World Library  
Flag as Inappropriate
Email this Article

Cadmium selenide

Article Id: WHEBN0002115745
Reproduction Date:

Title: Cadmium selenide  
Author: World Heritage Encyclopedia
Language: English
Subject: Cadmium telluride, Cadmium sulfide, Mercury selenide, Cadmium oxide, Cadmium
Publisher: World Heritage Encyclopedia

Cadmium selenide

Cadmium selenide
Unit cell, ball and stick model of cadmium selenide
Sample of nanocrystalline cadmium selenide in a vial
CAS number  YesY
ChemSpider  YesY
EC number
UN number 2570
RTECS number EV2300000
Gmelin Reference 13656
Jmol-3D images Image 1
Molecular formula CdSe
Molar mass 191.37 g mol−1
Appearance Black, translucent, adamantine crystals
Odor Odorless
Density 5.816 g cm-3
Melting point 1,268 °C; 2,314 °F; 1,541 K
Band gap 1.74 eV
Refractive index (nD) 2.5
Crystal structure Wurtzite
Space group C6v4-P63mc
GHS pictograms The skull-and-crossbones pictogram in the Globally Harmonized System of Classification and Labelling of Chemicals (GHS) The health hazard pictogram in the Globally Harmonized System of Classification and Labelling of Chemicals (GHS) The environment pictogram in the Globally Harmonized System of Classification and Labelling of Chemicals (GHS)
GHS signal word DANGER
GHS hazard statements H301, H312, H331, H373, H410
GHS precautionary statements P261, P273, P280, P301+310, P311, P501
EU Index 048-001-00-5
EU classification Toxic T Dangerous for the Environment (Nature) N
R-phrases R50/53
S-phrases (S2), S36/37, S45, S60, S61
Related compounds
Other anions Cadmium oxide,
Cadmium sulfide,
Cadmium telluride
Other cations Zinc selenide,
Mercury(II) selenide
Except where noted otherwise, data are given for materials in their standard state (at 25 °C (77 °F), 100 kPa)
 YesY   YesY/N?)

Cadmium selenide is an CdSe. It is a black to redish black solid that is classified as a II-VI semiconductor of the n-type. Much of the current research on cadmium selenide is focused on its nanoparticles.


Three crystalline forms of CdSe are known: wurtzite (hexagonal), sphalerite (cubic) and rock-salt (cubic). The sphalerite CdSe structure is unstable and converts to the wurtzite form upon moderate heating. The transition starts at about 130 °C, and at 700 °C it completes within a day. The rock-salt structure is only observed under high pressure.[3]


The production of cadmium selenide has been carried out in two different ways. The preparation of bulk crystalline CdSe is done by the High-Pressure Vertical Bridgman method or High-Pressure Vertical Zone Melting.[4]

Cadmium selenide may also be produced in the form of nanoparticles. (see applications for explanation) Several methods for the production of CdSe nanoparticles have been developed: arrested precipitation in solution, synthesis in structured media, high temperature pyrolysis, sonochemical, and radiolytic methods are just a few.[5][6]

Atomic resolution image of a CdSe nanoparticle.[6]

Production of cadmium selenide by arrested precipitation in solution is performed by introducing alkylcadmium and trioctylphosphine selenide (TOPSe) precursors into a heated solvent under controlled conditions.[7]

Me2Cd + TOPSe → CdSe + (byproducts)

CdSe nanoparticles can be modified by production of two phase materials with ZnS coatings. The surfaces can be further modified, e.g. with mercaptoacetic acid, to confer solubility. [8]

Synthesis in structured environments refers to the production of cadmium selenide in liquid crystal or surfactant solutions. The addition of surfactants to solutions often results in a phase change in the solution leading to a liquid crystallinity. A liquid crystal is similar to a solid crystal in that the solution has long range translational order. Examples of this ordering are layered alternating sheets of solution and surfactant, micelles, or even a hexagonal arrangement of rods.

High temperature pyrolysis synthesis is usually carried out using an aerosol containing a mixture of volatile cadmium and selenium precursors. The precursor aerosol is then carried through a furnace with an inert gas, such as hydrogen, nitrogen, or argon. In the furnace the precursors react to form CdSe as well as several by-products.[5]

CdSe nanoparticles

A photograph and representative spectrum of photoluminescence from colloidal CdSe quantum dots excited by UV light.

