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A nanowire is a nanostructure, with the diameter of the order of a nanometer (10−9 meters). It can also be defined as the ratio of the length to width being greater than 1000. Alternatively, nanowires can be defined as structures that have a thickness or diameter constrained to tens of nanometers or less and an unconstrained length. At these scales, quantum mechanical effects are important—which coined the term "quantum wires". Many different types of nanowires exist, including superconducting (e.g. YBCO), metallic (e.g. Ni, Pt, Au), semiconducting (e.g. silicon nanowires (SiNWs), InP, GaN) and insulating (e.g. SiO2, TiO2). Molecular nanowires are composed of repeating molecular units either organic (e.g. DNA) or inorganic (e.g. Mo6S9−xIx).
Typical nanowires exhibit aspect ratios (length-to-width ratio) of 1000 or more. As such they are often referred to as one-dimensional (1-D) materials. Nanowires have many interesting properties that are not seen in bulk or 3-D (three-dimensional) materials. This is because electrons in nanowires are quantum confined laterally and thus occupy energy levels that are different from the traditional continuum of energy levels or bands found in bulk materials.
Peculiar features of this quantum confinement exhibited by certain nanowires manifest themselves in discrete values of the electrical conductance. Such discrete values arise from a quantum mechanical restraint on the number of electrons that can travel through the wire at the nanometer scale. These discrete values are often referred to as the quantum of conductance and are integer multiples of
They are inverse of the well-known resistance unit h/e2, which is roughly equal to 25812.8 ohms, and referred to as the von Klitzing constant RK (after Klaus von Klitzing, the discoverer of exact quantization). Since 1990, a fixed conventional value RK-90 is accepted.
Examples of nanowires include inorganic molecular nanowires (Mo6S9−xIx, Li2Mo6Se6), which can have a diameter of 0.9 nm and be hundreds of micrometers long. Other important examples are based on semiconductors such as InP, Si, GaN, etc., dielectrics (e.g. SiO2,TiO2), or metals (e.g. Ni, Pt).
There are many applications where nanowires may become important in electronic, opto-electronic and nanoelectromechanical devices, as additives in advanced composites, for metallic interconnects in nanoscale quantum devices, as field-emitters and as leads for biomolecular nanosensors.
There are two basic approaches to synthesizing nanowires: top-down and bottom-up. A top-down approach reduces a large piece of material to small pieces, by various means such as lithography,milling or thermal oxidation. A bottom-up approach synthesizes the nanowire by combining constituent adatoms. Most synthesis techniques use a bottom-up approach. Initial synthesis via either method may often be followed by a nanowire thermal treatment step, often involving a form of self-limiting oxidation, to fine tune the size and aspect ratio of the structures.
Nanowire production uses several common laboratory techniques, including suspension, electrochemical deposition, vapor deposition, and VLS growth. Ion track technology enables growing homogeneous and segmented nanowires down to 8 nm diameter. As nanowire oxidation rate is controlled by diameter, thermal oxidation steps are often applied to tune their morphology.
A suspended nanowire is a wire produced in a high-vacuum chamber held at the longitudinal extremities. Suspended nanowires can be produced by:
A common technique for creating a nanowire is vapor-liquid-solid method (VLS), which was first reported by Wagner and Ellis in 1964 for silicon whiskers with diameters ranging from hundreds of nm to hundreds of µm.This process can produce high-quality crystalline nanowires of many semiconductor materials, for example, VLS–grown single crystalline silicon nanowires (SiNWs) with smooth surfaces could have excellent properties, such as ultra-large elasticity. This method uses a source material from either laser ablated particles or a feed gas such as silane.
VLS synthesis requires a catalyst. For nanowires, the best catalysts are liquid metal (such as gold) nanoclusters, which can either be self-assembled from a thin film by dewetting, or purchased in colloidal form and deposited on a substrate.
The source enters these nanoclusters and begins to saturate them. On reaching supersaturation, the source solidifies and grows outward from the nanocluster. Simply turning off the source can adjust the final length of the nanowire. Switching sources while still in the growth phase can create compound nanowires with super-lattices of alternating materials.
A single-step vapour phase reaction at elevated temperature synthesises inorganic nanowires such as Mo6S9−xIx. From another point of view, such nanowires are cluster polymers.
