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Permanent URI for this collectionhttps://hdl.handle.net/20.500.14288/6

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    PublicationOpen Access
    Highly sensitive optical sensor for hydrogen gas based on a polymer microcylinder ring resonator
    (Elsevier, 2020) Eryürek, Mustafa; Department of Physics; Department of Chemistry; Department of Electrical and Electronics Engineering; Bavili, Nima; Balkan, Timuçin; Morova, Berna; Uysallı, Yiğit; Kaya, Sarp; Kiraz, Alper; Researcher; Researcher; PhD Student; Faculty Member; Faculty Member; Department of Physics; Department of Chemistry; Department of Electrical and Electronics Engineering; Koç University Tüpraş Energy Center (KUTEM) / Koç Üniversitesi Tüpraş Enerji Merkezi (KÜTEM); Graduate School of Sciences and Engineering; College of Sciences; College of Engineering; N/A; N/A; N/A; N/A; 116541; 22542
    A highly sensitive platform is demonstrated for hydrogen gas (H-2) sensing based on a polymer microcylinder ring resonator (PMRR) obtained by an optical fiber coated with an inner nanofilm of amorphous palladium (Pd) and an outer polymer layer of polydimethylsiloxane (PDMS) permeable to H-2. The sensing scheme is based on monitoring the spectral shifts of high-quality optical resonances called whispering gallery modes (WGMs) that propagate in the vicinity of the outer rim of the PDMS layer without being affected by the absorption and scattering losses caused by the Pd nanofilm. WGMs are excited by a single-mode tapered optical fiber evanescently coupled to the PMRR. The observed reversible spectral shifts of the WGMs are induced by changes in the diameter of the PDMS layer caused by expansion or contraction of the Pd nanofilm exposed to varying concentrations of H-2. Maximum spectral shift sensitivity of 140 pm/% H-2, a minimum response time of 95 s, and minimum limit of detection of similar to 60 ppm were measured for sensors prepared with different thicknesses of the amorphous Pd nanofilm and tested in the H-2 concentration range up to 1%, having nitrogen gas (N-2) as a carrier. Experiments were also conducted with Pd nanofilms annealed in air or N-2 atmosphere after the deposition. In both cases, smaller sensitivities were observed due to the formation of larger grains within the film, resulting in slower diffusion and reduced solubility of H in the Pd layer. The impacts of oxygen gas and humidity on sensor performance were also studied.
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    PublicationOpen Access
    CdTe quantum dot sensitized hexaniobate nanoscrolls and their photoelectrochemical properties
    (Royal Society of Chemistry (RSC), 2012) Department of Chemistry; Öztuna, Feriha Eylül Saraç; Akkaya, Ceren Yılmaz; Acar, Havva Funda Yağcı; Ünal, Uğur; PhD Student; Faculty Member; Department of Chemistry; Koç University Surface Science and Technology Center (KUYTAM) / Koç Üniversitesi Yüzey Teknolojileri Araştırmaları Merkezi (KUYTAM); College of Sciences; N/A; N/A; 178902; N/A
    We have constructed hybrid quantum dot-layered niobate films with an electrophoretic deposition method. The structure and photoelectrochemical behaviour were demonstrated.
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    PublicationOpen Access
    Weakening the strength of CO binding on subsurface alloyed Pt(111)
    (Elsevier, 2019) Ogasawara, Hirohito; Department of Chemistry; N/A; Kaya, Sarp; Gürlek, Sezen; Panahi, Mohammad; Solati, Navid; Faculty Member; PhD Student; Department of Chemistry; Koç University Tüpraş Energy Center (KUTEM) / Koç Üniversitesi Tüpraş Enerji Merkezi (KÜTEM); College of Sciences; Graduate School of Sciences and Engineering; 116541; N/A; N/A; N/A
    The interaction of CO with Pt/3d/Pt(111) subsurface alloys (3d: Ni, Co, Fe) was investigated by combination of vibrational spectroscopy and temperature programmed desorption. The binding strength of CO is significantly reduced on Pt/Fe/Pt(111) and Pt/Co/Pt(111) and is sorted in the following order: Pt >Ni > Co approximate to Fe. Our analysis shows that the 3d admetal is stable in the subsurface region and CO is linearly bonded to the atop sites of the Pt(111) surface. At high CO coverage, compressed structures are obtained. At low CO coverage, the desorption activation energy of CO (similar to 143 kJ/mol for Pt(111)) drops to 124 kJ/mol for Pt/Ni/Pt(111), and goes further down to 111 and 110 kJ/mol for Pt/Co/Pt(111) and Pt/Fe/Pt(111), respectively. The enhancement in the surface activity is attributed to the modified backdonation to the antibonding states of adsorbed CO due to the downshifted 5d-band center of Pt upon embedding 3d metals in the subsurface region.
