Browsing by Subject "Tio2"

Now showing 1 - 4 of 4

Open Access
Au/TiO2 nanorod-based Schottky-type UV photodetectors
(Wiley, 2012-10-12) Karaagac, H.; Aygun, L. E.; Parlak, M.; Ghaffari, M.; Bıyıklı, Necmi; Okyay, Ali Kemal
TiO2 nanorods (NRs) were synthesized on fluorine-doped tin oxide (FTO) pre-coated glass substrates using hydrothermal growth technique. Scanning electron microscopy studies have revealed the formation of vertically-aligned TiO2 NRs with length of similar to 2 mu m and diameter of 110128 nm, homogenously distributed over the substrate surface. 130 nm thick Au contacts using thermal evaporation were deposited on the n-type TiO2 NRs at room temperature for the fabrication of NR-based Schottky-type UV photodetectors. The fabricated Schottky devices functioned as highly sensitive UV photodetectors with a peak responsivity of 134.8 A/W (lambda = 350 nm) measured under 3 V reverse bias. (c) 2012 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim
Open Access
Influence of the sol – gel preparation method on the photocatalytic NO oxidation performance of TiO2/Al2O3 binary oxides
(Elsevier, 2015-03-01) Soylu, A. M.; Polat, M.; Erdogan, D. A.; Erguven, H.; Ozensoy, E.; Vovk, E. I.
In the current work, TiO2/Al2O3 binary oxide photocatalysts were synthesized via two different sol-gel protocols (P1 and P2), where various TiO2 to Al2O3 mole ratios (0.5 and 1.0) and calcination temperatures (150-1000 degrees C) were utilized in the synthesis. Structural characterization of the synthesized binary oxide photocatalysts was also performed via BET surface area analysis, X-ray diffraction (XRD) and Raman spectroscopy. The photocatalytic NO(g) oxidation performances of these binary oxides were measured under UVA irradiation in a comparative fashion to that of a Degussa P25 industrial benchmark. TiO2/Al2O3 binary oxide photocatalysts demonstrate a novel approach which is essentially a fusion of NSR (NOx storage reduction) and PCO (photocatalytic oxidation) technologies. In this approach, rather than attempting to perform complete NOx reduction, NO(g) is oxidized on a photocatalyst surface and stored in the solidstate. Current results suggest that alumina domains can be utilized as active NOx capturing sites that can significantly eliminate the release of toxic NO2(g) into the atmosphere. Using either (P1) or (P2) protocols, structurally different binary oxide systems can be synthesized enabling much superior photocatalytic total NOx removal (i.e. up to 176% higher) than Degussa P25. Furthermore, such binary oxides can also simultaneously decrease the toxic NO2(g) emission to the atmosphere by 75% with respect to that of Degussa P25. There is a complex interplay between calcination temperature, crystal structure, composition and specific surface area, which dictate the ultimate photocatalytic activity in a coordinative manner. Two structurally different photocatalysts prepared via different preparation protocols reveal comparably high photocatalytic activities implying that the active sites responsible for the photocatalytic NO(g) oxidation and storage have a non-trivial nature.
Open Access
Photosensitivity enhancement with TiO2 in semitransparent light-sensitive skins of nanocrystal monolayers
(American Chemical Society, 2014) Akhavan S.; Yeltik, A.; Demir, Hilmi Volkan
We propose and demonstrate light-sensitive nanocrystal skins that exhibit broadband sensitivity enhancement based on electron transfer to a thin TiO2 film grown by atomic layer deposition. In these photosensors, which operate with no external bias, photogenerated electrons remain trapped inside the nanocrystals. These electrons generally recombine with the photogenerated holes that accumulate at the top interfacing contact, which leads to lower photovoltage buildup. Because favorable conduction band offset aids in transferring photoelectrons from CdTe nanocrystals to the TiO2 layer, which decreases the exciton recombination probability, TiO2 has been utilized as the electron-accepting material in these light-sensitive nanocrystal skins. A controlled interface thickness between the TiO2 layer and the monolayer of CdTe nanocrystals enables a photovoltage buildup enhancement in the proposed nanostructure platform. With TiO2 serving as the electron acceptor, we observed broadband sensitivity improvement across 350-475 nm, with an approximately 22% enhancement. Furthermore, time-resolved fluorescence measurements verified the electron transfer from the CdTe nanocrystals to the TiO2 layer in light-sensitive skins. These results could pave the way for engineering nanocrystal-based light-sensing platforms, such as smart transparent windows, light-sensitive walls, and large-area optical detection systems.
Open Access
SOx uptake and release properties of TiO2/Al2O3 and BaO/TiO2/Al2O3 mixed oxide systems as NOx storage materials
(Elsevier, 2012-04-30) Şentürk, G. S.; Vovk, E. I.; Zaikovskii, V. I.; Say, Z.; Soylu, A. M.; Bukhtiyarov, V. I.; Ozensoy, E.
Titania was used as a promoter to obtain novel materials in the form of TiO2/Al2O3 (Ti/Al) and BaO/TiO2/Al2O3 (Ba/Ti/Al, containing 8 wt% or 20 wt% BaO) that are relevant to NOx storage reduction (NSR) catalysis. Two different protocols (P1, P2) were utilized in the synthesis. Ti/Al(P1) manifests itself as crystallites of TiO2 on -Al2O3, while Ti/Al(P2) reveals an amorphous AlxTiyOz mixed oxide. The structures of the synthesized materials were investigated via TEM, EDX, BET analysis and XPS while the catalytic functionality/performance of these support materials upon SOx and subsequent NOx adsorption were investigated with TPD and in situ FTIR spectroscopy. Ti/Al(P1, P2) revealed a high affinity towards SOx. Overall thermal stabilities of the adsorbed SOx species and the total SOx uptake of the Ba-free samples increase in the following order: TiO2(anatase) -Al2O3 < Ti/Al(P1) < Ti/Al(P2). The superior SOx uptake of Ti/Al(P1, P2) support materials can be tentatively attributed to the increasing specific surface area upon TiO2 promotion and/or the changes in the surface acidity. Promotion of BaO/Al2O3 with TiO2 leads to the attenuation of the SOx uptake and a significant decrease in the thermal stability of the adsorbed SOx species. The relative SOx adsorption capacities of the investigated materials can be ranked as follows: 8Ba/Ti/Al(P1) < 8Ba/Ti/Al(P2) < 8Ba/Al ∼ 20Ba/Ti/Al(P1) < 20Ba/Al < 20Ba/Ti/Al(P2).