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Quantum Dots

Quantum dots are tiny particles or nanocrystals of a semiconducting material with diameters in the range of 2-10 nanometers (10-50 atoms). They were first discovered in 1980. 1 They display unique electronic properties, intermediate between those of bulk semiconductors and discrete molecules, that are partly the result of the unusually high surface-to-volume ratios for these particles.2-4 The most apparent result of this is fluorescence, wherein the nanocrystals can produce distinctive colors determined by the size of the particles.

Due to their small size, the electrons in these particles are confined in a small space (quantum box), and when the radii of the semiconductor nanocrystal is smaller than the exciton Bohr radius (exciton Bohr radius is the average distance between the electron in the conduction band and the hole it leaves behind in the valence band), there is quantization of the energy levels according to Pauli’s exclusion principle (Figure 1)5,6. The discrete, quantized energy levels of these quantum particles relate them more closely to atoms than bulk materials and have resulted in them being nicknamed 'artificial atoms. Generally, as the size of the crystal decreases, the difference in energy between the highest valence band and the lowest conduction band increases. More energy is then needed to excite the dot, and concurrently, more energy is released when the crystal returns to its ground state, resulting in a color shift from red to blue in the emitted light. As a result of this phenomenon, these nanomaterials can emit any color of light from the same material simply by changing the dot size. Additionally, because of the high level of control possible over the size of the nanocrystals produced, these semiconducting structures can be tuned during manufacturing to emit any color of light.7

Quantum dots can be classified into different types based on their composition and structure.

Quantum Confinement Effect

Figure 1.Splitting of energy levels in quantum dots due to the quantum confinement effect, semiconductor band gap increases with decrease in size of the nanocrystal.


Core-Type Quantum Dots

These nano dots can be single component materials with uniform internal compositions, such as chalcogenides (selenides, sulfides or tellurides) of metals like cadmium, lead or zinc, example, CdTe (Product No. 777951) or PbS (Product No. 747017). The photo- and electroluminescence properties of core-type nanocrystals can be fine-tuned by simply changing the crystallite size.

Core-Shell Quantum Dots

The luminescent properties of quantum dots arise from recombination of electron-hole pairs (exciton decay) through radiative pathways. However, the exciton decay can also occur through nonradiative methods, reducing the fluorescence quantum yield. One of the methods used to improve efficiency and brightness of semiconductor nanocrystals is growing shells of another higher band gap semiconducting material around them. These particles with small regions of one material embedded in another with a wider band gap are known as core-shell quantum dots (CSQDs) or core-shell semiconducting nanocrystals (CSSNCs). For example, quantum dots with CdSe in the core and ZnS in the shell (Product Nos. 748056, 790192) available from Sigma-Aldrich Materials Science exhibit greater than 50% quantum yield. Coating quantum dots with shells improves quantum yield by passivizing nonradiative recombination sites and also makes them more robust to processing conditions for various applications. This method has been widely explored as a way to adjust the photophysical properties of quantum dots.8-10

Alloyed Quantum Dots

The ability to tune optical and electronic properties by changing the crystallite size has become a hallmark of quantum dots. However, tuning the properties by changing the crystallite size could cause problems in many applications with size restrictions. Multicomponent dots offer an alternative method to tune properties without changing crystallite size. Alloyed semiconductor nanodots with both homogeneous and gradient internal structures allow tuning of the optical and electronic properties by merely changing the composition and internal structure without changing the crystallite size. For example, alloyed quantum dots of the compositions CdSxSe1-x/ZnS of 6nm diameter emits light of different wavelengths by just changing the composition (Product Nos. 753742, 753793) (Figure 2). Alloyed semiconductor quantum dots formed by alloying together two semiconductors with different band gap energies exhibited interesting properties distinct not only from the properties of their bulk counterparts but also from those of their parent semiconductors. Thus, alloyed nanocrystals possess novel and additional composition-tunable properties aside from the properties that emerge due to quantum confinement effects.11

Photoluminescence of alloyed CdSxSe1-x/ZnS quantum dots of 6 nm diameter

Figure 2.Photoluminescence of alloyed CdSxSe1-x/ZnS quantum dots of 6 nm diameter. The material emits different color of light by tuning the composition.

