Silica-Coated Gold Nanorod Supraparticles: A Tunable Platform for Surface Enhanced Raman Spectroscopy

Plasmonic nanoparticle assemblies are promising functional materials for surface-enhanced Raman spectroscopy (SERS). Gold nanorod (AuNR) assemblies are of particular interest due to the large, shape-induced local field enhancement and the tunable surface plasmon resonance of the AuNRs. Designing the optimal assembly structure for SERS, however, is challenging and requires a delicate balance between the interparticle distance, porosity, and wetting of the assembly. Here, a new type of functional assemblies–called supraparticles–fabricated through the solvent-evaporation driven assembly of silica-coated gold nanorods into spherical ensembles, in which the plasmonic coupling and the mass transport is tuned through the thickness and porosity of the silica shells are introduced. Etching of the AuNRs allowed fine-tuning of the plasmonic response to the laser excitation wavelength. Using a correlative SERS-electron microscopy approach, it is shown that all supraparticles successfully amplified the Raman signal of the crystal violet probe molecules, and that the Raman signal strongly increased when decreasing the silica shell thickness from 35 to 3 nm, provided that the supraparticles have a sufficiently high porosity. The supraparticles introduced in this study present a novel class of materials for sensing, and open up a wide parameter space to optimize their performance

Bridging the Gap: 3D Real-Space Characterization of Colloidal Assemblies via FIB-SEM Tomography

Insight in the structure of nanoparticle assemblies up to a single particle level is key to understand the collective properties of these assemblies, which critically depend on the individual particle positions and orientations. However, the characterization of large, micron sized assemblies containing small, 10-500 nanometer, sized colloids is highly challenging and cannot easily be done with the conventional light, electron or X-ray microscopy techniques. Here, we demonstrate that focused ion beam-scanning electron microscopy (FIB-SEM) tomography in combination with image processing enables quantitative real-space studies of ordered and disordered particle assemblies too large for conventional transmission electron tomography, containing particles too small for confocal microscopy. First, we demonstrate the high resolution structural analysis of spherical nanoparticle assemblies, containing small anisotropic gold nanoparticles. Herein, FIB-SEM tomography allows the characterization of assembly dimensions which are inaccessible to conventional transmission electron microscopy. Next, we show that FIB-SEM tomography is capable of characterizing much larger ordered and disordered assemblies containing silica colloids with a diameter close to the resolution limit of confocal microscopes. We determined both the position and the orientation of each individual (nano)particle in the assemblies by using recently developed particle tracking routines. Such high precision structural information is essential in the understanding and design of the collective properties of new nanoparticle based materials and processes.Comment: 17 pages, 4 figures, Supplemental Information at articles webpage: https://doi.org/10.1039/C8NR09753

In situ single particle characterization of the themoresponsive and co-nonsolvent behavior of PNIPAM microgels and silica@PNIPAM core-shell colloids

Poly(N-isopropylacrylamide) (PNIPAM) microgels and PNIPAM colloidal shells attract continuous strong interest due to their thermoresponsive behavior, as their size and properties can be tuned by temperature. The direct single particle observation and characterization of pure, unlabeled PNIPAM microgels in their native aqueous environment relies on imaging techniques that operate either at interfaces or in cryogenic conditions, thus limiting the observation of their dynamic nature. Liquid Cell (Scanning) Transmission Electron Microscopy (LC-(S) TEM) imaging allows the characterization of materials and dynamic processes such as nanoparticle growth, etching, and diffusion, at nanometric resolution in liquids. Here we show that via a facile post-synthetic in situ polymer labelling step with high-contrast marker core–shell Au@SiO2 nanoparticles (NPs) it is possible to determine the full volume of PNIPAM microgels in water. The labelling allowed for the successful characterization of the thermoresponsive behavior of PNIPAM microgels and core shell silica@PNIPAM hybrid microgels, as well as the co-nonsolvency of PNIPAM in aqueous alcoholic solutions. The interplay between electron beam irradiation and PNIPAM systems in water resulted in irreversible shrinkage due to beam induced water radiolysis products, which in turn also affected the thermoresponsive behavior of PNIPAM. The addition of 2-propanol as radical scavenger improved PNIPAM stability in water under electron beam irradiation

