Oleg Yu. Grafov
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Oleg Yu. Grafov has a total of 87 co-authors. Here are the top co-authors by number of shared publications:
- Philipp Yu. Gorobtsov
Kurnakov Institute of General and Inorganic Chemistry, Russian Academy of Sciences, Moscow, Russia
3 shared publications - Tatiana L. Simonenko
Kurnakov Institute of General and Inorganic Chemistry of the Russian Academy of Sciences, 31 Leninsky pr., 119991 Moscow, Russia
3 shared publications - Yurii I. Kuznetsov
A.N. Frumkin Institute of Physical Chemistry and Electrochemistry, Russian Academy of Sciences, Moscow 119071, Russia
3 shared publications - Andrey Yu. Luchkin
Frumkin Institute of Physical Chemistry and Electrochemistry, Russian Academy of Sciences
2 shared publications - Elizaveta Petrovna Simonenko
Kurnakov Institute of General and Inorganic Chemistry of the Russian Academy of Sciences, Moscow, Russia
2 shared publications - Galina Vladimirovna Redkina
Frumkin Institute of Physical Chemistry and Electrochemistry, Russian Academy of Sciences, Leninsky Prospect 31-4, 119071 Moscow, Russia
2 shared publications
Latest Publications
- 17 July 2024
- Published by Elsevier in International Journal of Adhesion and Adhesives
- Vol. 134
Conversion coatings for magnesium and steel alloys based on styrene-acrylic dispersion
- 17 July 2024
- Published by Elsevier in International Journal of Adhesion and Adhesives
- Vol. 134
Conversion coatings for magnesium and steel alloys based on styrene-acrylic dispersion
- 6 April 2024
- Published by Wiley in Journal of Applied Polymer Science
- Vol. 141 (24)
Immobilization of N,N‐diallyl‐N,N‐dimethylammonium chloride on polyethylene. Biocidal properties of the material
The immobilization of N,N‐diallyl‐N,N‐dimethylammonium chloride (DADMAC) on low‐density polyethylene (LDPE) films was carried out by the method of postradiation grafting using x‐ray radiation. The introduction of polycation exchanger links provided the appearance of hydrophilicity of the surface of the modified film. By measuring the wetting contact angle, IR and SEM, the island‐type character of the coating from grafted polyDADMAC was detected. The death of Gram‐negative bacteria Pseudomonas aeruginosa, Gram‐positive bacteria Staphylococcus aureus, and yeast (eukaryotes) Yarrowia lipolytica on the surface of the film with grafted polyDADMAC was demonstrated.
- 6 April 2024
- Published by Wiley in Journal of Applied Polymer Science
- Vol. 141 (24)
Immobilization of N,N‐diallyl‐N,N‐dimethylammonium chloride on polyethylene. Biocidal properties of the material
The immobilization of N,N‐diallyl‐N,N‐dimethylammonium chloride (DADMAC) on low‐density polyethylene (LDPE) films was carried out by the method of postradiation grafting using x‐ray radiation. The introduction of polycation exchanger links provided the appearance of hydrophilicity of the surface of the modified film. By measuring the wetting contact angle, IR and SEM, the island‐type character of the coating from grafted polyDADMAC was detected. The death of Gram‐negative bacteria Pseudomonas aeruginosa, Gram‐positive bacteria Staphylococcus aureus, and yeast (eukaryotes) Yarrowia lipolytica on the surface of the film with grafted polyDADMAC was demonstrated.
- Open Access
- 30 August 2023
- Published by A.N. Frumkin Institute of Physical Chemistry and Electrochemistry in Corrosion: material protection and research methods
- Vol. 1 (2) , 37-48-48
Modification of ultrathin conversion coatings for AMg3 aluminum alloy and their interaction with painting system
Модификация ультратонких конверсионных покрытий на алюминиевом сплаве АМг3 и их взаимодействие с лакокрасочным покрытием
- 30 August 2023
- Published by A.N. Frumkin Institute of Physical Chemistry and Electrochemistry in Corrosion: material protection and research methods
- Vol. 1 (2) , 37-48-48
Open AccessModification of ultrathin conversion coatings for AMg3 aluminum alloy and their interaction with painting system
Модификация ультратонких конверсионных покрытий на алюминиевом сплаве АМг3 и их взаимодействие с лакокрасочным покрытием
- Open Access
- 29 July 2023
- Published by MDPI AG in International Journal of Molecular Sciences
- Vol. 24 (15) , 12165
Nanostructured Aluminum Oxyhydroxide—A Prospective Support for Functional Porphyrin-Based Materials
A method for the grafting of unsymmetrical A2BC-type 5,15-bis(4-butoxyphenyl)-10-(4-carboxyphenyl)-20-(phenanthrenoimidazolyl)-porphyrin onto the surface of nanostructured aluminum oxyhydroxide modified with a single SiO2 layer (NAOM) was successfully developed. A straightforward procedure towards surface modification of NAOM allowed us to prepare a new porphyrin-containing hybrid material. The obtained 3D heterostructure was extensively characterized using XPS, TEM and diffuse reflectance spectroscopy. Structural and morphological peculiarities of the inorganic support before and after the immobilization procedure were studied and discussed in detail. The stability of the material against leaching and the porphyrin immobilization ratio ca. 14% by weight were also revealed.