VSS Growth Similar to VLS synthesis, VSS (vapor-solid-solid) synthesis of nanowires (NWs) proceeds through thermolytic decomposition of a silicon precursor (typically phenylsilane). Unlike VLS, the catalytic seed remains in solid state when subjected to high temperature annealing of the substrate. This such type of synthesis is widely used to synthesise metal silicide/germanide nanowires through VSS alloying between a copper substrate and a silicon/germanium precursor.
Solution-phase synthesis refers to techniques that grow nanowires in solution. They can produce nanowires of many types of materials. Solution-phase synthesis has the advantage that it can produce very large quantities, compared to other methods. In one technique, the polyol synthesis, ethylene glycol is both solvent and reducing agent. This technique is particularly versatile at producing nanowires of gold,lead, platinum, and silver.
The supercritical fluid-liquid-solid growth methodcan be used to synthesize semiconductor nanowires, e.g., Si and Ge. By using metal nanocrystals as seeds, Si and Ge organometallic precursors are fed into a reactor filled with a supercritical organic solvent, such as toluene. Thermolysis results in degradation of the precursor, allowing release of Si or Ge, and dissolution into the metal nanocrystals. As more of the semiconductor solute is added from the supercritical phase (due to a concentration gradient), a solid crystallite precipitates, and a nanowire grows uniaxially from the nanocrystal seed.
Nanowires can be also grown without the help of catalysts, which gives an advantage of pure nanowires and minimizes the number of technological steps. The simplest methods to obtain metal oxide nanowires use ordinary heating of the metals, e.g. metal wire heated with battery, by Joule heating in aircan be easily done at home. The vast majority of nanowire-formation mechanisms are explained through the use of catalytic nanoparticles, which drive the nanowire growth and are either added intentionally or generated during the growth. However the mechanisms for catalyst-free growth of nanowires (or whiskers) were known from 1950s. Spontaneous nanowire formation by non-catalytic methods were explained by the dislocation present in specific directions or the growth anisotropy of various crystal faces. More recently, after microscopy advancement, the nanowire growth driven by screw dislocations or twin boundaries were demonstrated. The picture on the right shows a single atomic layer growth on the tip of CuO nanowire, observed by in situ TEM microscopy during the non-catalytic synthesis of nanowire.
An emerging field is to use DNA strands as scaffolds for metallic nanowire synthesis. This method is investigated both for the synthesis of metallic nanowires in electronic components and for biosensing applications, in which they allow the transduction of a DNA strand into a metallic nanowire that can be electrically detected. Typically, ssDNA strands are stretched, whereafter they are decorated with metallic nanoparticles that have been functionalised with short complementary ssDNA strands.
Several physical reasons predict that the conductivity of a nanowire will be much less than that of the corresponding bulk material. First, there is scattering from the wire boundaries, whose effect will be very significant whenever the wire width is below the free electron mean free path of the bulk material. In copper, for example, the mean free path is 40 nm. Copper nanowires less than 40 nm wide will shorten the mean free path to the wire width.
Nanowires also show other peculiar electrical properties due to their size. Unlike single wall carbon nanotubes, whose motion of electrons can fall under the regime of ballistic transport (meaning the electrons can travel freely from one electrode to the other), nanowire conductivity is strongly influenced by edge effects. The edge effects come from atoms that lay at the nanowire surface and are not fully bonded to neighboring atoms like the atoms within the bulk of the nanowire. The unbonded atoms are often a source of defects within the nanowire, and may cause the nanowire to conduct electricity more poorly than the bulk material. As a nanowire shrinks in size, the surface atoms become more numerous compared to the atoms within the nanowire, and edge effects become more important.
Furthermore, the conductivity can undergo a quantization in energy: i.e. the energy of the electrons going through a nanowire can assume only discrete values, which are multiples of the conductance quantum G = 2e2/h (where e is the charge of the electron and h is the Planck constant. See also the Quantum Hall effect).
The conductivity is hence described as the sum of the transport by separate channels of different quantized energy levels. The thinner the wire is, the smaller the number of channels available to the transport of electrons.
This quantization has been demonstrated by measuring the conductivity of a nanowire suspended between two electrodes while pulling it: as its diameter reduces, its conductivity decreases in a stepwise fashion and the plateaus correspond to multiples of G.
The quantization of conductivity is more pronounced in semiconductors like Si or GaAs than in metals, due to their lower electron density and lower effective mass. It can be observed in 25 nm wide silicon fins, and results in increased threshold voltage. In practical terms, this means that a MOSFET with such nanoscale silicon fins, when used in digital applications, will need a higher gate (control) voltage to switch the transistor on.
