Sağlam, Özge
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Saglam, OEzge
Saglam, Özge
Saglam, Ozge
Saglam, Özge
Saglam, Ozge
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ozge.saglam@ieu.edu.tr
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05.10. Mechanical Engineering
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6CLEAN WATER AND SANITATION
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Documents
29
Citations
734
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12
Documents
34
Citations
794
Scholarly Output
20
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15
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61/110
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3
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0
WoS Citation Count
169
Scopus Citation Count
127
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7
WoS Citations per Publication
8.45
Scopus Citations per Publication
6.35
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9
Supervised Theses
3
| Journal | Count |
|---|---|
| Colloıds And Surfaces A-Physıcochemıcal And Engıneerıng Aspects | 2 |
| Chemıcal Communıcatıons | 1 |
| ChemnNanoMat | 1 |
| ChemPlusChem | 1 |
| Colloids and Surfaces A: Physicochemical and Engineering Aspects | 1 |
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Now showing 1 - 10 of 20
Article Citation - WoS: 10Citation - Scopus: 11Upconversion Properties of Tm3+-Er3+ Co-Doped Layered Perovskites and In-Vitro Cytotoxicity of Their Exfoliated Nanomaterials(Elsevier, 2021) Gunay, Bensu; Sariyar, Ece; Unal, Ugur; Karagonlar, Zeynep Firtina; Saglam, Ozge; Firtina Karagonlar, ZeynepThe upconversion behavior of Er3+/Tm3+ co-doped Ruddlesden-Popper type K(2)Ln(2)Ti(3)O(10) layered perovskites was investigated. The lanthanide pair was selected for achieving 980 nm-driven green, red, and NIR emission. The perovskites having different dopant compositions were synthesized by a conventional solid-state procedure by substitution of La3+ ions in the host lattice. Moreover, the single nanosheets having approximately 1.8 nm thickness and 2 mu m lateral size were obtained via chemical exfoliation. The non-doped and co-doped layered materials and the nanosheets derived from these materials were characterized by X-ray diffraction, Scanning Electron Microscopy, Atomic Force Microscopy and custom-made experimental set-up of upconversion emission spectroscopy. According to the XRD profiles, the perovskites had the layered orientation and water molecules in the interlayer domain because of their hygroscopic nature. The co-doped layered perovskites presented twophoton excited green and red emissions, identified as S-4(3/2) -> (4)I(15/2 )with H-2(11/2) -> (4)I(15/2 )and F-4(9/2) -> I-4(15/2) of the Er3+ transitions with a NIR emission. The intensity of red to green ratio emission of the materials increased with respect to the co-dopant concentration. The nanosheets' upconversion emission was weak in the visible region compared to their layered morphology. On the other hand, the NIR emission based on H-3(4) -> H-3(6) transition of the Tm3+ ions was preserved despite the acid and solvent treatments to break apart the layered orientation. MTT assay and Calcein/PI staining were conducted to evaluate cytotoxicity of non-doped and Er3+/Tm3+ co-doped K(2)Ln(2)Ti(3)O(10) perovskites and their exfoliated nanosheets on HEK 293 and HepG2 cell lines. Both assays indicated that although cell viability decreases with increasing concentration, good cell viability was observed at even 100 mu g/mL. In addition to their excellent luminescent and optical features, the nanomaterials also demonstrated low cytotoxicity increasing the potential for their use in laser-based biological applications.Master Thesis 2d Perovskite Nanosheets for Multifunctional Device Fabrication and Biological Applications(İzmir Ekonomi Üniversitesi, 2021) Günay, Bensu; Sağlam, Özge; Karagonlar, Zeynep FırtınaBu tezin amaçları, frekans yükseltme özelliğine sahip nanolevhalar kullanılarak yapılandırılmış çok işlevli bir cihaz tasarımı ve biyolojik uygulamalar için iki boyutlu nanolevhaların biyouyumluluğunun araştırılmasıdır. K2Ln2Ti3O10 yapıda katmanlı perovskitler frekans yükseltme ile kırmızı ışıma elde edebilmek için farklı sitokiyometrik oranlarda Tm3+/Er3+ iyonları ile katkılandırılarak sentezlenmiştir. 