An experimental study of molecular hydrogen adsorption on single gold nanoparticles of various sizes deposited on the surface of highly oriented pyrolytic graphite (HOPG) was carried out by means of scanning tunneling microscopy and spectroscopy. The effect of size on the HOPG/Au system was established. Hydrogen was dissociatively chemisorbed on the surface of gold nanoparticles with an average size of 5–6 nanometers. An increase in the size of nanoparticles to 10 nm or more led to hydrogen chemisorption being inhibited and unable to be detected.

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The adsorption of CO on the surface of Cu-based nanoparticles was studied in the presence of an external electric field by means of scanning tunneling microscopy (STM) and spectroscopy (STS). Nanoparticles were synthesized on the surface of a graphite support by the impregnation–precipitation method. The chemical composition of the surface of the nanoparticles was determined as a mixture of Cu2O, Cu4O3 and CuO oxides. CO was adsorbed from the gas phase onto the surface of the nanoparticles. During the adsorption process, the potential differences ΔV = +1 or −1 V were applied to the vacuum gap between the sample and the grounded tip. Thus, the system of the STM tip and sample surface formed an asymmetric capacitor, inside which an inhomogeneous electric field existed. The CO adsorption process is accompanied by the partial reduction of nanoparticles. Due to the orientation of the CO molecule in the electric field, the reduction was weak in the case of a positive potential difference, while in the case of a negative potential difference, the reduction rate increased significantly. The ability to control the adsorption process of CO by means of an external electric field was demonstrated. The size of the nanoparticle was shown to be the key factor affecting the adsorption process, and particularly, the strength of the local electric field close to the nanoparticle surface.

The morphological features of nanostructured films of tin, zinc, indium, and cerium oxides are established. The parameters of electron traps, such as adsorbed oxygen atoms and structural defects, respon sible for the sensory effect are determined. An increase in the conductance of indium oxide films upon annealing in vacuum is revealed.

The hydrogenation features of gold nanoparticles deposited on highly oriented pyrolytic graphite were determined, and composite nanostructures consisting of pure and hydrogenized gold were synthesized. Methods of scanning tunneling microscopy and spectroscopy have been successfully used to probe the bottom of the conductive band and to determine the shape of the electron energy barrier in hydrogenized gold. Considering models of surface and volume hydrogenation, we have shown that no hydrogen dissolution occurred in gold nanoparticles, but all changes in their electronic structure were associated with surface processes. The results of the quantum chemical simulation also corresponded with this conclusion.

The morphologies and local electronic structures of titanium coatings deposited on the surfaces of highly oriented pyrolytic graphite were determined. Chemical compositions of the oxides formed on the coating surfaces were established. A theoretical model was developed describing the changes in the TiO x oxides (1.75 < x < 2) band gap depending on the duration and temperature of the titanium film annealing procedure in oxygen. The effective activation energy of oxygen diffusion in TiO x (1.75 < x < 2) was determined, and the pre-exponential factor of the diffusion coefficient was estimated.

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