Chemistry / Kimya

Permanent URI for this collectionhttps://hdl.handle.net/11147/4072

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Now showing 1 - 10 of 17
  • Article
    Citation - WoS: 7
    Citation - Scopus: 10
    Enhanced Light–matter Interaction in a Hybrid Photonic–plasmonic Cavity
    (Springer, 2021) Gökbulut, Belkıs; İnanç, Arda; Topçu, Gökhan; Özçelik, Serdar; Demir, Mustafa Muammer; İnci, Mehmet Naci
    Strongly concentrated optical fields around a metal nanoparticle in the close vicinity of a dipole noticeably facilitate dramatic changes in the localized density of states due to hybrid photonic–plasmonic mode couplings as compared to that of the pure cavity mode fields. Significant variations of the field intensity in the presence of the metal nanoparticle elucidate enhanced light–matter interaction in a hybrid structure. The enhancement factor of the light–matter interaction is studied through the single-atom cooperativity parameter, which is directly proportional to the ratio of the fluorescence lifetimes of the off-resonant and on-resonant emission. A compact and cost-effective hybrid device, which includes a microfiber cavity, supporting whispering gallery modes, and a well-defined solid nanostructure, consisting of a gold nanoparticle core, overcoated by a silica shell, and decorated with CdS/CdSe quantum dots, is demonstrated to offer an outstanding potential for the enhancement of light–matter interaction. Surface plasmons of a gold nanoparticle, placed inside a hollow cylindrical nanostructure at the surface of a microfiber, are activated upon excitation of the dipoles of the quantum emitters, which are on-resonance with the whispering gallery mode. Time-resolved experiments demonstrate that the single-atom cooperativity parameter of the quantum dots is enhanced by a factor of about 4.8 in the presence of the gold nanoparticle being simultaneously in strong interaction with the cavity mode field and the metal nanoparticle’s surface plasmons.
  • Correction
    Correction To: Enhanced Light–matter Interaction in a Hybrid Photonic–plasmonic Cavity
    (Springer, 2022) Gökbulut, Belkıs; İnanç, Arda; Topçu, Gökhan; Özçelik, Serdar; Demir, Mustafa Muammer; İnci, Mehmet Naci
    In this article the statement in the Funding information section was incorrect. The correct Funding information is as follows. ‘Dr Belkıs Gökbulut acknowledges TUBITAK for the financial support provided under Contract Number 120F323’.
  • Article
    Citation - WoS: 14
    Citation - Scopus: 16
    Bodipy-Based Organic Color Conversion Layers for Wleds
    (Elsevier, 2020) Yüce, Hürriyet; Güner, Tuğrul; Dartar, Suay; Kaya, Beraat Umur; Emrullahoğlu, Mustafa; Demir, Mustafa Muammer
    The usage of organic dyes in phosphor conversion layer of WLED is an attractive approach since they have high molar extinction coefficient and photostability. Various types of organic pigments have been employed for this purpose such as BODIPY, perylene diimide, Rhodamine B, pyrene, Nile red, etc. Among those, BODIPY-based organic dyes appear to be promising candidate for white light generation. In this work, for the first time, red and green emitting BODIPY-based organic molecules have been used as colour conversion layer. These molecules were associated with PMMA in DMF solution and the resulting solution was subjected to electrospinning. Colorful electrospun mats were embedded into PDMS matrix and their free-standing PDMS composite films were used as color conversion layers over blue LED to produce white light such that CRI of 95 and CCT of 4200 K was achieved. These values show that BODIPY-based organic molecules containing fiber composites are promising candidates to be used as color conversion layers for white light applications.