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    PublicationOpen Access
    Development of highly luminescent and cytocompatible near-IR-emitting aqueous Ag2S quantum dots
    (Royal Society of Chemistry (RSC), 2012) Çizmeciyan, M. Natali; Erdem, Rengin; Özen, Can; Kurt, Adnan; N/A; Department of Physics; Department of Chemistry; Hocaoğlu, İbrahim; Sennaroğlu, Alphan; Acar, Havva Funda Yağcı; PhD Student; Faculty Member; Department of Physics; Department of Chemistry; Graduate School of Sciences and Engineering; College of Sciences; N/A; 23851; 178902
    Colloidally stable and highly luminescent near-IR emitting Ag2S quantum dots (NIRQDs) were prepared by a very simple aqueous method using 2-mercaptopropionic acid (2MPA) as a coating. Emission of Ag2S-2MPA NIRQDs can be tuned between 780 and 950 nm. These NIRQDs have photoluminescence quantum yields (PLQY) around 7–39% and exhibit excellent cytocompatibility even at 600 mg mL 1 in NIH/3T3 cells. With such improved properties, Ag2S-2MPA NIRQDs have a great potential in practical bio-applications.
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    PublicationOpen Access
    One-step aqueous synthesis of anionic and cationic AgInS2 quantum dots and their utility in improving the efficacy of ALA-based photodynamic therapy
    (American Chemical Society (ACS), 2022) Loizidou, Marilena; MacRobert, Alexander J.; Department of Chemistry; Acar, Havva Funda Yağcı; Hashemkhani, Mahshid; PhD Student; Department of Chemistry; College of Sciences; Graduate School of Sciences and Engineering; 178902; N/A
    Silver-indium-sulfide quantum dots (AIS QDs) have potential applications in many areas, including biomedicine. Their lack of regulated heavy metals, unlike many commercialized QDs, stands out as an advantage, but the necessity for alloyed or core-shell structures and related costly and sophisticated processes for the production of stable and high quantum yield aqueous AIS QDs are the current challenges. The present study demonstrates the one-step aqueous synthesis of simple AgInS2 QD compositions utilizing for the first time either a polyethyleneimine/2-mercaptopropionic acid (AIS-PEI/2MPA) mixture or only 2-mercaptopropionic acid (AIS-2MPA) as the stabilizing molecules, providing a AgInS2 portfolio consisting of cationic and anionic AIS QDs, respectively, and tuneable emission. Small AIS QDs with long-term stability and high quantum yields (19-23%) were achieved at a molar ratio of Ag/In/S 1/10/10 in water without any dopant or a semiconductor shell. The theranostic potential of these cationic and anionic AIS QDs was also evaluated in vitro. Non-toxic doses were determined, and fluorescence imaging potential was demonstrated. More importantly, these QDs were electrostatically loaded with zwitterionic 5-aminolevulinic acid (ALA) as a prodrug to enhance the tumor availability of ALA and to improve ALA-induced porphyrin photodynamic therapy (PDT). This is the first study investigating the influence of nanoparticle charge on ALA binding, release, and therapeutic efficacy. Surface charge was found to be more critical in cellular internalization and dark toxicity rather than drug loading and release. Both QDs provided enhanced ALA release at acidic pH but protected the prodrug at physiological pH, which is critical for tumor delivery of ALA, which suffers from low bioavailability. The PDT efficacy of the ALA-loaded AIS QDs was tested in 2D monolayers and 3D constructs of HT29 and SW480 human colon adenocarcinoma cancer cell lines. The incorporation of ALA delivery by the AIS QDs, which on their own do not cause phototoxicity, elicited significant cell death due to enhanced light-induced ROS generation and apoptotic/necrotic cell death, reducing the IC50 for ALA dramatically to about 0.1 and 0.01 mM in anionic and cationic AIS QDs, respectively. Combined with simple synthetic methods, the strong intracellular photoluminescence of AIS QDs, good biocompatibility of especially the anionic AIS QDs, and the ability to act as drug carriers for effective PDT signify that the AIS QDs, in particular AIS-2MPA, are highly promising theranostic QDs.
