EFluor Nanocrystal

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eFluor Nanocrystals under UV-excitation EFluor Nanocrystal Vials.jpg
eFluor Nanocrystals under UV-excitation

eFluor nanocrystals are a class of fluorophores made of semiconductor quantum dots. The nanocrystals can be provided as either primary amine, carboxylate, or non-functional groups on the surface, allowing conjugation to biomolecules of a researcher's choice. The nanocrystals can be conjugated to primary antibodies which are used for flow cytometry, immunohistochemistry, microarrays, in vivo imaging and microscopy.

Contents

Size

The optical emission properties of eFluor Nanocrystals are primarily dictated by their size, as discussed in the next section. There are at least two aspects to consider when discussing the "size" of a quantum dot: the physical size of the semiconductor structure, and the size of the entire quantum dot moiety including the associated ligands and hydrophilic coating. The size of the semiconductor structure is tabulated below, and reflects the diameter of the spherical quantum dot without ligands. eFluor Nanocrystals are rendered water-dispersable with a patented poly-ethylene glycol (PEG) lipid layer that functions as both a protective hydrophilic coating around the quantum dot, as well as reducing non-specific binding [1] By dynamic light scattering measurements, the hydrodynamic radius of all eFluor Nanocrystals ranges from 10 to 13 nm.

Nanocrystal NameEmission Wavelength (nm)Approximate 1st ExcitonDiameter (nm)Molecular Weight* (gmole)Extinction* (1st Exciton, M−1 cm−1)Composition
eFluor 490NC490 ± 3 nm4703.413,4915.95 E4CdSe/ZnS
eFluor 525NC525 ± 3 nm5054.3 [2] 13,0555.78 E4CdSe/ZnS
eFluor 545NC545 ± 3 nm525**20,2487.74 E4CdSe/ZnS
eFluor 565NC565 ± 3 nm5504.8 [2] 27,2251.05 E5CdSe/ZnS
eFluor 585NC585 ± 3 nm570**47,5591.57 E5CdSe/ZnS
eFluor 605NC605 ± 3 nm5906.1 [2] 95,0092.53 E5CdSe/ZnS
eFluor 625NC625 ± 3 nm6107.1 [2] 205,0744.58 E5CdSe/ZnS
eFluor 650NC650 ± 3 nm6408.7 [2] 740,2991.11 E6CdSe/ZnS
eFluor 700NC690 ± 10 nmN/A3.8115,3853.24 E6 (@ 350 nm)InGaP/ZnS
* Values based on literature relationships. [3]
** No measurement yet available

Properties and structure

Quantum dots are unique fluorophores relative to organic dyes, like fluorescein or rhodamine because they are composed of semiconductor metals, instead of a π-conjugated carbon-bonding framework. With organic dyes, the length of the π-conjugated framework (quantum confinement), as well as side-groups (electron donating/withdrawing or halogens) tend to dictate the absorption and emission spectra of the molecule. Semiconductor quantum dots also work on the concept of quantum confinement, (often referred to as "Particle in a Box" theory) where an exciton is formed inside the crystal lattice by an incident photon of higher energy. The electron and hole of the exciton have an interaction energy that is tuned by changing the physical size of the quantum dot. The absorption and emission colors are tuned such that smaller quantum dots confine the exciton into a tighter physical space and increase the energy. Alternatively, a larger quantum dot confines the exciton into a larger physical space, lowering the interaction energy of the electron and hole, and decreasing the energy of the system. As shown in the table above, the diameter of the CdSe quantum dots is related to the emission energy such that the smaller quantum dots emit photons toward the blue wavelength range (higher energy) and the larger quantum dots emit photons toward the red wavelength range (lower energy.)

Extinction and photoluminescence spectra for eFluor-605 nanocrystals EF 605 spectra.png
Extinction and photoluminescence spectra for eFluor-605 nanocrystals

To the right are representative absorption (blue) and emission (red) spectra for the eFluor-605 nanocrystal. The absorption spectrum of nanocrystals displays a number of peaks overlaid on background that rises exponentially toward the ultraviolet, where the lowest energy absorption peak arises from the 1S32-1Se transition, [4] and has been correlated to the physical size of the quantum dot. [3] Generally referred to as the "1st exciton," and is the primary absorption characteristic used to determine both size and concentration for most quantum dots.