CdSe-derived nanoparticles with sizes below 100 nm exhibit a property known as quantum confinement. Quantum confinement results when the electrons in a material are confined to a very small volume. Quantum confinement is size dependent, meaning the properties of CdSe nanoparticles are tunable based on their size.[9] One type of CdSe nanoparticle is a CdSe quantum dot. This discretization of energy states results in electronic transitions that vary by quantum dot size. Larger quantum dots have closer electronic states than smaller quantum dots which means that the energy required to excite an electron from HOMO to the LUMO is lower than the same electronic transition in a smaller quantum dot. This quantum confinement effect can be observed as a red shift in absorbance spectra for nanocrystals with larger diameters.

CdSe quantum dots have been implemented in a wide range of applications including solar cells,[10] light emitting diodes,[11] and biofluorescent tagging. CdSe-based materials also have potential uses in biomedical imaging. Human tissue is permeable to far infra-red light. By injecting appropriately prepared CdSe nanoparticles into injured tissue, it may be possible to image the tissue in those injured areas.[12][13]

Surface Chemistry of CdSe Quantum Dots

CdSe quantum dots are semiconductor nanocrystals composed of a CdSe core and a ligand shell. Ligands play important roles in the stability and solubility of the nanoparticles. During synthesis, ligands stabilize growth to prevent aggregation and precipitation of the nanocrystals. These capping ligands also affect the quantum dot’s electronic and optical properties by passivating surface electronic states.[14] An application that depends on the nature of the surface ligands is the synthesis of CdSe thin films.[15][16] The density of the ligands on the surface and the length of the ligand chain affect the separation between nanocrystal cores which in turn influence stacking and conductivity. Understanding the surface structure of CdSe quantum dots in order to investigate the structure’s unique properties and for further functionalization for greater synthetic variety requires a rigorous description of the ligand exchange chemistry on the quantum dot surface.

A prevailing belief is that trioctylphosphine oxide (TOPO) or trioctylphosphine (TOP), a neutral ligand derived from a common precursor used in the synthesis of CdSe dots, caps the surface of CdSe quantum dots. However, results from recent studies challenge this model. Using NMR, quantum dots have been shown to be nonstoichiometric meaning that the cadmium to selenide ratio is not one to one. CdSe dots have excess cadmium cations on the surface that can form bonds with anionic species such as carboxylate chains.[17] The CdSe quantum dot would be charge unbalanced if TOPO or TOP were indeed the only type of ligand bound to the dot.

The CdSe ligand shell may contain both X type ligands which form covalent bonds with the metal and L type ligands that form dative bonds. It has been shown that these ligands can undergo exchange with other ligands. Examples of X type ligands that have been studied in the context of CdSe nanocrystal surface chemistry are sulfides and thiocyanates (ref). Examples of L type ligands that have been studied are amines and phosphines (ref). A ligand exchange reaction in which tributylphosphine ligands were displaced by primary alkylamine ligands on chloride terminated CdSe dots has been reported.[18] Stoichiometry changes were monitored using proton and phosphorus NMR. Photoluminescence properties were also observed to change with ligand moiety. The amine bound dots had significantly higher photoluminescent quantum yields than the phosphine bound dots.


CdSe material is transparent to infra-red (IR) light and has seen limited use in photoresistors and in windows for instruments utilizing IR light. The material is also highly luminescent.[19]

Safety information

Cadmium is a toxic heavy metal and appropriate precautions should be taken when handling it and its compounds. Selenides are toxic in large amounts. Cadmium selenide is a known carcinogen to humans and medical attention should be sought if swallowed or if contact with skin or eyes occurs.[20][21]


