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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.Article Citation - WoS: 25Citation - Scopus: 26Identifying the Potentials for Charge Transport Layers Free N-P Homojunction-Based Perovskite Solar Cells(Pergamon-elsevier Science Ltd, 2022) Khan, Danish; Sajid, Sajid; Khan, Suliman; Park, Jongee; Ullah, IhsanPerovskite solar cells (PSCs) with no charge transport layers (CTLs) could be one of the major device architectures for the production of simple and low-cost devices. However, CTLs-free PSCs based on n-p homojunction have yet to show high power conversion efficiency (PCE), which is most likely due to inadequate light-and charge-management in the p-type perovskite. The device operation is examined using Solar Cell Capacitance Simulator (SCAPS)-software, and a novel n-p homojunction design is proposed to attempt efficient CTLs-free PSCs. Several aspects of p-type layer that can affect device performance, such as acceptor density, photon harvesting capability, defects density, and resistances to the transport of charge-carriers are scrutinized and adjusted. Furthermore, the effects of different work-functions of metal electrodes are examined. A suitable acceptor concentration is required for oriented charge transport. It is determined that a p-type perovskite with a thickness of 0.3 mu m is advantageous for high performance. A metal electrode with a high work-function is essential for efficient device. Consequently, a PCE of 15.60% is obtained with an optimal defect density of E15 cm(-3), indicating that n-p homojunction-based CTLs-free PSCs are promising since they simplify the device design and fabrication process while retaining an acceptable PCE.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: 4Citation - Scopus: 5In Vitro Evaluation of Tooth-Colored Yttria Stabilized Zirconia Ceramics(Taylor & Francis Ltd, 2021) Akarsu, Melis Kaplan; Basar, Ahmet Ozan; Sasmazel, Hilal Turkoglu; Park, Jongee; Ozturk, AbdullahEffects of MoCl3 and NiCl2, originally incorporated as coloring agent, on the cellular response of 3 mol% yttria stabilized zirconia (3Y-TZP) ceramics was investigated. MoCl3 and NiCl2-MoCl3 incorporated, tooth-colored 3Y-TZP ceramics were produced through cold isostatic pressing at 100 MPa followed by pressureless sintering at 1450 degrees C for 2 h. Aging was performed on the sintered ceramics using distilled water in a reactor at 134 degrees C at 2.3 bar pressure for 2 h. The phases developed during different stages of processing were identified by X-ray diffraction (XRD) analysis. In vitro cell culture studies were carried out using L929 fibroblast cell line. The cell viability and proliferation studies revealed that none of the specimens showed cytotoxicity with respect to coloring. Confocal laser scanning microscope (CLSM) analyses suggested that all of the specimens exhibited good in vitro cytocompatibility. Enhancement in cell attachment, adhesion, and proliferation was observed in all specimens via scanning electron microscope (SEM) analysis. Although the coloring process did not improve the proliferation performance of the aged specimens, the incorporation of transition metals enhanced the in vitro performance of 3Y-TZP ceramics.Article Calcium Phosphate Honeycomb Scaffolds With Tailored Microporous Walls Using Phase Separation-Assisted Digital Light Processing(MDPI, 2025) Kim, Gyu-Nam; Park, Jae-Hyung; Song, Jae-Uk; Koh, Young-Hag; Park, JongeeThe present study reports on the manufacturing of biphasic calcium phosphate (BCP) honeycomb scaffolds with tailored microporous walls using phase separation-assisted digital light processing (PS-DLP). To create micropores in BCP walls, camphene was used as the pore-forming agent for preparing BCP suspensions, since it could be completely dissolved in photopolymerizable monomers composed of triethylene glycol dimethacrylate (TEGDMA) and polyethylene glycol diacrylate (PEGDA) and then undergo phase separation when placed at 5 degrees C. Therefore, solid camphene crystals could be formed in phase-separated BCP layers and then readily removed via sublimation after the photopolymerization of