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Permanent URI for this collectionhttps://hdl.handle.net/20.500.14288/3

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    Non-invasive raman classification comparison with pXRF of monochrome and related qing porcelains: lead-rich-, lead-poor-, and alkali-based glazes
    (Multidisciplinary Digital Publishing Institute (MDPI), 2024) Colomban, Philippe; Gallet, Xavier; Fournery, Nicolas; Quette, Béatrice; Franci, Gülsu Şimşek; Koç University Surface Science and Technology Center (KUYTAM) / Koç Üniversitesi Yüzey Teknolojileri Araştırmaları Merkezi (KUYTAM)
    Chinese porcelain with an optically clear colored glaze, imported to Europe from the Kangxi period (1662–1722, Qing Dynasty) onwards was highly collected by the French Elite of the 18th century. The bright colors with a clear, shiny glaze were unlike anything produced in Europe at that time. The colors of enamelled artifacts (on biscuits or already glazed porcelain) can be fully monochrome or consist of associations of large monochromatic areas with or without application of gilding. Non-invasive portable XRF and mobile Raman analyses have previously shown their effectiveness in the characterization of (colored) glassy silicates. In this study, we compare the Raman signatures of twenty-one Chinese artifacts fully—or with major monochrome area (sancai)—decorated with blue, turquoise (or celectian blue), honey-yellow, green, eggplant, and red color. Different types of glazes are identified and confirmed by pXRF: lead-rich, lead-poor-alkali, lead-doped alkali, and alkali-based compositions. However, an unexpected low level of lead is observed in the turquoise glazes, likely to optimize the gloss. Raman spectroscopy appears more reliable to compare the Pb content than pXRF. This work presents Raman spectral signatures of glazes that can potentially be used for non-invasive object classification and counterfeit detection.
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    Roadmap for clinical translation of mobile microrobotics
    (Wiley-V C H Verlag Gmbh, 2024) Bozuyuk, Ugur; Wrede, Paul; Yildiz, Erdost; Department of Mechanical Engineering; Sitti, Metin; Department of Mechanical Engineering; College of Engineering; School of Medicine
    Medical microrobotics is an emerging field to revolutionize clinical applications in diagnostics and therapeutics of various diseases. On the other hand, the mobile microrobotics field has important obstacles to pass before clinical translation. This article focuses on these challenges and provides a roadmap of medical microrobots to enable their clinical use. From the concept of a "magic bullet" to the physicochemical interactions of microrobots in complex biological environments in medical applications, there are several translational steps to consider. Clinical translation of mobile microrobots is only possible with a close collaboration between clinical experts and microrobotics researchers to address the technical challenges in microfabrication, safety, and imaging. The clinical application potential can be materialized by designing microrobots that can solve the current main challenges, such as actuation limitations, material stability, and imaging constraints. The strengths and weaknesses of the current progress in the microrobotics field are discussed and a roadmap for their clinical applications in the near future is outlined. The clinical use of medical microrobots gets closer to reality with the rapidly growing biomedical research on them. However, the clinical translation of microrobots has several challenges and obstacles, including scalability, biocompatibility, and imaging. In this review article, a realistic roadmap for medical microrobots is conceptualized with the collaborative efforts of microrobot researchers and clinicians.
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    Silk as a biodegradable resist for field-emission scanning probe lithography
    (Institute of Physics (IOP) Publishing, 2020) Sadeghi, Sadra; Rangelow, Ivo W.; Department of Mechanical Engineering; Department of Electrical and Electronics Engineering; N/A; N/A; Department of Electrical and Electronics Engineering; Alaca, Burhanettin Erdem; Kumar, Baskaran Ganesh; Melikov, Rustamzhon; Doğru-Yüksel, Itır Bakış; Nizamoğlu, Sedat; Faculty Member; Other; PhD Student; PhD Student; Faculty Member; Department of Mechanical Engineering; Department of Electrical and Electronics Engineering; Koç University Surface Science and Technology Center (KUYTAM) / Koç Üniversitesi Yüzey Teknolojileri Araştirmalari Merkezi (KUYTAM); N/A; N/A; N/A; N/A; College of Engineering; College of Engineering; Graduate School of Sciences and Engineering; Graduate School of Sciences and Engineering; College of Engineering; 115108; N/A; N/A; N/A; 130295
    The patterning of silk allows for manufacturing various structures with advanced functionalities for optical and tissue engineering and drug delivery applications. Here, we propose a high-resolution nanoscale patterning method based on field-emission scanning probe lithography (FE-SPL) that crosslinks the biomaterial silk on conductive indium tin oxide (ITO) promoting the use of a biodegradable material as resist and water as a developer. During the lithographic process, Fowler-Nordheim electron emission from a sharp tip was used to manipulate the structure of silk fibroin from random coil to beta sheet and the emission formed nanoscale latent patterns with a critical dimension (CD) of similar to 50 nm. To demonstrate the versatility of the method, we patterned standard and complex shapes. This method is particularly attractive due to its ease of operation without relying on a vacuum or a special gaseous environment and without any need for complex electronics or optics. Therefore, this study paves a practical and cost-effective way toward patterning biopolymers at ultra-high level resolution.