  1. ^ "cadmium selenide - PubChem Public Chemical Database". The PubChem Project. USA: Nation Center for Biotechnology Information. Descriptors Computed from Structure. 
  2. ^ a b "cadmium selenide (CHEBI:50834)". Chemical Entities of Biological Interest (ChEBI). UK: European Bioinformatics Institute. IUPAC Names. 
  3. ^ Lev Isaakovich Berger (1996). Semiconductor materials. CRC Press. p. 202.  
  4. ^ II-VI compound crystal growth, HPVB & HPVZM basics
  5. ^ a b Didenko, Yt; Suslick, Ks (Sep 2005). "Chemical aerosol flow synthesis of semiconductor nanoparticles.". Journal of the American Chemical Society 127 (35): 12196–7.  
  6. ^ a b Haitao Zhang, Bo Hu, Liangfeng Sun, Robert Hovden, Frank W. Wise, David A. Muller, and Richard D. Robinson (Sep 2011). "Surfactant Ligand Removal and Rational Fabrication of Inorganically Connected Quantum Dots". Nanoletters.  
  7. ^ Murray, C. B.; Norris, D. J.; Bawendi, M. G. (1993). "Synthesis and characterization of nearly monodisperse CdE (E = sulfur, selenium, tellurium) semiconductor nanocrystallites". Journal of the American Chemical Society 115 (19): 8706.  
  8. ^ Somers, Rebecca C.; Bawendi, Moungi G.; Nocera, Daniel G. (2007). "CdSe nanocrystal based chem-/bio- sensors". Chemical Society Reviews 36: 579–591.  
  9. ^ Nanotechnology Structures - Quantum Confinement
  10. ^ Robel, I.; Subramanian, V.; Kuno, M.; Kamat, P.V. (2006). J. Am. Chem. Soc 128: 2385–2393. 
  11. ^ Colvin, V. L.; Schlamp, M. C.; Alivisatos, A. P. (1994). "Light-emitting diodes made from cadmium selenide nanocrystals and a semiconducting polymer". Nature 370 (6488): 354.  
  12. ^ Chan, W. C.; Nie, S. M. (1998). "Quantum Dot Bioconjugates for Ultrasensitive Nonisotopic Detection". Science 281 (5385): 2016–8.  
  13. ^ Bruchez, M.;Moronne, M.; Gin, P.; Weiss, S.; Alivisatos, A. P. (1998). "Semiconductor nanocrystals as fluorescent biological labels". Science 281 (5385): 2013–6.  
  14. ^ Murray, C. B.; Kagan, C. R.; Bawendi, M. G. (2000). Annu. Rev. Mater. Sci. 30: 545–610. 
  15. ^ Murray, C. B.; Kagan, C. R.; Bawendi, M. G. (1995). Science 270: 1335–1338. 
  16. ^ Islam, M. A.; Xia, Y. Q.; Telesca, D. A.; Steigerwald, M. L.; Herman, I. P. (2004). Chem. Mater 16: 49–54. 
  17. ^ Owen, J. S.; Park, J.; Trudeau, P.E.; Alivisatos, A. P. (2008). J. Am. Chem. Soc 130: 12279–12281. 
  18. ^ Anderson, N. A.; Owen, J. S. (2013). Chem. Mater 25: 69–76. 
  19. ^ Efros, Al. L.; Rosen, M. (2000). "The electronic structure of semiconductor nanocrystals". Annual Review of Materials Science 30: 475–521.  
  20. ^ Additional safety information available at, search 'cadmium selenide' (must register to use).
  21. ^ Additional safety information available at

Related materials

Additional links

This article was sourced from Creative Commons Attribution-ShareAlike License; additional terms may apply. World Heritage Encyclopedia content is assembled from numerous content providers, Open Access Publishing, and in compliance with The Fair Access to Science and Technology Research Act (FASTR), Wikimedia Foundation, Inc., Public Library of Science, The Encyclopedia of Life, Open Book Publishers (OBP), PubMed, U.S. National Library of Medicine, National Center for Biotechnology Information, U.S. National Library of Medicine, National Institutes of Health (NIH), U.S. Department of Health & Human Services, and, which sources content from all federal, state, local, tribal, and territorial government publication portals (.gov, .mil, .edu). Funding for and content contributors is made possible from the U.S. Congress, E-Government Act of 2002.
Crowd sourced content that is contributed to World Heritage Encyclopedia is peer reviewed and edited by our editorial staff to ensure quality scholarly research articles.
By using this site, you agree to the Terms of Use and Privacy Policy. World Heritage Encyclopedia™ is a registered trademark of the World Public Library Association, a non-profit organization.

Copyright © World Library Foundation. All rights reserved. eBooks from Project Gutenberg are sponsored by the World Library Foundation,
a 501c(4) Member's Support Non-Profit Organization, and is NOT affiliated with any governmental agency or department.