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List of semiconductor materials
View on WikipediaSemiconductor materials are nominally small band gap insulators. The defining property of a semiconductor material is that it can be compromised by doping it with impurities that alter its electronic properties in a controllable way.[1] Because of their application in the computer and photovoltaic industry—in devices such as transistors, lasers, and solar cells—the search for new semiconductor materials and the improvement of existing materials is an important field of study in materials science.
Most commonly used semiconductor materials are crystalline inorganic solids. These materials are classified according to the periodic table groups of their constituent atoms.
Different semiconductor materials differ in their properties. Thus, in comparison with silicon, compound semiconductors have both advantages and disadvantages. For example, gallium arsenide (GaAs) has six times higher electron mobility than silicon, which allows faster operation; wider band gap, which allows operation of power devices at higher temperatures, and gives lower thermal noise to low power devices at room temperature; its direct band gap gives it more favorable optoelectronic properties than the indirect band gap of silicon; it can be alloyed to ternary and quaternary compositions, with adjustable band gap width, allowing light emission at chosen wavelengths, which makes possible matching to the wavelengths most efficiently transmitted through optical fibers. GaAs can be also grown in a semi-insulating form, which is suitable as a lattice-matching insulating substrate for GaAs devices. Conversely, silicon is robust, cheap, and easy to process, whereas GaAs is brittle and expensive, and insulation layers cannot be created by just growing an oxide layer; GaAs is therefore used only where silicon is not sufficient.[2]
By alloying multiple compounds, some semiconductor materials are tunable, e.g., in band gap or lattice constant. The result is ternary, quaternary, or even quinary compositions. Ternary compositions allow adjusting the band gap within the range of the involved binary compounds; however, in case of combination of direct and indirect band gap materials there is a ratio where indirect band gap prevails, limiting the range usable for optoelectronics; e.g. AlGaAs LEDs are limited to 660 nm by this. Lattice constants of the compounds also tend to be different, and the lattice mismatch against the substrate, dependent on the mixing ratio, causes defects in amounts dependent on the mismatch magnitude; this influences the ratio of achievable radiative/nonradiative recombinations and determines the luminous efficiency of the device. Quaternary and higher compositions allow adjusting simultaneously the band gap and the lattice constant, allowing increasing radiant efficiency at wider range of wavelengths; for example AlGaInP is used for LEDs. Materials transparent to the generated wavelength of light are advantageous, as this allows more efficient extraction of photons from the bulk of the material. That is, in such transparent materials, light production is not limited to just the surface. Index of refraction is also composition-dependent and influences the extraction efficiency of photons from the material.[3]
Types of semiconductor materials
[edit]- Group III elemental semiconductors, (B)
- Group IV elemental semiconductors, (C, Si, and Ge)
- Group IV compound semiconductors
- Group VI elemental semiconductors, (Se and Te)
- III–V semiconductors: Crystallizing with high degree of stoichiometry, most can be obtained as both n-type and p-type. Many have high carrier mobilities and direct energy gaps, making them useful for optoelectronics. (See also: Template:III-V compounds.)
- II–VI semiconductors: usually p-type, except ZnTe and ZnO which are n-type
- I–VII semiconductors
- IV–VI semiconductors
- V–VI semiconductors
- II–V semiconductors
- I–III–VI2 semiconductors
- Oxides
- Layered semiconductors
- Magnetic semiconductors
- Organic semiconductors
- Charge-transfer complexes
- Some of MOFs.
- Others
Compound semiconductors
[edit]This section needs additional citations for verification. (September 2021) |
A compound semiconductor is a semiconductor compound composed of chemical elements of at least two different species. These semiconductors form for example in periodic table groups 13–15 (old groups III–V), for example of elements from the Boron group (old group III, boron, aluminium, gallium, indium) and from group 15 (old group V, nitrogen, phosphorus, arsenic, antimony, bismuth). The range of possible formulae is quite broad because these elements can form binary (two elements, e.g. gallium(III) arsenide (GaAs)), ternary (three elements, e.g. indium gallium arsenide (InGaAs)) and quaternary alloys (four elements) such as aluminium gallium indium phosphide (AlInGaP)) alloy and Indium arsenide antimonide phosphide (InAsSbP). The properties of III-V compound semiconductors are similar to their group IV counterparts. The higher ionicity in these compounds, and especially in the II-VI compound, tends to increase the fundamental bandgap with respect to the less ionic compounds.[4]
Fabrication
[edit]Metalorganic vapor-phase epitaxy (MOVPE) is the most popular deposition technology for the formation of compound semiconducting thin films for devices.[citation needed] It uses ultrapure metalorganics and/or hydrides as precursor source materials in an ambient gas such as hydrogen.
Other techniques of choice include:
- Molecular-beam epitaxy (MBE)
- Hydride vapor-phase epitaxy (HVPE)
- Liquid phase epitaxy (LPE)
- Metal-organic molecular-beam epitaxy (MOMBE)
- Atomic layer deposition (ALD)
Table of semiconductor materials
[edit]| Group | Elem. | Material | Formula | Band gap (eV) | Gap type | Description |
|---|---|---|---|---|---|---|
| IV | 1 | Silicon | Si | 1.12[5][6] | indirect | Used in conventional crystalline silicon (c-Si) solar cells, and in its amorphous form as amorphous silicon (a-Si) in thin-film solar cells. Most common semiconductor material in photovoltaics; dominates worldwide PV market; easy to fabricate; good electrical and mechanical properties. Forms high quality thermal oxide for insulation purposes. Most common material used in the fabrication of integrated circuits. |
| IV | 1 | Germanium | Ge | 0.67[5][6] | indirect | Used in early radar detection diodes and first transistors, with lesser purity required than silicon. A substrate for high-efficiency multijunction photovoltaic cells. Very similar lattice constant to gallium arsenide. High-purity crystals used for gamma spectroscopy. May grow whiskers, which impair reliability of some devices. |
| IV | 1 | Diamond | C | 5.47[5][6] | indirect | Excellent thermal conductivity. Superior mechanical and optical properties.
