Publications by authors named "Robin N Klupp Taylor"

Plasmonic nanoparticles have intriguing optical properties which make them suitable candidates for sensing or theranostic applications. Anisotropic patchy particles, where metal is locally deposited on the surface of a core particle, exhibit plasmon resonances that can be specifically adjusted for these applications. However, many existing synthesis routes are complex, yield too little material, or provide particles with limited optical tunability.

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Anisotropic nanoparticles offer considerable promise for applications but also present significant challenges in terms of their characterization. Recent developments in the electroless deposition of silver patches directly onto colloidal silica particles have opened up a simple and scalable synthesis method for patchy particles with tunable optical properties. Due to the reliance on patch nucleation and growth, however, the resulting coatings are distributed in coverage and thickness and some core particles remain uncoated.

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The natural world is a colorful environment. Stunning displays of coloration have evolved throughout nature to optimize camouflage, warning, and communication. The resulting flamboyant visual effects and remarkable dynamic properties, often caused by an intricate structural design at the nano- and microscale, continue to inspire scientists to unravel the underlying physics and to recreate the observed effects.

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The ability to confine and manipulate light below the diffraction limit is a major goal of future multifunctional optoelectronic/plasmonic systems. Here, we demonstrate the design and realization of a tunable and localized electrical source of excitons coupled to surface plasmons based on a polymer light-emitting field-effect transistor (LEFET). Gold nanorods that are integrated into the channel support localized surface plasmons and serve as nanoantennas for enhanced electroluminescence.

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Nanostructured particles containing noble metals can have highly tunable localized surface plasmon resonances and are therefore of particular interest for numerous applications. Nanoshells comprising a dielectric core and gold or silver shell are a widely researched systems because of the strong dependence of their optical properties on the ratio of core diameter to shell thickness. Although seeded-growth procedures have been developed to produce these particles, the many reported studies show significant variation in the nanoshell morphologies and hence optical properties.

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Patchy particles comprise regions of differing material or chemical functionality on otherwise isotropic cores. To meet the great potential of these anisotropic structures in a wide range of application fields, completely new approaches are sought for the scalable and tunable production of patchy particles, particularly those with nanoscale dimensions. In this paper the synthesis of patchy particles via a simple colloidal route is investigated.

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This work addresses the determination of arbitrarily shaped particle size distributions (PSDs) from PbS and PbSe quantum dot (QD) optical absorbance spectra in order to arrive at a relationship between band gap energy and particle size over a large size range. Using a modified algorithm which was previously developed for ZnO, we take only bulk absorption data from the literature and match the PSDs derived from QD absorbance spectra with those from transmission electron microscopical (TEM) image analysis in order to arrive at the functional dependence of the band gap on particle size. Additional samples sized solely from their absorbance spectra with our algorithm show excellent agreement with TEM results.

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Here we report that silver nanoparticle necklaces can be readily formed by treatment of colloidal silica with ammoniacal silver complex solution followed by washing, deposition and ageing. We investigate the morphology of the produced materials and elucidate the key variables that influence this promising new approach to one-dimensional nanostructuring.

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The formation of spherical superparamagnetic colloidal aggregates of magnetite nanoparticles by emulsification of a ferrofluid and subsequent solvent evaporation has been systematically studied. The colloidal aggregates occur as a dense sphere with magnetite nanoparticles randomly packed and preserved particle-particle separation due to chemisorbed oleic acid. The voids between nanoparticles are filled with solvent and free oleic acid.

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Patchy particles possessing heterogeneous surface composition show great promise as self-organizing building blocks for new classes of hierarchical functional structures. A major hurdle is the scalable synthesis of stable patches on nanosized core particles with arbitrarily defined patch number and coverage. So far, few methods have been reported which could be expected to meet these challenges.

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The visual appearance of the artificial world is largely governed by films or composites containing particles with at least one dimension smaller than a micron. Over the past century and a half, the optical properties of such materials have been scrutinized and a broad range of colorant products, based mostly on empirical microstructural improvements, developed. With the advent of advanced synthetic approaches capable of tailoring particle shape, size and composition on the nanoscale, the question of what is the optimum particle for a certain optical property can no longer be answered solely by experimentation.

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Polymers and coordinating solvents have been shown to serve as templating agents to assist the precipitation of ZnO nanoparticles and address their morphology. In this work we show for the first time that a difference in the coordination strength between the polymer (poly-N-vinylpyrrolidone (PVP)) and the two Zn(II) precursor salts (nitrate and acetate) is able to promote or suppress the formation of mesocrystalline structures and even more importantly to tune their three-dimensional organization. On the basis of FTIR and (13)C NMR spectroscopic studies, we propose that not only the polymer (PVP) but also the solvent (DMF) play a key role as directing agents.

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Here we demonstrate, for the first time, the heterogeneous nucleation and growth of silver patches on submicrometer silica spheres. While patches can be grown directly onto native silica particles, it is shown that a higher patch yield can be obtained by first treating the silica with a mixture of an alkanolamine and silver nitrate. Variation of the pretreatment and subsequent coating reactions allowed the patch yield, number, size, thickness, and shape to be adjusted.

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