2.5% Tm3+-20% Er3+ ile katkılı katmanlı malzemenin yanal boyutu 300 nm ile 2.5 µm arasında elde edilmiştir. Nanolevhaların kalınlığı 2-3 nm arasında belirlenmiştir ve tek nanolevhaların başarılı bir şekilde elde edildiği gösterilmiştir. Frekans yükseltme özelliğine sahip Tm3+/Yb3+ ve Er3+/Yb3+ ile katkılı nanolevhalar katman-katman tekniği ile 20 kez kaplanmıştır ve hazırlanan filmler sırasıyla 1G4 ›3H6 geçişi ile mavi ışıma ve 4S3/2›4I15/2 ve 2H11/2›4I15/2 geçişleri ile yeşil ışımalar göstermiştir. Öte yandan, Tm3+/Er3+ ortak katkılı nanolevha yapılı filmler, frekans yükseltme işlemi sırasında kırmızı ve yeşil emisyon sergilemiştir. Er3+/Yb3+ ortak katkılı nanolevhaların biriktirilmiş filmleri durumunda, yeşil ve kırmızı frekans yükseltme emisyonlarında iki foton süreçleri yer almıştır. 60 katman ile üretilen filmler ayrıca üç farklı nanolevhalar kullanılarak hazırlanmıştır. Film oluştururken nanolevhaların kombinasyonu CIE diagramında beyaz emisyon sergilemiştir. Ayrıca nanolevhaların sitotoksisitesi HepG2 ve HEK 293 hücre hatları kullanılarak analiz edilmiştir. HEK 293 hücre hattı için Tm3+/Er3+ katkılı katmanlı malzemenin toksisitesi %45,7 iken, nanolevhaların toksisitesi %73,6 olarak belirlenmiştir.Article Citation - WoS: 11Citation - Scopus: 11Isomerism Control of Diethylstilbestrol by Metal Surface Induced O-H Cleavage(Royal Soc Chemistry, 2018) Oh, Seung Cheol; Lloyd, Julian A.; Fischer, Sybille; Saglam, OEzge; Papageorgiou, Anthoula C.; Diller, Katharina; Duncan, David A.Diethylstilbestrol (DES) is studied on Ag(111) and Cu(111) surfaces using X-ray photoelectron spectroscopy (XPS) and scanning tunnelling microscopy (STM). We find that DES molecules on the silver surface adsorb intact and adopt a trans-conformation. On the more reactive copper surface, O-H bond cleavage results in molecular adsorption in the cis-conformation, thus providing the means of obtaining different adsorption geometries. The difference in isomerism is reflected in the observed self-assemblies which exhibit room-temperature stability.Article Citation - WoS: 12Tuning the Ease of Formation of On-Surface Metal-Adatom Coordination Polymers Featuring Diketones(Royal Soc Chemistry, 2018) Papageorgiou, Anthoula C.; Li, Jiang; Oh, Seung Cheol; Zhang, Bodong; Sağlam, Özge; Guo, Yuanyuan; Reichert, JoachimWe use pyrene-4,5,9,10-tetraketone molecules with substituents of varying bulkiness in the 2,7 positions to probe the generality and versatility of the previously reported on-surface coordination of two diketones with a single metal atom, leading to one-dimensional coordination polymers. Three different low index surfaces of group 11 metals (Cu, Ag and Au) are used to provide both the support and the metal atoms for metal-organic coordination. By real space visualisation with single molecule resolution employing scanning tunnelling microscopy we investigate the molecular self-assembly and show how this can be substantiated with the formation of metal-organic linear and cyclic oligomers, depending on the employed substrate.Article Citation - WoS: 50Citation - Scopus: 54Synthesis of Pyrene-Fused Pyrazaacenes on Metal Surfaces: Toward One-Dimensional Conjugated Nanostructures(Amer Chemical Soc, 2016) Jiang, Li; Papageorgiou, Anthoula C.; Oh, Seung Cheol; Sağlam, Özge; Reichert, Joachim; Duncan, David A.; Zhang, Yi-QiWe investigated the synthesis of one-dimensional nanostructures via Schiff base (imine) formation on three close-packed coinage metal (Au, Ag, and Cu) surfaces under ultrahigh vacuum conditions. We demonstrate the feasibility of forming pyrene-fused pyrazaacene-based oligomers on the Ag(111) surface by thermal annealing of tetraketone and tetraamine molecules, which were designed to afford cyclocondensation products. Direct visualization by scanning tunneling microscopy of reactants, intermediates, and products with submolecular resolution and the analysis' of