High carrier mobilities[7] and high electric breakdown field[8] at room temperature as excellent electronics characteristics. Extremely high nanomechanical resonator quality factor.[9] |
| IV | 1 | Gray tin, α-Sn | Sn | 0[10][11] | semimetal | Low temperature allotrope (diamond cubic lattice). |
| IV | 2 | Silicon carbide, 3C-SiC | SiC | 2.3[5] | indirect | Used for early yellow LEDs |
| IV | 2 | Silicon carbide, 4H-SiC | SiC | 3.3[5] | indirect | Used for high-voltage and high-temperature applications |
| IV | 2 | Silicon carbide, 6H-SiC | SiC | 3.0[5] | indirect | Used for early blue LEDs |
| VI | 1 | Sulfur, α-S | S8 | 2.6[12] | ||
| VI | 1 | Gray (trigonal) selenium | Se | 1.83–2.0[13][14] | indirect | Used in selenium rectifiers and solar cells.[15] Band gap depends on fabrication conditions. |
| VI | 1 | Red selenium | Se | 2.05 | indirect | [16] |
| VI | 1 | Tellurium | Te | 0.33[17] | ||
| III-V | 2 | Boron nitride, cubic | BN | 6.36[18] | indirect | Potentially useful for ultraviolet LEDs |
| III-V | 2 | Boron nitride, hexagonal | BN | 5.96[18] | quasi-direct | Potentially useful for ultraviolet LEDs |
| III-V | 2 | Boron nitride nanotube | BN | 5.5[19] | ||
| III-V | 2 | Boron phosphide | BP | 2.1[20] | indirect | |
| III-V | 2 | Boron arsenide | BAs | 1.82 | direct | Ultrahigh thermal conductivity for thermal management; Resistant to radiation damage, possible applications in betavoltaics. |
| III-V | 2 | Boron arsenide | B12As2 | 3.47 | indirect | Resistant to radiation damage, possible applications in betavoltaics. |
| III-V | 2 | Aluminium nitride | AlN | 6.28[5] | direct | Piezoelectric. Not used on its own as a semiconductor; AlN-close GaAlN possibly usable for ultraviolet LEDs. Inefficient emission at 210 nm was achieved on AlN. |
| III-V | 2 | Aluminium phosphide | AlP | 2.45[6] | indirect | |
| III-V | 2 | Aluminium arsenide | AlAs | 2.16[6] | indirect | |
| III-V | 2 | Aluminium antimonide | AlSb | 1.6/2.2[6] | indirect/direct | |
| III-V | 2 | Gallium nitride | GaN | 3.44[5][6] | direct | Problematic to be doped to p-type, p-doping with Mg and annealing allowed first high-efficiency blue LEDs[3] and blue lasers. Very sensitive to ESD. Insensitive to ionizing radiation. GaN transistors can operate at higher voltages and higher temperatures than GaAs, used in microwave power amplifiers. When doped with e.g. manganese, becomes a magnetic semiconductor. |
| III-V | 2 | Gallium phosphide | GaP | 2.26[5][6] | indirect | Used in early low to medium brightness cheap red/orange/green LEDs. Used standalone or with GaAsP. Transparent for yellow and red light, used as substrate for GaAsP red/yellow LEDs. Doped with S or Te for n-type, with Zn for p-type. Pure GaP emits green, nitrogen-doped GaP emits yellow-green, ZnO-doped GaP emits red. |
| III-V | 2 | Gallium arsenide | GaAs | 1.42[5][6] | direct | Second most common in use after silicon, commonly used as substrate for other III-V semiconductors, e.g. InGaAs and GaInNAs. Brittle. Lower hole mobility than Si, P-type CMOS transistors unfeasible. High impurity density, difficult to fabricate small structures. Used for near-IR LEDs, fast electronics, and high-efficiency solar cells. Very similar lattice constant to germanium, can be grown on germanium substrates. |
| III-V | 2 | Gallium antimonide | GaSb | 0.73[5][6] | direct | Used for infrared detectors and LEDs and thermophotovoltaics. Doped n with Te, p with Zn. |
| III-V | 2 | Indium nitride | InN | 0.7[5] | direct | Possible use in solar cells, but p-type doping difficult. Used frequently as alloys. |
| III-V | 2 | Indium phosphide | InP | 1.35[5] | direct | Commonly used as substrate for epitaxial InGaAs. Superior electron velocity, used in high-power and high-frequency applications. Used in optoelectronics. |
| III-V | 2 | Indium arsenide | InAs | 0.36[5] | direct | Used for infrared detectors for 1–3.8 μm, cooled or uncooled. High electron mobility. InAs dots in InGaAs matrix can serve as quantum dots. Quantum dots may be formed from a monolayer of InAs on InP or GaAs. Strong photo-Dember emitter, used as a terahertz radiation source. |
| III-V | 2 | Indium antimonide | InSb | 0.17[5] | direct | Used in infrared detectors and thermal imaging sensors, high quantum efficiency, low stability, require cooling, used in military long-range thermal imager systems. AlInSb-InSb-AlInSb structure used as quantum well. Very high electron mobility, electron velocity and ballistic length. Transistors can operate below 0.5V and above 200 GHz. Terahertz frequencies maybe achievable. |
| II-VI | 2 | Cadmium selenide | CdSe | 1.74[6] | direct | Nanoparticles used as quantum dots. Intrinsic n-type, difficult to dope p-type, but can be p-type doped with nitrogen. Possible use in optoelectronics. Tested for high-efficiency solar cells. |
| II-VI | 2 | Cadmium sulfide | CdS | 2.42[6] | direct | Used in photoresistors and solar cells; CdS/Cu2S was the first efficient solar cell. Used in solar cells with CdTe. Common as quantum dots. Crystals can act as solid-state lasers. Electroluminescent. When doped, can act as a phosphor. |
| II-VI | 2 | Cadmium telluride | CdTe | 1.49[6] | direct | Used in solar cells with CdS. Used in thin film solar cells and other cadmium telluride photovoltaics; less efficient than crystalline silicon but cheaper. High electro-optic effect, used in electro-optic modulators. Fluorescent at 790 nm. Nanoparticles usable as quantum dots. |
| II-VI, oxide | 2 | Zinc oxide | ZnO | 3.37[6] | direct | Photocatalytic. Band gap is tunable from 3 to 4 eV by alloying with magnesium oxide and cadmium oxide. Intrinsic n-type, p-type doping is difficult. Heavy aluminium, indium, or gallium doping yields transparent conductive coatings; ZnO:Al is used as window coatings transparent in visible and reflective in infrared region and as conductive films in LCD displays and solar panels as a replacement of indium tin oxide. Resistant to radiation damage. Possible use in LEDs and laser diodes. Possible use in random lasers. |
| II-VI | 2 | Zinc selenide | ZnSe | 2.7[6] | direct | Used for blue lasers and LEDs. Easy to n-type doping, p-type doping is difficult but can be done with e.g. nitrogen. Common optical material in infrared optics. |
| II-VI | 2 | Zinc sulfide | ZnS | 3.54/3.91[6] | direct | Band gap 3.54 eV (cubic), 3.91 (hexagonal). Can be doped both n-type and p-type. Common scintillator/phosphor when suitably doped. |
| II-VI | 2 | Zinc telluride | ZnTe | 2.3[6] | direct | Can be grown on AlSb, GaSb, InAs, and PbSe. Used in solar cells, components of microwave generators, blue LEDs and lasers. Used in electrooptics. Together with lithium niobate used to generate terahertz radiation. |
| I-VII | 2 | Cuprous chloride | CuCl | 3.4[21] | direct | |
| I-VI | 2 | Copper(I) sulfide | Cu2S | 1.2[20] | indirect | p-type, Cu2S/CdS was the first efficient thin film solar cell |
| IV-VI | 2 | Lead selenide | PbSe | 0.26[17] | direct | Used in infrared detectors for thermal imaging. Nanocrystals usable as quantum dots. Good high temperature thermoelectric material. |
