The imaging of non-conducting materials by scanning electron microscopy (SEM) is most often performed after depositing few nanometers thick conductive layers on the samples. It is shown in this work, that even a 5 nm thick sputtered gold layer can dramatically alter the morphology and the surface structure of many different types of aerogels. Silica, polyimide, polyamide, calcium-alginate and cellulose aerogels were imaged in their pristine forms and after gold sputtering utilizing low voltage scanning electron microscopy (LVSEM) in order to reduce charging effects. The morphological features seen in the SEM images of the pristine samples are in excellent agreement with the structural parameters of the aerogels measured by nitrogen adsorption-desorption porosimetry. In contrast, the morphologies of the sputter coated samples are significantly distorted and feature nanostructured gold. These findings point out that extra care should be taken in order to ensure that gold sputtering does not cause morphological artifacts. Otherwise, the application of low voltage scanning electron microscopy even yields high resolution images of pristine non-conducting aerogels.
Porous gold nanoparticles (PGNs) are usually prepared in an immobilized form on a solid substrate, which is not practical in many applications. In this work, a simple method is reported for the preparation and stabilization of mesoporous gold particles of a few hundred nanometers in size in aqueous suspension. Nanoparticles of Ag-Au alloy were fabricated on CaF 2 and Si/SiO 2 substrates by the solid-state dewetting method. Silver was selectively dissolved (dealloyed), and the resulting porous gold nanoparticles were chemically removed from the substrate either in a concerted step with dealloying, or in a subsequent step. Nitric acid was used for the one-step dealloying and detachment of the particles from CaF 2 substrate. The consecutive use of HNO 3 and HF resulted in the dealloying and the subsequent detachment of the particles from Si/SiO 2 substrate. The PGNs were recovered from the aqueous suspensions by centrifugation. The Au content of the suspensions was monitored by using elemental analysis (ICP-OES), and recovery was optimized. The morphology and the optical characteristics of the support-free PGNs were analyzed by scanning electron microscopy (SEM), dynamic light scattering spectroscopy (DLS), and near-infrared spectrophotometry (NIR). The obtained PGNs are spherical disk-shaped with a mean particle size of 765 ± 149 nm. The suspended, support-free PGNs display an ideally narrow dipole plasmon peak at around 1450 nm in the NIR spectral region. Thus, the new colloidal PGNs are ideal candidates for biomedical applications, for instance photothermal therapy.
In this study, metallic nanoislands were prepared by thermal annealing of gold thin film produced by vacuum evaporation on a glass substrate to investigate the surface-enhanced Raman scattering (SERS) effect on them. The influence of the analyte on the enhancement factor of SERS was studied with riboflavin and rhodamine 6G dye. Two laser excitation sources at 532 and 633 nm wavelengths were used for SERS measurements. We found that the enhancement factors of the gold nanoisland SERS substrates were influenced by the analytes’ adsorption tendency onto their surfaces. The SERS amplification was also found to be dependent on the electronic structure of the molecules; higher enhancement factors were obtained for rhodamine 6G with 532 nm excitation, while for riboflavin the 633 nm source performed better.
Porous gold nanoparticles (PGNs) are very popular due to their high surface/volume ratio, moreover they have stronger plasmonic properties than their solid counterparts. These properties make the porous gold nanoparticles very useful for lots of applications, for instance chemical sensors, cancer therapy applications. For applications, however, it is indispensable that the resonance frequency (RF) of a plasmonic structure to be tuneable. In this work we show that the RF can be set in a wide range as desired by coating the PGNs by mixed oxide layers. By changing the composition of the coating layer, that is the mixture ratio, the RF can be shifted practically continuously in a wide range determined by the refractive index of the used oxides. As a demonstration, PGNs were coated with mixed alumina-titania oxide layers (5–7 nm) using plasma-enhanced atomic layer deposition method. The oxide layer, beside as a tuning tool, also stabilises the structure of the PGNs when are exposed to elevated temperature. This is shown by the influence of the temperature (from $$350\, ^{\circ }\hbox {C}$$
350
∘
C
up to $$900\, ^{\circ }\hbox {C}$$
900
∘
C
) on the morphology, and as a consequence the optical extinction spectra, of the oxide coated PGNs.
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