Browsing by Subject "Oxide minerals"

Now showing 1 - 8 of 8

Open Access
A baseball-bat-like CdTe/TiO2 nanorods-based heterojunction core–shell solar cell
(Elsevier, 2013) Karaagac, H.; Parlak, M.; Aygun, L. E.; Ghaffari, M.; Bıyıklı, Necmi; Okyay, Ali Kemal
Rutile TiO2 nanorods on fluorine-doped thin oxide glass substrates via the hydrothermal technique were synthesized and decorated with a sputtered CdTe layer to fabricate a core-shell type n-TiO2/p-CdTe solar cell. Absorbance spectrum verified the absorption contribution of both TiO2 and CdTe to the absorption process. The solar cell parameters, such as open circuit voltage, short circuit current density, fill factor and power conversion efficiency were found to be 0.34 V, 1.27 mA cm-2, 28% and 0.12%, respectively. .
Open Access
Excitation dependent recombination studies on SnO2/TiO2 electrospun nanofibers
(Royal Society of Chemistry, 2015) Babu, V. J.; Vempati S.; Ertas Y.; Uyar, Tamer
Poly(vinyl acetate) (PVAc)/TiO2 nanofibers, PVAc/SnO2 nanoribbons and PVAc/SnO2-TiO2 nanoribbons were produced via electrospinning. TiO2 nanofibers and SnO2 nanoribbons were obtained by removal of the polymeric matrix (PVAc) after calcination at 450 °C. Interestingly, PVAc/SnO2-TiO2 nanoribbons were transformed into SnO2-TiO2 nanofibers after calcination under the similar conditions. Fiber morphology and elemental mapping confirmed through SEM and TEM microscope techniques respectively. The X-ray diffraction measurements suggested the presence of anatase TiO2 and rutile SnO2 and both were present in the SnO2-TiO2 mixed system. Systematic photoluminescence studies were performed on the electrospun nanostructures at different excitation wavelengths (λex1 = 325, λex2 = 330, λex3 = 350, λex4 = 397 and λex5 = 540 nm). We emphasize that the defects in the SnO2-TiO2 based on the defect levels present in TiO2 and SnO2 and anticipate that these defect levels may have great potential in understanding and characterizing various semiconducting nanostructures.
Open Access
Imaging capability of pseudomorphic high electron mobility transistors, AlGaN/GaN, and Si micro-Hall probes for scanning Hall probe microscopy between 25 and 125 °c
(American Vacuum Society, 2009) Akram, R.; Dede, M.; Oral, A.
The authors present a comparative study on imaging capabilities of three different micro-Hall probe sensors fabricated from narrow and wide band gap semiconductors for scanning hall probe microscopy at variable temperatures. A novel method of quartz tuning fork atomic force microscopy feedback has been used which provides extremely simple operation in atmospheric pressures, high-vacuum, and variable-temperature environments and enables very high magnetic and reasonable topographic resolution to be achieved simultaneously. Micro-Hall probes were produced using optical lithography and reactive ion etching process. The active area of all different types of Hall probes were 1×1 μ m2. Electrical and magnetic characteristics show Hall coefficient, carrier concentration, and series resistance of the hall sensors to be 10 mG, 6.3× 1012 cm-2, and 12 k at 25 °C and 7 mG, 8.9× 1012 cm-2 and 24 k at 125 °C for AlGaNGaN two-dimensional electron gas (2DEG), 0.281 mG, 2.2× 1014 cm-2, and 139 k at 25 °C and 0.418 mG, 1.5× 1014 cm-2 and 155 k at 100 °C for Si and 5-10 mG, 6.25× 1012 cm-2, and 12 k at 25 °C for pseudomorphic high electron mobility transistors (PHEMT) 2DEG Hall probe. Scan of magnetic field and topography of hard disc sample at variable temperatures using all three kinds of probes are presented. The best low noise image was achieved at temperatures of 25, 100, and 125 °C for PHEMT, Si, and AlGaNGaN Hall probes, respectively. This upper limit on the working temperature can be associated with their band gaps and noise associated with thermal activation of carriers at high temperatures.
Open Access
Photocatalytic conversion of nitric oxide on titanium dioxide: cryotrapping of reaction products for online monitoring by mass spectrometry
(American Chemical Society, 2016) Lu, W.; Olaitan, A. D.; Brantley, M. R.; Zekavat, B.; Erdogan, D. A.; Ozensoy, E.; Solouki, T.