| IV-VI | 2 | Lead(II) sulfide | PbS | 0.37[22] | Mineral galena, first semiconductor in practical use, used in cat's whisker detectors; the detectors are slow due to high dielectric constant of PbS. Oldest material used in infrared detectors. At room temperature can detect SWIR, longer wavelengths require cooling. | |
| IV-VI | 2 | Lead telluride | PbTe | 0.32[5] | Low thermal conductivity, good thermoelectric material at elevated temperature for thermoelectric generators. | |
| IV-VI | 2 | Tin(II) sulfide | SnS | 1.3/1.0[23] | direct/indirect | Tin sulfide (SnS) is a semiconductor with direct optical band gap of 1.3 eV and absorption coefficient above 104 cm−1 for photon energies above 1.3 eV. It is a p-type semiconductor whose electrical properties can be tailored by doping and structural modification and has emerged as one of the simple, non-toxic and affordable material for thin film solar cells since a decade. |
| IV-VI | 2 | Tin(IV) sulfide | SnS2 | 2.2[24] | SnS2 is widely used in gas sensing applications. | |
| IV-VI | 2 | Tin telluride | SnTe | 0.18 | direct | Complex band structure. |
| V-VI, layered | 2 | Bismuth telluride | Bi2Te3 | 0.13[5] | Efficient thermoelectric material near room temperature when alloyed with selenium or antimony. Narrow-gap layered semiconductor. High electrical conductivity, low thermal conductivity. Topological insulator. | |
| II-V | 2 | Cadmium phosphide | Cd3P2 | 0.5[25] | ||
| II-V | 2 | Cadmium arsenide | Cd3As2 | 0 | N-type intrinsic semiconductor. Very high electron mobility. Used in infrared detectors, photodetectors, dynamic thin-film pressure sensors, and magnetoresistors. Recent measurements suggest that 3D Cd3As2 is actually a zero band-gap Dirac semimetal in which electrons behave relativistically as in graphene.[26] | |
| II-V | 2 | Zinc phosphide | Zn3P2 | 1.5[27] | direct | Usually p-type. |
| II-V | 2 | Zinc diphosphide | ZnP2 | 2.1[28] | ||
| II-V | 2 | Zinc arsenide | Zn3As2 | 1.0[29] | The lowest direct and indirect bandgaps are within 30 meV or each other.[29] | |
| II-V | 2 | Zinc antimonide | Zn3Sb2 | Used in infrared detectors and thermal imagers, transistors, and magnetoresistors. | ||
| Oxide | 2 | Titanium dioxide, anatase | TiO2 | 3.20[30] | indirect | Photocatalytic, n-type |
| Oxide | 2 | Titanium dioxide, rutile | TiO2 | 3.0[30] | direct | Photocatalytic, n-type |
| Oxide | 2 | Titanium dioxide, brookite | TiO2 | 3.26[30] | [31] | |
| Oxide | 2 | Copper(I) oxide | Cu2O | 2.17[32] | One of the most studied semiconductors. Many applications and effects first demonstrated with it. Formerly used in rectifier diodes, before silicon. | |
| Oxide | 2 | Copper(II) oxide | CuO | 1.2 | N-type semiconductor.[33] | |
| Oxide | 2 | Uranium dioxide | UO2 | 1.3 | High Seebeck coefficient, resistant to high temperatures, promising thermoelectric and thermophotovoltaic applications. Formerly used in URDOX resistors, conducting at high temperature. Resistant to radiation damage. | |
| Oxide | 2 | Tin dioxide | SnO2 | 3.7 | Oxygen-deficient n-type semiconductor. Used in gas sensors. | |
| Oxide | 3 | Barium titanate | BaTiO3 | 3 | Ferroelectric, piezoelectric. Used in some uncooled thermal imagers. Used in nonlinear optics. | |
| Oxide | 3 | Strontium titanate | SrTiO3 | 3.3 | Ferroelectric, piezoelectric. Used in varistors. Conductive when niobium-doped. | |
| Oxide | 3 | Lithium niobate | LiNbO3 | 4 | Ferroelectric, piezoelectric, shows Pockels effect. Wide uses in electrooptics and photonics. | |
| Oxide, V-VI | 2 | monoclinic Vanadium(IV) oxide | VO2 | 0.7[34] | optical | Stable below 67 °C |
| Layered | 2 | Lead(II) iodide | PbI2 | 2.4[35] | PbI2 is a layered direct bandgap semiconductor with bandgap of 2.4 eV in its bulk form, whereas its 2D monolayer has an indirect bandgap of ~2.5 eV, with possibilities to tune the bandgap between 1–3 eV | |
| Layered | 2 | Molybdenum disulfide | MoS2 | 1.23 eV (2H)[36] | indirect | |
| Layered | 2 | Gallium selenide | GaSe | 2.1 | indirect | Photoconductor. Uses in nonlinear optics. Used as 2D-material. Air sensitive.[37][38][39] |
| Layered | 2 | Indium selenide | InSe | 1.26–2.35 eV[39] | direct (indirect in 2D) | Air sensitive. High electrical mobility in few- and mono-layer form.[37][38][39] |
| Layered | 2 | Tin sulfide | SnS | >1.5 eV | direct | |
| Layered | 2 | Bismuth sulfide | Bi2S3 | 1.3[5] | ||
| Magnetic, diluted (DMS)[40] | 3 | Gallium manganese arsenide | GaMnAs | |||
| Magnetic, diluted (DMS) | 3 | Lead manganese telluride | PbMnTe | |||
| Magnetic | 4 | Lanthanum calcium manganate | La0.7Ca0.3MnO3 | Colossal magnetoresistance | ||
| Magnetic | 2 | Iron(II) oxide | FeO | 2.2[41] | Antiferromagnetic. Band gap for iron oxide nanoparticles was found to be 2.2 eV and on doping the band gap found to be increased up to 2.5 eV | |
| Magnetic | 2 | Nickel(II) oxide | NiO | 3.6–4.0 | direct[42][43] | Antiferromagnetic |
| Magnetic | 2 | Europium(II) oxide | EuO | Ferromagnetic | ||
| Magnetic | 2 | Europium(II) sulfide | EuS | Ferromagnetic | ||
| Magnetic | 2 | Chromium(III) bromide | CrBr3 | |||
| other | 3 | Copper indium selenide, CIS | CuInSe2 | 1 | direct | |
| other | 3 | Silver gallium sulfide | AgGaS2 | Nonlinear optical properties | ||
| other | 3 | Zinc silicon phosphide | ZnSiP2 | 2.0[20] | ||
| other | 2 | Arsenic trisulfide Orpiment | As2S3 | 2.7[44] | direct | Semiconductive in both crystalline and glassy state |
| other | 2 | Arsenic sulfide Realgar | As4S4 | Semiconductive in both crystalline and glassy state | ||
| other | 2 | Platinum silicide | PtSi | Used in infrared detectors for 1–5 μm. Used in infrared astronomy. High stability, low drift, used for measurements. Low quantum efficiency. | ||
| other | 2 | Bismuth(III) iodide | BiI3 | |||
| other | 2 | Mercury(II) iodide | HgI2 | Used in some gamma-ray and x-ray detectors and imaging systems operating at room temperature. | ||
| other | 2 | Thallium(I) bromide | TlBr | 2.68[45] | Used in some gamma-ray and x-ray detectors and imaging systems operating at room temperature. Used as a real-time x-ray image sensor. | |
| other | 2 | Silver sulfide | Ag2S | 0.9[46] | ||
| other | 2 | Iron disulfide | FeS2 | 0.95[47] | Mineral pyrite. Used in later cat's whisker detectors, investigated for solar cells. | |
| other | 4 | Copper zinc tin sulfide, CZTS | Cu2ZnSnS4 | 1.49 | direct | Cu2ZnSnS4 is derived from CIGS, replacing the Indium/Gallium with earth abundant Zinc/Tin. |
| other | 4 | Copper zinc antimony sulfide, CZAS | Cu1.18Zn0.40Sb1.90S7.2 | 2.2[48] | direct | Copper zinc antimony sulfide is derived from copper antimony sulfide (CAS), a famatinite class of compound. |
| other | 3 | Copper tin sulfide, CTS | Cu2SnS3 | 0.91[20] | direct | Cu2SnS3 is p-type semiconductor and it can be used in thin film solar cell application. |
Table of semiconductor alloy systems
[edit]The following semiconducting systems can be tuned to some extent, and represent not a single material but a class of materials.
