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1.
Int J Mol Sci ; 24(18)2023 Sep 13.
Artigo em Inglês | MEDLINE | ID: mdl-37762351

RESUMO

Thin-film nanocrystalline hematite electrodes were fabricated by electrochemical deposition and loaded with electrodeposited zinc oxide in various amounts. Under visible light illumination, these electrodes demonstrate high activity in the photoelectrochemical degradation of methanol, ethylene glycol and, in particular, glycerol. Results of intensity-modulated photocurrent spectroscopy show that the photoelectrocatalysis efficiency is explained by the suppression of the electron-hole pair recombination and an increase in the rate of photo-induced charge transfer. Thus, zinc oxide can be considered an effective modifying additive for hematite photoanodes.


Assuntos
Óxido de Zinco , Filmes Cinematográficos , Eletrodos , Elétrons
2.
Micromachines (Basel) ; 14(4)2023 Mar 24.
Artigo em Inglês | MEDLINE | ID: mdl-37420958

RESUMO

At present, a new class of 2D nanomaterials, MXenes, is of great scientific and applied interest, and their application prospects are very broad, including as effective doping components for receptor materials of MOS sensors. In this work we have studied the influence on the gas-sensitive properties of nanocrystalline zinc oxide synthesized by atmospheric pressure solvothermal synthesis, with the addition of 1-5% of multilayer two-dimensional titanium carbide Ti2CTx, obtained by etching Ti2AlC with NaF solution in hydrochloric acid. It was found that all the obtained materials have high sensitivity and selectivity with respect to 4-20 ppm NO2 at a detection temperature of 200 °C. It is shown that the selectivity towards this compound is best for the sample containing the highest amount of Ti2CTx dopant. It has been found that as the MXene content increases, there is an increase in nitrogen dioxide (4 ppm) from 1.6 (ZnO) to 20.5 (ZnO-5 mol% Ti2CTx). reactions which the responses to nitrogen dioxide increase. This may be due to the increase in the specific surface area of the receptor layers, the presence of MXene surface functional groups, as well as the formation of the Schottky barrier at the interface between the phases of the components.

3.
Biosensors (Basel) ; 13(4)2023 Mar 31.
Artigo em Inglês | MEDLINE | ID: mdl-37185520

RESUMO

ZnO/Fe2O3 nanocomposites with different concentration and thickness of the Fe2O3 layer were obtained by two-stage aerosol vapor deposition (AACVD). It was shown that the ZnO particles have a wurtzite structure with an average size of 51-66 nm, and the iron oxide particles on the ZnO surface have a hematite structure and an average size of 23-28 nm. According to EDX data, the iron content in the films was found to be 1.3-5.8 at.%. The optical properties of the obtained films were studied, and the optical band gap was found to be 3.16-3.26 eV. Gas-sensitive properties at 150-300 °C were studied using a wide group of analyte gases: CO, NH3, H2, CH4, C6H6, ethanol, acetone, and NO2. A high response to 100 ppm acetone and ethanol at 225-300 °C and a high and selective response to 300-2000 ppb NO2 at 175 °C were established. The effect of humidity on the magnitude and shape of the signal obtained upon NO2 detection was studied.


Assuntos
Nanocompostos , Óxido de Zinco , Óxido de Zinco/química , Dióxido de Nitrogênio , Acetona , Gases , Biomarcadores , Pulmão
4.
Dalton Trans ; 48(23): 8410-8417, 2019 Jun 21.
Artigo em Inglês | MEDLINE | ID: mdl-31115411

RESUMO

A set of silver(i) 3,5-bis(trifluoromethyl) pyrazolate adducts with 1,10-phenanthroline (L2), 2,9-dimethyl-1,10-phenanthroline (neocuproine, L3) and 2,9-dimethyl-4,7-diphenyl-1,10-phenanthroline (bathocuproine, L4) was synthesized starting from trimeric silver pyrazolate Ag3Pz3. Reactions with sterically hindered L3 and L4 cause the destruction of the original trimeric core, yielding a dinuclear Ag2Pz2 cycle with an unprecedented chair configuration for L3, while bathocuproine L4 leads to the drastic rearrangement of the silver pyrazolate core into cationic Ag(L4)2 and anionic Ag5Pz6 subunits. All complexes obtained exhibit phosphorescence in the solid state. Time-dependent density functional theory calculations demonstrate their different possible emission processes, explaining their emission behavior as well as their lifetimes.

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