To incorporate nanowire technology into industrial applications, researchers in 2008 developed a method of welding nanowires together: a sacrificial metal nanowire is placed adjacent to the ends of the pieces to be joined (using the manipulators of a scanning electron microscope); then an electric current is applied, which fuses the wire ends. The technique fuses wires as small as 10 nm.
For nanowires with diameters less than 10 nm, existing welding techniques, which require precise control of the heating mechanism and which may introduce the possibility of damage, will not be practical. Recently scientists discovered that single-crystalline ultrathin gold nanowires with diameters ~3–10 nm can be "cold-welded" together within seconds by mechanical contact alone, and under remarkably low applied pressures (unlike macro- and micro-scale cold welding process). High-resolution transmission electron microscopy and in situ measurements reveal that the welds are nearly perfect, with the same crystal orientation, strength and electrical conductivity as the rest of the nanowire. The high quality of the welds is attributed to the nanoscale sample dimensions, oriented-attachment mechanisms and mechanically assisted fast surface diffusion. Nanowire welds were also demonstrated between gold and silver, and silver nanowires (with diameters ~5–15 nm) at near room temperature, indicating that this technique may be generally applicable for ultrathin metallic nanowires. Combined with other nano- and microfabrication technologies, cold welding is anticipated to have potential applications in the future bottom-up assembly of metallic one-dimensional nanostructures.
The study of nanowire mechanics has boomed since the advent of the Atomic Force Microscope (AFM), and associated technologies which have enabled direct study of the response of the nanowire to an applied load.Specifically, a nanowire can be clamped from one end, and the free end displaced by an AFM tip. In this cantilever geometry, the height of the AFM is precisely known, and the force applied is precisely known. This allows for construction of a force vs. displacement curve, which can be converted to a stress vs. strain curve if the nanowire dimensions are known. From the stress-strain curve, the elastic constant known as the Young’s Modulus can be derived, as well as the toughness, and degree of strain-hardening.
The elastic component of the stress-strain curve described by the Young’s Modulus, has been reported for nanowires, however the modulus depends very strongly on the microstructure. Thus a complete description of the modulus dependence on diameter is lacking. Analytically, continuum mechanics has been applied to estimate the dependence of modulus on diameter: in tension, where is the bulk modulus, is the thickness of a shell layer in which the modulus is surface dependent and varies from the bulk, is the surface modulus, and is the diameter. This equation implies that the modulus increases as the diameter decreases. However, various computational methods such as molecular dynamics have predicted that modulus should decrease as diameter decreases.
Experimentally, gold nanowires have been shown to have a Young’s modulus which is effectively diameter independent.Similarly, nano-indentation was applied to study the modulus of silver nanowires, and again the modulus was found to be 88 GPa, very similar to the modulus of bulk Silver (85 GPa) These works demonstrated that the analytically determined modulus dependence seems to be suppressed in nanowire samples where the crystalline structure highly resembles that of the bulk system.
In contrast, Si solid nanowires have been studied, and shown to have a decreasing modulus with diameterThe authors of that work report a Si modulus which is half that of the bulk value, and they suggest that the density of point defects, and or loss of chemical stoichiometry may account for this difference.
The plastic component of the stress strain curve (or more accurately the onset of plasticity) is described by the yield strength. The strength of a material is increased by decreasing the number of defects in the solid, which occurs naturally in nanomaterials where the volume of the solid is reduced. As a nanowire is shrunk to a single line of atoms, the strength should theoretically increase all the way to the molecular tensile strength.Gold nanowires have been described as ‘ultrahigh strength’ due to the extreme increase in yield strength, approaching the theoretical value of E/10. This huge increase in yield is determined to be due to the lack of dislocations in the solid. Without dislocation motion, a ‘dislocation-starvation’ mechanism is in operation. The material can accordingly experience huge stresses before dislocation motion is possible, and then begins to strain-harden. For these reasons, nanowires (historically described as 'whiskers') have been used extensively in composites for increasing the overall strength of a material. Moreover, nanowires continue to be actively studied, with research aiming to translate enhanced mechanical properties to novel devices in the fields of MEMS or NEMS.
