Scopus İndeksli Yayınlar Koleksiyonu

Permanent URI for this collectionhttps://hdl.handle.net/20.500.12573/395

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  • Article
    Citation - WoS: 6
    Citation - Scopus: 5
    Photoluminescent and Superhydrophobic Nanocomposites of Perovskite Nanocrystals
    (Elsevier, 2024-03) Ocal, Sema Karabel; Celik, Nusret; Onses, M. Serdar; Mutlugun, Evren; Karabel Ocal, Sema
    Perovskite nanocrystals (PNCs) have found extensive utility across diverse technological applications in optoelectronics; nevertheless, their susceptibility to environmental instability poses a significant constraint on their practicality. Within this investigation, we present a novel and facile approach for the development of highly stable superhydrophobic PNCs. These engineered superhydrophobic perovskite nanocrystal composites, referred to as HSNPs@PNCs, demonstrate remarkable optoelectronic attributes, provided that their inherent instability can be effectively mitigated. HSNPs@PNCs manifest an impressive water contact angle of 172 degrees and an exceedingly low sliding angle of 1 degrees, thus showcasing their exceptional superhydrophobicity. Of particular note is the extraordinary stability exhibited by HSNPs@PNCs despite aqueous environments, thermal fluctuations, and UV exposure. Remarkably, even after a prolonged 30 -day immersion in water, this nanocomposite maintains an outstanding emission efficiency of 75 %. Furthermore, the method of application through a spray deposition technique circumvents sample size limitations, thereby amplifying their suitability for industrial applications. Moreover, this study extends the practicality of HSNPs@PNCs by enabling their homogeneous coating onto various surfaces such as glass, fabric, and aluminum, yielding luminescent superhydrophobic surfaces. This approach liberates the substrates from constraints, significantly broadening the potential spectrum of applications for these materials within diverse industrial and technological domains.
  • Article
    Citation - Scopus: 151
    Highly Flexible, Electrically Driven, Top-Emitting, Quantum Dot Light-Emitting Stickers
    (American Chemical Society, 2014-07-18) Yang, Xuyong; Mutlugün, Evren; Dang, Cuong H.; Dev, Kapil; Gao, Yuan; Tan, Swee Tiam; Volkan Demir, Hilmi Volkan; Demir, Hilmi Volkan
    Flexible information displays are key elements in future optoelectronic devices. Quantum dot light-emitting diodes (QLEDs) with advantages in color quality, stability, and cost-effectiveness are emerging as a candidate for single-material, full color light sources. Despite the recent advances in QLED technology, making high-performance flexible QLEDs still remains a big challenge due to limited choices of proper materials and device architectures as well as poor mechanical stability. Here, we show highly efficient, large-area QLED tapes emitting in red, green, and blue (RGB) colors with top-emitting design and polyimide tapes as flexible substrates. The brightness and quantum efficiency are 20 000 cd/m2 and 4.03%, respectively, the highest values reported for flexible QLEDs. Besides the excellent electroluminescence performance, these QLED films are highly flexible and mechanically robust to use as electrically driven light-emitting stickers by placing on or removing from any curved surface, facilitating versatile LED applications. Our QLED tapes present a step toward practical quantum dot based platforms for high-performance flexible displays and solid-state lighting. © 2014 American Chemical Society. © 2021 Elsevier B.V., All rights reserved.
  • Article
    Citation - Scopus: 47
    Air-Stable, Nanostructured Electronic and Plasmonic Materials From Solution-Processable, Silver Nanocrystal Building Blocks
    (American Chemical Society service@acs.org, 2014-02-10) Fafarman, Aaron T.; Hong, Sunghoon; Oh, Soongju; Caglayan, Humeyra; Ye, Xingchen; Diroll, Benjamin T.; Kagan, Cherie R.
    Herein we describe a room-temperature, chemical process to transform silver nanocrystal solids, deposited from colloidal solutions, into highly conductive, corrosion-resistant, optical and electronic materials with nanometer-scale architectures. After assembling the nanocrystal solids, we treated them with a set of simple, compact, organic and inorganic reagents: ammonium thiocyanate, ammonium chloride, potassium hydrogen sulfide, and ethanedithiol. We find that each reagent induces unique changes in the structure and composition of the resulting solid, giving rise to films that vary from insulating to, in the case of thiocyanate, conducting with a remarkably low resistivity of 8.8 × 10-6 ·cm, only 6 times that of bulk silver. We show that thiocyanate mediates the spontaneous sintering of nanocrystals into structures with a roughness of less than 1/10th of the wavelength of visible light. We demonstrate that these solution-processed, low-resistivity, optically smooth films can be patterned, using imprint lithography, into conductive electrodes and plasmonic mesostructures with programmable resonances. We observe that thiocyanate-treated solids exhibit significantly retarded atmospheric corrosion, a feature that dramatically increases the feasibility of employing silver for electrical and plasmonic applications. © 2014 American Chemical Society. © 2014 Elsevier B.V., All rights reserved.