WoS İndeksli Yayınlar Koleksiyonu
Permanent URI for this collectionhttps://hdl.handle.net/20.500.12573/394
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Article Citation - WoS: 4Citation - Scopus: 4Transparent Films Made of Highly Scattering Particles(Amer Chemical Soc, 2020-01-13) Erdem, Talha; Yang, Lan; Xu, Peicheng; Altintas, Yemliha; O'Neil, Thomas; Caciagli, Alessio; Eiser, ErikaToday, colloids are widely employed in various products from creams and coatings to electronics. The ability to control their chemical, optical, or electronic features by controlling their size and shape explains why these materials are so widely preferred. Nevertheless, altering some of these properties may also lead to some undesired side effects, one of which is an increase in optical scattering upon concentration. Here, we address this strong scattering issue in films made of binary colloidal suspensions. In particular, we focus on raspberry-type polymeric particles made of a spherical polystyrene core decorated by small hemispherical domains of acrylate with an overall positive charge, which display an unusual stability against aggregation in aqueous solutions. Their solid films display a brilliant red color due to Bragg scattering but appear completely white on account of strong scattering otherwise. To suppress the scattering and induce transparency, we prepared films by hybridizing them with oppositely charged PS particles with a size similar to that of the bumps on the raspberries. We report that the smaller PS particles prevent raspberry particle aggregation in solid films and suppress scattering by decreasing the spatial variation of the refractive index inside the film. We believe that the results presented here provide a simple strategy to suppress strong scattering of larger particles to be used in optical coatings.Article Citation - WoS: 53Citation - Scopus: 59Thickness-Tunable Self-Assembled Colloidal Nanoplatelet Films Enable Ultrathin Optical Gain Media(Amer Chemical Soc, 2020-07-31) Erdem, Onur; Foroutan, Sina; Gheshlaghi, Negar; Guzelturk, Burak; Altintas, Yemliha; Demir, Hilmi VolkanWe propose and demonstrate construction of highly uniform, multilayered superstructures of CdSe/CdZnS core/shell colloidal nanoplatelets (NPLs) using liquid interface self-assembly. These NPLs are sequentially deposited onto a solid substrate into slabs having monolayer-precise thickness across tens of cm(2) areas. Because of near-unity surface coverage and excellent uniformity, amplified spontaneous emission (ASE) is observed from an uncharacteristically thin film having 6 NPL layers, corresponding to a mere 42 nm thickness. Furthermore, systematic studies on optical gain of these NPL superstructures having thicknesses ranging from 6 to 15 layers revealed the gradual reduction in gain threshold with increasing number of layers, along with a continuous spectral shift of the ASE peak (similar to 18 nm). These observations can be explained by the change in the optical mode confinement factor with the NPL waveguide thickness and propagation wavelength. This bottom-up construction technique for thickness-tunable, three-dimensional NPL superstructures can be used for large-area device fabrication.Article Citation - WoS: 37Citation - Scopus: 39Spectrally Wide-Range Efficient, and Bright Colloidal Light-Emitting Diodes of Quasi-2D Nanoplatelets Enabled by Engineered Alloyed Heterostructures(Amer Chemical Soc, 2020-08-25) Altintas, Yemliha; Liu, Baiquan; Hernandez-Martinez, Pedro Ludwig; Gheshlaghi, Negar; Shabani, Farzan; Sharma, Manoj; Demir, Hilmi VolkanRecently, there has been tremendous interest in the synthesis and optoelectronic applications of quasi-two-dimensional colloidal nanoplatelets (NPLs). Thanks to the ultranarrow emission linewidth, high-extinction coefficient, and high photostability, NPLs offer an exciting opportunity for high-performance optoelectronics. However, until now, the applications of these NPLs are limited to available discrete emission ranges, limiting the full potential of these exotic materials as efficient light emitters. Here, we introduce a detailed systematic study on the synthesis of NPLs based on the alloying mechanisms in core/shell, core/alloyed shell, alloyed core/shell, and alloyed core/alloyed shell heterostructures. Through the engineering of the band gap supported by the theoretical calculations, we carefully designed and successfully synthesized the NPL emitters with continuously tunable emission. Unlike conventional NPLs showing discrete emission, here, we present highly efficient core/shell NPLs with fine spectral tunability from green to deep-red spectra. As an important demonstration of these efficient emitters, the first-time implementation of yellow NPL light-emitting diodes (LEDs) has been reported with record device performance, including the current efficiency surpassing 18.2 cd A(-1), power efficiency reaching 14.8 lm W-1, and record luminance exceeding 46 900 cd m(-2). This fine and wide-range color tunability in the visible range from stable and efficient core/shell NPLs is expected to be extremely important for the optoelectronic applications of the family of colloidal NPL emitters.Article Citation - WoS: 16Citation - Scopus: 17Solid-State Encapsulation and Color Tuning in Films of Cesium Lead Halide Perovskite Nanocrystals for White Light Generation(Amer Chemical Soc, 2019-01-30) Torun, Ilker; Altintas, Yemliha; Yazici, Ahmet Faruk; Mutlugun, Evren; Onses, M. SerdarPerovskite nanocrystals (PNCs) are highly demanding nanomaterials for solid-state lighting applications. A challenge for their exploitation in practical