| Group | Elem. | Material class | Formula | Band gap (eV) | Gap type | Description | |
|---|---|---|---|---|---|---|---|
| Lower | Upper | ||||||
| IV-VI | 3 | Lead tin telluride | Pb1−xSnxTe | 0 | 0.29 | Used in infrared detectors and for thermal imaging | |
| IV | 2 | Silicon-germanium | Si1−xGex | 0.67 | 1.11[5] | direct/indirect | Adjustable band gap, allows construction of heterojunction structures. Certain thicknesses of superlattices have direct band gap.[49] |
| IV | 2 | Silicon-tin | Si1−xSnx | 1.0 | 1.11 | indirect | Adjustable band gap.[50] |
| III-V | 3 | Aluminium gallium arsenide | AlxGa1−xAs | 1.42 | 2.16[5] | direct/indirect | Direct band gap for x<0.4 (corresponding to 1.42–1.95 eV); can be lattice-matched to GaAs substrate over entire composition range; tends to oxidize; n-doping with Si, Se, Te; p-doping with Zn, C, Be, Mg.[3] Can be used for infrared laser diodes. Used as a barrier layer in GaAs devices to confine electrons to GaAs (see e.g. QWIP). AlGaAs with composition close to AlAs is almost transparent to sunlight. Used in GaAs/AlGaAs solar cells. |
| III-V | 3 | Indium gallium arsenide | InxGa1−xAs | 0.36 | 1.43 | direct | Well-developed material. Can be lattice matched to InP substrates. Use in infrared technology and thermophotovoltaics. Indium content determines charge carrier density. For x=0.015, InGaAs perfectly lattice-matches germanium; can be used in multijunction photovoltaic cells. Used in infrared sensors, avalanche photodiodes, laser diodes, optical fiber communication detectors, and short-wavelength infrared cameras. |
| III-V | 3 | Indium gallium phosphide | InxGa1−xP | 1.35 | 2.26 | direct/indirect | Used for HEMT and HBT structures and high-efficiency multijunction solar cells for e.g. satellites. Ga0.5In0.5P is almost lattice-matched to GaAs, with AlGaIn used for quantum wells for red lasers. |
| III-V | 3 | Aluminium indium arsenide | AlxIn1−xAs | 0.36 | 2.16 | direct/indirect | Buffer layer in metamorphic HEMT transistors, adjusting lattice constant between GaAs substrate and GaInAs channel. Can form layered heterostructures acting as quantum wells, in e.g. quantum cascade lasers. |
| III-V | 3 | Aluminium gallium antimonide | AlxGa1−xSb | 0.7 | 1.61 | direct/indirect | Used in HBTs, HEMTs, resonant-tunneling diodes and some niche optoelectronics. Also used as a buffer layer for InAs quantum wells. |
| III-V | 3 | Aluminium indium antimonide | AlxIn1−xSb | 0.17 | 1.61 | direct/indirect | Used as a buffer layer in InSb-based quantum wells and other devices grown on GaAs and GaSb substrates. Also used as the active layer in some mid-infrared LEDs and photodiodes. |
| III-V | 3 | Gallium arsenide nitride | GaAsN | ||||
| III-V | 3 | Gallium arsenide phosphide | GaAsP | 1.43 | 2.26 | direct/indirect | Used in red, orange and yellow LEDs. Often grown on GaP. Can be doped with nitrogen. |
| III-V | 3 | Aluminium arsenide antimonide | AlAsSb | 1.61 | 2.16 | indirect | Used as a barrier layer in infrared photodetectors. Can be lattice matched to GaSb, InAs and InP. |
| III-V | 3 | Gallium arsenide antimonide | GaAsSb | 0.7 | 1.42[5] | direct | Used in HBTs and in tunnel junctions in multi-junction solar cells. GaAs0.51Sb0.49 is lattice matched to InP. |
| III-V | 3 | Aluminium gallium nitride | AlGaN | 3.44 | 6.28 | direct | Used in blue laser diodes, ultraviolet LEDs (down to 250 nm), and AlGaN/GaN HEMTs. Can be grown on sapphire. Used in heterojunctions with AlN and GaN. |
| III-V | 3 | Aluminium gallium phosphide | AlGaP | 2.26 | 2.45 | indirect | Used in some green LEDs. |
| III-V | 3 | Indium gallium nitride | InGaN | 2 | 3.4 | direct | InxGa1–xN, x usually between 0.02 and 0.3 (0.02 for near-UV, 0.1 for 390 nm, 0.2 for 420 nm, 0.3 for 440 nm). Can be grown epitaxially on sapphire, SiC wafers or silicon. Used in modern blue and green LEDs, InGaN quantum wells are effective emitters from green to ultraviolet. Insensitive to radiation damage, possible use in satellite solar cells. Insensitive to defects, tolerant to lattice mismatch damage. High heat capacity. |
| III-V | 3 | Indium arsenide antimonide | InAsSb | 0.17 | 0.36 | direct | Primarily used in mid- and long-wave infrared photodetectors due to its small bandgap, which reaches a minimum of around 0.08 eV in InAs0.4Sb0.6 at room temperature. |
| III-V | 3 | Indium gallium antimonide | InGaSb | 0.17 | 0.7 | direct | Used in some transistors and infrared photodetectors. |
| III-V | 4 | Aluminium gallium indium phosphide | AlGaInP | direct/indirect | Also InAlGaP, InGaAlP, AlInGaP; for lattice matching to GaAs substrates the In mole fraction is fixed at about 0.48, the Al/Ga ratio is adjusted to achieve band gaps between about 1.9 and 2.35 eV; direct or indirect band gaps depending on the Al/Ga/In ratios; used for wavelengths between 560 and 650 nm; tends to form ordered phases during deposition, which has to be prevented[3] | ||
| III-V | 4 | Aluminium gallium arsenide phosphide | AlGaAsP | ||||
| III-V | 4 | Indium gallium arsenide phosphide | InGaAsP | ||||
| III-V | 4 | Indium gallium arsenide antimonide | InGaAsSb | Use in thermophotovoltaics. | |||
| III-V | 4 | Indium arsenide antimonide phosphide | InAsSbP | Use in thermophotovoltaics. | |||
| III-V | 4 | Aluminium indium arsenide phosphide | AlInAsP | ||||
| III-V | 4 | Aluminium gallium arsenide nitride | AlGaAsN | ||||
| III-V | 4 | Indium gallium arsenide nitride | InGaAsN | ||||
| III-V | 4 | Indium aluminium arsenide nitride | InAlAsN | ||||
| III-V | 4 | Gallium arsenide antimonide nitride | GaAsSbN | ||||
| III-V | 5 | Gallium indium nitride arsenide antimonide | GaInNAsSb | ||||
| III-V | 5 | Gallium indium arsenide antimonide phosphide | GaInAsSbP | Can be grown on InAs, GaSb, and other substrates. Can be lattice matched by varying composition. Possibly usable for mid-infrared LEDs. | |||
| II-VI | 3 | Cadmium zinc telluride, CZT | CdZnTe | 1.4 | 2.2 | direct | Efficient solid-state x-ray and gamma-ray detector, can operate at room temperature. High electro-optic coefficient. Used in solar cells. Can be used to generate and detect terahertz radiation. Can be used as a substrate for epitaxial growth of HgCdTe. |
| II-VI | 3 | Mercury cadmium telluride | HgCdTe | 0 | 1.5 | Known as "MerCad". Extensive use in sensitive cooled infrared imaging sensors, infrared astronomy, and infrared detectors. Alloy of mercury telluride (a semimetal, zero band gap) and CdTe. High electron mobility. The only common material capable of operating in both 3–5 μm and 12–15 μm atmospheric windows. Can be grown on CdZnTe. | |