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    PublicationOpen Access
    Synthesis and characterization of mesoporous zirconium oxide thin films
    (Institute of Physics (IOP) Publishing, 2010) Department of Chemistry; Miko, Annamaria; Demirel, Adem Levent; Somer, Mehmet Suat; Teaching Faculty; Faculty Member; Faculty Member; Department of Chemistry; College of Sciences; N/A; 6568; 178882
    Zirconium oxide (ZrO2) has generated wide interest because of its potential in applications such as solid oxide fuel cells, catalysts and optical devices. In these applications, it is important to control the grain size of the material and increase the surface area by introducing porosity with tailored pore size. This paper presents a synthesis route for the preparation of mesoporous zirconia using spin-coating method combined with block copolymer templating evaporation induced self assembly (EISA). The hybrid mesophase was formed by zirconium oxychloride precursor ZrOCl2 center dot 8H(2)O and Brij 700 poly-ethylene oxide based block copolymer template C18H37(OCH2CH2). FT-IR and Raman measurements of the hybrid mesophase provided information on the possible intermolecular interactions between the precursor and the copolymer template. The results indicate a weak ion-dipole interaction between the inorganic precursor and the organic template after the solvent evaporation, possibly directly between the zirconium and the oxygen of the poly-ethylene oxide chain. The removal of the organic block copolymer by heat treatment resulted in mesoporous zirconia with pore size of similar to 4-8 nm and crystalline grain size of similar to 10-17 nm. The morphology in thin films depended significantly on the solvent quality and the block copolymer concentration. Tailoring the surface morphology and the grain size resulted in super-hydrophilic mesoporous zirconia thin films in contrast to water contact angle of 50 degrees on conventional tetragonal zirconium oxide.
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    PublicationOpen Access
    Silk-hydrogel lenses for light-emitting diodes
    (Nature Publishing Group (NPG), 2017) Melikov, Rustamzhon; Press, Daniel Aaron; Kumar, Baskaran Ganesh; Dogru, Itir Bakis; Sadeghi, Sadra; Chirea, Mariana; Department of Chemistry; Department of Electrical and Electronics Engineering; Yılgör, İskender; Nizamoğlu, Sedat; Faculty Member; Faculty Member; Department of Chemistry; Department of Electrical and Electronics Engineering; College of Sciences; College of Engineering; 24181; 130295
    Today the high demand for electronics leads to massive production of waste, thus green materials based electronic devices are becoming more important for environmental protection and sustainability. The biomaterial based hydrogels are widely used in tissue engineering, but their uses in photonics are limited. In this study, silk fibroin protein in hydrogel form is explored as a bio-friendly alternative to conventional polymers for lens applications in light-emitting diodes. The concentration of silk fibroin protein and crosslinking agent had direct effects on optical properties of silk hydrogel. The spatial radiation intensity distribution was controlled via dome- and crater-type silk-hydrogel lenses. The hydrogel lens showed a light extraction efficiency over 0.95 on a warm white LED. The stability of silk hydrogel lens is enhanced approximately three-folds by using a biocompatible/biodegradable poly(ester-urethane) coating and more than three orders of magnitude by using an edible paraffin wax coating. Therefore, biomaterial lenses show promise for green optoelectronic applications.