The photoluminescence spectra of quantum dots are also unique relative to organic dyes in that they are typically Gaussian-shaped curves with no red-tailing to the spectrum. The width of the photoluminescence peak represents the heterogeneity in size dispersion of the quantum dots, where a large size dispersion will lead to broad emission peaks, and tight size-dispersion will lead to narrow emission peaks, often quantified by the full width at half maximum (FWHM) value. eFluor Nanocrystals are specified at ≤30 nm FWHM for the CdSe nanocrystals, and ≤70 nm FWHM for the InGaP eFluor 700 nanocrystals.

Related Research Articles

Exciton Quasiparticle which is a bound state of an electron and an electron hole

An exciton is a bound state of an electron and an electron hole which are attracted to each other by the electrostatic Coulomb force. It is an electrically neutral quasiparticle that exists in insulators, semiconductors and some liquids. The exciton is regarded as an elementary excitation of condensed matter that can transport energy without transporting net electric charge.

Photoluminescence light emission from substances after they absorb photons

Photoluminescence is light emission from any form of matter after the absorption of photons. It is one of many forms of luminescence and is initiated by photoexcitation, hence the prefix photo-. Following excitation various relaxation processes typically occur in which other photons are re-radiated. Time periods between absorption and emission may vary: ranging from short femtosecond-regime for emission involving free-carrier plasma in inorganic semiconductors up to milliseconds for Phosphorescence processes in molecular systems; and under special circumstances delay of emission may even span to minutes or hours.

Band gap Energy range in a solid where no electron states can exist

In solid-state physics, a band gap, also called an energy gap, is an energy range in a solid where no electronic states can exist. In graphs of the electronic band structure of solids, the band gap generally refers to the energy difference between the top of the valence band and the bottom of the conduction band in insulators and semiconductors. It is the energy required to promote a valence electron bound to an atom to become a conduction electron, which is free to move within the crystal lattice and serve as a charge carrier to conduct electric current. It is closely related to the HOMO/LUMO gap in chemistry. If the valence band is completely full and the conduction band is completely empty, then electrons cannot move in the solid; however, if some electrons transfer from the valence to the conduction band, then current can flow. Therefore, the band gap is a major factor determining the electrical conductivity of a solid. Substances with large band gaps are generally insulators, those with smaller band gaps are semiconductors, while conductors either have very small band gaps or none, because the valence and conduction bands overlap.

Quantum dot Zero-dimensional, nano-scale semiconductor particles with novel optical and electronic properties

Quantum dots (QDs) are 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.

Fluorescence spectroscopy

Fluorescence spectroscopy is a type of electromagnetic spectroscopy that analyzes fluorescence from a sample. It involves using a beam of light, usually ultraviolet light, that excites the electrons in molecules of certain compounds and causes them to emit light; typically, but not necessarily, visible light. A complementary technique is absorption spectroscopy. In the special case of single molecule fluorescence spectroscopy, intensity fluctuations from the emitted light are measured from either single fluorophores, or pairs of fluorophores.

Fluorophore

A fluorophore is a fluorescent chemical compound that can re-emit light upon light excitation. Fluorophores typically contain several combined aromatic groups, or planar or cyclic molecules with several π bonds.

Potential well

A potential well is the region surrounding a local minimum of potential energy. Energy captured in a potential well is unable to convert to another type of energy because it is captured in the local minimum of a potential well. Therefore, a body may not proceed to the global minimum of potential energy, as it would naturally tend to due to entropy.

Cadmium selenide

Cadmium selenide is an inorganic compound with the formula CdSe. It is a black to red-black solid that is classified as a II-VI semiconductor of the n-type. Much of the current research on this salt is focused on its nanoparticles.

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.

Quantum dot solar cell Type of solar cell based on quantum dot devices

A quantum dot solar cell (QDSC) is a solar cell design that uses quantum dots as the absorbing photovoltaic material. It attempts to replace bulk materials such as silicon, copper indium gallium selenide (CIGS) or cadmium telluride (CdTe). Quantum dots have bandgaps that are tunable across a wide range of energy levels by changing their size. In bulk materials, the bandgap is fixed by the choice of material(s). This property makes quantum dots attractive for multi-junction solar cells, where a variety of materials are used to improve efficiency by harvesting multiple portions of the solar spectrum.