Nanowires can be used for MOSFETs (MOS field-effect transistors). MOS transistors are used widely as fundamental building elements in today's electronic circuits.As predicted by Moore's law, the dimension of MOS transistors is shrinking smaller and smaller into nanoscale. One of the key challenges of building future nanoscale MOS transistors is ensuring good gate control over the channel. Due to the high aspect ratio, if the gate dielectric is wrapped around the nanowire channel, we can get good control of channel electrostatic potential, thereby turning the transistor on and off efficiently.
Due to the unique one-dimensional structure with remarkable optical properties, the nanowire also opens new opportunities for realizing high efficiency photovoltaic devices.Compared with its bulk counterparts, the nanowire solar cells are less sensitive to impurities due to bulk recombination, and thus silicon wafers with lower purity can be used to achieve acceptable efficiency, leading to the a reduction on material consumption.
To create active electronic elements, the first key step was to chemically dope a semiconductor nanowire. This has already been done to individual nanowires to create p-type and n-type semiconductors.
The next step was to find a way to create a p–n junction, one of the simplest electronic devices. This was achieved in two ways. The first way was to physically cross a p-type wire over an n-type wire. The second method involved chemically doping a single wire with different dopants along the length. This method created a p-n junction with only one wire.
After p-n junctions were built with nanowires, the next logical step was to build logic gates. By connecting several p-n junctions together, researchers have been able to create the basis of all logic circuits: the AND, OR, and NOT gates have all been built from semiconductor nanowire crossings.
In August 2012, researchers reported constructing the first NAND gate from undoped silicon nanowires. This avoids the problem of how to achieve precision doping of complementary nanocircuits, which is unsolved. They were able to control the Schottky barrier to achieve low-resistance contacts by placing a silicide layer in the metal-silicon interface.
It is possible that semiconductor nanowire crossings will be important to the future of digital computing. Though there are other uses for nanowires beyond these, the only ones that actually take advantage of physics in the nanometer regime are electronic.
In addition, nanowires are also being studied for use as photon ballistic waveguides as interconnects in quantum dot/quantum effect well photon logic arrays. Photons travel inside the tube, electrons travel on the outside shell.
When two nanowires acting as photon waveguides cross each other the juncture acts as a quantum dot.
Conducting nanowires offer the possibility of connecting molecular-scale entities in a molecular computer. Dispersions of conducting nanowires in different polymers are being investigated for use as transparent electrodes for flexible flat-screen displays.
Because of their high Young's moduli, their use in mechanically enhancing composites is being investigated. Because nanowires appear in bundles, they may be used as tribological additives to improve friction characteristics and reliability of electronic transducers and actuators.
Because of their high aspect ratio, nanowires are also uniquely suited to dielectrophoretic manipulation,which offers a low-cost, bottom-up approach to integrating suspended dielectric metal oxide nanowires in electronic devices such as UV, water vapor, and ethanol sensors.
Nanowire lasers are nano-scaled lasers with potential as optical interconnects and optical data communication on chip. Nanowire lasers are built from III–V semiconductor heterostructures, the high refractive index allows for low optical loss in the nanowire core. Nanowire lasers are subwavelength lasers of only a few hundred nanometers. GHz offering possibilities for optical chip level communications.Nanowire lasers are Fabry–Perot resonator cavities defined by the end facets of the wire with high-reflectivity, recent developments have demonstrated repetition rates greater than 200
In an analogous way to FET devices in which the modulation of conductance (flow of electrons/holes) in the semiconductor, between the input (source) and the output (drain) terminals, is controlled by electrostatic potential variation (gate-electrode) of the charge carriers in the device conduction channel, the methodology of a Bio/Chem-FET is based on the detection of the local change in charge density, or so-called “field effect”, that characterizes the recognition event between a target molecule and the surface receptor.
This change in the surface potential influences the Chem-FET device exactly as a ‘gate’ voltage does, leading to a detectable and measurable change in the device conduction. When these devices are fabricated using semiconductor nanowires as the transistor element the binding of a chemical or biological species to the surface of the sensor can lead to the depletion or accumulation of charge carriers in the "bulk" of the nanometer diameter nanowire i.e. (small cross section available for conduction channels). Moreover, the wire, which serves as a tunable conducting channel, is in close contact with the sensing environment of the target, leading to a short response time, along with orders of magnitude increase in the sensitivity of the device as a result of the huge S/V ratio of the nanowires.
While several inorganic semiconducting materials such as Si, Ge, and metal oxides (e.g. In2O3, SnO2, ZnO, etc.) have been used for the preparation of nanowires, Si is usually the material of choice when fabricating nanowire FET-based chemo/biosensors.
