28 results
Search Results
Now showing 1 - 10 of 28
Article Citation - WoS: 8Effect of H2o Ratio on Photocatalytic Activity of Sol-Gel Tio2 Powder(Ice Publishing, 2013) Agartan, Lutfi; Kapusuz, Derya; Park, Jongee; Ozturk, AbdullahEffect of water/tetraethyl orthotitanate molar ratio (R) on the formation and morphology of sol-gel-derived titania powder has been studied. Solutions for R of 3 and 5 have been prepared. Initial viscosity of the solutions and viscosity of the gels prepared by aging the solutions for some time were measured. Results revealed that lower gel viscosities lead to better crystallization of the aerogel. Aerogels were dried at 80 degrees C for 24 h and then calcined at 300 degrees C for 1 h to obtain titania powders. The structural and morphological analyses of the powders were performed using X-ray diffraction and scanning electron microscopic characterization techniques. Titania particles obtained after calcination composed of only anatase phase and were in the size range of 9-50 nm. The photocatalytic activity of the powders was evaluated in terms of the degradation of methylene blue (MB) solution under UV (ultraviolet) illumination. A diffuse reflectance spectroscopy was used for the band gap energy measurements. Results revealed that R had a profound effect on the particle morphology and photocatalytic activity of sol-gel-derived titania powders. The titania powders prepared from the solution for R of 5 degraded 99.47% of MB solution under UV illumination in 90 min.Article Citation - WoS: 44Citation - Scopus: 43Sol-Gel Synthesis and Photocatalytic Activity of B and Zr Co-Doped Tio2(Pergamon-elsevier Science Ltd, 2013) Kapusuz, Derya; Park, Jongee; Ozturk, AbdullahEffects of boron (B) and/or zirconium (Zr) doping on photocatalytic activity of sol-gel derived titania (TiO2) powders were investigated. A conventional, non-hydrous sol-gel technique was applied to synthesize the B, Zr doped/co-doped TiO2 powders. Doping was made at molar ratios of Ti/B=1 and Ti/Zr=10. Sol-gel derived xero-gels were calcined at 500 degrees C for 3 h. The crystal chemistry and the morphology of the undoped and B, Zr doped/co-doped TiO2 nanoparticles were investigated using X-ray diffractometer and scanning electron microscope. Nano-scale (9-46 nm) TiO2 crystallites were obtained after calcination. Doping and co-doping decreased the crystallite size. Photocatalytic activity was measured through the degradation of methylene blue (MB) under 1 h UV-irradiation using a UV-vis spectrophotometer. Results revealed that B doping into anatase caused the formation of oxygen vacancies, whereas Zr addition caused Ti substitution. Both B and Zr ions had a profound effect on the particle morphology and photocatalytic activity of TiO2. The photocatalytic activity of B and Zr doped TiO2 particles increased from 27% to 77% and 57%, respectively. The best activity (88.5%) was achieved by co-doping. (C) 2013 Elsevier Ltd. All rights reserved.Conference Object Citation - WoS: 1PRODUCTION OF SILVER LOADED PHOTOCATALYTIC TIO2 POWDERS BY BALL MILLING(Tanger Ltd, 2011) Aysin, Basak; Park, Jongee; Ozturk, AbdullahThe present study was undertaken to improve photocatalytic efficiency of TiO2 powder by silver doping and/or particle size reduction through mechanical ball milling. A planetary ball mill was employed to reduce the particle size of TiO2 powders to nanoscale and silver loading to TiO2 powders. Silver nitrate was used as silver source to obtain about 1% Ag load. Slurry taken from ball mill was separated by centrifugal separator into nano and micro sols. Separated nanosol was taken into the furnace to be dried at 103 degrees C and calcined at 400 degrees C for 1 hour to assist silver loading. X-Ray powder diffraction (XRD) was employed to identify the crystalline phases present in the powders produced. XRD results revealed that doped TiO2 powders were consisted of only anatase phase of TiO2. Changes in lattice parameters of TiO2 structure after doping were determined also by XRD. Scanning Electron Microscope (SEM) and particle size analyzer were used for examining the size reduction effect of ball milling process. Photocatalytic performance of the powders was evaluated by Methylene Orange (MO) test under UV light illumination using UV-Spectrophotometer.Article Citation - WoS: 11Citation - Scopus: 10Synthesis and Characterization of Hydrothermally Grown Potassium Titanate Nanowires(Korean Assoc Crystal Growth, inc, 2015) Kapusuz, Derya; Kalay, Y. Eren; Park, Jongee; Ozturk, Abdullah; Metallurgical and Materials EngineeringPotassium titanate (KT) nanowires were synthesized by a one-step hydrothermal reaction between TiO2 and aqueous KOH solution. The effects of KOH