Multiple exciton generation

In solar cell research, carrier multiplication is the phenomenon wherein the absorption of a single photon leads to the excitation of multiple electrons from the valence band to conduction band. In the theory of a conventional solar cell, each photon is only able to excite one electron across the band gap of the semiconductor, and any excess energy in that photon is dissipated as heat. In a material with carrier multiplication, high-energy photons excite on average more than one electron across the band gap, and so in principle the solar cell can produce more useful work.

Fluorescence is used in the life sciences generally as a non-destructive way of tracking or analysing biological molecules by means of fluorescence. Some proteins or small molecules in cells are naturally fluorescent, which is called intrinsic fluorescence or autofluorescence. Alternatively, specific or general proteins, nucleic acids, lipids or small molecules can be "labelled" with an extrinsic fluorophore, a fluorescent dye which can be a small molecule, protein or quantum dot. Several techniques exist to exploit additional properties of fluorophores, such as fluorescence resonance energy transfer, where the energy is passed non-radiatively to a particular neighbouring dye, allowing proximity or protein activation to be detected; another is the change in properties, such as intensity, of certain dyes depending on their environment allowing their use in structural studies.

Photoluminescence excitation is a specific type of photoluminescence and concerns the interaction between electromagnetic radiation and matter. It is used in spectroscopic measurements where the frequency of the excitation light is varied, and the luminescence is monitored at the typical emission frequency of the material being studied. Peaks in the PLE spectra often represent absorption lines of the material. PLE spectroscopy is a useful method to investigate the electronic level structure of materials with low absorption due to the superior signal-to-noise ratio of the method compared to absorption measurements.

Core–shell semiconductor nanocrystal

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.

Blinking colloidal nanocrystals is a phenomenon observed during studies of single colloidal nanocrystals that show that they randomly turn their photoluminescence on and off even under continuous light illumination. This has also been described as luminescence intermittency. Similar behavior has been observed in crystals made of other materials. For example, porous silicon also exhibits this affect.

The semiconductor luminescence equations (SLEs) describe luminescence of semiconductors resulting from spontaneous recombination of electronic excitations, producing a flux of spontaneously emitted light. This description established the first step toward semiconductor quantum optics because the SLEs simultaneously includes the quantized light–matter interaction and the Coulomb-interaction coupling among electronic excitations within a semiconductor. The SLEs are one of the most accurate methods to describe light emission in semiconductors and they are suited for a systematic modeling of semiconductor emission ranging from excitonic luminescence to lasers.

The Elliott formula describes analytically, or with few adjustable parameters such as the dephasing constant, the light absorption or emission spectra of solids. It was originally derived by Roger James Elliott to describe linear absorption based on properties of a single electron–hole pair. The analysis can be extended to a many-body investigation with full predictive powers when all parameters are computed microscopically using, e.g., the semiconductor Bloch equations or the semiconductor luminescence equations.

Terahertz spectroscopy detects and controls properties of matter with electromagnetic fields that are in the frequency range between a few hundred gigahertz and several terahertz. In many-body systems, several of the relevant states have an energy difference that matches with the energy of a THz photon. Therefore, THz spectroscopy provides a particularly powerful method in resolving and controlling individual transitions between different many-body states. By doing this, one gains new insights about many-body quantum kinetics and how that can be utilized in developing new technologies that are optimized up to the elementary quantum level.

Quantum dots (QDs) are semiconductor nanoparticles with a size less than 10 nm. They exhibited size-dependent properties especially in the optical absorption and the photoluminescence (PL). Typically, the fluorescence emission peak of the QDs can be tuned by changing their diameters. So far, QDs were consisted of different group elements such as CdTe, CdSe, CdS in the II-VI category, InP or InAs in the III-V category, CuInS2 or AgInS2 in the I–III–VI2 category, and PbSe/PbS in the IV-VI category. These QDs are promising candidates as fluorescent labels in various biological applications such as bioimaging, biosensing and drug delivery.

Perovskite nanocrystal

Perovskite nanocrystals are a class of semiconductor nanocrystals, which exhibit unique characteristics that separate them from traditional quantum dots. Perovskite nanocrystals have an ABX3 composition where A = cesium, methylammonium (MA), or formamidinium (FA); B = lead or tin; and X = chloride, bromide, or iodide.

References

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