise quantum mechanical mechanisms of generation and recombination are governed by conservation of energyand conservation of momentum.
As the probability that electrons and holes meet together is proportional to the product of their amounts, the product is in steady state nearly constant at a given temperature, providing that there is no significant electric field (which might "flush" carriers of both types, or move them from neighbour regions containing more of them to meet together) or externally driven pair generation. The product is a function of the temperature, as the probability of getting enough thermal energy to produce a pair increases with temperature, being approximately 1/exp(band gap / kT), where k is
Boltzmann's constantand T is absolute temperature.
The probability of meeting is increased by carrier traps – impurities or dislocations which can trap an electron or hole and hold it until a pair is completed. Such carrier traps are sometimes purposely added to reduce the time needed to reach the steady state.
The property of semiconductors that makes them most useful for constructing electronic devices is that their conductivity may easily be modified by introducing impurities into their
crystal lattice. The process of adding controlled impurities to a semiconductor is known as "doping". The amount of impurity, or dopant, added to an "intrinsic" (pure) semiconductor varies its level of conductivity. Doped semiconductors are often referred to as "extrinsic".
The materials chosen as suitable dopants depend on the atomic properties of both the dopant and the material to be doped. In general, dopants that produce the desired controlled changes are classified as either electron acceptors or donors. A donor atom that activates (that is, becomes incorporated into the crystal lattice) donates weakly-bound valence electrons to the material, creating excess negative
charge carriers. These weakly-bound electrons can move about in the crystal lattice relatively freely and can facilitate conduction in the presence of an electric field. (The donor atoms introduce some states under, but very close to the conduction band edge. Electrons at these states can be easily excited to conduction band, becoming free electrons, at room temperature.) Conversely, an activated acceptor produces a hole. Semiconductors doped with donor impurities are called "n-type", while those doped with acceptor impurities are known as "p-type". The n and p type designations indicate which charge carrier acts as the material's majority carrier. The opposite carrier is called the minority carrier, which exists due to thermal excitation at a much lower concentration compared to the majority carrier.
For example, the pure semiconductor
siliconhas four valence electrons. In silicon, the most common dopants are IUPACgroup 13 (commonly known as "group III") and group 15 (commonly known as "group V") elements. Group 13 elements all contain three valence electrons, causing them to function as acceptors when used to dope silicon. Group 15 elements have five valence electrons, which allows them to act as a donor. Therefore, a silicon crystal doped with boroncreates a p-type semiconductor whereas one doped with phosphorusresults in an n-type material.
The concentration of dopant introduced to an intrinsic semiconductor determines its concentration and indirectly affects many of its electrical properties. The most important factor that doping directly affects is the material's carrier concentration. In an intrinsic semiconductor under thermal equilibrium, the concentration of electrons and holes is equivalent. That is,
If we have a non-intrinsic semiconductor in thermal equilibrium the relation becomes:
:Where is the concentration of conducting electrons, is the electron hole concentration, and is the material's intrinsic carrier concentration. Intrinsic carrier concentration varies between materials and is dependent on temperature. Silicon's , for example, is roughly 1.6×1010 cm-3 at 300
In general, an increase in doping concentration affords an increase in conductivity due to the higher concentration of carriers available for conduction. Degenerately (very highly) doped semiconductors have conductivity levels comparable to metals and are often used in modern
integrated circuits as a replacement for metal. Often superscript plus and minus symbols are used to denote relative doping concentration in semiconductors. For example, denotes an n-type semiconductor with a high, often degenerate, doping concentration. Similarly, would indicate a very lightly doped p-type material. It is useful to note that even degenerate levels of doping imply low concentrations of impurities with respect to the base semiconductor. In crystalline intrinsic silicon, there are approximately 5×1022 atoms/cm³. Doping concentration for silicon semiconductors may range anywhere from 1013 cm-3 to 1018 cm-3. Doping concentration above about 1018 cm-3 is considered degenerate at room temperature. Degenerately doped silicon contains a proportion of impurity to silicon in the order of parts per thousand. This proportion may be reduced to parts per billion in very lightly doped silicon. Typical concentration values fall somewhere in this range and are tailored to produce the desired properties in the device that the semiconductor is intended for.
