Polina Konstantinovna Ignat’eva
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Polina Konstantinovna Ignat’eva has a total of 9 co-authors. Here are the top co-authors by number of shared publications:
- Andrey Konstantinovich Gatin
N.N. Semenov Federal Research Center for Chemical Physics of Russian Academy of Sciences (FRCCP RAS), Kosygina Street 4, 119991 Moscow, Russia
2 shared publications - Dinara Tastaibek
Department of Materials Science, Nanotechnology and Engineering Physics, Mining and Metallurgical Institute, Satbayev University (KazNRTU), Satbaeva Street 22, 050013 Almaty, Kazakhstan
2 shared publications - Maxim Vyacheslavovich Grishin
N.N. Semenov Federal Research Center for Chemical Physics of Russian Academy of Sciences (FRCCP RAS), Kosygina Street 4, 119991 Moscow, Russia
2 shared publications - Sergey Yurievich Sarvadiy
N.N. Semenov Federal Research Center for Chemical Physics of Russian Academy of Sciences (FRCCP RAS), Kosygina Street 4, 119991 Moscow, Russia
2 shared publications - Denis A. Yavsin
Ioffe Physico-Technical Institute, Russian Academy of Sciences, Politechnicheskaya Street 26, 194021 Saint Petersburg, Russia
1 shared publication - Ekaterina I. Rudenko
N.N. Semenov Federal Research Center for Chemical Physics of Russian Academy of Sciences (FRCCP RAS), Kosygina Street 4, 119991 Moscow, Russia
1 shared publication
Latest Publications
- Open Access
- 7 May 2026
- Published by MDPI AG in Nanomaterials
- Vol. 16 (10) , 570
Structure Inhomogeneity of Gold Nanoparticles and Its Effect on H2 Dissociative Chemisorption
Significant differences in hydrogen adsorption on amorphous and crystalline gold nanoparticles deposited on highly oriented pyrolytic graphite (HOPG) were revealed. Crystalline nanoparticles were synthesized via the impregnation–precipitation method followed by annealing at 700 K, whereas amorphous ones were obtained using the laser electrodispersion method. The morphology and electronic structure of single nanoparticles were investigated with high spatial resolution using scanning tunneling microscopy and spectroscopy (STM/STS) in ultra-high vacuum both before and after exposure to molecular hydrogen at doses of 400–6000 L. Experiments performed at room temperature showed that the surface coverage by the adsorbate in both cases begins at the Au-HOPG interface, spreads towards the center of the particle, and corresponds to the island growth model. However, amorphous nanoparticles have fewer growth sites at the periphery compared to crystalline ones. The local electronic structure of amorphous nanoparticles is more inhomogeneous compared to crystalline ones, demonstrating variation across different points on the nanoparticle surface. It was shown that dissociative chemisorption of hydrogen takes place on amorphous gold nanoparticles with a size of 4–6 nm. Chemisorption is completely inhibited when the nanoparticle size is reduced to 2 nm or less.
- 7 May 2026
- Published by MDPI AG in Nanomaterials
- Vol. 16 (10) , 570
Open AccessStructure Inhomogeneity of Gold Nanoparticles and Its Effect on H2 Dissociative Chemisorption
Significant differences in hydrogen adsorption on amorphous and crystalline gold nanoparticles deposited on highly oriented pyrolytic graphite (HOPG) were revealed. Crystalline nanoparticles were synthesized via the impregnation–precipitation method followed by annealing at 700 K, whereas amorphous ones were obtained using the laser electrodispersion method. The morphology and electronic structure of single nanoparticles were investigated with high spatial resolution using scanning tunneling microscopy and spectroscopy (STM/STS) in ultra-high vacuum both before and after exposure to molecular hydrogen at doses of 400–6000 L. Experiments performed at room temperature showed that the surface coverage by the adsorbate in both cases begins at the Au-HOPG interface, spreads towards the center of the particle, and corresponds to the island growth model. However, amorphous nanoparticles have fewer growth sites at the periphery compared to crystalline ones. The local electronic structure of amorphous nanoparticles is more inhomogeneous compared to crystalline ones, demonstrating variation across different points on the nanoparticle surface. It was shown that dissociative chemisorption of hydrogen takes place on amorphous gold nanoparticles with a size of 4–6 nm. Chemisorption is completely inhibited when the nanoparticle size is reduced to 2 nm or less.
- Open Access
Effects of Surface Rearrangement on H and O Adsorption on Cu and Pd Nanoparticles
Atomic effects determining the adsorption of hydrogen and oxygen atoms on (111), (100), (110), and (211) surfaces of Cu and Pd have been studied using quantum chemical simulations. The deformation of the (111) and (100) surfaces during adatom bonding enhances the bond strength at active sites with high coordination numbers. In contrast, the deformation of the (110) and (211) surfaces does not exhibit a strong tendency. The atomic contribution of the nearest-neighbor environment depends on the square magnitude of the interaction matrix element, . A high value increases the proportion of repulsive interactions within the metal adsorption complexes, leading to a decrease in the coordination number of the most stable adsorption site.Open AccessEffects of Surface Rearrangement on H and O Adsorption on Cu and Pd Nanoparticles
Atomic effects determining the adsorption of hydrogen and oxygen atoms on (111), (100), (110), and (211) surfaces of Cu and Pd have been studied using quantum chemical simulations. The deformation of the (111) and (100) surfaces during adatom bonding enhances the bond strength at active sites with high coordination numbers. In contrast, the deformation of the (110) and (211) surfaces does not exhibit a strong tendency. The atomic contribution of the nearest-neighbor environment depends on the square magnitude of the interaction matrix element, . A high value increases the proportion of repulsive interactions within the metal adsorption complexes, leading to a decrease in the coordination number of the most stable adsorption site.