Nanoparticles (NPs) with either plasmonic or upconverting properties have been selectively coated onto the surfaces of polystyrene (PS) spheres, imparting their optical properties to the PS colloids. These NP coated PS spheres have many potential applications, such as in medicine as drug-delivery systems or diagnostic tools. To prepare the NP coated PS spheres, gold or core-shell NaYF4Tm0.5Yb30/NaYF4 NPs were synthesized and separately combined with amino-functionalized PS spheres. The mechanism by which the NPs adhered to the PS spheres is attributed to interactions of the NP and a polyvinylpyrrolidone additive with the surfaces of the PS spheres. Two-photon fluorescence microscopy and SERS analysis demonstrate the potential applications of these NP coated PS spheres.

Atomic layer deposition has attracted much attention recently in fabricating noble metal nanoparticles for a wide range of applications. We have explored synthesizing palladium nanoparticles via atomic layer deposition on self-assembled monolayers modified silicon substrate. Using alkyltrichlorosilanes as the passivating agents, our results show the method is capable of fabricating Pd nanoparticles with well controlled density and particle diameter on the modified silicon substrate.

Physical vapor deposition, in combination with gas-aggregation (PVD-GA), is a controllable method for creation of diverse nanoparticle structures. Given the size effects that dominate the physics of nanoparticles, a particular advantage of the PVD-GA technique is the compatibility with in situ mass filtering of the nanocluster beam.

In the current work, PVD-GA has been utilized to deposit Ag and Si nanoparticles. Nanoparticles were analyzed using in situ quadrupole mass spectrometry (charge/mass ratio), atomic force microscopy (nanoparticle height), and transmission electron microscopy (nanocluster diameter & crystallinity). The results for particle size distribution were cross-correlated, with excellent agreement.

Different growth methods & conditions were explored, resulting in controlled differences in the measured particle size distributions and surface coverage. A novel growth configuration utilizing a conventional sputter source in combination with a linear magnetron allowed a significant (fivefold) increase in Ag cluster yield.

Hydrothermal nanoparticle synthesis uses high temperature and pressure water to control the chemical processes that lead to specific compositions and structures. Analyses of the chemistry associated with this process have been mainly restricted to bulk thermodynamics in the form of quantities such as solubilities and empirical models based on experimental observations. In this paper we demonstrate for NiO and NiFe2O4 particles how effective reference chemical potentials derived from first principles calculations can be used to predict cluster shapes, nucleation barriers and surface reactivity. Implications for controlling the nanoparticle size and shape by adjusting pH and temperature will be discussed, as well as implications of these results in forming nanostructured materials by cluster condensation.

The enhancement of the plasmonic signatures, indicated by the shifting of the localized surface plasmon resonances, of three-dimensional, hollow, gold nanocages with respect to substrate nature and cage density is reported. The effect of substrate nature was investigated using absorbance, reflection, and transmission by ultraviolet-visible and near-infrared spectrophotometry. The gold nanocages were deposited on substrates as monolayers primarily by Langmuir-Blodgett technique. The density of the deposited monolayers and the nature of the surface of the substrates were determined using AFM and SEM/TEM imaging. The position of the LSPR signatures, primarily the dipolar plasmonic resonances, with respect to changing environment and nanostructure characteristics determined the tuneability of the plasmonic enhancements.

Alkyl-terminated Si nanocrystals (NCs) are synthesized at room temperature by hydride reduction of SiCl4 within inverse micelles. Highly monodisperse Si NCs (2 – 6 nm) are produced by variation of the cationic quaternary ammonium salts used to form the inverse micelles. Transmission electron microscopy imaging confirms the NCs are highly crystalline, while FTIR spectra confirm that the NCs are passivated by covalent attachment of alkanes, with minimal surface oxidation. The photoluminescence intensity of the Si NCs exhibits an inverse relationship with the mean NC diameter, with a quantum yield of 12 % recorded for 2 nm NCs.