Several examples of the use of silicon nanowire(SiNW) sensing devices include the ultra sensitive, real-time sensing of biomarker proteins for cancer, detection of single virus particles, and the detection of nitro-aromatic explosive materials such as 2,4,6 Tri-nitrotoluene (TNT) in sensitives superior to these of canines.Silicon nanowires could also be used in their twisted form, as electromechanical devices, to measure intermolecular forces with great precision.
Generally, the charges on dissolved molecules and macromolecules are screened by dissolved counterions, since in most cases molecules bound to the devices are separated from the sensor surface by approximately 2–12 nm (the size of the receptor proteins or DNA linkers bound to the sensor surface). As a result of the screening, the electrostatic potential that arises from charges on the analyte molecule decays exponentially toward zero with distance. Thus, for optimal sensing, the Debye length must be carefully selected for nanowire FET measurements. One approach of overcoming this limitation employs fragmentation of the antibody-capturing units and control over surface receptor density, allowing more intimate binding to the nanowire of the target protein. This approach proved useful for dramatically enhancing the sensitivity of cardiac biomarkers (e.g. Troponin) detection directly from serum for the diagnosis of acute myocardial infarction.
Carbon nanotubes (CNTs) are tubes made of carbon with diameters typically measured in nanometers.
Cathodoluminescence is an optical and electromagnetic phenomenon in which electrons impacting on a luminescent material such as a phosphor, cause the emission of photons which may have wavelengths in the visible spectrum. A familiar example is the generation of light by an electron beam scanning the phosphor-coated inner surface of the screen of a television that uses a cathode ray tube. Cathodoluminescence is the inverse of the photoelectric effect, in which electron emission is induced by irradiation with photons.
Molecular-beam epitaxy (MBE) is an epitaxy method for thin-film deposition of single crystals. The MBE process was developed in the late 1970s at Bell Telephone Laboratories by J. R. Arthur and Alfred Y. Cho. MBE is widely used in the manufacture of semiconductor devices, including transistors, and it is considered one of the fundamental tools for the development of nanotechnologies. MBE is used to fabricate diodes and MOSFETs at microwave frequencies, and to manufacture the lasers used to read optical discs.
Gallium nitride (GaN) is a binary III/V direct bandgap semiconductor commonly used in light-emitting diodes since the 1990s. The compound is a very hard material that has a Wurtzite crystal structure. Its wide band gap of 3.4 eV affords it special properties for applications in optoelectronic, high-power and high-frequency devices. For example, GaN is the substrate which makes violet (405 nm) laser diodes possible, without use of nonlinear optical frequency-doubling.
Thermoelectric materials show the thermoelectric effect in a strong or convenient form.
Quantum dots (QDs) are tiny semiconductor particles a few nanometres in size, having optical and electronic properties that differ from larger particles due to quantum mechanics. They are a central topic in nanotechnology. When the quantum dots are illuminated by UV light, an electron in the quantum dot can be excited to a state of higher energy. In the case of a semiconducting quantum dot, this process corresponds to the transition of an electron from the valence band to the conductance band. The excited electron can drop back into the valence band releasing its energy by the emission of light. This light emission (photoluminescence) is illustrated in the figure on the right. The color of that light depends on the energy difference between the conductance band and the valence band.
In mesoscopic physics, a quantum wire is an electrically conducting wire in which quantum effects influence the transport properties. Usually such effects appear in the dimension of nanometers, so they are also referred to as nanowires.
Indium gallium nitride is a semiconductor material made of a mix of gallium nitride (GaN) and indium nitride (InN). It is a ternary group III/group V direct bandgap semiconductor. Its bandgap can be tuned by varying the amount of indium in the alloy. InxGa1−xN has a direct bandgap span from the infrared for InN to the ultraviolet of GaN. The ratio of In/Ga is usually between 0.02/0.98 and 0.3/0.7.
Hybrid solar cells combine advantages of both organic and inorganic semiconductors. Hybrid photovoltaics have organic materials that consist of conjugated polymers that absorb light as the donor and transport holes. Inorganic materials in hybrid cells are used as the acceptor and electron transporter in the structure. The hybrid photovoltaic devices have a potential for not only low-cost by roll-to-roll processing but also for scalable solar power conversion.