Effect on band structure
Doping a semiconductor crystal introduces allowed energy states within the band gap but very close to the energy band that corresponds with the dopant type. In other words, donor impurities create states near the conduction band while acceptors create states near the valence band. The gap between these energy states and the nearest energy band is usually referred to as dopant-site bonding energy or and is relatively small. For example, the for
boronin silicon bulk is 0.045 eV, compared with silicon's band gap of about 1.12 eV. Because is so small, it takes little energy to ionize the dopant atoms and create free carriers in the conduction or valence bands. Usually the thermal energy available at room temperature is sufficient to ionize most of the dopant.
Dopants also have the important effect of shifting the material's Fermi level towards the energy band that corresponds with the dopant with the greatest concentration. Since the Fermi level must remain constant in a system in
thermodynamic equilibrium, stacking layers of materials with different properties leads to many useful electrical properties. For example, the p-n junction's properties are due to the energy band bending that happens as a result of lining up the Fermi levels in contacting regions of p-type and n-type material.
This effect is shown in a "
band diagram". The band diagram typically indicates the variation in the valence band and conduction band edges versus some spatial dimension, often denoted "x". The Fermi energy is also usually indicated in the diagram. Sometimes the "intrinsic Fermi energy", "Ei", which is the Fermi level in the absence of doping, is shown. These diagrams are useful in explaining the operation of many kinds of semiconductor devices.
Preparation of semiconductor materials
Semiconductors with predictable, reliable electronic properties are necessary for
mass production. The level of chemical purity needed is extremely high because the presence of impurities even in very small proportions can have large effects on the properties of the material. A high degree of crystalline perfection is also required, since faults in crystal structure (such as dislocations, twins, and stacking faults) interfere with the semiconducting properties of the material. Crystalline faults are a major cause of defective semiconductor devices. The larger the crystal, the more difficult it is to achieve the necessary perfection. Current mass production processes use crystal ingotsbetween four and twelve inches (300 mm) in diameter which are grown as cylinders and sliced into wafers.
Because of the required level of chemical purity and the perfection of the crystal structure which are needed to make semiconductor devices, special methods have been developed to produce the initial semiconductor material. A technique for achieving high purity includes growing the crystal using the
Czochralski process. An additional step that can be used to further increase purity is known as zone refining. In zone refining, part of a solid crystal is melted. The impurities tend to concentrate in the melted region, while the desired material recrystalizes leaving the solid material more pure and with fewer crystalline faults.
In manufacturing semiconductor devices involving
heterojunctions between different semiconductor materials, the lattice constant, which is the length of the repeating element of the crystal structure, is important for determining the compatibility of materials.
Electronic band structure
Semiconductor device fabrication
List of semiconductor materials
Wide bandgap semiconductors
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*cite book|last=Muller|first=Richard S.|coauthors=Theodore I. Kamins|title=Device Electronics for Integrated Circuits |edition= 2d|year= 1986|publisher= Wiley|location= New York|isbn= 0-471-88758-7
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*Ben G. Steetman and Sanjay Kumar Banerjee (2006), Solid State Electronic Devices, Pearson Education Inc. ISBN 0-13-149726-X
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* [http://www.newark.com/semiconductors-prototyping Newark - Source for Semiconductors and Prototyping ]
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* [http://hyperphysics.phy-astr.gsu.edu/hbase/solids/semcn.html Semiconductor Concepts at Hyperphysics]
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* [http://ece-www.colorado.edu/~bart/book/book/ Principles of Semiconductor Devices] by Bart Van Zeghbroeck, University of Colorado. An online textbook
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