Quantum Dots Applications

The unique size and composition tunable electronic property of these very small, semiconducting quantum dots make them very appealing for a variety of applications and new technologies.12

Quantum dots are particularly significant for optical applications owing to their bright, pure colors along with their ability to emit rainbow of colors coupled with their high efficiencies, longer lifetimes and high extinction coefficient. Examples include LEDs and solid state lighting, displays and photovoltaics.7,13,14

Being zero dimensional, quantum dots have a sharper density of states than higher-dimensional structures. Their small size also means that electrons do not have to travel as far as with larger particles, thus electronic devices can operate faster. Examples of applications taking advantage of these unique electronic properties include transistors, solar cells, ultrafast all-optical switches and logic gates, and quantum computing, among many others.13-15

The small size of dots allow them to go anywhere in the body making them suitable for different bio-medical applications like medical imaging, biosensors, etc. At present, fluorescence based biosensors depend on organic dyes with a broad spectral width, which limits their effectiveness to a small number of colors and shorter lifetimes to tag the agents. On the other hand, quantum dots can emit the whole spectrum, are brighter and have little degradation over time thus proving them superior to traditional organic dyes used in biomedical applications.16

Materials
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References:

1.
Sreenivasan M. 1981. Cytology of a Spontaneous TriploidCoffea CanephoraPierre ex Froehner. Caryologia. 34(3):345-349. https://doi.org/10.1080/00087114.1981.10796901
2.
Kastner MA. 1993. Artificial Atoms. Physics Today. 46(1):24-31. https://doi.org/10.1063/1.881393
3.
Ashoori RC. 1996. Electrons in artificial atoms. Nature. 379(6564):413-419. https://doi.org/10.1038/379413a0
4.
Collier CP, Vossmeyer T, Heath JR. 1998. NANOCRYSTAL SUPERLATTICES. Annu. Rev. Phys. Chem.. 49(1):371-404. https://doi.org/10.1146/annurev.physchem.49.1.371
5.
Reimann SM, Manninen M. Electronic structure of quantum dots. Rev. Mod. Phys.. 74(4):1283-1342. https://doi.org/10.1103/revmodphys.74.1283
6.
Bawendi MG, Steigerwald ML, Brus LE. 1990. The Quantum Mechanics of Larger Semiconductor Clusters ("Quantum Dots"). Annu. Rev. Phys. Chem.. 41(1):477-496. https://doi.org/10.1146/annurev.pc.41.100190.002401
7.
Yoffe AD. 2001. Semiconductor quantum dots and related systems: Electronic, optical, luminescence and related properties of low dimensional systems. Advances in Physics. 50(1):1-208. https://doi.org/10.1080/00018730010006608
8.
Rao CNR, Müller A, Cheetham AK. 2004. The Chemistry of Nanomaterials. https://doi.org/10.1002/352760247x
9.
Dorfs D, Eychmüller A. 2006. Multishell Semiconductor Nanocrystals. Zeitschrift für Physikalische Chemie. 220(12):1539-1552. https://doi.org/10.1524/zpch.2006.220.12.1539
10.
Smith AM, Nie S. 2009. Next-generation quantum dots. Nat Biotechnol. 27(8):732-733. https://doi.org/10.1038/nbt0809-732
11.
Vastola G, Zhang Y, Shenoy VB. 2012. Experiments and modeling of alloying in self-assembled quantum dots. Current Opinion in Solid State and Materials Science. 16(2):64-70. https://doi.org/10.1016/j.cossms.2011.10.004
12.
Vahala KJ. 2003. Optical microcavities. Nature. 424(6950):839-846. https://doi.org/10.1038/nature01939
13.
Nirmal M, Brus L. 1999. Luminescence Photophysics in Semiconductor Nanocrystals. Acc. Chem. Res.. 32(5):407-414. https://doi.org/10.1021/ar9700320
14.
Sargent EH. 2012. Colloidal quantum dot solar cells. Nature Photon. 6(3):133-135. https://doi.org/10.1038/nphoton.2012.33
15.
Zhao Y, Burda C. Development of plasmonic semiconductor nanomaterials with copper chalcogenides for a future with sustainable energy materials. Energy Environ. Sci.. 5(2):5564-5576. https://doi.org/10.1039/c1ee02734d
16.
Medintz IL, Uyeda HT, Goldman ER, Mattoussi H. 2005. Quantum dot bioconjugates for imaging, labelling and sensing. Nature Mater. 4(6):435-446. https://doi.org/10.1038/nmat1390
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