Nanochemistry is the combination of chemistry and nanoscience. Nanochemistry is associated with synthesis of building blocks which are dependent on size, surface, shape and defect properties. Nanochemistry is being used in chemical, materials and physical, science as well as engineering, biological and medical applications. Nanochemistry and other nanoscience fields have the same core concepts but the usages of those concepts are different.
Indium(III) oxide (In2O3) is a chemical compound, an amphoteric oxide of indium.
Nanoelectronics refers to the use of nanotechnology in electronic components. The term covers a diverse set of devices and materials, with the common characteristic that they are so small that inter-atomic interactions and quantum mechanical properties need to be studied extensively. Some of these candidates include: hybrid molecular/semiconductor electronics, one-dimensional nanotubes/nanowires or advanced molecular electronics.
Strain engineering refers to a general strategy employed in semiconductor manufacturing to enhance device performance. Performance benefits are achieved by modulating strain in the transistor channel, which enhances electron mobility and thereby conductivity through the channel.
Mesoscopic physics is a subdiscipline of condensed matter physics that deals with materials of an intermediate length.The lower limit can also be defined as being the size of individual atoms. At the micrometre level are bulk materials. Both mesoscopic and macroscopic objects contain many atoms. Whereas average properties derived from its constituent materials describe macroscopic objects, as they usually obey the laws of classical mechanics, a mesoscopic object, by contrast, is affected by thermal fluctuations around the average, and its electronic behavior may require modeling at the level of quantum mechanics.
Organic photovoltaic devices (OPVs) are fabricated from thin films of organic semiconductors, such as polymers and small-molecule compounds, and are typically on the order of 100 nm thick. Because polymer based OPVs can be made using a coating process such as spin coating or inkjet printing, they are an attractive option for inexpensively covering large areas as well as flexible plastic surfaces. A promising low cost alternative to conventional solar cells made of crystalline silicon, there is a large amount of research being dedicated throughout industry and academia towards developing OPVs and increasing their power conversion efficiency.
The vapor–liquid–solid method (VLS) is a mechanism for the growth of one-dimensional structures, such as nanowires, from chemical vapor deposition. The growth of a crystal through direct adsorption of a gas phase on to a solid surface is generally very slow. The VLS mechanism circumvents this by introducing a catalytic liquid alloy phase which can rapidly adsorb a vapor to supersaturation levels, and from which crystal growth can subsequently occur from nucleated seeds at the liquid–solid interface. The physical characteristics of nanowires grown in this manner depend, in a controllable way, upon the size and physical properties of the liquid alloy.
As the devices continue to shrink further into the sub-100 nm range following the trend predicted by Moore’s law, the topic of thermal properties and transport in such nanoscale devices becomes increasingly important. Display of great potential by nanostructures for thermoelectric applications also motivates the studies of thermal transport in such devices. These fields, however, generate two contradictory demands: high thermal conductivity to deal with heating issues in sub-100 nm devices and low thermal conductivity for thermoelectric applications. These issues can be addressed with phonon engineering, once nanoscale thermal behaviors have been studied and understood.
Local oxidation nanolithography (LON) is a tip-based nanofabrication method. It is based on the spatial confinement on an oxidation reaction under the sharp tip of an atomic force microscope.
Core–shell semiconducting nanocrystals (CSSNCs) are a class of materials which have properties intermediate between those of small, individual molecules and those of bulk, crystalline semiconductors. They are unique because of their easily modular properties, which are a result of their size. These nanocrystals are composed of a quantum dot semiconducting core material and a shell of a distinct semiconducting material. The core and the shell are typically composed of type II–VI, IV–VI, and III–V semiconductors, with configurations such as CdS/ZnS, CdSe/ZnS, CdSe/CdS, and InAs/CdSe Organically passivated quantum dots have low fluorescence quantum yield due to surface related trap states. CSSNCs address this problem because the shell increases quantum yield by passivating the surface trap states. In addition, the shell provides protection against environmental changes, photo-oxidative degradation, and provides another route for modularity. Precise control of the size, shape, and composition of both the core and the shell enable the emission wavelength to be tuned over a wider range of wavelengths than with either individual semiconductor. These materials have found applications in biological systems and optics.
Silicon nanowires, also referred to as SiNWs, are a type of semiconductor nanowire most often formed from a silicon precursor by etching of a solid or through catalyzed growth from a vapor or liquid phase. Such nanowires have promising applications in lithium ion batteries, thermoelectrics and sensors. Initial synthesis of SiNWs is often accompanied by thermal oxidation steps to yield structures of accurately tailored size and morphology.
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