| II-VI | 3 | Mercury zinc telluride | HgZnTe | 0 | 2.25 | Used in infrared detectors, infrared imaging sensors, and infrared astronomy. Better mechanical and thermal properties than HgCdTe but more difficult to control the composition. More difficult to form complex heterostructures. | |
| II-VI | 3 | Mercury zinc selenide | HgZnSe | ||||
| II-V | 4 | Zinc cadmium phosphide arsenide | (Zn1−xCdx)3(P1−yAsy)2[51] | 0[26] | 1.5[52] | Various applications in optoelectronics (incl. photovoltaics), electronics and thermoelectrics.[53] | |
| other | 4 | Copper indium gallium selenide, CIGS | Cu(In,Ga)Se2 | 1 | 1.7 | direct | CuInxGa1–xSe2. Polycrystalline. Used in thin film solar cells. |
See also
[edit]References
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- ^ Milton Ohring Reliability and failure of electronic materials and devices Academic Press, 1998, ISBN 0-12-524985-3, p. 310.
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List of semiconductor materials
View on GrokipediaBasics of Semiconductor Materials
Definition and Key Properties
Semiconductors are a class of materials characterized by electrical conductivity intermediate between that of conductors and insulators, typically arising from a narrow energy band gap that permits thermal excitation of electrons across the gap at moderate temperatures.[8] This band gap, denoted as , represents the energy difference between the top of the valence band—where electrons are bound in atomic orbitals—and the bottom of the conduction band, where electrons can move freely to contribute to current.[9] In semiconductors, generally ranges from 0.1 to 4 eV, enabling partial population of the conduction band and thus controllable conductivity without external doping.[10][11] Key properties of semiconductors include the band gap energy , which governs the material's response to temperature and light; carrier concentration, quantifying the density of charge carriers (electrons and holes); electron and hole mobility, measuring how readily carriers drift under an electric field; and strong temperature dependence of conductivity.[12]/10%3A_Electronic_Properties_of_Materials_-_Superconductors_and_Semiconductors/10.05%3A_Semiconductors-_Band_Gaps_Colors_Conductivity_and_Doping) In intrinsic (undoped) semiconductors, the intrinsic carrier concentration —the equilibrium density of electrons in the conduction band (equal to holes in the valence band)—is given by where and are the effective densities of states in the conduction and valence bands, respectively, is Boltzmann's constant, and is the absolute temperature.[9][13] Mobility influences the overall conductivity , where is the elementary charge, and are electron and hole concentrations, and and are their respective mobilities; higher mobility enables faster device switching and lower power loss.[12] Conductivity in semiconductors increases exponentially with temperature due to enhanced thermal generation of carriers, contrasting with the behavior in other materials.[14] Unlike metals, which exhibit high conductivity from overlapping valence and conduction bands with no band gap—resulting in a partially filled conduction band and conductivity that often decreases with rising temperature due to increased scattering—semiconductors require thermal or optical energy to generate carriers. Insulators, by comparison, possess large band gaps exceeding 5 eV, rendering carrier excitation negligible at room temperature and yielding extremely low conductivity.[15] The semiconductor behavior was first observed in 1833 by Michael Faraday, who noted that the resistance of silver sulfide decreased with increasing temperature, an anomalous effect relative to metals.[16] Practical theoretical understanding emerged in the 20th century through quantum mechanics, particularly with Alan Wilson's 1931 band theory model explaining electron behavior in periodic lattices.[17][18]Doping and Conductivity Types
Doping involves the intentional introduction of impurities, known as dopants, into a semiconductor crystal lattice to alter its electrical conductivity by creating additional charge carriers. These dopants are classified as donors or acceptors: donors contribute electrons to the conduction band, while acceptors create holes in the valence band. In semiconductors, donor impurity levels are typically shallow, positioned approximately 0.01–0.1 eV below the conduction band edge, allowing thermal ionization at room temperature to release electrons. Similarly, acceptor levels lie about 0.01–0.1 eV above the valence band edge, facilitating the capture of electrons and generation of holes.[19][20] Semiconductors exhibit intrinsic or extrinsic conductivity based on purity and doping. Intrinsic semiconductors are undoped, featuring equal concentrations of electrons (n = p = n_i) generated thermally across the band gap, resulting in low conductivity limited by the intrinsic carrier concentration n_i. Extrinsic semiconductors, however, are doped to dominate with one carrier type: n-type doping introduces donors (e.g., group V elements in group IV hosts), making electrons the majority carriers (n >> p), while p-type doping adds acceptors (e.g., group III elements), where holes predominate (p >> n). Doping shifts the Fermi level; in n-type materials, it moves closer to the conduction band, increasing electron population, whereas in p-type, it approaches the valence band, enhancing hole density. This follows Fermi-Dirac statistics, which govern the probabilistic occupation of energy states by carriers.[20][21] In extrinsic semiconductors at room temperature, assuming complete ionization of dopants, the majority carrier concentration approximates the dopant density: for n-type, electron concentration , where is the donor concentration, and for p-type, hole concentration , with as the acceptor concentration. These approximations hold when doping levels far exceed the intrinsic carrier density () and minority carriers are negligible. The charge neutrality condition maintains overall electrical balance and is expressed as: where and represent ionized donors and acceptors, respectively. Doping elevates carrier concentrations from intrinsic levels (around 10^{10} cm^{-3} for silicon at 300 K) to 10^{15}–10^{18} cm^{-3}, boosting conductivity by orders of magnitude—typically 10^5 to 10^8 times higher—through enhanced charge transport while preserving the semiconductor's band structure.[21]Traditional Semiconductor Materials
Elemental Semiconductors
