The femtosecond laser ablation of a gold target in aqueous solutions has been used to produce colloidal Au nanoparticles with controlled surface chemistry. A detailed chemical analysis showed that the nanoparticles formed were partially oxidized by the oxygen present in solution. The hydroxylation of these Au-O compounds, followed by a proton loss to give surface Au-O -, resulted in the negative charging of the nanoparticles. The partial oxidation of the gold nanoparticle surface enhances its chemical reactivity and consequently has a strong impact on its growth. In particular, the oxidized surface reacted efficiently with Cland OHto augment its net surface charge. This limited the coalescence of the particles, due to electrostatic repulsion, and led to a significant reduction of their size. Taking advantage of the repulsion effect, efficient size control was achieved using different salts (7 ( 5 nm for 10 mM KCl, 5.5 ( 4 nm for 10 mM NaCl, 8 ( 5 nm for NaOH, pH 9.4), a considerable improvement comparatively to particles prepared in deionized water, using identical ablation conditions, where particles of 1-250 nm were produced. The partially oxidized gold surface was also suitable for surface modification through both covalent and electrostatic interactions during particle formation. Using solutions of N-propylamine, we showed an efficient control of nanoparticle size (5-8 ( 4-7 nm) by the involvement of these interactions. The results obtained help to develop methodologies for the control of laser-ablation-based nanoparticle growth and the functionalization of nanoparticle surfaces by specific interactions.

The diffusion and coalescence of metal nanoparticles play important roles in many phenomena. Here, we offer a new integrated overview of the main factors that control the nanoparticle coalescence process. Three factors are considered in our description of the coalescence process: nanoparticle diffusion across the surface, their physical and thermodynamic properties, and the mechanism of coalescence. We demonstrate that the liquid-like properties of the surface layers of the nanoparticles play an essential role in this process. We present experimental evidence for our opinion, based on the high-resolution electron microscopic analysis of several different types of nanoparticles.

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Femtosecond laser radiation has been used to ablate a gold target in aqueous beta-cyclodextrin (CD) solutions to produce stable gold nanoparticle colloids with extremely small size (2 to 2.4 nm) and size dispersion (1 to 1.5 nm). On the basis of XPS and zeta-potential measurements, we propose a model involving chemical interactions between the gold and the CDs. The model includes both the hydrophobic interaction of the Au0 with the interior cavity of the CD and the hydrogen bonding of O- groups on the partially oxidized gold surface with -OH groups of the CDs.

The interaction between multiwalled carbon nanotubes (MWCNTs) and aqueous poly(diallyl dimethylammonium) chloride (PDDA) was studied by X-ray photoelectron (XPS) and photoacoustic Fourier transform infrared (PA-FTIR) spectroscopies. We have found that the mild sonication of MWCNTs in aqueous PDDA results in a significant improvement of CNT dispersibility and greatly enhances their adhesion to Au and Si substrates. The MWCNT-PDDA interaction is due to the presence of an unsaturated contaminant in the PDDA chain, as confirmed by both XPS and PA-FTIR, which enters into a pi-pi interaction with the CNTs. Electrostatic group repulsions of the coated CNTs then provide the dispersibility and adhesion.

3D Pt nanoflowers, which are composed of numerous single‐crystal nanowires, are successfully synthesized by a facile chemical procedure, at room temperature, without surfactant or template. The Pt nanoflowers adhere to carbon paper, exhibiting an enlarged electroactive surface area comparable to that of a commercial Pt/C electrode.

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The X-ray photoelectron spectroscopic characterizations of Pt nanoparticles evaporated onto untreated and Ar+-treated highly oriented pyrolytic graphite surfaces, with, respectively, low and high surface defect densities have been studied using multicomponent analysis with symmetric line shapes:  each Pt4f spectral component (f7/2 and f5/2) was deconvoluted into three symmetric peaks. On analyzing the relationships among the Pt4f, C1s, and O1s spectra, we attribute these peaks to the existence of surface oxidation on the platinum nanoparticles and to the different electronic configurations of surface and bulk Pt atoms. We use the varying intensities of these component peaks, as a function of deposited Pt, to explain the changing shape of the Pt4f asymmetric envelope with nanoparticle size.