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    An electrochemical gelation method for patterning conductive PEDOT:PSS hydrogels
    (2019) Feig, Vivian Rachel; Tran, Helen; Lee, Minah; Liu, Kathy; Huang, Zhuojun; Mackanic, David G.; Bao, Zhenan; Department of Mechanical Engineering; Beker, Levent; Faculty Member; Department of Mechanical Engineering; College of Engineering; 308798
    Due to their high water content and macroscopic connectivity, hydrogels made from the conducting polymer PEDOT:PSS are a promising platform from which to fabricate a wide range of porous conductive materials that are increasingly of interest in applications as varied as bioelectronics, regen-erative medicine, and energy storage. Despite the promising properties of PEDOT:PSS-based porous materials, the ability to pattern PEDOT:PSS hydrogels is still required to enable their integration with multifunctional and multichannel electronic devices. In this work, a novel electrochemical gelation (“electrogelation”) method is presented for rapidly patterning PEDOT:PSS hydrogels on any conductive template, including curved and 3D surfaces. High spatial resolution is achieved through use of a sacrificial metal layer to generate the hydrogel pattern, thereby enabling high-performance conducting hydrogels and aerogels with desirable material properties to be introduced into increasingly complex device architectures
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    Development of color tunable aqueous cds-cysteine quantum dots with improved efficiency and investigation of cytotoxicity
    (Amer Scientific Publishers, 2010) N/A; N/A; Department of Chemistry; Department of Chemistry; Öztürk, Sinan S.; Selçukbiricik, Fatih; Acar, Havva Funda Yağcı; Master Student; N/A; Faculty Member; Department of Chemistry; Graduate School of Sciences and Engineering; College of Sciences; College of Sciences; N/A; N/A; 178902
    Cysteine capped aqueous CdS quantum dots with improved luminescence and excellent colloidal-luminescence stability were developed in a simple one pot aqueous method from safer precursors at low temperatures. Investigation of size and luminescence as a function of cysteine amount, pH and temperature revealed an optimum value for all these variables to maximize the quantum yield. Cysteine:Cd ratio of 2, reaction pH of 9.5 and synthesis at room temperature-30 degrees C emerged as the best conditions for the highest QY of 19%. Yet, QY can be improved up to 55% if QDs are cleaned from excess cysteine and ions and redispersed in pH 7 medium. Size of the QDs, therefore the color of luminescence, can be tuned by the reaction temperature in this simple process. Higher temperatures provide larger particles. Cell uptake and cell viability studies in a wide range of doses and different incubation times with MCF-7 and HeLa cell lines revealed cell dependent differences. MCF-7 cells uptake more ODs but are much more viable than HeLa cells. At low doses such as 0.025 mg QD/ml all cells are viable. At 24 h incubation times MCF-7 cells demonstrate viability above 75% up to 0.15 mg QD/ml. On the other hand HeLa cells loose viability with increasing dose.