their statistical distribution in dependence of stoichiometry and annealing temperature together with the inspection of complementary X-ray photoelectron spectroscopy signatures provide unique insight in the reaction mechanism, its limitations, and the role of the supporting substrate. In contrast to the reaction on Ag(111), the reactants desorb from the Au(111) surface before reacting, whereas they decompose on the Cu(111) Surface during the relevant thermal treatment.Review Citation - WoS: 23Citation - Scopus: 24Fighting Bacterial Pathogens With Carbon Nanotubes: Focused Review of Recent Progress(Royal Soc Chemistry, 2023) Asaftei, Mihaela; Lucidi, Massimiliano; Cirtoaje, Cristina; Holban, Alina-Maria; Charitidis, Costas A. A.; Yang, Fang; Wu, Aiguo; Sağlam, Özge; Stanciu, Stefan G.The fast and global spread of bacterial resistance to currently available antibiotics results in a great and urgent need for alternative antibacterial agents and therapeutic strategies. Recent studies on the application of nanomaterials as antimicrobial agents have demonstrated their potential for the management of infectious diseases. Among the diverse palette of nanomaterials currently used in biomedical applications, carbon nanotubes (CNTs) have gained massive interest given their many valuable properties, such as high thermal and electrical conductivity, tensile strength, flexibility convenient aspect ratio, and low fabrication costs. All these features are augmented by facile conjugation with functional groups. CNTs are currently available in many configurations, with two main categories being single-walled and multi-walled CNTs, depending on the number of rolled-up single-layer carbon atoms sheets making up the nanostructure. Both classes have been identified over the past years as promising antibacterial agents but the current level of understanding of their efficiency still harbors many pending questions. This mini-review surveys recent progress on the topic of antibacterial effects of CNTs and examines the proposed mechanisms of action(s) of different CNT typologies, placing the main focus on past studies addressing the antibacterial activity on Staphylococcus aureus and Escherichia coli, two prototypical Gram-positive and Gram-negative pathogens, respectively.Article Citation - WoS: 7Citation - Scopus: 8Ag-Intercalation of Tm3+/Er3+ Co-Doped Layered Perovskites and Their Exfoliated 2d Nanosheets With an Enhanced Antibiofilm and Antibacterial Activity(Elsevier, 2022) Gunay, Bensu; Doger, Hilal; Karagonlar, Zeynep Firtina; Saglam, OzgeThere is a significant demand for antibiofilm and antimicrobial materials in the medical device industry. It is well established that Ag-based compounds have a high antimicrobial efficiency. Without being in a lattice, silver's antimicrobial action is mainly mediated by the release of Ag+ ions from the compound. These ions at high levels are toxic to most bacterial species. However, rapidly released Ag+ ions tend to aggregate and lose their anti-bacterial effect over time. Thus, utilizing a new approach for using silver as an antimicrobial agent based on imparting the antimicrobial action through contact, rather than releasing Ag+ ions could be beneficial. Here we report that Ag+ ions intercalation of Tm/Er co-doped layered perovskites and their 2D nanosheets exhibit antibacterial and antibiofilm activities against the human opportunistic pathogens Escherichia coli and Bacillus subtilis. Specifically, flocculation of nanosheets with Ag+ ions had efficient antibacterial and antibiofilm activity at 100 mu g/mL. In addition, the flocculated product demonstrated low in vitro cytotoxicity against the Huh7 hepatocellular carcinoma cell line and HEK 293 embryonic kidney cell line. Our results indicate that Ag-intercalated layered perovskites and the flocculation of the nanosheets hold great promise to be used for anti-microbial and antibiofilm purposes in biomedical engineering applications.Article Citation - WoS: 4Citation - Scopus: 5Concentration Based Multicolor Upconversion Emission of Lanthanides Co -Doped Ruddlesden-Popper Type Layered Perovskites(Elsevier, 