The electronic structure of a gold film deposited on W was studied during the adsorption of sodium atoms. An analysis of the photoemission spectra from the valence band and core levels of Au 4f and Na 2p upon synchrotron excitation in the photon energy range of 80–600 eV showed that Na adsorption leads to the formation of NaxAuy intermetallic compounds of various stoichiometry under the Na monolayer.

Photoelectron spectroscopy was used to study the electronic structure in situ in an ultrahigh vacuum before and after the adsorption of sodium atoms on the surface of tungsten oxidized at an oxygen pressure of 1 Torr and a temperature of 950 K. The photoemission spectra from the valence band and the W 4f, O 2s, and Na 2p core states were studied under synchrotron excitation in the photon energy range 80–600 eV. It is found that a tungsten oxide film is formed which contains various tungsten oxides with an oxidation state of 6+ to 4+. The deposition of a 1.1 monolayer of sodium atoms on the surface of oxidized tungsten leads to the reduction of the W6+ states to W4+ and the reaction with oxygen in the hydroxyl composition, which is reflected in the change in the spectrum of the W 4f and O 2s core states. It is shown that the cathodoluminescence spectrum is associated with the luminescence of tungsten oxide.

Using the method of photoelectron spectroscopy, an in situ study in ultrahigh vacuum of the electronic structure of a clean surface of tungsten oxidized at an oxygen pressure of 1 Torr and temperature of 1000 K was carried out. The spectra of photoemission from the valence band and core levels O 1s, O 2s, W 4f under synchrotron excitation in the photon energy range 80  600 eV are studied. It was found that a semiconductor film of tungsten oxide is formed, which contains various tungsten oxides with an oxidation state of 6+ to 4+. On the surface, mainly tungsten oxides with an oxidation state of 6+ are formed, the proportion of which gradually decreases with distance from the surface with an increase in tungsten oxides with an oxidation state of 4+.