- 29 July 2023
- Published by MDPI AG in International Journal of Molecular Sciences
- Vol. 24 (15) , 12165
Open AccessNanostructured Aluminum Oxyhydroxide—A Prospective Support for Functional Porphyrin-Based Materials
A method for the grafting of unsymmetrical A2BC-type 5,15-bis(4-butoxyphenyl)-10-(4-carboxyphenyl)-20-(phenanthrenoimidazolyl)-porphyrin onto the surface of nanostructured aluminum oxyhydroxide modified with a single SiO2 layer (NAOM) was successfully developed. A straightforward procedure towards surface modification of NAOM allowed us to prepare a new porphyrin-containing hybrid material. The obtained 3D heterostructure was extensively characterized using XPS, TEM and diffuse reflectance spectroscopy. Structural and morphological peculiarities of the inorganic support before and after the immobilization procedure were studied and discussed in detail. The stability of the material against leaching and the porphyrin immobilization ratio ca. 14% by weight were also revealed.
- Open Access
Chamber Protection of Zinc with Ethylhexanoic Acid
Chamber protection is a promising and quickly developing method of vapor-phase protection of metals against atmospheric corrosion by inhibitors. It was shown that chamber treatment with 2-ethylhexanoic acid (EHA) efficiently inhibits the initiation of zinc corrosion. The optimum conditions (temperature and duration) of zinc treatment with vapors of this compound were determined. If these conditions are met, adsorption films of EHA with thicknesses up to 100 nm are formed on the metal surface. It was found that their protective properties increase during the first day as zinc is exposed to air after chamber treatment. The anticorrosive action of adsorption films is due both to the surface being shielded from the corrosive environment and to the inhibition of corrosion processes on the active surface of the metal. Corrosion inhibition was caused by the ability of EHA to convert zinc to the passive state and inhibit its local anionic depassivation.
Open AccessChamber Protection of Zinc with Ethylhexanoic Acid
Chamber protection is a promising and quickly developing method of vapor-phase protection of metals against atmospheric corrosion by inhibitors. It was shown that chamber treatment with 2-ethylhexanoic acid (EHA) efficiently inhibits the initiation of zinc corrosion. The optimum conditions (temperature and duration) of zinc treatment with vapors of this compound were determined. If these conditions are met, adsorption films of EHA with thicknesses up to 100 nm are formed on the metal surface. It was found that their protective properties increase during the first day as zinc is exposed to air after chamber treatment. The anticorrosive action of adsorption films is due both to the surface being shielded from the corrosive environment and to the inhibition of corrosion processes on the active surface of the metal. Corrosion inhibition was caused by the ability of EHA to convert zinc to the passive state and inhibit its local anionic depassivation.
- Open Access
- 14 February 2023
- Published by MDPI AG in Chemosensors
- Vol. 11 (2) , 138
Microplotter Printing of Hierarchically Organized NiCo2O4 Films for Ethanol Gas Sensing
Using a combination of chemical coprecipitation and hydrothermal treatment of the resulting dispersed system, a hierarchically organized NiCo2O4 nanopowder was obtained, consisting of slightly elongated initial oxide nanoparticles self-organized into nanosheets about 10 nm thick, which in turn are combined into hierarchical cellular agglomerates of about 2 μm. Fourier-transform infrared spectroscopy (FTIR), X-ray diffraction analysis (XRD), selected area electron diffraction (SAED) and high-resolution transmission electron microscopy (HR-TEM) allowed to confirm the formation of NiCo2O4 powder with the desired crystal structure via additional heat treatment of the intermediate product. Energy-dispersive X-ray spectroscopy (EDX) was used to confirm the target metal ratio, and the uniform distribution of the elements (Ni, Co and O) was shown by mapping. The resulting nanopowder was employed to prepare functional inks suitable for microplotter printing of the NiCo2O4 film. It was found that an oxide film morphology is fully inherited from the hierarchically organized oxide nanopowder used. Atomic force microscopy (AFM) revealed the film thickness (15 μm) and determined the maximum height difference of 500 nm over an area of 25 μm2. Kelvin probe force microscopy (KPFM) showed that the surface potential was shifted to the depths of the oxide film, and the work function value of the material surface was 4.54 eV, which is significantly lower compared to those reported in the literature. The electronic state of the elements in the NiCo2O4 film under study was analyzed by X-ray photoelectron spectroscopy (XPS). Chemosensor measurements showed that the printed receptor layer exhibited selectivity and high signal reproducibility for ethanol detection. As the relative humidity increases from 0 to 75%, the response value is reduced; however, the sensor response profile and signal-to-noise ratio remain without significant changes.