Measuring interactions between colloidal (nano)particles

Colloidal dispersions, which are liquids with finely dispersed particles of between 1 nanometer and 10 micrometer in size, are ubiquitous in nature and in man-made applications. The stability of colloidal particles and the processes underlying their assembly into functional materials are governed by the interaction forces between the particles, and knowledge of these interaction forces is thus crucial to understand and predict their properties. In this thesis we explore methods to measure these interaction forces experimentally, with a focus on measurements of nanoparticles because their interactions are particularly difficult to predict using theory. We first review the different techniques which have been used to perform such measurements and their relevance to nanoparticles, and subsequently study two conceptually different methods by which interaction forces may be extracted from real-space microscopy data. This is done firstly through the analysis of equilibrium distribution functions which may be obtained from a single snap-shot of the particle positions. We demonstrate such measurements for a number of different (nano)particle systems using different 3D optical and electron micron microscopy techniques. Finally, we demonstrate using simulations and experiments that for micron-sized colloids interaction forces may be extracted without relying on equilibrium conditions through measurement of the particle dynamics using high-speed 2D and 3D optical microscopy, and extend this method to allow for measurement of particles with anisotropic (dipolar) interaction forces out of equilibrium

Single Au Atom Doping of Silver Nanoclusters

Ag29 nanoclusters capped with lipoic acid (LA) can be doped with Au. The doped clusters show enhanced stability and increased luminescence efficiency. We attribute the higher quantum yield to an increase in the rate of radiative decay. With mass spectrometry, the Au-doped clusters were found to consist predominantly of Au1Ag28(LA)12 3-. The clusters were characterized using X-ray absorption spectroscopy at the Au L3-edge. Both the extended absorption fine structure (EXAFS) and the near edge structure (XANES) in combination with electronic structure calculations confirm that the Au dopant is preferentially located in the center of the cluster. A useful XANES spectrum can be recorded for lower concentrations, or in shorter time, than the more commonly used EXAFS. This makes XANES a valuable tool for structural characterization

Single Au Atom Doping of Silver Nanoclusters

Ag29 nanoclusters capped with lipoic acid (LA) can be doped with Au. The doped clusters show enhanced stability and increased luminescence efficiency. We attribute the higher quantum yield to an increase in the rate of radiative decay. With mass spectrometry, the Au-doped clusters were found to consist predominantly of Au1Ag28(LA)12 3-. The clusters were characterized using X-ray absorption spectroscopy at the Au L3-edge. Both the extended absorption fine structure (EXAFS) and the near edge structure (XANES) in combination with electronic structure calculations confirm that the Au dopant is preferentially located in the center of the cluster. A useful XANES spectrum can be recorded for lower concentrations, or in shorter time, than the more commonly used EXAFS. This makes XANES a valuable tool for structural characterization

In Situ Study of the Wet Chemical Etching of SiO2 and Nanoparticle@SiO2 Core−Shell Nanospheres

The recent development of liquid cell (scanning) transmission electron microscopy (LC-(S)TEM) has opened the unique possibility of studying the chemical behavior of nanomaterials down to the nanoscale in a liquid environment. Here, we show that the chemically induced etching of three different types of silica-based silica nanoparticles can be reliably studied at the single particle level using LC-(S)TEM with a negligible effect of the electron beam, and we demonstrate this method by successfully monitoring the formation of silica-based heterogeneous yolk-shell nanostructures. By scrutinizing the influence of electron beam irradiation, we show that the cumulative electron dose on the imaging area plays a crucial role in the observed damage and needs to be considered during experimental design. Monte-Carlo simulations of the electron trajectories during LC-(S)TEM experiments allowed us to relate the cumulative electron dose to the deposited energy on the particles, which was found to significantly alter the silica network under imaging conditions of nanoparticles. We used these optimized LC-(S)TEM imaging conditions to systematically characterize the wet etching of silica and metal(oxide)-silica core-shell nanoparticles with cores of gold and iron oxide, which are representative of many other core-silica-shell systems. The LC-(S)TEM method reliably reproduced the etching patterns of Stöber, water-in-oil reverse microemulsion (WORM), and amino acid-catalyzed silica particles that were reported before in the literature. Furthermore, we directly visualized the formation of yolk-shell structures from the wet etching of Au@Stöber silica and Fe3O4@WORM silica core-shell nanospheres