  • Article
    Citation - WoS: 6
    Citation - Scopus: 8
    Enhanced Spontaneous Emission Rate in a Low-Q Hybrid Photonic-Plasmonic Nanoresonator
    (American Chemical Society, 2019) Gökbulut, Belkıs; İnanç, Arda; Topçu, Gökhan; Ünlütürk, Seçil Sevim; Özçelik, Serdar; Demir, Mustafa Muammer; İnci, Mehmet Naci
    In this paper, CdTe quantum dots (QDs)-doped single electrospun polymer nanofibers are partially coated with gold nanoparticles to form distinct hybrid photonic-plasmonic nanoresonators to investigate the critical role of the cavity-confined hybrid mode on the modification of the spontaneous emission dynamics of the fluorescent emitters in low-Q photonic cavities. A total enhancement factor of 11.2 is measured via a time-resolved experimental technique, which shows that there is an increase of about three times in the spontaneous emission rate for the QDs-doped gold nanoparticle-decorated nanofibers as they are compared with those uncoated ones. The physical mechanism affecting the spontaneous emission rate of the encapsulated QDs in such a hybrid photonic-plasmonic nanoresonator is explained to be due to regeneration of the mode field in the nanofiber cavity upon the interaction of the dipoles with the surface plasmons of distinctive gold nanoparticles that surround the outer surface of the nanofiber.
  • Article
    Citation - WoS: 9
    Citation - Scopus: 10
    Polymeric Planar Microcavities Doped With a Europium Complex
    (MDPI, 2020) Lova, Paola; Olivieri, Marco; Surace, Alba; Topçu, Gökhan; Emirdağ Eanes, Mehtap; Demir, Mustafa Muammer; Comoretto, Davide
    Organo-metallic europium complex tetrakis (dibenzoyl methide) triethylammonium (EuD(4)TEA) shows a sharp emission spectrum, which makes it interesting for photonic applications. In this work, we embedded it into all-polymeric planar microcavities and investigated the effect of the photonic environment on its emission spectrum. To this end, submicron-sized EuD(4)TEA crystals were loaded into a blend of polystyrene and carboxylic terminated polystyrene matrix, which served to stabilize the emitter in the polymer and to make the composite processable. The new composite was then casted by spin-coating as a defect layer in a polymeric planar microcavity. Spectroscopic studies demonstrate that fine spectral tuning of the cavity mode on the sharp organometal luminescence is possible and produces spectral redistribution of the fluorophore emission, along with a remarkable cavity quality factor.
  • Article
    Citation - Scopus: 2
    Enthalpy-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 Muammer
    CdSe0.75S0.25 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.
  • Article
    Citation - WoS: 45
    Polymers and Inorganics: a Happy Marriage?
    (Polymer Society of Korea, 2007) Wegner, Gerhard; Demir, Mustafa Muammer; Faatz, Michael; Gorna, Katazyrna; Munoz-Espi, Rafael; Guillemet, Baptiste; Gröhn, Franziska
    The most recent developments in two areas: (a) synthesis of inorganic particles with control over size and shape by polymer additives, and (b) synthesis of inorganic-polymer hybrid materials by bulk polymerization of blends of monomers with nanosized crystals are reviewed. The precipitations of inorganics, such as zinc oxide or calcium carbonate, in presence and under the control of bishydrophilic block or comb copolymers, are relevant to the field of Biomineralization. The application of surface modified latex particles, used as controlling agents, and the formation of hybrid crystals in which the latex is embedded in otherwise perfect crystals, are discussed. The formation of nano sized spheres of amorphous calcium carbonate, stabilized by surfactant-like polymers, is also discussed. Another method for the preparation of nanosized inorganic functional particles is the controlled pyrolysis of metal salt complexes of poly (acrylic acid), as demonstrated by the syntheses of lithium cobalt oxide and zinc/magnesium oxide. Bulk polymerization of methyl methacrylate blends, with for example, nanosized zinc oxide, revealed that the mechanisms of free radical polymerization respond to the presence of these particles. The termination by radical-radical interaction and the gel effect are suppressed in favor of degenerative transfer, resulting in a polymer with enhanced thermal stability. The optical properties of the resulting polymer-particle blends are addressed based on the basic discussion of the miscibility of polymers and nanosized particles.