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    Fluorescent protein integrated white LEDs for displays
    (Iop Publishing Ltd, 2016) N/A; Department of Electrical and Electronics Engineering; N/A; N/A; Department of Molecular Biology and Genetics; Department of Electrical and Electronics Engineering; Press, Daniel Aaron; Melikov, Rustamzhon; Çonkar, Deniz; Karalar, Elif Nur Fırat; Nizamoğlu, Sedat; Researcher; PhD Student; PhD Student; Faculty Member; Faculty Member; Department of Molecular Biology and Genetics; Department of Electrical and Electronics Engineering; College of Engineering; Graduate School of Sciences and Engineering; Graduate School of Sciences and Engineering; College of Sciences; College of Engineering; N/A; N/A; N/A; 206349; 130295
    The usage time of displays (e.g., TVs, mobile phones, etc) is in general shorter than their functional life time, which worsens the electronic waste (e-waste) problem around the world. The integration of biomaterials into electronics can help to reduce the e-waste problem. In this study, we demonstrate fluorescent protein integrated white LEDs to use as a backlight source for liquid crystal (LC) displays for the first time. We express and purify enhanced green fluorescent protein (eGFP) and monomeric Cherry protein (mCherry), and afterward we integrate these proteins as a wavelength-converter on a blue LED chip. The protein-integrated backlight exhibits a high luminous efficacy of 248 lm/W-opt and the area of the gamut covers 80% of the NTSC color gamut. The resultant colors and objects in the image on the display can be well observed and distinguished. Therefore, fluorescent proteins show promise for display applications.
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    Size driven barrier to chirality reversal in electric control of magnetic vortices in ferromagnetic nanodiscs
    (Royal Soc Chemistry, 2023) Aldulaimi, W. A. S.; Okatan, M. B.; Sendur, K.; Misirlioglu, I. B.; Department of Electrical and Electronics Engineering; Onbaşlı, Mehmet Cengiz; Faculty Member; Department of Electrical and Electronics Engineering; College of Engineering; 258783
    New high density storage media and spintronic devices come about with a progressing demand for the miniaturization of ferromagnetic structures. Vortex ordering of magnetic dipoles in such structures has been repeatedly observed as a stable state, offering the possibility of chirality in these states as a means to store information at high density. Electric pulses and magnetoelectric coupling are attractive options to control the chirality of such states in a deterministic manner. Here, we demonstrate the chirality reversal of vortex states in ferromagnetic nanodiscs via pulsed electric fields using a micromagnetic approach and focus on the analysis of the energetics of the reversal process. A strong thickness dependence of the chirality reversal in the nanodiscs is found that emanates from the anisotropy of the demagnetizing fields. Our results indicate that chiral switching of the magnetic moments in thin discs can give rise to a transient vortex-antivortex lattice not observed in thicker discs. This difference in the chirality reversal mechanism emanates from profoundly different energy barriers to overcome in thin and thicker discs. We also report the polarity-chirality correlation of a vortex that appears to depend on the aspect ratio of the nanodiscs.
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    Structural control of InP/ZnS core/shell quantum dots enables high-quality white LEDs
    (Iop Publishing Ltd, 2018) Ow-Yang, Cleva W; Department of Electrical and Electronics Engineering; N/A; N/A; N/A; N/A; Department of Electrical and Electronics Engineering; Kumar, Baskaran Ganesh; Sadeghi, Sadra; Melikov, Rustamzhon; Aria, Mohammad Mohammadi; Jalali, Houman Bahmani; Nizamoğlu, Sedat; Other; PhD Student; PhD Student; PhD Student; PhD Student; Faculty Member; Department of Electrical and Electronics Engineering; College of Engineering; Graduate School of Sciences and Engineering; Graduate School of Sciences and Engineering; Graduate School of Sciences and Engineering; Graduate School of Sciences and Engineering; College of Engineering; N/A; N/A; N/A; N/A; N/A; 130295
    Herein, we demonstrate that the structural and optical control of InP-based quantum dots (QDs) can lead to high-performance light-emitting diodes (LEDs). Zinc sulphide (ZnS) shells passivate the InP QD core and increase the quantum yield in green-emitting QDs by 13-fold and redemitting QDs by 8-fold. The optimised QDs are integrated in the liquid state to eliminate aggregation-induced emission quenching and we fabricated white LEDs with a warm, neutral and cool-white appearance by the down-conversion mechanism The QD-functionalized white LEDs achieve luminous efficiency (LE) up to 14.7 lm W-1 and colour-rendering index up to 80. The structural and optical control of InP/ZnS core/shell QDs enable 23-fold enhancement in LE of white LEDs compared to ones containing only QDs of InP core.