Nikolai G. Khlebtsov

On the measurement of gold nanoparticle sizes by the dynamic light scattering method

The application of the dynamic light scattering (DLS) method for determining the size distribution of colloidal gold nanoparticles in a range of 1–100 nm is discussed. It is shown that rotational diffusion of nonspherical strongly scattering particles with sizes of larger than 30–40 nm results in the appearance of a false peak in a size range of about 5–10 nm. In this case, the uncritical application of the DLS method may yield particle volume or number size distributions different from those obtained by transmission electron microscopy. For weakly scattering particles with diameters of smaller that 20 nm, the DLS method demonstrates an additional peak of intensity distribution in the region of large sizes that is related to particle aggregates or byproduct particles rather than individual nanoparticles. Practical methods for solving the problem of false peaks are discussed. It is established that the width of the DLS distribution does not correspond to transmission electron microscopy data and is overestimated. The advantages and drawbacks of the methods are compared and it is noted that, at present, the DLS method is the only instrument suitable for nonperturbative and sensitive diagnostics of relatively slow aggregation processes with characteristic times on the order of 1 min. In particular, this method can be used to diagnose gold nanoparticle conjugate aggregation initiated by biospecific interactions on their surface.

Determination of the Size, Concentration, and Refractive Index of Silica Nanoparticles from Turbidity Spectra

The size and concentration of silica cores determine the size and concentration of silica/gold nanoshells in final preparations. Until now, the concentration of silica/gold nanoshells with Stobers silica core has been evaluated through the material balance assumption. Here, we describe a method for simultaneous determination of the average size and concentration of silica nanospheres from turbidity spectra measured within the 400-600 nm spectral band. As the refractive index of silica nanoparticles is the key input parameter for optical determination of their concentration, we propose an optical method and provide experimental data on a direct determination of the refractive index of silica particles n = 1.475 +/- 0.005. Finally, we exemplify our method by determining the particle size and concentration for 10 samples and compare the results with transmission electron microscopy (TEM), atomic force microscopy (AFM), and dynamic light scattering data.

A Multilayer Model for Gold Nanoparticle Bioconjugates: Application to Study of Gelatin and Human IgG Adsorption Using Extinction and Light Scattering Spectra and the Dynamic Light Scattering Method

A new model of colloidal gold (CG) bioconjugates is proposed. The model consists of a gold core and a primary polymer shell formed during conjugate synthesis. Additionally, the conjugate includes a secondary shell formed during its interaction with target molecules. Each of the inhomogeneous shells is modeled by the arbitrary number of discrete layers. Using Mie theory for multilayered spheres, we calculated the extinction and static light scattering (SLS, at 90°) spectra, as well as differential spectra ΔA(λ), ΔI(λ) describing the effects of primary and secondary shells. Our calculations are performed for the conjugates with gold particle diameters d = 10–160 nm and two 5-nm shells. The primary shell consists of two 2.5-nm layers with the refractive indices of 1.50 and 1.45; the secondary shell, of two 2- and 3-nm layers with the refractive indices of 1.45 and 1.40. The differential spectra are related to the adsorption of target molecules and possess a characteristic resonance that is shifted to the red region of spectra compared to the usual localized plasmon resonances of gold particles. The maximal values of differential resonances ΔAmax and ΔImax are observed for gold particles with diameters about 40–60 nm (extinction spectra) or 70–90 nm (the SLS spectra). The adsorption of human gamma-globulin (hIgG) and gelatin onto 15- and 34-nm gold particles was studied using the SLS and extinction spectra in combination with the dynamic light scattering measurements. It is shown that the thickness of adsorbed layer is equal to 5–6 nm for hIgG and to 15–18 nm for gelatin. The experimental extinction and SLS spectra for CG + hIgG conjugates are well explained by a simple model with the gold core and homogeneous polymer coating. For the CG + gelatin conjugates, we used the new model with inhomogeneous polymer coating, which is modeled by 10 discrete layers with the total thickness of 16–18 nm and exponential spatial profile of shell refractive index.

Large-scale high-quality 2D silica crystals: dip-drawing formation and decoration with gold nanorods and nanospheres for SERS analysis

High-quality colloidal crystals (CCs) are important for use in photonic research and as templates for large-scale plasmonic SERS substrates. We investigated how variations in temperature, colloid concentration, and dip-drawing parameters (rate, incubation time, etc) affect the structure of 2D CCs formed by highly monodisperse silica nanoparticles (SiNPs) synthesized in an l-arginine solution and regrown by a modified Stöber method. The best quality 2D CCs were obtained with aqueous 12 wt% colloids at a temperature of 25 °C, an incubation time of 1 min, and a drawing rate of 50 mm min(-1). Assembling of gold nanorods (GNRs) on 2D CCs resulted in the formation of ring-like chains with a preferential tail-to-tail orientation along the hexagonal boundaries. To the best of our knowledge, this is the first time that such nanostructures have been prepared. Owing to the preferential tail-to-tail packing of GNRs, 2D SiNP CC + GNR substrates demonstrated an analytical SERS enhancement of about 8000, which was 10 to 15 times higher than that for self-assembled GNRs on a silicon wafer. In addition, the analytical SERS enhancement was almost 60 times lower after replacing the nanorods in 2D SiNP CC + GNR substrates with 25 nm gold nanospheres.