monomer networks embedding BCP particles by DLP. This approach allowed for tight control over the microporosity of BCP walls by adjusting the camphene content. As the camphene content increased from 40 to 60 vol%, the microporosity increased from similar to 38 to similar to 59 vol%. Consequently, the overall porosity of dual-scale porosity scaffolds increased from similar to 51 to similar to 67 vol%, while their compressive strength decreased from similar to 70.4 to similar to 13.7 MPa. The mass transport ability increased remarkably with an increase in microporosity.Article Citation - WoS: 6Citation - Scopus: 6Diethanolamine Modified Perovskite-Substrate Interface for Realizing Efficient Esl-Free Pscs(Mdpi, 2023) Sajid, Sajid; Alzahmi, Salem; Wei, Dong; Ben Salem, Imen; Park, Jongee; Obaidat, Ihab M.Simplifying device layout, particularly avoiding the complex fabrication steps and multiple high-temperature treatment requirements for electron-selective layers (ESLs) have made ESL-free perovskite solar cells (PSCs) attractive. However, the poor perovskite/substrate interface and inadequate quality of solution-processed perovskite thin films induce inefficient interfacial-charge extraction, limiting the power conversion efficiency (PCEs) of ESL-free PSCs. A highly compact and homogenous perovskite thin film with large grains was formed here by inserting an interfacial monolayer of diethanolamine (DEA) molecules between the perovskite and ITO substrate. In addition, the DEA created a favorable dipole layer at the interface of perovskite and ITO substrate by molecular adsorption, which suppressed charge recombination. Comparatively, PSCs based on DEA-treated ITO substrates delivered PCEs of up to 20.77%, one of the highest among ESL-free PSCs. Additionally, this technique successfully elongates the lifespan of ESL-free PSCs as 80% of the initial PCE was maintained after 550 h under AM 1.5 G irradiation at ambient temperature.Article Citation - WoS: 19Citation - Scopus: 19Antisolvent-Fumigated Grain Growth of Active Layer for Efficient Perovskite Solar Cells(Pergamon-elsevier Science Ltd, 2021) Sajid, Sajid; Khan, Suliman; Khan, Ayub; Khan, Danish; Issakhov, Alibek; Park, JongeeHigh efficiency of perovskite solar cell can be obtained through various approaches, including materials and interface engineering, device modification and fabrication techniques. In all approaches, the quality of the perovskite layer has a significant impact on the efficiency of the perovskite solar cell. Antisolvent dripping is widely used in almost all fabrication methodologies to achieve a high-quality perovskite layer. However, in the conventional antisolvent dripping, there are several factors (antisolvent volume, time and point of dripping, etc.) to be strictly followed. Due to these difficult and critical tricks, researchers often get perovskite layers with pinholes, small grains, and wide grain boundaries that deteriorate the performance of the perovskite solar cells. In order to produce perovskite films with large-scale grains, narrow boundaries and smooth surface morphology, a sealed antisolvent-fumigated process is implemented. There is no need to make any substantial efforts to achieve optimal conditions for the fabrication of high-quality perovskite layers using the antisolvent-fumigated strategy. Consequently, the efficiency of perovskite solar cell improves dramatically from 18.65% to 21.45%. Our findings present a new and convenient method for fabricating highly efficient perovskite solar cells.Article Citation - WoS: 17Citation - Scopus: 17Effects of Fluorination and Thermal Shock on the Photocatalytic Activity of Bi2o3< Nanopowders(Elsevier, 2021) Bouziani, Asmae; Park, Jongee; Ozturk, AbdullahFluorinated Bi2O3 (F-Bi2O3) nanopowder was prepared via fluorination followed by thermal shock of alpha-Bi2O3 nanopowder. The XRD, FTIR, SEM, and DRS characterization techniques were employed to investigate the effects of fluorine (F) insertion into the alpha-Bi2O3 host and the thermal shock from different temperatures. The crystal structure, optical and photocatalytic properties of the F-Bi2O3 nanopowders prepared were researched. The