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    PublicationOpen Access
    Protocol on synthesis and characterization of copper-doped InP/ZnSe quantum dots as ecofriendly luminescent solar concentrators with high performance and large area
    (Elsevier, 2021) Department of Electrical and Electronics Engineering; N/A; N/A; Department of Chemistry; Nizamoğlu, Sedat; Sadeghi, Sadra; Eren, Güncem Özgün; Shahzad, Mehwish; Faculty Member; PhD Student; Department of Electrical and Electronics Engineering; Department of Chemistry; College of Engineering; Graduate School of Sciences and Engineering; 130295; N/A; N/A; N/A
    Luminescent solar concentrators (LSCs) are simple and cost-effective solar energy-harvesting devices. Indium phosphide (InP)-based colloidal quantum dots (QDs) are promising QDs for efficient LSC devices due to their environmentally benign nature. One major challenge in LSC devices is reabsorption losses. To minimize the reabsorption, Stokes shift engineering is a critical process to designing the QD material. Here, we present a protocol that contains the preparation of structurally engineered copper-doped InP/ZnSe QDs and their LSC application.
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    PublicationOpen Access
    Self-assembled poly(2-ethyl-2-oxazoline) fibers in aqueous solutions
    (Royal Society of Chemistry (RSC), 2012) N/A; Department of Chemistry; Güner, Pınar Tatar; Miko, Annamaria; Schweinberger, Florian F.; Demirel, Adem Levent; Teaching Faculty; Teaching Faculty; Faculty Member; Department of Chemistry; Graduate School of Sciences and Engineering; College of Sciences; 188227; N/A; N/A; 6568
    Poly(2-ethyl-2-oxazoline) (PEOX) formed self-assembled fibers in aqueous solutions above the cloud point temperature (T-c) through a slow crystallization process. The fiber formation above T-c happened both in pure water and in the presence of salting-in (SCN-) and salting-out (CH3COO-) ions. The crystal structure and the melting temperature of the PEOX fibers were determined.
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    PublicationOpen Access
    A new class of porous materials for efficient CO2 separation: ionic liquid/graphene aerogel composites
    (Elsevier, 2021) Department of Chemical and Biological Engineering; N/A; Department of Chemistry; Zeeshan, Muhammad; Yalçın, Kaan; Keskin, Seda; Uzun, Alper; Öztuna, Feriha Eylül Saraç; Ünal, Uğur; PhD Student; Faculty Member; Faculty Member; Department of Chemical and Biological Engineering; Department of Chemistry; Koç University Tüpraş Energy Center (KUTEM) / Koç Üniversitesi Tüpraş Enerji Merkezi (KÜTEM); Koç University Surface Science and Technology Center (KUYTAM) / Koç Üniversitesi Yüzey Teknolojileri Araştırmaları Merkezi (KUYTAM); Graduate School of Sciences and Engineering; College of Engineering; College of Sciences; N/A; N/A; 40548; 59917; N/A; 42079
    Here, we report a new post-synthesis modification strategy for functionalizing reduced graphene aerogels (rGAs) towards an exceptional CO2 separation performance. 1-N-butyl-3-methylimidazolium hexafluorophosphate ([BMIM][PF6]) was impregnated on a rGA, prepared by reducing GA at 700 degrees C, at various ionic liquid (IL) loadings of 5, 10, 30, and 50 wt%. The resulting composites were characterized in deep detail by X-ray photoelectron spectroscopy, X-ray diffraction, N-2 physical adsorption measurements, scanning electron microscopy, Fourier transform infrared and Raman spectroscopies, and thermogravimetric analysis. Results indicated the presence of interactions between the rGA surface and the anion of the IL, potentially improving the CO2 affinity. Volumetric gas adsorption measurements using these materials showed that the deposition of [BMIM][PF6] on rGA surface at an IL loading of 50 wt% boosts the CO2/CH4 selectivity by more than 20-times, exceeding an absolute value of 120, a remarkably higher CO2/CH4 selectivity compared to that of other functionalized materials under similar operating conditions. Tunability of both the IL structure and the surface characteristics of rGA offer a tremendous degree of flexibility for the rational design of these IL/rGA composites towards high performance in gas separation applications.