concentration and reaction time on hydrothermal formation and KT nanowire growth were investigated. The nanowire growth mechanism was elucidated using a combined study of powder X-ray diffraction, and scanning and transmission electron microscopy. The results revealed that hydrothermal growth was initiated by the formation of amorphous-like Ti-O-K sheets in anatase. Increasing hydrothermal reaction time caused the transformation of anatase to Ti-O-K sheets, from which potassium hexa-titanate (K2Ti6O13) nuclei formed and grew to establish one-dimensional morphology through preferential growth along the b-axis. It was revealed that the hydrothermal reactions followed a quite different mechanism than the well-known calcination route. Potassium tetra-titanate (K2Ti4O9) crystals formed in the amorphous region using the hexa-titanate phase as a nucleation site for heterogeneous crystallization. Increasing the KOH concentration in the solution accelerated the hydrothermal reaction rate.Article Citation - WoS: 10Alkaline Hydrothermal Synthesis, Characterization, and Photocatalytic Activity of Tio2 Nanostructures: the Effect of Initial Tio2 Phase(Amer Scientific Publishers, 2019) Erdogan, Nursev; Park, Jongee; Choi, Woohyuk; Kim, Soo Young; Ozturk, AbdullahOne-dimensional (1D) titanate nanostructures were synthesized by hydrothermal route, using commercially available TiO2 (P25) and anatase powders as precursor materials and strong NaOH solution as catalyzer. The prepared titanates were calcined, followed by protonation to produce TiO2 nanostructures having enhanced photocatalytic and photovoltaic properties. The synthesized TiO2 1D nanostructures were characterized using field-emission scanning electron microscope, high-resolution electron microscope, X-ray diffraction analysis, and UV-Vis photospectroscopy to understand the effect of initial TiO2 phase on morphological and crystallographic features, and bandgap. Methylene blue degradation test was applied to evaluate the photoactivity of the products obtained after different stages of the process. The findings indicate that 1D TiO2 nanostructures form by different mechanisms from dissolved aggregates during hydrothermal process, depending on the crystal structure of the initial precursor used. Photocatalytic test results reveal that protonated titanates have considerable adsorption capability, while photocatalytic degradation depends on TiO2 transformation.Article Citation - WoS: 31Citation - Scopus: 37Effect of Initial Water Content and Calcination Temperature on Photocatalytic Properties of Tio2 Nanopowders Synthesized by the Sol-Gel Process(Elsevier Sci Ltd, 2015) Agartan, Lutfi; Kapusuz, Derya; Park, Jongee; Ozturk, AbdullahThe effects of initial water content and calcination temperature on sol gel synthesized TiO2 powders were studied. Mother solutions had water/Ti-precursor mole ratios (R ratio) of 1, 5, 10, and 50. Dried aerogels were calcined for 3 h at temperatures of 300, 400, and 500 degrees C to obtain crystallized TiO2 nanopowders in the range of 15-30 nm. PE-scanning electron microscopy and X-ray diffraction techniques were employed to investigate the morphological and structural properties of the nanopowders synthesized. Profound effect of gel viscosity was observed on the formation mechanism and extent of crystallinity in the powders. Methylene blue degradation test results suggest, photocatalytic performance is enhanced as initial water content and calcination temperature increased. Band-gap energy of the powders ranged from 3.09 to 3.27 eV. Overall, this study shows that initial water content and calcination regime have a profound effect on the phase assembly, crystallite size, band-gap energy, and photocatalytic performance of sol gel synthesized TiO2 nanopowders. (C) 2015 Elsevier Ltd and Techna Group S.r.l. All rights reserved.Conference Object Citation - WoS: 2Citation - Scopus: 4Influence of Boron And/Or Zirconium Doping on Morphology and Optical Properties of Titania(Tanger Ltd, 2011) Kapusuz, Derya; Park, Jongee; Ozturk, Abdullah; Metallurgical and Materials EngineeringSol-gel derived B (boron) and Zr (zirconium) doped TiO2 (Titania) nanoparticles were synthesized. Microstructural, photocatalytic and crystallographic properties of the doped particles were investigated. Highest photocatalytic activity was achieved by 10 wt% Zr doping. 