Elemental semiconductors consist of pure elements, primarily from Group IV of the periodic table, that exhibit semiconducting properties due to their band structures allowing controlled electrical conductivity. These materials are characterized by moderate band gaps, enabling applications in electronics where charge carriers can be thermally excited or manipulated. Silicon and germanium are the quintessential examples, valued for their crystalline diamond lattice structures and compatibility with doping to achieve n-type or p-type conduction. Silicon (Si) is the cornerstone of the semiconductor industry, possessing an indirect band gap of 1.12 eV at 300 K, which supports efficient carrier generation for devices operating at room temperature.[22] Its widespread use in integrated circuits stems from natural abundance, excellent thermal stability up to 150°C, and the ability to form high-quality native oxides for passivation.[23] Electron mobility in silicon reaches 1500 cm²/V·s, facilitating fast switching in transistors.[22] Germanium (Ge), with an indirect band gap of 0.67 eV at 300 K, offers higher intrinsic carrier concentrations and superior carrier mobilities compared to silicon, with electron mobility up to 3900 cm²/V·s.[22][24] It played a pivotal role in early transistor prototypes and continues to be employed in photodetectors and high-speed electronics due to its responsiveness in the infrared spectrum.[23] Beyond Group IV, carbon in the diamond allotrope serves as a wide-band-gap elemental semiconductor with an indirect band gap of 5.5 eV, enabling operation in harsh environments like high-power and high-temperature devices, though it requires doping to manifest semiconducting behavior effectively.[25] Gray tin (α-Sn), stable below 13°C, features a narrow direct band gap of approximately 0.08 eV, bordering on semimetallic properties and exhibiting high carrier mobilities in the range of 1000–3000 cm²/V·s.[26] Selenium (Se), a Group VI element, has a direct band gap of about 1.8 eV and notable photoconductivity, historically utilized in photocells and xerography for its sensitivity to visible light.[27] The historical trajectory of elemental semiconductors underscores silicon's dominance: germanium powered the first transistors in the late 1940s and proliferated through the 1950s, but silicon supplanted it by the late 1950s owing to superior high-temperature stability and processability, leading to germanium's phase-out for mainstream applications by the 1970s.[23][28]| Element | Lattice Constant (Å) | Melting Point (°C) | Band Gap (eV at 300 K) | Band Gap Type | Electron Mobility (cm²/V·s) |
|---|---|---|---|---|---|
| Silicon (Si) | 5.431 | 1414 | 1.12 | Indirect | 1500 |
| Germanium (Ge) | 5.657 | 938 | 0.67 | Indirect | 3900 |
| Carbon (diamond) | 3.567 | Sublimes (~3550) | 5.5 | Indirect | ~2200 |
| Tin (gray, α-Sn) | 6.489 | 232 (white allotrope) | 0.08 | Direct | 1000–3000 |
| Selenium (Se) | a=4.364, c=4.954 (trigonal) | 221 | 1.8 | Direct | ~10–100 (photoconductive) |
Binary Compound Semiconductors
Binary compound semiconductors are materials formed by combining elements from two different groups of the periodic table, primarily III-V, II-VI, IV-VI, and I-VII groups, resulting in compounds with tunable electronic properties suitable for optoelectronic and photovoltaic applications. These materials often exhibit direct band gaps, enabling efficient light emission and absorption, and typically crystallize in zincblende or wurtzite structures, which influence their lattice parameters and suitability for epitaxial growth. Unlike elemental semiconductors, binary compounds introduce partial ionicity, affecting bonding character and defect formation, with lattice matching critical for heteroepitaxy to minimize strain and defects in device fabrication.[29][30][31]III-V Compounds
III-V binary semiconductors, such as gallium arsenide (GaAs), indium phosphide (InP), and gallium nitride (GaN), are pivotal for high-performance electronics and optoelectronics due to their direct band gaps and high carrier mobilities. GaAs features a zincblende structure with a lattice constant of 5.653 Å and a direct band gap of 1.42 eV at room temperature, alongside an electron mobility of 8500 cm²/V·s, making it ideal for light-emitting diodes (LEDs), lasers, metal-semiconductor field-effect transistors (MESFETs), and heterojunction bipolar transistors (HBTs).[29][32] InP, also zincblende-structured with a lattice constant of 5.869 Å, has a direct band gap of 1.35 eV and serves as a substrate for fiber-optic telecommunications devices owing to its compatibility with lattice-matched alloys for lasers and detectors operating near 1.55 μm.[29][33] GaN adopts a wurtzite structure (lattice parameters a=3.189 Å, c=5.185 Å) with a direct band gap of 3.4 eV, enabling blue LEDs and lasers; its development earned the 2014 Nobel Prize in Physics for efficient blue light emission, revolutionizing energy-efficient lighting.[29][34]II-VI Compounds
II-VI binaries like zinc selenide (ZnSe), cadmium telluride (CdTe), and mercury telluride (HgTe) offer wider band gaps and are valued for visible and infrared optoelectronics, though they exhibit higher ionicity leading to more polar bonding compared to III-V materials. ZnSe possesses a zincblende structure (lattice constant 5.668 Å) and a direct band gap of 2.7 eV, positioning it for green laser applications in optoelectronic devices.[29][35] CdTe, also zincblende (lattice constant 6.482 Å), has a direct band gap of 1.5 eV and achieves solar cell efficiencies up to 22% in thin-film photovoltaics due to its high absorption coefficient and stability.[29][36] HgTe is a semimetal with a zero band gap in its zincblende form, but its structure allows tunability through strain or alloying for infrared detection applications.[29][37]Other Groups
IV-VI compounds, exemplified by lead sulfide (PbS), feature narrow band gaps suitable for infrared technologies; PbS has a rock-salt structure and a band gap of 0.41 eV, enabling room-temperature IR detectors with high sensitivity.[38] I-VII compounds like copper chloride (CuCl) provide wide band gaps for ultraviolet optoelectronics; CuCl exhibits a zincblende structure and a direct band gap of 3.4 eV, supporting applications in excitonic devices and lasers.[39]| Material | Group | Structure | Lattice Constant (Å) | Band Gap (eV, direct) | Key Application |
|---|---|---|---|---|---|
| GaAs | III-V | Zincblende | 5.653 | 1.42 | LEDs, lasers, high-speed electronics |
| InP | III-V | Zincblende | 5.869 | 1.35 | Telecom optoelectronics |