Details of coupling a catalytic reaction chamber to a liquid nitrogen-cooled cryofocuser/triple quadrupole mass spectrometer for online monitoring of nitric oxide (NO) photocatalytic reaction products are presented. Cryogenic trapping of catalytic reaction products, via cryofocusing prior to mass spectrometry analysis, allows unambiguous characterization of nitrous oxide (N2O) and nitrogen oxide species (i.e., NO and nitrogen dioxide (NO2)) at low concentrations. Results are presented, indicating that the major photocatalytic reaction product of NO in the presence of titanium dioxide (TiO2) P25 and pure anatase catalysts when exposed to ultraviolet (UV) light (at a wavelength of 365 nm) is N2O. However, in the presence of rutile-rich TiO2 catalyst and UV light, the conversion of NO to N2O was less than 5% of that observed with the P25 or pure anatase TiO2 catalysts.
Open Access
Three-dimensional interaction force and tunneling current spectroscopy of point defects on rutile TiO2(110)
(American Institute of Physics Inc., 2016) Baykara, M. Z.; Mönig, H.; Schwendemann, T. C.; Ünverdi, Ö.; Altman, E. I.; Schwarz, U. D.
The extent to which point defects affect the local chemical reactivity and electronic properties of an oxide surface was evaluated with picometer resolution in all three spatial dimensions using simultaneous atomic force/scanning tunneling microscopy measurements performed on the (110) face of rutile TiO2. Oxygen atoms were imaged as protrusions in both data channels, corresponding to a rarely observed imaging mode for this prototypical metal oxide surface. Three-dimensional spectroscopy of interaction forces and tunneling currents was performed on individual surface and subsurface defects as a function of tip-sample distance. An interstitial defect assigned to a subsurface hydrogen atom is found to have a distinct effect on the local density of electronic states on the surface, but no detectable influence on the tip-sample interaction force. Meanwhile, spectroscopic data acquired on an oxygen vacancy highlight the role of the probe tip in chemical reactivity measurements.
Open Access
TiO2 thin film transistor by atomic layer deposition
(SPIE, 2013) Okyay, Ali Kemal; Oruç, Feyza B.; Çimen, Furkan; Aygün, Levent E.
In this study, TiO2 films were deposited using thermal Atomic Layer Deposition (ALD) system. It is observed that asdeposited ALD TiO 2 films are amorphous and not suitable as TFT channel material. In order to use the film as channel material, a post-annealing process is needed. Annealed films transform into a polycrystalline form containing mixed anatase and rutile phases. For this purpose, devices are annealed at 475°C and observed that their threshold voltage value is 6.5V, subthreshold slope is 0.35 V/dec, Ion/Ioff ratios 2.5×106 and mobility value is 0.672 cm2/V.s. Optical response measurements showed that devices exhibits decent performance at ultraviolet region where TiO 2 has band to band absorption mechanism. © 2013 SPIE.
Open Access
A versatile bio-inspired material platform for catalytic applications: Micron-sized "buckyball-shaped" TiO2 structures
(Royal Society of Chemistry, 2015) Erdogan, D. A.; Solouki, T.; Ozensoy, E.
A simple sol-gel synthesis method is presented for the production of micron-sized buckyball-like TiO2 architectures using naturally occurring Lycopodium clavatum (LC) spores as biotemplates. We demonstrate that by simply altering the calcination temperature and titanium(iv) isopropoxide : ethanol volume ratio, the crystal structure and surface composition of the buckyball-like TiO2 overlayer can be readily fine-tuned. After the removal of the biological scaffold, the unique surface morphology and pore structure of the LC biotemplate can be successfully transferred to the inorganic TiO2 overlayer. We also utilize photocatalytic degradation of Rhodamine B dye samples to demonstrate the photocatalytic functionality of these micron-sized buckyball-like TiO2 architectures. Moreover, we show that the photocatalytic activity of TiO2 overlayers can be modified in a controlled manner by varying the relative surface coverages of anatase and rutile domains. These results open a potential gateway for the synthesis of a variety of bio-inspired materials with unique surface properties and shapes comprised of reducible metal oxides, metal sulfides, mixed-metal oxides, and/or perovskites.
Open Access
Visualization of one-dimensional diffusion and spontaneous segregation of hydrogen in single crystals of VO2
(Institute of Physics Publishing, 2016-07) Kasirga, T. S.; Coy, J. M.; Park, J. H.; Cobden, D. H.
Hydrogen intercalation in solids is common, complicated, and very difficult to monitor. In a new approach to the problem, we have studied the profile of hydrogen diffusion in single-crystal nanobeams and plates of VO2, exploiting the fact that hydrogen doping in this material leads to visible darkening near room temperature connected with the metal-insulator transition at 65 ï¿½C. We observe hydrogen diffusion along the rutile c-axis but not perpendicular to it, making this a highly one-dimensional diffusion system. We obtain an activated diffusion coefficient ∼ 0.01 e-0.6eV/kBT cm2s-1, applicable in metallic phase. In addition, we observe dramatic supercooling of the hydrogen-induced metallic phase and spontaneous segregation of the hydrogen into stripes implying that the diffusion process is highly nonlinear, even in the absence of defects. Similar complications may occur in hydrogen motion in other materials but are not revealed by conventional measurement techniques.