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We report on co-doping of high-quality AlN single crystals by group II Beryllium acceptors by means of diffusion from the vapour phase at a temperature of 1850 °C. We discovered that Be is characterized by the high diffusion length, allowing one to produce Be co-doping of sub-mm-thick AlN wafers. We show that Be diffusion led to the quenching of the visible (VIS) 450 nm (2.75 eV) and deep ultraviolet (UV) 265 nm (4.7 eV) optical absorption bands with simultaneous induction of the absorption band peaked at 248 nm (5 eV). By means of electron paramagnetic resonance (EPR), we also found that the presence of Be impurities compensated the donor type paramagnetic centers. Correlation of the EPR data with the optical absorption allowed us to conclude that Be produced in the AlN via diffusion acted predominantly as an acceptor, inducing the shift of the Fermi level to the lower part of the AlN bandgap. This shift of the Fermi level results in recharging of the deep level defects in the AlN bandgap, which explains the observed quenching of the VIS and UV absorption bands.

Porous silica materials offer wide range of possibilities for enhancement of the productivity of oil reservoirs. However the mechanism of adsorption of polar components of crude oil on silica surface is poorly understood that hinders technological improvement of supports and oil extraction. We have synthesized opal films with the silica microspheres size of about 360 ± 20 nm, specific surface area of 5.2 m 2 × g −1 and pore size of 230 nm. We have fractionated and characterized oil and oil asphaltenes from heavy (Ashalchinskoe) oil. By pulsed electron paramagnetic resonance (EPR) and double electron-nuclear resonance (ENDOR) in the W-band frequency range (microwave frequency of 94 GHz, magnetic field of 3.4 T) we have studied the adsorption of oil asphaltenes on the surface of opal samples using the intrinsic for asphaltenes paramagnetic vanadylporphyrins (VO) complexes. 1 H ENDOR spectra are found to be different for initial and the adsorbed samples in their central parts (that is a sign of asphaltenes VO disaggregation) whereas no significant changes in the W-band EPR spectra were detected. Contrasting to alumina support, no strong electron-proton interaction with the protons on the surface of SiO2 (presumably, silanol groups) was found and infiltration of the oiled opal films with gasoline changes the central part of 1 H ENDOR spectra. It shows that the proton containing groups on the surface of amorphous SiO2 sample can significantly change the asphaltene adsorption properties and ENDOR of the intrinsic for oil paramagnetic centers could be used for the characterization of surface state in porous media in situ or operando. PACS: 76.70.Dx, 75.10.Dg, 61.43.Bn.

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