| GaN | III-V | Wurtzite | a=3.189, c=5.185 | 3.4 | Blue LEDs |
| ZnSe | II-VI | Zincblende | 5.668 | 2.7 | Green lasers |
| CdTe | II-VI | Zincblende | 6.482 | 1.5 | Solar cells |
| HgTe | II-VI | Zincblende | - | 0 | IR detectors (tunable) |
| PbS | IV-VI | Rock-salt | - | 0.41 | IR detectors |
| CuCl | I-VII | Zincblende | - | 3.4 | UV optoelectronics |
Advanced and Emerging Semiconductor Materials
Alloy Systems
Semiconductor alloys are formed by combining two or more binary compounds to create materials with tunable electronic and optical properties, primarily through compositional variation that enables band gap engineering. These alloys are essential in optoelectronics and high-performance electronics, allowing precise control over parameters like lattice constant and band gap to achieve device-specific requirements, such as emission wavelengths in lasers or absorption spectra in solar cells. Unlike fixed-composition binaries, alloys exhibit compositional flexibility, often described by formulas like A_{1-x}B_xC, where x varies to adjust properties while minimizing defects through lattice matching.[42] Binary alloys, such as Si_{1-x}Ge_x, provide a foundational example of property tuning in group IV materials. The band gap of Si_{1-x}Ge_x varies continuously from 0.67 eV for pure Ge (x=1) to 1.12 eV for pure Si (x=0), remaining indirect throughout the composition range, which facilitates integration with silicon-based technologies. Strain engineering in Si_{1-x}Ge_x layers enhances carrier mobility, making it critical for channel materials in advanced MOSFETs and heterojunction bipolar transistors, where compressive strain reduces effective mass and boosts performance in high-speed circuits.[42][43] Ternary alloys extend this tunability to III-V compounds, exemplified by Al_xGa_{1-x}As and In_xGa_{1-x}As. In Al_xGa_{1-x}As, the direct band gap spans approximately 1.42 eV (x=0, GaAs) to 2.2 eV (near AlAs compositions), with the alloy remaining nearly lattice-matched to GaAs substrates across the full range due to the close lattice constants of AlAs (5.661 Å) and GaAs (5.653 Å), enabling defect-free epitaxial growth. This matching is vital for heterostructures in visible and near-infrared lasers, where the refractive index contrast supports optical confinement in quantum well devices. Similarly, In_xGa_{1-x}As offers a tunable band gap from 0.35 eV (InAs, x=1) to 1.43 eV (GaAs, x=0), leveraging high electron mobility (up to 10,000 cm²/V·s) for high-speed electronics like field-effect transistors in telecommunications. Quaternary alloys introduce additional degrees of freedom by varying two compositions, as in Al_xGa_{1-x}As_yP_{1-y} and CuIn_xGa_{1-x}Se_2 (CIGS). The Al_xGa_{1-x}As_yP_{1-y} system allows independent tuning of band gap (1.0–2.2 eV) and lattice constant to match GaAs or other substrates, historically enabling efficient red and yellow LEDs through liquid-phase epitaxy growth. In CIGS, the band gap adjusts from 1.0 eV (CuInSe_2) to 1.7 eV (CuGaSe_2) via the Ga ratio x, optimizing absorption for thin-film solar cells that have achieved laboratory efficiencies exceeding 23% as of 2025, with the graded composition enhancing open-circuit voltage and carrier collection.[44] A key feature of these alloys is band gap bowing, a nonlinear deviation from Vegard's law due to atomic-scale interactions, described by the empirical relation: where and are the band gaps of the end binaries, and b is the bowing parameter. For In_xGa_{1-x}As, b ≈ 0.15 eV reflects weak nonlinearity, allowing predictable tuning for infrared detectors, though higher values (e.g., 0.5–1.0 eV in other systems) can complicate design by shifting emission energies unexpectedly.[45] Despite these advantages, alloy systems face challenges including phase separation from immiscibility at certain compositions, which leads to compositional inhomogeneities and reduced performance, and lattice mismatch inducing misfit dislocations that act as recombination centers. These defects degrade carrier lifetimes and increase leakage currents, necessitating advanced growth techniques like molecular beam epitaxy to maintain uniformity and minimize threading dislocations in heterostructures.[46][47]Organic, 2D, and Novel Semiconductors
Organic semiconductors encompass a diverse class of materials, including conjugated polymers and small molecules, that enable flexible and low-cost electronics due to their solution-processable nature and mechanical pliability. Conjugated polymers such as polythiophene exhibit a band gap of approximately 2.0 eV, making them suitable for applications in flexible electronics and organic light-emitting diodes (OLEDs), where charge transport occurs primarily via hopping mechanisms with mobilities typically below 1 cm²/V·s. Small molecules like pentacene, with a band gap ranging from 1.5 to 2.2 eV and hole mobilities up to 3.0 cm²/V·s in thin-film organic field-effect transistors (OFETs), further exemplify their role in high-performance organic transistors, though air instability remains a challenge. These materials' π-conjugated structures facilitate delocalized charge carriers, but their amorphous or polycrystalline morphologies limit coherent transport compared to inorganic counterparts. Two-dimensional (2D) semiconductors, derived from layered van der Waals materials, offer atomic-scale thickness and tunable electronic properties arising from quantum confinement effects, enabling advanced nanoelectronics. Transition metal dichalcogenides like monolayer MoS₂ feature a direct band gap of about 1.8 eV, supporting high-on/off ratio transistors scalable to channel lengths below 3 nm, as demonstrated in devices with contact pitches as small as 42 nm. Black phosphorus, or phosphorene, provides a tunable band gap from 0.3 eV in bulk to 2.0 eV in monolayers, with electron and hole mobilities reaching approximately 1000 cm²/V·s, positioning it as a promising p-type channel material for 2D complementary metal-oxide-semiconductor (CMOS) logic inverters when paired with n-type MoS₂. The reduced dimensionality in these materials enhances gate control and suppresses short-channel effects, though integration challenges persist. Perovskite semiconductors, particularly hybrid organic-inorganic variants, stand out for their defect tolerance and facile solution processing, which allow high-quality films via low-temperature methods like spin-coating. Methylammonium lead iodide (MAPbI₃) possesses a band gap of 1.55 eV and has enabled perovskite solar cells with efficiencies up to approximately 22%. Broader perovskite compositions have achieved certified power conversion efficiencies exceeding 25% as of 2025, attributed to long charge carrier diffusion lengths despite moderate defect densities.