6 research outputs found
Controlled Growth of Gold Nanoparticles Preorganized in LangmuirâBlodgett Monolayers
A method
is described for the in situ growth of substrate-supported
organized gold nanoparticles. Upon exposure to an aqueous solution
of a gold salt and a mild reducing agent, the particle size can be
significantly increased without any loss of superstructure organization.
Furthermore, no secondary nucleation is observed. The surface-supported
regrowth procedure can be combined with the LangmuirâBlodgett
technique to produce a rich library of plasmonic nanoparticle assemblies.
Controlled particle regrowth plays a crucial role in this assembly
method because only relatively small metallic nanoparticles can be
directly dispersed in polymeric LangmuirâBlodgett films. The
versatility of the method is demonstrated through the fabrication
of several specific nanoparticle structures, including contiguous
plasmonic rings, coreâsatellite structures, and necklace assemblies.
Plasmon extinction spectra are presented for the various nanoparticle
superstructures and illustrate the importance of controlling both
particle size and assembly architecture in achieving targeted optical
properties. The reported approach constitutes a viable bottom-up assembly
route for the fabrication of surface-supported nanoparticle superstructures
for plasmonic applications
Nanoparticle Size Control in Microemulsion Synthesis
Quasi-monodisperse
populations of (H<sub>3</sub>O)ÂY<sub>3</sub>F<sub>10</sub>·<i>x</i>H<sub>2</sub>O nanocrystals
of varying size are prepared in Igepal-stabilized microemulsions.
Correlations between microemulsion composition, micelle hydrodynamic
radius, and final nanoparticle size are established and shed light
on the mechanism of particle size control. Under the conditions considered
here, size control appears to be primarily governed by the number
of micelles and the quantities of precursor ions. More specifically,
the number of NPs formed can be successfully correlated with the number
of micelles present and final NP size is, in turn, determined by the
number of nuclei and the total amount of material available for nanocrystal
formation. This insight into nanoparticle formation facilitates the
selection of appropriate synthetic conditions for the preparation
of populations of a targeted size
Controlled 2D Organization of Gold Nanoparticles in Block Copolymer Monolayers
The organization of organic-capped
gold nanoparticles in PS-<i>b</i>-PMMA monolayers is investigated.
The preferred location
of the particles within the block copolymer template is found to depend
on both nanoparticle size and the length of the aliphatic capping
agent. In the case of relatively short ligands, the particles behave
as hard spheres and their incorporation in the polymer matrix can
be qualitatively rationalized by entropic considerations. Three distinct
arrangements are observed. Particles that are small, relative to the
radius of gyration of the host polymer, evenly disperse within the
PS domains, whereas the largest particles are considered form ordered,
island-like aggregates. Particles of intermediate size exhibit the
most striking arrangement, being relegated to the PS-PMMA interface
to form organized ring structures. The tendency of these particles
to assemble at the interface is sufficiently strong to force a modification
of the polymer morphology to accommodate the particles at higher loadings.
As the number of particles is increased, the circular PS-<i>b</i>-PMMA surface micelles elongate to form nanostrands
Size-Dependent Extinction Coefficients and Transition Energies of Near-Infrared ÎČâAg<sub>2</sub>Se Colloidal Quantum Dots
Our investigations of silver selenide
colloidal quantum dots, emitting
in the biologically important near-infrared region, demonstrate the
size-dependence of their optical properties. Ag<sub>2</sub>Se nanocrystals
were prepared in the orthorhombic phase with their average radius
varying from 0.95 to 4.7 nm as observed by transmission electron microscopy.
The high purity of the samples, established by energy-dispersive X-ray
spectroscopy and X-ray diffraction, allowed for the accurate determination
of the Ag<sub>2</sub>Se content of colloidal suspensions by a thermogravimetric
method. The energy of the first observed transition is found to decrease
asymptotically with colloidal quantum dot size, tending toward a value
of 1.1 eV, a value significantly above the ÎČ-Ag<sub>2</sub>Se
bulk bandgap. Furthermore, the molar extinction coefficient of this
absorption is proportional to <i>r</i><sub>0</sub><sup>2.7±0.2</sup>, where <i>r</i><sub>0</sub> is the cQD radius. At higher
energies, the extinction coefficient eventually follows the classically
predicted cubic power law with <i>r</i><sub>0</sub>
Size-Modulation of Plasmonic Nanorings Obtained by the Self-Assembly of Gold Nanoparticles and Block Copolymers
Metal nanoparticles exhibit interesting
optical properties due
to the collective excitation of conduction electrons called the plasmon.
Within appropriate metal nanostructures, cooperative plasmon modes
appear and the resonance plasmon frequency is modified. This article
reports a simple method for the formation of such structures, in the
form of self-assembled nanorings. Rings of alkanethiol-capped gold
nanoparticles are obtained by the LangmuirâBlodgett technique
and a block copolymer (PS-<i>b</i>-P2VP) template. With
this approach, organized nanoparticle arrangements covering a large
surface area are obtained. Furthermore, geometric parameters such
as ring diameter, ring-to-ring separation, and ring width can be systematically
varied by the addition of homopolymer or in situ nanoparticle regrowth.
Optical extinction spectra recorded for the nanoparticle rings depend
both on ring diameter and particle size. In particular, after in situ
particle regrowth, the plasmon extinction spectrum exhibits a red-shift
that increases with ring diameter. Theoretical spectra generated with
the discrete dipole approximation indicate that this spectral shift
can be attributed to plasmon coupling that extends over an increasing
number of particles as the ring is enlarged
Comprehensive Solid-State Characterization of Rare Earth Fluoride Nanoparticles
The combination of multinuclear solid-state
NMR spectroscopy and
powder X-ray diffraction has been applied to characterize the octahedron-shaped
crystalline nanoparticle products resulting from an inverse micelle
synthesis. Rietveld refinements of the powder X-ray diffraction data
from the nanoparticles revealed their general formula to be (H<sub>3</sub>O)ÂY<sub>3</sub>F<sub>10</sub>·<i>x</i>H<sub>2</sub>O. <sup>1</sup>H magic-angle spinning (MAS) NMR experiments
provided information on sample purity and served as an excellent probe
of the zeolithic incorporation of atmospheric water. <sup>19</sup>F MAS NMR experiments on a series of monodisperse nanoparticle samples
of various sizes yielded spectra featuring three unique <sup>19</sup>F resonances arising from three different fluorine sites within the
(H<sub>3</sub>O)ÂY<sub>3</sub>F<sub>10</sub>·<i>x</i>H<sub>2</sub>O crystal structure. Partial removal of zeolithic water
from the internal cavities and tunnels of the nanoparticles led to
changes in the integrated peak intensities in the <sup>19</sup>F MAS
NMR spectra; the origin of this behavior is discussed in terms of <sup>19</sup>F longitudinal relaxation. <sup>19</sup>Fâ<sup>89</sup>Y variable-amplitude cross-polarization (VACP) NMR experiments on
both stationary samples and samples under MAS conditions indicated
that two distinct yttrium environments are present, and on the basis
of the relative peak intensities, the population of one of the two
sites is closely linked to the nanoparticle size. Both <sup>19</sup>F MAS and <sup>19</sup>Fâ<sup>89</sup>Y VACP/MAS experiments
indicated small amounts of an impurity present in certain nanoparticles;
these are postulated to be spherical amorphous YF<sub>3</sub> nanoparticles.
We discuss the importance of probing molecular-level structure in
addition to microscopic structure and how the combination of these
characterization methods is crucial for understanding nanoparticle
design, synthesis, and application