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Effects of Ag Additive in Low Temperature CO Detection with In(2)O(3) Based Gas Sensors

Nanocomposites In(2)O(3)/Ag obtained by ultraviolet (UV) photoreduction and impregnation methods were studied as materials for CO sensors operating in the temperature range 25–250 °C. Nanocrystalline In(2)O(3) and In(2)O(3)/Ag nanocomposites were characterized by X-ray diffraction (XRD), single-poin...

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Detalles Bibliográficos
Autores principales: Naberezhnyi, Daniil, Rumyantseva, Marina, Filatova, Darya, Batuk, Maria, Hadermann, Joke, Baranchikov, Alexander, Khmelevsky, Nikolay, Aksenenko, Anatoly, Konstantinova, Elizaveta, Gaskov, Alexander
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6215304/
https://www.ncbi.nlm.nih.gov/pubmed/30297657
http://dx.doi.org/10.3390/nano8100801
Descripción
Sumario:Nanocomposites In(2)O(3)/Ag obtained by ultraviolet (UV) photoreduction and impregnation methods were studied as materials for CO sensors operating in the temperature range 25–250 °C. Nanocrystalline In(2)O(3) and In(2)O(3)/Ag nanocomposites were characterized by X-ray diffraction (XRD), single-point Brunauer-Emmet-Teller (BET) method, scanning electron microscopy (SEM), transmission electron microscopy (TEM), and high angle annular dark field scanning transmission electron microscopy (HAADF-STEM) with energy dispersive X-ray (EDX) mapping. The active surface sites were investigated using Fourier-transform infrared spectroscopy (FTIR), X-ray photoelectron spectroscopy (XPS), electron paramagnetic resonance (EPR) spectroscopy and thermo-programmed reduction with hydrogen (TPR-H(2)) method. Sensor measurements in the presence of 15 ppm CO demonstrated that UV treatment leads to a complete loss of In(2)O(3) sensor sensitivity, while In(2)O(3)/Ag-UV nanocomposite synthesized by UV photoreduction demonstrates an increased sensor signal to CO at T < 200 °C. The observed high sensor response of the In(2)O(3)/Ag-UV nanocomposite at room temperature may be due to the realization of an additional mechanism of CO oxidation with participation of surface hydroxyl groups associated via hydrogen bonds.