One of the methods to grow nanoscale three-dimensional (3D) Au patterns is to perform local electron-beam-induced deposition (EBID) using the Me2Au(acac) precursor inside the chamber of a scanning electron microscope (SEM). However, due to the organometallic nature of the chemical, the concentration of the metallic constituent in the as-deposited structure is dramatically low, at around 10 at. % of Au. Ex-situ post-annealing of Me2Au(acac) EBIDs is a very promising purification approach, resulting in an Au content of > 92 at. % after annealing at 600 °C. However, in most of the cases it also distorts the geometrical shape of the heat-treated structure, preserving of which is essential for the application. In this paper we present a systematic study of the dependence between the annealing parameters and resulting purity in combination with the shape of the Au structure. Optimized heat treatment conditions for the creation of well-purified high aspect ratio Au pillar array are presented; and for planar continuous structures, the importance of the parameter height to area ratio is identified.

Nanoparticle functionalization and assembly is undergoing a period of challenging yet exciting development. Much of this research effort has been focused on the development of new functionalities that might enable strategically-directed assembly of nanoparticles into structures that can be utilized in other important applications.

In order to determine the success of such experiments, researchers often prepare a dried sample and study the assembly patterns with electron microscopy. However, these imaging techniques can be expensive and do not provide a complete illustration of what the three dimensional nanoparticle assemblies truly look like in solution. Moreover, sample preparation presents its own challenges. Most notably, sample preparation may cause alteration to the individual assemblies or unwanted aggregation of the assemblies upon removal of the solution.

To address these concerns, assemblies of anisotropic nanoparticles were tracked free-floating in solution with differential interference contrast (DIC) microscopy. DIC microscopy is an optical technique based on interferometry with high lateral resolution and shallow depth of field. After functionalizing gold and silver nanoparticles for self-assembly, aliquots of the nanoparticle solutions were examined in real-time. Nanoparticle assemblies were observed undergoing rotations, internal vibrations, structural modifications, and interactions with other assemblies. Observations of the dynamic behaviors of nanoparticle assemblies serve as a complement to imaging with electron microscopy and provide new insights into the actual assembly process.

In nonaqueous emulsion, moisture-sensitive polymerizations are performed in order to generate nanoparticles, which are not accessible by common aqueous emulsion polymerization. A nonaqueous emulsion, consisting of two immiscible aprotic organic solvents, is stabilized by amphiphilic block copolymers, such as PIb-PEO or PIb-PMMA copolymer, and lead to formation of nanosized dispersed droplets. They act as dispersed “nanoreactors” for the one-step synthesis of poly(urethane) nanoparticles in a polyadditon reaction as well as poly(L-lactide) nanoparticles through ring-opening polymerization, catalyzed by a moisture-sensitive catalyst. The well-dispersed particles possess average diameters below 100 nm and have narrow size distributions owing to the long-term stability of the dispersed droplets in the continuous phase.

We report a transformative, all inorganic method-based synthesis of supported bimetallic alloy nanoparticles. We use Pd3Ag as a proof of concept. The method involves breaking down bulk Pd3Ag alloy into the nanoparticles in liquid lithium, converting metallic Li to LiOH, transferring Pd3Ag nanoparticles/LiOH mixture onto non-water soluble supports, followed by leaching off the LiOH with water under ambient conditions. The size of the resulting Pd3Ag nanoparticles was found narrowly distributed around 2.3 nm characterized by transmission electron microscope (TEM). In addition, studies by X-ray diffraction (XRD) showed that the resulting Pd3Ag nanoparticles inherited similar structure as the starting bulk Pd3Ag.

Semiconductor nanocrystals or quantum dots are becoming increasingly popular in research fields as wide ranging as cancer therapies, solar energy and disease detection. Colloidal synthesis provides a low-cost method of producing high quality quantum dots with narrow size distributions. The controllable nature of colloidal synthesis allows researchers to design the size, shape and surface functionalization of the resulting particles.

Here we investigate a simple low temperature method to produce CdSe quantum dots. The quantum dots were grown in solution by dissolving the CdO precursor in a mixture of macadamia oil, and oleic acid. Elemental Se was heated separately before the two mixtures were combined under an inert atmosphere. The injection temperature, reaction temperature and oleic acid concentration were all varied.

Optical absorption and photoluminescence spectroscopies showed the size of the quantum dots increased with time, temperature and oleic acid concentration. Dynamic light scattering has shown the hydrodynamic particle size to range from 7 to 22nm and the samples for up to 6 months.