2020) Saglam, OzgeYb3+ ions initiated upconversion properties of Ruddlesden-Popper type layered materials were studied to elucidate the tunability of the visible emission under 980 nm excitation. The substitution of lanthanum ions in the host layer perovskites with different concentrations of Yb3+/Er3+ and Yb3+/Tm3+ as the sensitizer/activator pairs was performed via the solid-state procedure. The upconversion spectra of the samples have depicted that the materials relatively lower dopant concentrations of Yb3+/Er3+ have the green color, which was shifted to the red region due to both heavy activator and sensitizer concentrations because of the dominant F-4(9/2) -> I-4(15/2) transition rather than the H-2(11/2), S-4(3/2) -> I-4(15/2) transitions. The tunability of upconversion emission of Yb3+/ Tm3+ introduced materials was limited in the visible region compared to the Yb3+/Er3+ pair despite the fact that the wide variety of the lanthanide concentrations were studied and the layered materials were structured successfully. On the other hand, the first intense NIR emission was achieved for the layered perovskites co-doped with Yb3+/Tm3+ due to the H-3(4)-> H-3(6) relaxation.Article Citation - WoS: 2Citation - Scopus: 2Langmuir-Blodgett Deposition and Physicochemical Surface Characterization of Two-Dimensional Perovskite Nanosheets on Ito-Pet Substrates(Elsevier B.V., 2023) Küçükcan B.; Günay B.; Gordesli-Duatepe F.P.; Sağlam Ö.; Sağlam, Özge; Gordesli-Duatepe, Fatma Pinar; Küçükcan, Begümnur; Günay, BensuWe successfully obtained Ca2NaNb4O13? single perovskite nanosheets by delaminating x = 4 Dion-Jacobson type KCa2NaNb4O13 layered materials. These nanosheets were then deposited onto conductive, transparent, and flexible indium tin oxide-polyethylene terephthalate (ITO-PET) substrates using the Langmuir-Blodgett (LB) technique. The polar and apolar (dispersive) surface tension components of LB nanofilms composed of Ca2NaNb4O13? perovskite nanosheets and the work of adhesion between the nanofilms and silicon and ITO-PET substrates were determined through contact angle measurements combined with mathematical modeling based on surface thermodynamics. The results showed that the apolar surface tension components had similar values for all surfaces studied, while the polar surface tension components of the nanofilms deposited on the substrates had higher values than those of the bare substrates. The higher polar interaction observed between the nanofilm and ITO-PET resulted in higher total work of adhesion of the nanofilm to the ITO-PET surface in water, while the total work of adhesion computed between the nanofilm and Si was higher in air. © 2023 Elsevier B.V.Article Citation - WoS: 21In Vacuo Porphyrin Metalation on Ag(111) Via Chemical Vapor Deposition of Ru-3(co)(12): Mechanistic Insights(Amer Chemical Soc, 2016) Papageorgiou, Anthoula C.; Diller, Katharina; Fischer, Sybille; Allegretti, Francesco; Klappenberger, Florian; Oh, Seung Cheol; Saglam, OzgePorphyrin molecules offer a very stable molecular environment for the incorporation of numerous metal ions inside their cavity, which enables a plethora of applications. The fabrication and characterization of surface confined metal organic architectures by employing porphyrins are of particular interest. Here, we report on a comprehensive study of chemical vapor deposition (CVD) of triruthenium dodecacarbonyl as metal precursor for the on-surface metalation of different porphyrin species with Ru under ultrahigh vacuum conditions. By employing synchrotron radiation X-ray photoelectron spectroscopy (XPS), near edge X-ray absorption fine structure (NEXAFS), and scanning tunneling microscopy (STM), we investigated the metalation process and particularly the role of the support: the close packed Ag(111) surface. It was found that the surface is active in the metalation process under the employed conditions: it decomposes the metal precursor and delivers metal centers to the porphyrin macrocycles. The generality of the metalation process is illustrated for tetraphenylporphyrin, its high temperature derivatives, and porphine.
