|
Chemical
Synthesis
The synthesis
of nearly monodisperse collections of well-passivated nanoparticles
is essential in order to study the intrinsic effects of particle
size and composition on the magnetic and optical properties of these
materials. . We currently synthesize a variety of inorganic compounds
using solution-phase chemical techniques: Bi, Bi1-xSbx,
PbSe, Bi2S3, Co, CoPt and Mn-doped Pb chalcogenides.
For our semiconductor and semimetal nanoparticle materials, we use
a high-temperature coprecipitation from organometallic precursors.
This class of synthesis techniques results in highly-crystalline
nanoparticles, passivated with a monolayer of organic molecules.
The passivation is required not only to terminate the chemical bonds
on the particle's surface, but to also allow the particles to be
dissolved and manipulated in solution and precipitated by evaporation
of the solvent. The passivation prevents agglomeration and oxidation
of the particles. Coupled with a post-synthesis size selection procedure,
particles with size variation of less than 5% can be isolated in
solution. A variety of different capping ligands can be employed
including phosphines, amines and carboxylate acids, and these surface
ligands can be changed in post-synthesis procedures. In addition,
these particle colloids can be dried and redissolved in various
organic solvents, deposited to from close-packed ordered arrays
of nanoparticles or incorporated into a polymer matrices.
An alternative
chemical synthesis method we sometimes use is the reverse micelle
technique. Briefly, reverse micelles are nanometer-sized droplets
of water encased by a surfactant and suspended in oil. The reverse
micelles can be used to synthesize size-controlled inorganic crystallites
by carrying out aqueous chemical reactions (coprecipitation or reduction)
in the water droplets. The reverse micelles restrict the growth
of the particle and prevent aggregation.
References
C. B. Murray, C. R. Kagan, and M. G. Bawendi, "Synthesis and
characterization of monodisperse nanocrystals and close-packed nanocrystal
assemblies," Annu. Rev. Mater. Sci., vol. 30, pp. 545-610,
2000.
L. Brus, "Chemical approaches to semiconductor nanocrystals,"
J. Phys. Chem. Solids, vol. 59, pp. 459-465, 1998.
M. P. Pileni, "Reverse micelles as microreactors," J.
Phys. Chem., vol. 97, pp. 6961, 1993.
|