Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection
Permanent URI for this collectionhttps://hdl.handle.net/11147/7148
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Article Citation - WoS: 4Citation - Scopus: 4Polymer-Bonded Cdte Quantum Dot-Nitroxide Radical Nanoprobes for Fluorescent Sensors(Springer, 2022) Karabıyık, Merve; Ebil, ÖzgençA novel functional polymer-bonded quantum dots (QDs)-nitroxide radical complex was demonstrated. In the first part of the study, the synthesis of polymer thin films via initiated chemical vapor deposition (iCVD), functionalization of polymer thin films with amine functional groups, and attachment of QDs to polymer surface were demonstrated. Fourier transform infrared spectroscopy and energy-dispersive X-ray spectroscopy together with fluorescence spectroscopy studies revealed that aliphatic primary amine (propylamine) was very effective for the functionalization of iCVD deposited poly(glycidyl methacrylate) (pGMA) and its copolymer with diethylaminoethyl methacrylate (p(GMA-co-DEAEMA)) and also QD attachment to functionalized polymer surface. In the second part of the study, the synthesis and attachment of Quantum Dot-4Amino TEMPO (QD-4AT) nanoprobes to functionalized pGMA thin films and feasibility of using them as fluorescent sensor structures were investigated. It was found that high initial 4AT concentration and long (24 h) interaction times are beneficial for nanoprobe synthesis. Electron paramagnetic resonance (EPR) spectroscopy analysis revealed the existence of covalent bond between QD and 4AT when 1-ethyl-3-(3-dimethylaminopropyl) carbodiimide was used during synthesis. EPR analysis together with fluorescence microscopy investigation confirmed the successful attachment of nanoprobes to polymer surface. Time-depended fluorescence quenching analysis revealed that more than 50% reduction in fluorescence intensity within 15 min demonstrating the potential of polymer bonded QD-4AT nanoprobes in various sensor applications.Article Citation - WoS: 3Citation - Scopus: 5Physically Unclonable Security Patterns Created by Electrospinning, and Authenticated by Two-Step Validation Method(IOP Publishing, 2022) Taşcıoğlu, Didem; Atçı, Arda; Sevim Ünlütürk, Seçil; Özçelik, SerdarCounterfeiting is a growing economic and social problem. For anticounterfeiting, random and inimitable droplet/fiber patterns were created by the electrospinning method as security tags that are detectable under UV light but invisible in daylight. To check the authenticity of the original security patterns created; images were collected with a simple smartphone microscope and a database of the recorded original patterns was created. The originality of the random patterns was checked by comparing them with the patterns recorded in the database. In addition, the spectral signature of the patterns in the droplet/fiber network was obtained with a simple and hand-held spectrometer. Thus, by reading the spectral signature from the pattern, the spectral information of the photoluminescent nanoparticles was verified and thus a second-step verification was established. In this way, anticounterfeiting technology that combines ink formula, unclonable security pattern creation and two-level verification is developed.Article Citation - WoS: 8Citation - Scopus: 8Effects of Long-Range Disorder and Electronic Interactions on the Optical Properties of Graphene Quantum Dots(American Physical Society, 2017) Altıntaş, Abdulmenaf; Çakmak, K. E.; Güçlü, Alev DevrimWe theoretically investigate the effects of long-range disorder and electron-electron interactions on the optical properties of hexagonal armchair graphene quantum dots consisting of up to 10 806 atoms. The numerical calculations are performed using a combination of tight-binding, mean-field Hubbard, and configuration interaction methods. Imperfections in the graphene quantum dots are modeled as a long-range random potential landscape, giving rise to electron-hole puddles. We show that, when the electron-hole puddles are present, the tight-binding method gives a poor description of the low-energy absorption spectra compared to mean-field and configuration interaction calculation results. As the size of the graphene quantum dot is increased, the universal optical conductivity limit can be observed in the absorption spectrum. When disorder is present, the calculated absorption spectrum approaches the experimental results for isolated monolayers of graphene sheets.Article Citation - Scopus: 2Enthalpy-Driven Selective Loading of Cdse0.75s0.25 Nanoalloys in Triblock Copolymer Polystyrene-B(Elsevier Ltd., 2016) Aşkın, Görkem; Çeçen, Volkan; Ünlütürk, Seçil Sevim; Özçelik, Serdar; Demir, Mustafa MuammerCdSe0.75S0.25 nanoalloys were blended with asymmetric triblock copolymer of polystyrene-b-polyisoprene-b-polystyrene(PS-SIS) in tetrahydrofuran. The fraction of styrene block varies from 14 to 22% with respect to isoprene by mass. The morphology of the copolymer cast film experiences a phase change from cylinder to lamella. CdSe0.75S0.25 nanoalloys were prepared by two-phase method. The surface of the nanoalloys was capped by either oleic acid (OA) or n-tri-octylphosphonic acid (TOPO) in situ. The mean diameter of the alloyed particles is around 12 nm in both systems. The chemical nature of the nanoalloy surface was found to influence the dispersion of the particles over polymer volume. The size of the nanoalloy domains in PS is 50 nm, on average, consisting of approximately 0.7 wt% nanoalloys. However, the size of the nanoalloy domains is smaller when they are loaded into PS-SIS. The structure formation is predominantly determined by enthalpic compatibilization. Atomic force microscopy results suggest that the nanoalloys capped with TOPO sequester into PS-rich domains and enlarge the domain. On the other hand, the ones capped with OA prefer to locate in polyisoprene domains. The increase of particles over 1.0 wt% distorts the lamella structure.