- 14 February 2023
- Published by MDPI AG in Chemosensors
- Vol. 11 (2) , 138
Open AccessMicroplotter Printing of Hierarchically Organized NiCo2O4 Films for Ethanol Gas Sensing
Using a combination of chemical coprecipitation and hydrothermal treatment of the resulting dispersed system, a hierarchically organized NiCo2O4 nanopowder was obtained, consisting of slightly elongated initial oxide nanoparticles self-organized into nanosheets about 10 nm thick, which in turn are combined into hierarchical cellular agglomerates of about 2 μm. Fourier-transform infrared spectroscopy (FTIR), X-ray diffraction analysis (XRD), selected area electron diffraction (SAED) and high-resolution transmission electron microscopy (HR-TEM) allowed to confirm the formation of NiCo2O4 powder with the desired crystal structure via additional heat treatment of the intermediate product. Energy-dispersive X-ray spectroscopy (EDX) was used to confirm the target metal ratio, and the uniform distribution of the elements (Ni, Co and O) was shown by mapping. The resulting nanopowder was employed to prepare functional inks suitable for microplotter printing of the NiCo2O4 film. It was found that an oxide film morphology is fully inherited from the hierarchically organized oxide nanopowder used. Atomic force microscopy (AFM) revealed the film thickness (15 μm) and determined the maximum height difference of 500 nm over an area of 25 μm2. Kelvin probe force microscopy (KPFM) showed that the surface potential was shifted to the depths of the oxide film, and the work function value of the material surface was 4.54 eV, which is significantly lower compared to those reported in the literature. The electronic state of the elements in the NiCo2O4 film under study was analyzed by X-ray photoelectron spectroscopy (XPS). Chemosensor measurements showed that the printed receptor layer exhibited selectivity and high signal reproducibility for ethanol detection. As the relative humidity increases from 0 to 75%, the response value is reduced; however, the sensor response profile and signal-to-noise ratio remain without significant changes.
- Open Access
PtM/CNT (M = Mo, Ni, CoCr) Electrocatalysts with Reduced Platinum Content for Anodic Hydrogen Oxidation and Cathodic Oxygen Reduction in Alkaline Electrolytes
Bimetallic catalysts containing platinum and transition metals (PtM, M = Mo, Ni, CoCr) were synthesized on carbon nanotubes (CNTs) functionalized in an alkaline medium. Their platinum content is 10–15% by mass. PtM/CNTNaOH are active in both the hydrogen oxidation reaction (HOR) and the oxygen reduction reaction (ORR) in alkaline electrolytes. Although catalysts based on a single transition metal are inactive in the HOR, their activity in the cathode process of ORR increases relative to CNTNaOH. When using the rotating ring-disk electrode method for ORR, PtM/CNT showed a high selectivity in reducing oxygen directly to water. In HOR, the PtM/CNT catalyst had an activity comparable to that of a commercial monoplatinum catalyst. The results obtained show that it is possible to use the PtM/CNT catalyst in an alkaline fuel cell both as an anode and as a cathode.
Open AccessPtM/CNT (M = Mo, Ni, CoCr) Electrocatalysts with Reduced Platinum Content for Anodic Hydrogen Oxidation and Cathodic Oxygen Reduction in Alkaline Electrolytes
Bimetallic catalysts containing platinum and transition metals (PtM, M = Mo, Ni, CoCr) were synthesized on carbon nanotubes (CNTs) functionalized in an alkaline medium. Their platinum content is 10–15% by mass. PtM/CNTNaOH are active in both the hydrogen oxidation reaction (HOR) and the oxygen reduction reaction (ORR) in alkaline electrolytes. Although catalysts based on a single transition metal are inactive in the HOR, their activity in the cathode process of ORR increases relative to CNTNaOH. When using the rotating ring-disk electrode method for ORR, PtM/CNT showed a high selectivity in reducing oxygen directly to water. In HOR, the PtM/CNT catalyst had an activity comparable to that of a commercial monoplatinum catalyst. The results obtained show that it is possible to use the PtM/CNT catalyst in an alkaline fuel cell both as an anode and as a cathode.