  • Article
    Citation - WoS: 12
    Probing Nanoscale Domains of J-Aggregates Deposited on a Mica Surface
    (American Chemical Society, 2004) Demir, Mustafa Muammer; Özçelik, Serdar; Birkan, Burak
    J-aggregates of 1,1′,3,3′-tetraethyl-5,5′,6,6′- tetrachlorobenzimidazolocarbocyanine (TTBC) were deposited on a mica surface and probed by atomic force microscopy operated at tapping mode in air. Optical spectra showed that J-aggregates were formed in aqueous solutions. Atomic force microscopy images revealed that J-aggregates deposited on mica surfaces mainly present single domains with a mean height of 2.00 ± 0.25 nm and an average diameter of 100 ± 20 nm. Quantitative analysis of the morphology of images indicated that the single domain of J-aggregates exhibits very uniform height and diameter distributions with polydispersity indices of 1.02 and 1.04, respectively. Based on the results, we propose a two-dimensional nanostructure in which TTBC J-aggregates could be arranged in a monolayer.
  • Article
    Citation - WoS: 36
    Citation - Scopus: 36
    Surfactant-Assisted Formation of Organophilic Ceo2 Nanoparticles
    (Elsevier Ltd., 2012) Tunusoğlu, Özge; Muñoz-Espí, Rafael; Akbey, Ümit; Demir, Mustafa Muammer
    We report a simple one-pot method to prepare organically functionalized CeO 2 nanoparticles by controlled chemical precipitation. The particles were nucleated by mixing aqueous solutions of Ce(NO 3) 3·6H 2O and ammonia at room temperature. Different small organic molecules were chosen as capping agents and injected into the reaction medium at the beginning of the synthesis: 3-(mercaptopropyl) trimethoxy silane (MPS), hexadecyltrimethyl ammonium bromide (CTAB), 3-mercapto propionic acid (3-MPA), and thioglycolic acid (TGA). The resulting nanocrystals were quasi-spherical and had a narrow mean size distribution with an average size smaller than 10nm. Dynamic nuclear polarization enhanced NMR (DNP-NMR) and FTIR measurements suggested a chemical grafting of the surfactant and a homogeneous surface modification. The colloidal stabilities were characterized by dynamic light scattering and zeta potential measurements. The stabilization by aliphatic groups was tested with a frequently used hydrophobic monomer, methyl methacrylate. According to the results, CTAB is the most effective of the used stabilizing surfactant. The mechanism of formation of the organophilic CeO 2 nanoparticles is discussed.
  • Article
    Citation - WoS: 35
    Citation - Scopus: 45
    Types of the Scaling in Hyper Saline Geothermal System in Northwest Turkey
    (Elsevier Ltd., 2014) Demir, Mustafa Muammer; Baba, Alper; Atilla, Vedat; İnanlı, Mustafa
    Tuzla is an active geothermal area located in northwestern Turkey, 80km south of the city of Canakkale and 5km from the Aegean Coast. The geothermal brine from this area, which is dominated by NaCl, has a typical temperature of 173°C. Rapid withdrawal of fluid to ambient surface conditions during sampling causes precipitation of various compounds known as scaling. Scaling is one of the important problems in Tuzla geothermal system that reduces the efficiency of the geothermal power plant and causes economical loss. The aim of this study was to determine the type of scaling as a first step towards preventing its formation. The scales formed in the geothermal system were divided into two groups according to location: the ones that formed in downhole and the ones that accumulated along the surface pipeline. Both scales were examined in terms of their elemental composition, structure and morphology using XRF, XRD, and SEM, respectively. The former was found to be mainly composed of PbS (Galena) and CaCO3 (aragonite or calcite). In contrast, the latter was heterogeneous in nature and consisted of mainly saponite like amorphous structure along with submicrometer-sized amorphous silica particles, layered double magnesium and iron hydroxide, and NaCl.