XRD results confirmed the substitution of O2- with F-. The FTIR results revealed that the coordination of Bi atoms changed upon F- substitution. The incorporation of F into the alpha-Bi2O3 host and thermal shock did not influence the morphology but modified the band structure of alpha-Bi2O3, leading to a red-shift in the optical absorption edge. Also, the bandgap narrowed from 2.8 eV to 2.6 eV. The density functional theory calculation proved that the F 2p orbitals were positioned in the valence band (VB), resulting in broader and more spread bands for F-Bi2O3. The results suggested that the photoexcited charge carrier mobility in the valence band (VB) and conduction band (CB) are enhanced upon F insertion into alpha-Bi2O3. The photocatalytic efficiency of the synthesized nanopowders was assessed by the degradation of Bromocresol Green (BG) under visible light illumination. Photocatalytic activity improved upon fluorination. The F-Bi2O3 nanopowders thermally shocked from higher temperatures showed negligible photocatalytic performance. The best photocatalytic performance of 70% BG degradation was realized after 180 min visible irradiation for the F-Bi2O3 nanopowder thermal shocked from 500 degrees C.Article Citation - WoS: 11Citation - Scopus: 14Tribological Behavior of Alumina-Added Apatite-Wollastonite Glass-Ceramics in Simulated Body Fluid(Elsevier Science Sa, 2010) Park, Jongee; You, Sang-Hee; Shin, Dong-Woo; Ozturk, AbdullahTribological properties of an alumina-added apatite-wollastonite glass-ceramic produced by controlled heat treatment of a glass in the system MgO-CaO-SiO(2)-P(2)O(5)-Al(2)O(3) have been evaluated and compared with those of selected commercial dental ceramics, Duceragold and IPS Empress. Tribological tests were performed in dry condition and in simulated body fluid (SBF) using a pin-on-disk apparatus. The friction coefficient and specific wear rate of the tested materials were measured in dry and in artificial saliva (simulated body fluid: SBF) in order to elucidate the appropriateness of the alumina-added apatite-wollastonite (A-W) glass-ceramic for dental applications. Wear rate of the materials investigated varied from 0.96 x 10(-4) mm(3) N(-1) m to 41.37 x 10(-4) mm(3) N(-1) m depending on the bioenvironmental test conditions. The results of this study revealed that the alumina-added A-W glass-ceramic becomes more wear resistant as sintering temperature is increased and exhibits tribological properties similar to those of the commercial dental materials investigated. (C) 2010 Elsevier B.V. All rights reserved.Article Citation - WoS: 18Citation - Scopus: 19Synthesis and Enhanced Photocatalytic Activity of Nitrogen-Doped Triphasic Tio2 Nanoparticles(Elsevier Science Sa, 2019) Erdogan, Nursev; Bouziani, Asmae; Park, Jongee; Micusik, Matej; Kim, Soo Young; Majkova, Eva; Ozturk, AbdullahTiO2 nanoparticles of the single anatase phase, binary anatase-brookite phases, and ternary anatase-brookite-rutile phases were synthesized using an HNO3-catalyzed hydrothermal process. The types and amounts of phases varied depending on the hydrothermal synthesis conditions. The results revealed that N dissolves in different amounts and chemical states, depending on the phases present and their proportions in the nano particles. Brookite and rutile nanoparticles oriented through one direction were found to be crystallized by the surface transformation from anatase. Photocatalytic activity tests, evaluated by degradation of methylene blue (MB) under ultraviolet (UV) and visible light illumination, revealed that the N-doped TiO2 nanoparticles containing a ternary-phase mixture had the best photocatalytic activity. The MB degradation of the visible light-active nanoparticles was three times better than that of a commercially available well-known TiO2 powder, P25 under UV illumination. The enhanced photoactivity was attributed to the following: i) a high surface area, ii) suppression of the recombination of electron-hole pairs with ternary-phase mixture crystallized in heterojunctions, iii) larger anatase phase content, and iv) narrower band gap and facilitation of charge separation by dissolved N atoms.
