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

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Department: search.filters.department.N/ASubject: search.filters.subject.Materials science, multidisciplinary

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Now showing 1 - 5 of 5
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    PublicationOpen Access
    Plasmon-coupled photocapacitor neuromodulators
    (American Chemical Society (ACS), 2020) Ülgüt, Burak; Çetin, Arif E.; N/A; N/A; Department of Molecular Biology and Genetics; Department of Electrical and Electronics Engineering; Department of Chemical and Biological Engineering; Melikov, Rustamzhon; Srivastava, Shashi Bhushan; Karatüm, Onuralp; Doğru-Yüksel, Itır Bakış; Jalali, Houman Bahmani; Sadeghi, Sadra; Dikbaş, Uğur Meriç; Kavaklı, İbrahim Halil; Nizamoğlu, Sedat; PhD Student; Researcher; PhD Student; PhD Student; Master Student; Faculty Member; Faculty Member; Department of Molecular Biology and Genetics; Department of Electrical and Electronics Engineering; Department of Chemical and Biological Engineering; Graduate School of Sciences and Engineering; College of Sciences; College of Engineering; N/A; N/A; N/A; N/A; N/A; N/A; N/A; 40319; 130295
    Efficient transduction of optical energy to bioelectrical stimuli is an important goal for effective communication with biological systems. For that, plasmonics has a significant potential via boosting the light-matter interactions. However, plasmonics has been primarily used for heat-induced cell stimulation due to membrane capacitance change (i.e., optocapacitance). Instead, here, we demonstrate that plasmonic coupling to photocapacitor biointerfaces improves safe and efficacious neuromodulating displacement charges for an average of 185% in the entire visible spectrum while maintaining the faradic currents below 1%. Hot-electron injection dominantly leads the enhancement of displacement current in the blue spectral window, and the nanoantenna effect is mainly responsible for the improvement in the red spectral region. The plasmonic photocapacitor facilitates wireless modulation of single cells at three orders of magnitude below the maximum retinal intensity levels, corresponding to one of the most sensitive optoelectronic neural interfaces. This study introduces a new way of using plasmonics for safe and effective photostimulation of neurons and paves the way toward ultrasensitive plasmon-assisted neurostimulation devices.
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    PublicationOpen Access
    Predicting new iron garnet thin films with perpendicular magnetic anisotropy
    (Elsevier, 2020) N/A; Department of Electrical and Electronics Engineering; Zanjani, Saeedeh Mokarian; Onbaşlı, Mehmet Cengiz; Faculty Member; Department of Electrical and Electronics Engineering; Graduate School of Sciences and Engineering; College of Engineering; N/A; 258783
    Magnetic iron garnets are insulators with low Gilbert damping with many applications in spintronics. Many emerging spintronic applications require perpendicular magnetic anisotropy (PMA) although garnets have only a few PMA types (i.e. terbium and samarium garnet). More and stable PMA garnet options are needed for investigating new spintronic phenomena. In this study, we predict 20 new epitaxial magnetic iron garnet film/substrate pairs with stable PMA at room temperature. The effective anisotropy energies of 10 different garnet films that are lattice-matched to 5 different commercially available garnet substrates (total 50 film/substrate pairs) have been calculated using shape, magnetoelastic and magnetocrystalline anisotropy terms. Strain type, tensile or compressive depending on substrate choice, as well as the sign and the magnitude of the magnetostriction constants of garnets determine if a garnet film may possess PMA. We show the conditions in which Samarium, Gadolinium, Terbium, Holmium, Dysprosium and Thulium garnets may possess PMA on the investigated garnet substrate types. New PMA garnet films with tunable saturation moment and field may improve spin-orbit torque memory and compensated magnonic thin film devices.
