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Chad E Talley

Publications and source records attributed to Chad E Talley.

7 recordsLinked to original sources
PubMed2006

Synthesis, characterization, and tunable optical properties of hollow gold nanospheres.

Nearly monodisperse hollow gold nanospheres (HGNs) with tunable interior and exterior diameters have been synthesized by sacrificial galvanic replacement of cobalt nanoparticles. It is possible to tune the peak of the surface plasmon band absorption between 550 and 820 nm by carefully controlling particle size and wall thickness. Cobalt particle size is tunable by simultaneously changing the concentration of sodium borohydride and sodium citrate, the reducing and capping agent, respectively. The thickness of the gold shell can be varied by carefully controlling the addition of gold salt. With successful demonstration of ensemble as well as single HGN surface-enhanced Raman scattering, these HGNs have shown great potential for chemical and biological sensing applications, especially those requiring nanostructures with near-IR absorption.

Journal Article↗
PubMed2006

Improving nanoprobes using surface-enhanced Raman scattering from 30-nm hollow gold particles.

We report the development of nanoprobes that exploit the surface-enhanced Raman scattering (SERS) from nonaggregated, hollow, gold nanospheres (HGNSs). The homogeneity of the HGNSs leads to a nearly 10-fold improvement in signal consistency over standard silver SERS substrates, which translates into a significant increase in sensitivity and dynamic range for the model application of pH sensing. Moreover, the small size (30-nm diameter) of these SERS-active nanoparticles represents a major step in advancing sensing technology based on SERS, making this technology more amenable to intracellular sensing.

DNA Probes↗
PubMed2006

Bio-assay based on single molecule fluorescence detection in microfluidic channels.

A rapid bioassay is described based on the detection of colocalized fluorescent DNA probes bound to DNA targets in a pressure-driven solution flowing through a planar microfluidic channel. By employing total internal reflection excitation of the fluorescent probes and illumination of almost the entire flow channel, single fluorescent molecules can be efficiently detected leading to the rapid analysis of nearly the entire solution flowed through the device. Cross-correlation between images obtained from two spectrally distinct probes is used to determine the target concentration and efficiently reduces the number of false positives. The rapid analysis of DNA targets in the low pM range in less than a minute is demonstrated.

DNA↗
PubMed2005

Surface-enhanced Raman scattering from individual au nanoparticles and nanoparticle dimer substrates.

Surface-enhanced Raman scattering (SERS) intensities for individual Au nanospheres, nanoshells, and nanosphere and nanoshell dimers coated with nonresonant molecules are measured, where the precise nanoscale geometry of each monomer and dimer is identified through in situ atomic force microscopy. The observed intensities correlate with the integrated quartic local electromagnetic field calculated for each specific nanostructure geometry. In this study, we find that suitably fabricated nanoshells can provide SERS enhancements comparable to nanosphere dimers.

Dimerization↗
PubMed2004

Intracellular pH sensors based on surface-enhanced raman scattering.

We present the development of nanoscale pH sensors based on functionalized silver nanoparticles and surface-enhanced Raman scattering (SERS). The SERS spectrum from individual silver nanoparticle (50-80 nm in diameter) clusters functionalized with 4-mercaptobenzoic acid shows a characteristic response to the pH of the surrounding solution and is sensitive to pH changes in the range of 6-8. Measurements from nanoparticles incorporated in living Chinese hamster ovary cells demonstrate that the nanoparticle sensors retain their robust signal and sensitivity to pH when incorporated into a cell.

Animals↗
PubMed2004

Experimental and computational studies of the metal-metal stretching vibration in X(3)MMX(3) compounds (X = alkoxide, alkyl, amide).

Raman spectra of a number of triply bonded M(2)X(6) (M = Mo, W; X = alkoxide, alkyl) compounds have been obtained. Several exhibit a band assignable to the metal-metal stretching vibration nu(M)(M). This band was not identified in earlier studies of the M(2)(NMe(2))(6) compounds. We have attempted to correlate the Raman vibrational data with structural data from single-crystal X-ray diffraction studies. Diffraction studies of the M(2)(O-1-4-pentyl[2.2.2]bicyclooctyl)(6) species show a crowded environment around the dimetal core, but the M-M-O angles differ substantially from 90 degrees. Thus, this angle does not solely determine the extent to which the metal-metal and ligand-based vibrational modes couple and, in turn, our ability to observe nu(M)(M). Computational studies of model systems confirm the assignment of the band as being nu(M)(M), although the predicted vibrational energies are consistently too high by ca. 7%. The computational results suggest that a nu(M)(M) band may be present in the published spectra of the M(2)(NMe(2))(6) pair.

Journal Article↗