5 wt% doping was the optimum value for effective B doping. B ions were found to form oxygen vacancies behaving as interstitial defects whereas Zr ions substituted Ti4+ ions in the lattice.Article Citation - WoS: 23Citation - Scopus: 27Facile synthesis of CsPbBr3/PbSe composite clusters(Taylor & Francis Ltd, 2018) Thang Phan Nguyen; Ozturk, Abdullah; Park, Jongee; Sohn, Woonbae; Tae Hyung Lee; Jang, Ho Won; Kim, Soo YoungIn this work, CsPbBr3 and PbSe nanocomposites were synthesized to protect perovskite material from self-enlargement during reaction. UV absorption and photoluminescence (PL) spectra indicate that the addition of Se into CsPbBr3 quantum dots modified the electronic structure of CsPbBr3, increasing the band gap from 2.38 to 2.48 eV as the Cs:Se ratio increased to 1:3. Thus, the emission color of CsPbBr3 perovskite quantum dots was modified from green to blue by increasing the Se ratio in composites. According to X-ray diffraction patterns, the structure of CsPbBr3 quantum dots changed from cubic to orthorhombic due to the introduction of PbSe at the surface. Transmission electron microscopy and X-ray photoemission spectroscopy confirmed that the atomic distribution in CsPbBr3/PbSe composite clusters is uniform and the composite materials were well formed. The PL intensity of a CsPbBr3/PbSe sample with a 1:1 Cs: Se ratio maintained 50% of its initial intensity after keeping the sample for 81 h in air, while the PL intensity of CsPbBr3 reduced to 20% of its initial intensity. Therefore, it is considered that low amounts of Se could improve the stability of CsPbBr3 quantum dots.Article Citation - WoS: 49Citation - Scopus: 55Synthesis of Α-fe2o3< Heterogeneous Composites by the Sol-Gel Process and Their Photocatalytic Activity(Elsevier Science Sa, 2020) Bouziani, Asmae; Park, Jongee; Ozturk, Abdullahalpha-Fe2O3/TiO2 heterogeneous composites were synthesized by the sol-gel process to increase the photocatalytic activity of TiO2. The structural, morphological, and optical characteristics of the composites were determined by X-ray diffraction, scanning electron microscope, and UV-vis diffuse reflectance spectroscopy. Results revealed that the incorporation of alpha-Fe2O3 to TiO2 widened the visible light absorption ability of TiO2. It was realized that the calcination temperature plays a crucial role in morphology development hence photocatalytic activity of the alpha-Fe2O3/TiO2 heterogeneous composites. The photocatalytic activity of the composites calcined at various temperatures was evaluated for the degradation of Methylene Blue (MB) and Phenol (Ph) in aqueous medium under UV and sun-like illuminations. The alpha-Fe2O3-TiO2 composites exhibits superior photocatalytic efficiency to degrade both MB and Ph as compared to both pristine TiO2 and pristine alpha-Fe2O3 under sun-like illumination. The alpha-Fe2O3/TiO2 composite degraded approximately 90 % of MB and 50 % of Ph in 180 min sun-like illumination. Improvement in photocatalytic activity is attributed to the separation of photogenerated electron/hole pairs through the interaction of alpha-Fe(2)O(3 )and TiO2.Article Citation - WoS: 44Citation - Scopus: 54Preparation and Photocatalytic Activity of G-c3n4< Heterojunctions Under Solar Light Illumination(Elsevier Sci Ltd, 2020) Gundogmus, Pelin; Park, Jongee; Ozturk, AbdullahThe solar light sensitive g-C3N4/TiO2 heterojunction photocatalysts containing 20, 50, 80, and 90 wt% graphitic carbon nitride (g-C3N4) were prepared by growing Titania (TiO2) nanoparticles on the surfaces of g-C3N4 particles via one step hydrothermal process. The hydrothermal reactions were allowed to take place at 110 degrees C at autogenous pressure for 1 h. Raman spectroscopy analyses confirmed that an interface developed between the surfaces of TiO2 and g-C3N4 nanoparticles. The photocatalyst containing 80 wt% g-C3N4 was subsequently heat treated 1 h at temperatures between 350 and 500 degrees C to improve the photocatalytic efficiency. Structural and optical properties of the prepared g-C3N4/TiO2 heterojunction nanocomposites were compared with those of the pristine TiO2 and pristine g-C(3)N(4 )powders. Photocatalytic activity of all the nanocomposites and the pristine TiO2 andg-C3N4 powders were assessed by the Methylene Blue (MB) degradation test under solar light illumination. g-C3N4/TiO2 heterojunction photocatalysts exhibited better photocatalytic activity for the degradation of MB than both pristine TiO2 and g-C3N4. The photocatalytic efficiency of the g-C3N4/TiO2 heterojunction photocatalyst heat treated at 400 degrees C for 1 his 1.45 times better than that of the pristine TiO2 powder, 2.20 times better than that of the pristine g-C3N4 powder, and 1.24 times better than that of the commercially available TiO2 powder (Degussa P25). The improvement in photocatalytic efficiency was related to i) the generation of reactive oxidation species induced by photogenerated electrons, ii) the reduced recombination rate for electron-hole pairs, and iii) large specific surface area.
- «
- 1 (current)
- 2
- 3
- »