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    PublicationOpen Access
    Fast and selective adsorption of methylene blue from water using [BMIM][PF6]-incorporated UiO-66 and NH2-UiO-66
    (American Chemical Society (ACS), 2020) Department of Chemical and Biological Engineering; N/A; Kulak, Harun; Keskin, Seda; Uzun, Alper; Kavak, Safiyye; Polat, Hüsamettin Mert; Faculty Member; Department of Chemical and Biological Engineering; 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; N/A; 40548; 59917; N/A; N/A
    Incorporation of ionic liquids (ILs) into metal-organic frameworks (MOFs) offers a broad potential in various applications. However, their applications in wastewater treatment have remained unexplored. Here, we investigate their potential in wastewater treatment and demonstrate a new concept of IL incorporation in ligand-functionalized MOFs, introducing IL/FMOFs. The composites were prepared by incorporating 1-n-butyl-3-methylimidazolium hexafluorophosphate, [BMIM][PF6], into UiO-66 and NH2-UiO-66 and tested for the adsorption of methylene blue (MB) and methyl orange (MO) from aqueous solutions. Data showed that NH2-functionalization and [BMIM][PF6] incorporation improved MB removal performance of UiO-66 by 16- and 48-times, as the capacity increased from 84.8 to 144.7 mg g(-1) and 174.1 mg g(-1), respectively. When considering both modifications together, [BMIM][PF6]/NH2-UiO-66 was almost 300 times faster than that of UiO-66, and the capacity exceeded 200 mg g(-1). Data further suggested that IL incorporation almost doubled MB/MO selectivity because of the strong electrostatic interactions and hydrogen bonding between [PF6](-) and MB, and pi-pi interactions between the [BMIM](+) cation and MB molecules. These results are the first to demonstrate the prospect of combining ligand functionalization with IL incorporation for modifying MOFs, introducing IL/FMOF composites for fast and selective removal of pollutants from wastewater.
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    PublicationOpen Access
    Cation exchange mediated synthesis of bright Au@ZnTe core-shell nanocrystals
    (Institute of Physics (IOP) Publishing, 2021) Şahin, Mehmet; N/A; Department of Electrical and Electronics Engineering; Sadeghi, Sadra; Melikov, Rustamzhon; Nizamoğlu, Sedat; PhD Student; PhD Student; Faculty Member; Department of Electrical and Electronics Engineering; Graduate School of Sciences and Engineering; College of Engineering; N/A; N/A; 130295
    The synthesis of heterostructured core-shell nanocrystals has attracted significant attention due to their wide range of applications in energy, medicine and environment. To further extend the possible nanostructures, non-epitaxial growth is introduced to form heterostructures with large lattice mismatches, which cannot be achieved by classical epitaxial growth techniques. Here, we report the synthetic procedure of Au@ZnTe core-shell nanostructures by cation exchange reaction for the first time. For that, bimetallic Au@Ag heterostructures were synthesized by using PDDA as stabilizer and shape-controller. Then, by addition of Te and Zn precursors in a step-wise reaction, the zinc and silver cation exchange was performed and Au@ZnTe nanocrystals were obtained. Structural and optical characterization confirmed the formation of the Au@ZnTe nanocrystals. The optimization of the synthesis led to the bright nanocrystals with a photoluminescence quantum yield up to 27%. The non-toxic, versatile synthetic route, and bright emission of the synthesized Au@ZnTe nanocrystals offer significant potential for future bio-imaging and optoelectronic applications.
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    PublicationOpen Access
    Quantum dot to nanorod transition for efficient white-light-emitting diodes with suppressed absorption losses
    (American Chemical Society (ACS), 2022) Melikov, Rustamzhon; N/A; Department of Electrical and Electronics Engineering; N/A; Önal, Asım; Sadeghi, Sadra; Karatüm, Onuralp; Nizamoğlu, Sedat; Eren, Güncem Özgün; PhD Student; Faculty Member; Department of Electrical and Electronics Engineering; College of Engineering; Graduate School of Sciences and Engineering; N/A; N/A; N/A; 130295; N/A
    Colloidal nanocrystals have great potential for next-generation solid-state lighting due to their outstanding emission and absorption tunability via size and morphology, narrow emission linewidth, and high photoluminescence quantum yield (PLQY). However, the losses due to self-and interabsorption among multitudes of nanocrystals significantly decrease external quantum yield levels of light-emitting diodes (LEDs). Here, we demonstrate efficient white LEDs via CdSe/CdS dot to ""dot-in-rod"" transition that enabled a large Stokes shift of 780 meV and significantly reduced absorption losses when used in conjunction with near-unity PLQY ZnCdSe/ZnSe quantum dots (QDs) emitting at the green spectral range. The optimized incorporation of nanocrystals in a liquid state led to the white LEDs with an ultimate external quantum efficiency (EQE) of 42.9%, with a net increase of EQE of 10.3% in comparison with white LEDs using CdSe/CdS dots. Therefore, combinations of nanocrystals with different nanomorphologies hold high promise for efficient white LEDs.