Tin Acetylacetonate as a Precursor for Producing Gas-Sensing SnO2 Thin Films
- Authors: Simonenko E.P.1,2, Simonenko N.P.1,2, Mokrushin A.S.1, Vasiliev A.A.3, Vlasov I.S.2, Volkov I.A.2, Maeder T.2,4, Sevastyanov V.G.1, Kuznetsov N.T.1
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Affiliations:
- Kurnakov Institute of General and Inorganic Chemistry
- Moscow Institute of Physics and Technology (State University)
- National Research Center “Kurchatov Institute”
- École Polytechnique Fédérale de Lausanne, EPFL STI IMT LMIS1
- Issue: Vol 63, No 7 (2018)
- Pages: 851-860
- Section: Synthesis and Properties of Inorganic Compounds
- URL: https://journal-vniispk.ru/0036-0236/article/view/168801
- DOI: https://doi.org/10.1134/S0036023618070197
- ID: 168801
Cite item
Abstract
To expand the range of precursors used in the sol–gel technology for applying nanostructured SnO2 thin films promising as components of semiconductor chemical gas sensors, the efficiency of using tin acetylacetonate solutions with various precursor concentrations was demonstrated. It was determined that finely divided SnO2 with a crystallite size of 3–4 nm (cassiterite) can be obtained by hydrolysis by atmospheric moisture in the course of solvent evaporation at room temperature. Using tin acetylacetonate solutions with various precursor concentrations for applying SnO2 thin films by dip coating to the surface of rough ceramic Al2O3-based substrates with platinum interdigital electrodes and a microheater resulted in significant differences in microstructure, continuity, thickness, and porosity of the produced coatings. In a lower-concentration (0.13 mol/L) tin acetylacetonate solution, a multilayer dense continuous SnO2 coating was applied, whereas in a higher-concentration (0.25 mol/L) solution, the formed layer comprised aggregated nanoparticles 30–60 nm in size and had much more defects and higher porosity. The sensitivity of the obtained thin-film nanostructures to the most practically important gaseous analytes: CO, H2, CH4, CO2, and NO2. The produced two-dimensional nanomaterials were shown to be promising for detecting carbon monoxide at 200–300°C in dry air.
About the authors
E. P. Simonenko
Kurnakov Institute of General and Inorganic Chemistry; Moscow Institute of Physics and Technology (State University)
Author for correspondence.
Email: ep_simonenko@mail.ru
Russian Federation, Moscow, 119991; Dolgoprudnyi, Moscow oblast, 141701
N. P. Simonenko
Kurnakov Institute of General and Inorganic Chemistry; Moscow Institute of Physics and Technology (State University)
Email: ep_simonenko@mail.ru
Russian Federation, Moscow, 119991; Dolgoprudnyi, Moscow oblast, 141701
A. S. Mokrushin
Kurnakov Institute of General and Inorganic Chemistry
Email: ep_simonenko@mail.ru
Russian Federation, Moscow, 119991
A. A. Vasiliev
National Research Center “Kurchatov Institute”
Email: ep_simonenko@mail.ru
Russian Federation, Moscow, 123182
I. S. Vlasov
Moscow Institute of Physics and Technology (State University)
Email: ep_simonenko@mail.ru
Russian Federation, Dolgoprudnyi, Moscow oblast, 141701
I. A. Volkov
Moscow Institute of Physics and Technology (State University)
Email: ep_simonenko@mail.ru
Russian Federation, Dolgoprudnyi, Moscow oblast, 141701
T. Maeder
Moscow Institute of Physics and Technology (State University); École Polytechnique Fédérale de Lausanne, EPFL STI IMT LMIS1
Email: ep_simonenko@mail.ru
Russian Federation, Dolgoprudnyi, Moscow oblast, 141701; BM 3108 (Bâtiment BM), Station 17, Lausanne, CH-1015
V. G. Sevastyanov
Kurnakov Institute of General and Inorganic Chemistry
Email: ep_simonenko@mail.ru
Russian Federation, Moscow, 119991
N. T. Kuznetsov
Kurnakov Institute of General and Inorganic Chemistry
Email: ep_simonenko@mail.ru
Russian Federation, Moscow, 119991
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