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This article is about crystalline nanoparticles. For other nanocrystalline materials, see Nanocrystalline.

A nanocrystal is a material particle having at least one dimension smaller than 100 nanometres[1] (a nanoparticle) and composed of atoms in either a single- or poly-crystalline arrangement.[2]

The size of nanocrystals distinguishes them from larger crystals. For example, silicon nanocrystals can provide efficient light emission while bulk silicon does not[3] and may be used for memory components.[4]

When embedded in solids, nanocrystals may exhibit much more complex melting behaviour than conventional solids[5] and may form the basis of a special class of solids.[6] They can behave as single-domain systems (a volume within the system having the same atomic or molecular arrangement throughout) that can help explain the behaviour of macroscopic samples of a similar material without the complicating presence of grain boundaries and other defects.[citation needed]

Semiconductor nanocrystals having dimensions smaller than 10 nm are also described as quantum dots.


The traditional method to prepare nanocrystals of a new material requires choosing molecular precursors, surfactants, and solvents using optimized reaction conditions causing the atoms to self-assemble into monodisperse nanocrystals.[7]

A newer, simpler strategy uses preformed nanocrystals as templates and chemical transformation to change the composition.[7]

Solution-based mechanisms can chemically transform nanomaterials, allowing atoms to be easily and precisely incorporated, removed, or replaced from preformed templates. The approach uses oxidation, reduction, alloying, or atomic exchange reactions. In ionic nanocrystals, cation exchange can be driven by solvation energy differences between template and solvated ions. Ion solubilities can be controlled by adding selective coordinating species to the solution. In metal nanocrystals, atomic exchange reactions reflect reduction potential differences between the template metal and solvated metal ions. This galvanic replacement method involves a redox reaction. Placing a nanocrystal in a solution containing metal ions with a higher reduction potential oxidizes the templates' surface, dissolving its metal ions. The released electrons reduce the ions from the solution, which deposit at the template's surface.[7]

Galvanic replacement also applies to ionic compounds. In oxide nanocrystals, a redox-couple reaction can occur between multivalent metallic ions. E.g., higher–oxidation state ions in manganese oxide nanocrystals have been replaced with solvated lower–oxidation state iron ions.[7]

Atomic diffusion is a key parameter in such reactions. Chemical transformation tools provide complete composition control only within the atomic diffusion length. High nanocrystal surface-to-volume ratios expose the entire lattice to diffusion. The effective particle size range for these tools depends on the material, but can reach hundreds of nanometers.[7]


Nanocrystals made with zeolite are used to filter crude oil onto diesel fuel at an ExxonMobil oil refinery in Louisiana at a cost less than conventional methods.[8]

See also[edit]


  1. ^ B. D. Fahlman (2007). Material Chemistry. 1. Springer: Mount Pleasant, Michigan. pp. 282–283. 
  2. ^ J. L. Burt (2005). "Beyond Archimedean solids: Star polyhedral gold nanocrystals". J. Cryst. Growth. 285: 681. doi:10.1016/j.jcrysgro.2005.09.060. 
  3. ^ L. Pavesi (2000). "Optical gain in silicon nanocrystals". Nature. 408: 440. doi:10.1038/35044012. 
  4. ^ S. Tiwari (1996). "A silicon nanocrystal based memory". Appl. Phys. Lett. 68: 1377. doi:10.1063/1.116085. 
  5. ^ J. Pakarinen (2009). "Partial melting mechanisms of embedded nanocrystals". Phys. Rev. B. 79: 085426. doi:10.1103/physrevb.79.085426. 
  6. ^ D. V. Talapin (2012). "Nanocrystal solids: A modular approach to materials design". MRS Bulletin. 37: 63. doi:10.1557/mrs.2011.337. 
  7. ^ a b c d e Ibanez, M.; Cabot, A. (2013). "All Change for Nanocrystals". Science. 340 (6135): 935–936. doi:10.1126/science.1239221. PMID 23704562. 
  8. ^ P. Dutta and S. Gupta (eds.) (2006). Understanding of Nano Science and Technology (1 ed.). Global Vision Publishing House. p. 72. ISBN 81-8220-188-8. 

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