[48] As of late 2025, triple-junction perovskite solar cells have achieved efficiencies up to 27%.[49] All-inorganic counterparts, such as cesium lead iodide (CsPbI₃), maintain similar defect tolerance through shallow trap states and antibonding orbital interactions in the conduction band, facilitating efficient photovoltaics and light-emitting devices, though phase instability under ambient conditions requires passivation strategies. Topological insulators and semimetals represent novel classes protected by symmetry and band topology, exhibiting insulating bulk states with conductive surface or edge channels ideal for dissipationless spintronics. Bismuth selenide (Bi₂Se₃) features a bulk band gap of 0.3 eV with topologically protected surface states enabling spin-momentum locking, which supports spin-orbit torque switching in heterostructures for low-power magnetic memory applications. Weyl semimetals like tantalum arsenide (TaAs) host pairs of topological Weyl nodes—massless fermion excitations—that enable unique quantum phenomena, including chiral anomaly effects observable in high magnetic fields, with potential for fault-tolerant quantum computing via robust edge modes. Emerging trends in these materials emphasize overcoming stability and scalability hurdles to realize commercial viability. Organic semiconductors and perovskites suffer from environmental degradation, including moisture-induced hydrolysis in MAPbI₃ and photo-oxidation in polythiophenes, necessitating encapsulation or compositional tuning for operational lifetimes beyond 1000 hours. For 2D materials, post-2020 advances in wafer-scale synthesis, such as epitaxial growth of single-crystal MoS₂ monolayers on sapphire substrates yielding uniform films over 4-inch wafers with carrier mobilities exceeding 50 cm²/V·s, have accelerated integration into flexible circuits and tandem solar cells.Reference Tables
Table of Elemental and Binary Semiconductors
This section provides a tabular reference for key physical parameters of elemental and binary semiconductors, focusing on those commonly used in electronics and optoelectronics. The parameters include the material formula, crystal structure, band gap energy at 300 K, band gap type (direct or indirect), lattice constant, electron and hole mobilities, and primary applications. These values represent standard measurements under ambient conditions, though actual properties can vary with temperature, doping, and crystal quality—for instance, band gaps typically decrease with increasing temperature due to lattice expansion.[22][50]| Material | Crystal Structure | Band Gap (eV, 300 K) | Type | Lattice Constant (Å) | Electron Mobility (cm²/V·s) | Hole Mobility (cm²/V·s) | Primary Applications |
|---|---|---|---|---|---|---|---|
| Si | Diamond cubic | 1.12 | Indirect | 5.431 | 1500 | 450 | Integrated circuits, solar cells |
| Ge | Diamond cubic | 0.66 | Indirect | 5.657 | 3900 | 1900 | Infrared detectors, transistors |
| GaAs | Zincblende | 1.42 | Direct | 5.653 | 8500 | 400 | Optoelectronics, high-speed electronics, LEDs |
| GaP | Zincblende | 2.26 | Indirect | 5.451 | 100 | 100 | Light-emitting diodes (green), phosphors |
| InP | Zincblende | 1.34 | Direct | 5.869 | 5400 | 150 | Telecommunications lasers, photodetectors |
| GaSb | Zincblende | 0.72 | Direct | 6.096 | 5000 | 1000 | Infrared detectors, thermoelectrics |
| InAs | Zincblende | 0.35 | Direct | 6.058 | 30000 | 450 | Infrared detectors, high-speed transistors |
| InSb | Zincblende | 0.17 | Direct | 6.479 | 77000 | 850 | Hall effect sensors, magnetoresistors |
| ZnSe | Zincblende | 2.70 | Direct | 5.668 | 1000 | 50 | Blue LEDs, laser diodes |
| CdTe | Zincblende | 1.50 | Direct | 6.482 | 1050 | 100 | Solar cells, infrared detectors |
| CdS | Wurtzite | 2.42 | Direct | 4.136 (a), 6.714 (c) | 400 | 40 | Photoconductors, solar cells |
Table of Alloy and Emerging Systems
Alloy semiconductor systems enable precise tuning of electronic and optical properties through compositional variation, allowing band gap engineering for specific device requirements. These materials often exhibit nonlinear band gap dependence on composition, characterized by a bowing parameter in the expression , where is the alloy fraction and , are the band gaps of the binary endpoints. Lattice constants typically vary linearly with , facilitating epitaxial growth on substrates like GaAs or InP. Representative examples from III-V families are detailed below, focusing on tunable parameters and primary applications in optoelectronics and high-speed electronics.| Alloy System | Band Gap Range (eV) | Lattice Constant Range (Å) | Bowing Parameter (eV) | Key Applications |
|---|---|---|---|---|
| 1.42 (x=0) to 2.16 (x=1) | 5.653 to 5.661 | 0.37–0.67 | Heterostructure lasers, high-electron-mobility transistors (HEMTs)[52] | |
| 0.36 (x=1) to 1.42 (x=0) | 5.653 to 6.058 | 0.48 | Infrared detectors, quantum cascade lasers, high-speed photodetectors[52] | |
| 1.42 (x=0) to 2.26 (x=1) | 5.653 to 5.451 | 0.19–0.25 | Light-emitting diodes (LEDs), visible lasers[52] | |
| 1.35 (x=1) to 1.42 (x=0) | 5.653 to 5.870 | 0.67 | Red diode lasers, solar cell barriers[52] | |
| 0.36 (x=0) to 2.16 (x=1) | 5.661 to 6.058 | 0.63 | Buffer layers in HEMTs, mid-infrared optoelectronics[52] | |
| (CIGS) | 1.0 (x=1) to 1.7 (x=0) | ~5.8 (varies slightly) | 0.223 | Thin-film photovoltaics with efficiencies up to 23%[53] |
| Material | Structure | Band Gap (eV) | Electron Mobility (cm²/V·s) | Key Applications |
|---|---|---|---|---|
| (methylammonium lead iodide) | Perovskite (3D hybrid organic-inorganic) | 1.55 | 10–100 | Perovskite solar cells, with MAPbI3-based devices achieving up to 20.5% efficiency (as of 2025); used in early tandems but superseded by stabler compositions for records up to 33.6%[54][55] |
| (monolayer) | 2D TMD (transition metal dichalcogenide) | 1.8 (direct) | Up to 200 | Field-effect transistors (FETs), photodetectors, spintronics[56] |
| Black phosphorus (phosphorene, few-layer) | 2D puckered (orthorhombic) | 0.3 (bulk) to ~2.0 (monolayer) | >1000 (hole) | High-mobility p-type transistors, mid-infrared detectors |
| (monolayer) | 2D TMD | 2.0–2.1 (direct) | ~40–50 | Optoelectronic devices, valleytronics, flexible sensors[57] |
| Pentacene (organic) | Molecular crystal (polymorph) | ~2.0 | 0.1–5 | Organic thin-film transistors (OTFTs), organic photovoltaics[58] |