In Situ Study of the Wet Chemical Etching of SiO2 and Nanoparticle@SiO2 Core−Shell Nanospheres

The recent development of liquid cell (scanning) transmission electron microscopy (LC-(S)TEM) has opened the unique possibility of studying the chemical behavior of nanomaterials down to the nanoscale in a liquid environment. Here, we show that the chemically induced etching of three different types of silica-based silica nanoparticles can be reliably studied at the single particle level using LC-(S)TEM with a negligible effect of the electron beam, and we demonstrate this method by successfully monitoring the formation of silica-based heterogeneous yolk-shell nanostructures. By scrutinizing the influence of electron beam irradiation, we show that the cumulative electron dose on the imaging area plays a crucial role in the observed damage and needs to be considered during experimental design. Monte-Carlo simulations of the electron trajectories during LC-(S)TEM experiments allowed us to relate the cumulative electron dose to the deposited energy on the particles, which was found to significantly alter the silica network under imaging conditions of nanoparticles. We used these optimized LC-(S)TEM imaging conditions to systematically characterize the wet etching of silica and metal(oxide)-silica core-shell nanoparticles with cores of gold and iron oxide, which are representative of many other core-silica-shell systems. The LC-(S)TEM method reliably reproduced the etching patterns of Stöber, water-in-oil reverse microemulsion (WORM), and amino acid-catalyzed silica particles that were reported before in the literature. Furthermore, we directly visualized the formation of yolk-shell structures from the wet etching of Au@Stöber silica and Fe3O4@WORM silica core-shell nanospheres

Observation of Undamped 3D Brownian Motion of Nanoparticles Using Liquid-Cell Scanning Transmission Electron Microscopy

In theory, liquid-cell (scanning) transmission electron microscopy (LC(S)TEM) is the ideal method to measure 3D diffusion of nanoparticles (NPs) on a single particle level, beyond the capabilities of optical methods. However, particle diffusion experiments have been especially hard to explain in LC(S)TEM as the observed motion thus far has been slower than theoretical predictions by 3–8 orders of magnitude due to electron beam effects. Here, direct experimental evidence of undamped diffusion for two systems is shown; charge-neutral 77 nm gold nanoparticles in glycerol and negatively charged 350 nm titania particles in glycerol carbonate. The high viscosities of the used media and a low electron dose rate allow observation of Brownian motion that is not significantly altered by the electron beam. The resulting diffusion coefficient agrees excellently with a theoretical value assuming free diffusion. It is confirmed that the particles are also moving in the direction parallel to the electron beam by simulating STEM images using Monte Carlo simulations. Simulations and experiments show blurring of the particles when these move out of focus. These results make clear that direct observation of 3D diffusion of NPs is possible, which is of critical importance for the study of interparticle interactions or in situ colloidal self-assembly using LC(S)TEM

Observation of Undamped 3D Brownian Motion of Nanoparticles Using Liquid-Cell Scanning Transmission Electron Microscopy

In theory, liquid-cell (scanning) transmission electron microscopy (LC(S)TEM) is the ideal method to measure 3D diffusion of nanoparticles (NPs) on a single particle level, beyond the capabilities of optical methods. However, particle diffusion experiments have been especially hard to explain in LC(S)TEM as the observed motion thus far has been slower than theoretical predictions by 3–8 orders of magnitude due to electron beam effects. Here, direct experimental evidence of undamped diffusion for two systems is shown; charge-neutral 77 nm gold nanoparticles in glycerol and negatively charged 350 nm titania particles in glycerol carbonate. The high viscosities of the used media and a low electron dose rate allow observation of Brownian motion that is not significantly altered by the electron beam. The resulting diffusion coefficient agrees excellently with a theoretical value assuming free diffusion. It is confirmed that the particles are also moving in the direction parallel to the electron beam by simulating STEM images using Monte Carlo simulations. Simulations and experiments show blurring of the particles when these move out of focus. These results make clear that direct observation of 3D diffusion of NPs is possible, which is of critical importance for the study of interparticle interactions or in situ colloidal self-assembly using LC(S)TEM