Porous silver-coated pNIPAM--AAc hydrogel nanocapsules.

This paper describes the preparation and characterization of a new type of core-shell nanoparticle in which the structure consists of a hydrogel core encapsulated within a porous silver shell. The thermo-responsive hydrogel cores were prepared by surfactant-free emulsion polymerization of a selected mixture of -isopropylacrylamide (NIPAM) and acrylic acid (AAc). The hydrogel cores were then encased within either a porous or complete silver shell for which the localized surface plasmon resonance (LSPR) extends from visible to near-infrared (NIR) wavelengths (i.

Ultrasmall hollow gold-silver nanoshells with extinctions strongly red-shifted to the near-infrared.

Hollow gold-silver nanoshells having systematically varying sizes between 40 and 100 nm were prepared. These particles consist of a hollow spherical silver shell surrounded by a thin gold layer. By varying the volume of the gold stock solution added to suspensions of small silver-core templates, we tailored the hollow gold-silver nanoshells to possess strong tunable optical extinctions that range from the visible to the near-IR spectral regions, with extinctions routinely centered at ∼950 nm.

Gold, palladium, and gold-palladium alloy nanoshells on silica nanoparticle cores.

The synthesis of gold, palladium, and gold-palladium alloy nanoshells (approximately 15-20 nm thickness) was accomplished by the reduction of gold and palladium ions onto dielectric silica core particles (approximately 100 nm in diameter) seeded with small gold nanoparticles (approximately 2-3 nm in diameter). The size, morphology, elemental composition, and optical properties of the nanoshells were characterized using field-emission scanning electron microscopy, transmission electron microscopy, energy-dispersive X-ray spectroscopy, X-ray diffraction, and ultraviolet-visible spectroscopy. The results demonstrate the successful growth of gold, palladium, and gold-palladium alloy nanoshells, where the optical properties systematically vary with the relative content of gold and palladium.

Visualizing the lower critical solution temperature phase transition of individual poly(nipam)-based hydrogel particles using near-infrared multispectral imaging microscopy.

This manuscript reports the use of near-infrared multispectral imaging (NIR-MSI) microscopy to provide the first direct observation and spectral measurement of individual poly(n-isopropylacrylamide-co-acrylic acid) (NIPAM-co-AAc) hydrogel particles. The high sensitivity and high spatial resolution (approximately 0.9 microm/pixel) of the NIR-MSI microscope, coupled with its ability to measure images and spectra directly and simultaneously, allows the unprecedented in situ monitoring of the size, morphology, and spectroscopic properties of individual hydrogel particles, which respond strongly to external stimuli (e.

Visualizing the size, shape, morphology, and localized surface plasmon resonance of individual gold nanoshells by near-infrared multispectral imaging microscopy.

We have successfully utilized the newly developed near-infrared multispectral imaging (NIR-MSI) microscope to observe and measure directly the localized surface plasmon absorption (LSPR) of individual gold nanoshells. The NIR-MSI is suited for this task because it can simultaneously record spectral and spatial information of a sample with high sensitivity (single pixel resolution) and high spatial resolution (approximately 0.9 microm/pixel).

Preparation, characterization, and optical properties of gold, silver, and gold-silver alloy nanoshells having silica cores.

This report describes the structural and optical properties of a series of spherical shell/core nanoparticles in which the shell is comprised of a thin layer of gold, silver, or gold-silver alloy, and the core is comprised of a monodispersed silica nanoparticle. The silica core particles were prepared using the Stöber method, functionalized with terminal amine groups, and then seeded with small gold nanoparticles (approximately 2 nm in diameter). The gold-seeded silica particles were coated with a layer of gold, silver, or gold-silver alloy via solution-phase reduction of an appropriate metal ion or mixture of metal ions.