AREAS OF INTEREST:
- Properties of Colloids and Colloid Assemblies
- Nonlinear and Ultrafast Properties of Nanoparticles
RESEARCH:
Sarah came to Rice in 1995 with a B. Sc. Eng. in Engineering
Physics from Queen's University in Kingston, Ontario, Canada. She
received a Master's degree in Applied Physics at Rice in May, 1998.
Her master's thesis focussed on assembling gold nanoparticles using silica
nanoparticles as substrates. Other groups have assembled nanoparticles
on flat, planar substrates. However, by using silica nanoparticles
as substrates, there were hundreds of cm2 of surface area available
in every mL of solution instead of just the one monolayer that is on a
planar substrate. Concentrated solutions of assemblies with long
path lengths were made for optical measurements.
The first type of assembly used molecules to link
gold nanoparticles to each other. Silica nanoparticles of nominally
125 nm diameter were made using the Stober method. The silica nanoparticles
were functionalized with 3-aminopropyltrime thoxysilane,
which resulted in amine-terminated silica nanoparticles. The amine
groups reacted with gold nanoparticles and bound them on the silica nanoparticle
surface, as can be seen in the TEM image in Figure 1(a) (both scale bars
are 50 nm. The optical absorption spectrum of these structures, shown
in Figure 1(b) is dominated by the plasmon resonance absorption of the
gold nanoparticles at 520 nm. Next a bifunctional molecule, 4-aminobenzenethiol,
was added to the solution. One of the functional groups reacted with
the bound gold nanoparticles, leaving the other functional group exposed.
When more gold nanoparticles were added, those gold nanoparticles bound
to the exposed functional groups. Gold nanoparticles linked to each
other can be seen on the silica nanoparticle substrate in Figure 1(c).
The UV/visible absorption spectrum of these nanostructures shows a longer
wavelength component due to interactions between the plasmon resonances
of the linked gold nanoparticles. More details about this work can
be found in a Chemical Physics Letters paper which is scheduled to be published
in February, 1999.
Certain small gold nanoparticles self assemble into
clusters >and attach to functionalized silica nanoparticle surfaces in the correct solvent.
The small gold nanoparticles were made by reducing gold chloride with tetrakishydroxymethylphosphonium
chloride (Langmuir 1993, 9, 2301). When the aqueous
gold nanoparticle solution was diluted with ethanol, the gold nanoparticles
associated more closely. When functionalized silica nanoparticles
were added to this mixture, gold nanoparticle clusters attached to the
silica nanoparticles, as seen in the TEM image of Figure 2. The most
regular cluster shapes were attached to silica nanoparticles functionalized
with a mixture of a small amount of aminopropyltrimethoxysilane and a larger
amount of propyltrimethoxy silane (which is inert to the gold nanoparticles).
This work has been published in Langmuir (Langmuir 1998,14, 5396).
Recently, Sarah has been studying the ultrafast optical
properties of metal nanoshells. A cavity-dumped Ti:sapphire laser
that provides 60 femtosecond pulses at ~850 nm is used for these measurements.
By directing an intense pump beam on a solution or film of nanoshells,
the electrons in the metal shell are excited. A less intense probe
beam is transmitted through the nanoshells to measure the pump-induced
changes in the transmission. Richard
Averitt began this work by studying transient bleaching and transient
absorption from metal nanoshells. He successfully explained the observed
sign and magnitude of the signals by calculating the change in the dielectric
function of the gold shell. The current studies focus on how the
medium surrounding the nanoshells affects the cooling of the hot electrons
in the gold shell.
Sarah is most easily reached via electronic mail: westcott@rice.edu