Applied Surface Science 416 (2017) 988–995

A.A. Ionin, S.I. Kudryashov, A.O. Levchenko, L.V. Nguyen, I.N. Saraeva, A.A. Rudenko, E.I. Ageev, D.V. Potorochin, V.P. Veiko, E.V. Borisov, D.V. Pankin, D.A. Kirilenko, P.N. Brunkov

«Correlated topographic and structural modification on Si surface during multi-shot femtosecond laser exposures: Si nanopolymorphs as potential local structural nanomarkers»

Applied Surface Science 416 (2017) 988–995

DOI: 10.1016/j.apsusc.2017.04.215


High-pressure Si-XII and Si-III nanocrystalline polymorphs, as well as amorphous Si phase, appear consequently during multi-shot femtosecond-laser exposure of crystalline Si wafer surface above its spallation threshold along with permanently developing quasi-regular surface texture (ripples, microcones), residual hydrostatic stresses and subsurface damage, which are characterized by scanning and transmission electron microscopy, as well as by Raman micro-spectroscopy. The consequent yields of these structural Si phases indicate not only their spatially different appearance, but also potentially enable to track nanoscale, transient laser-induced high-pressure, high-temperature physical processes – local variation of ablation mechanism and rate, pressurization/pressure release, melting/resolidification, amorphization, annealing – versus cumulative laser exposure and the related development of the surface topography.



24 апреля состоялся совместный семинар РЦ ОЛМИВ, Кафедры лазерной химии и лазерного материаловедения и представителей ИХС РАН им. Гребенщикова.

На семинаре выступили:

О.А.Шилова, д.х.н., Институт химии силикатов  им. Гребенщикова и  В.Н.Щелушкин, рук. технологической группы, группа компаний Солэкс, г. Рязань.

Обсуждались вопросы выполнения совместных научно-исследовательских работ в области исследования новых материалов, в частности, для солнечной энергетики.


Polyhedron Volume 130, Pages 176-183

Y. Kondratenko, V. Fundamenskya, I. Ignatyev, A. Zolotarev, T. Kochina, V. Ugolkov

Synthesis and crystal structure of two zinc-containing complexes of triethanolamine

Polyhedron Volume 130, Pages 176-183

DOI: 10.1016/j.poly.2017.04.022

Two new zinc-containing complexes [Zn2(TEA)(C6H5COO)3] (1) and ([Zn(TEA)(H2O)2]SO4)·H2O (2) were synthesized and characterized by IR spectroscopy, elemental analysis, DSC and TG analysis. Their structure was determined by single-crystal X-ray diffraction. In the binuclear, mixed-ligand [Zn2(TEA)(C6H5COO)3] complex, one zinc atom is six-coordinated by nitrogen and three oxygen atoms of tetradentate triethanolamine (TEA) and two oxygen atoms of two different benzoate ligands, forming the distorted octahedron of the ZnNO5 type. The second zinc atom is five-coordinated, forming the distorted trigonal bipyramid. Two zinc atoms are bridged by two carboxylate groups of two benzoate ligands and one oxygen atom of the deprotonated hydroxyethyl group of TEA. Cationic complex 2 consists of [Zn(TEA)(H2O)2]2+ cations and SO42- anions. The coordination polyhedron around the zinc atom corresponds to a distorted octahedron (ZnNO5 type). The TEA ligand is tetradentately coordinated to the cation, forming three chelate rings. The coordination sphere of the Zn cation is completed by two aqua ligands.

REVIEWS  ON  ADVANCED  MATERIALS   SCIENCE Volume 47, No. 1, Pages 71-77

O.Yu. Kurapova, V.G. Konakov, A.S. Grashchenko, N.N. Novik, S.N. Golubev and I.A. Ovid’ko


REVIEWS  ON  ADVANCED  MATERIALS   SCIENCE Volume 47, No. 1, Pages 71-77


This paper addresses fabrication, structure, and hardness characteristics of nanotwinned (ntw) copper-graphene composites. The composites were fabricated by electrodeposition from 1M CuSO4·6H2O mixed water-alcohol solution containing graphene-graphite mixture stabilized by non-ionic surfactant. We fabricated two-layer solids each consisting of ntw copper layer and ntw copper-graphene layer. The synthesized two-layer specimens were examined in nanoindentation tests and showed high hardness values up to 3 GPa. The maximum hardness value of 3 GPa is higher than those of pure ntw copper and copper-graphene composites, taken from the literature.

Dalton Transactions Issue 12, Pages 3895-3905

Anastasia I. Solomatina, Irina O. Aleksandrova, Antti J. Karttunen, Sergey P. Tunik, Igor O. Koshevoy

Dibenzothiophene-platinated complexes: probing the effect of ancillary ligands on the photophysical performance

Dalton Transactions Issue 12, Pages 3895-3905

DOI: 10.1039/C7DT00349H


Cyclometalation of dibenzothienyl-pyridine (HPyDBT) afforded a series of platinum(II) complexes Pt(PyDBT)(L)Cl (L = DMSO, 1; P(p-C6H4-X)3 (X = H, 2; CF3, 3; OMe, 4; NPh2, 5); 1,3,5-triaza-7-phosphaadamantane, 6; 2,6-dimethylphenyl isocyanide, 7). Chelating bidentate LL ligands formed cationic compounds [Pt(PyDBT)(LL)]+ (LL = 1,2-bis(diphenylphosphino)benzene, 8; 2,2’-bipyridine, 9; 1,10-phenanthroline, 10). Oxidation of a thienyl sulfur atom allowed for the isolation of the sulfone derivative Pt(PyDBT)(PPh3)Cl (11). The title complexes were characterized crystallographically (except 7). Investigation of their photophysical behavior revealed solid state phosphorescence with quantum yields up to 0.45 for neat powders. The ancillary ligands L show a minor influence on the emission energies of the neutral compounds, but affect dramatically the intensity of luminescence. In contrast, the cationic species with diimine ligands demonstrate a significant contribution of the LL fragments into the emissive T1 states that leads to a certain mixing of 3IL and 3LL’CT transitions and causes a substantial bathochromic shift of emission.