applications is the insufficient ambient and water stability associated with their ionic nature. Here we report a novel route for solid-state encapsulation of films of perovskite nanocrystals (PNCs) through vapor-phase deposition of a thin and hydrophobic layer of fluoroalkyltrichlorosilanes (FAS). High quality nanoscale crystals of CsPbBr3 were synthesized with well established colloidal methods and coated on solid substrates. The films of PNCs were then subjected to vapor of FAS for short durations of time (<60 s) in ambient atmosphere, resulting in deposition of a thin (<20 nm) hydrophobic layer. Besides providing a barrier for water and humidity, the vapor-phase deposition of FAS was accompanied by the blue shift of the emission wavelength of the PNCs. The color shift results from the partial exchange of Br with Cl anions, which emerge during the self-hydrolysis of the silane molecules. Throughout this process, we demonstrate the enhanced water stability of the films of PNCs and fine tunability of the wavelength in films from 516 nm to 488 nm. The fabrication of a white-light-emitting diode and tunability of the color coordinates with the duration of the FAS deposition were demonstrated. The rapid, scalable, and inexpensive solid-state encapsulation approach shows great promise for films of halide perovskites.Article Citation - WoS: 25Citation - Scopus: 25Self-Resonant Microlasers of Colloidal Quantum Wells Constructed by Direct Deep Patterning(Amer Chemical Soc, 2021-05-24) Gheshlaghi, Negar; Foroutan-Barenji, Sina; Erdem, Onur; Altintas, Yemliha; Shabani, Farzan; Humayun, Muhammad Hamza; Demir, Hilmi VolkanHere, the first account of self-resonant fully colloidal mu-lasers made from colloidal quantum well (CQW) solution is reported. A deep patterning technique is developed to fabricate well-defined high aspect-ratio on-chip CQW resonators made of grating waveguides and in-plane reflectors. The fabricated waveguide-coupled laser, enabling tight optical confinement, assures in-plane lasing. CQWs of the patterned layers are closed-packed with sharp edges and residual-free lifted-off surfaces. Additionally, the method is successfully applied to various nanoparticles including colloidal quantum dots and metal nanoparticles. It is observed that the patterning process does not affect the nanocrystals (NCs) immobilized in the attained patterns and the different physical and chemical properties of the NCs remain pristine. Thanks to the deep patterning capability of the proposed method, patterns of NCs with subwavelength lateral feature sizes and micron-scale heights can possibly be fabricated in high aspect ratios.Article Citation - WoS: 101Citation - Scopus: 104Giant Alloyed Hot Injection Shells Enable Ultralow Optical Gain Threshold in Colloidal Quantum Wells(Amer Chemical Soc, 2019-08-22) Altintas, Yemliha; Gungor, Kivanc; Gao, Yuan; Sak, Mustafa; Quliyeva, Ulviyya; Bappi, Golam; Demir, Hilmi VolkanAs an attractive materials system for high- Record-low optical gain threshold in giant-shell COWs performance optoelectronics, colloidal nanoplatelets (NPLs) benefit from atomic-level precision in thickness, minimizing emission inhomogeneous broadening. Much progress has been made to enhance their photoluminescence quantum yield (PLQY) and photostability. However, to date, layer-by-layer growth of shells at room temperature has resulted in defects that limit PLQY and thus curtail the 0.2 performance of NPLs as an optical gain medium. Here, we introduce a hot-injection method growing giant alloyed shells using an approach that reduces core/shell lattice mismatch and suppresses Auger recombination. Near-unity PLQY is achieved with a narrow full-width-at-half-maximum (20 nm), accompanied by emission tunability (from 610 to 650 nm). The biexciton lifetime exceeds 1 ns, an order of magnitude longer than in conventional colloidal quantum dots (CQDs). Reduced Auger recombination enables record-low amplified spontaneous emission threshold of 2.4 mu J cm(-2) under one-photon pumping. This is lower by a factor of 2.5 than the best previously reported value in nanocrystals (6 /kJ cm(-2) for CdSe/CdS NPLs). Here, we also report single-mode lasing operation with a 0.55 mu J cm(-2) threshold under two-photoexcitation, which is also the best among nanocrystals (compared to 0.76 mu J cm(-2) from CdSe/CdS CQDs in the Fabry-Perot cavity). These findings indicate that hot-injection growth of thick alloyed shells makes ultrahigh performance NPLs.Article Citation - WoS: 21Citation - Scopus: 21Efficient Forster Resonance Energy Transfer Donors of In(Zn)P/ZnS Quantum Dots(Amer Chemical Soc, 2017-01-26) Altintas, Yemliha; Talpur, Mohammad Younis; Mutlugun, Evren; Altlntas, YemlihaWe demonstrate a detailed investigation of the effect of the type and concentration of zinc precursor on the optical properties of In(Zn)P/ZnS quantum dots. We achieved up to 87% quantum yield along with 54 nm emission bandwidth for the green emitters with changing the concentration of the Zn precursors. Employing efficient green emitters as the donor species, we demonstrated an efficient Forster resonance energy transfer (FRET) couple of green and red emitting InP-based quantum dots. With a FRET efficiency level of 70.3% achieved (analyzed from the donor lifetime with and without an acceptor), we further demonstrated the enhancement of the acceptor emission nearly twofold due to the energy transfer. Our results provide new insights toward the understanding of the excitonic interactions among donor and acceptor quantum dots of the III-V family for light harvesting applications.Article Citation - WoS: 44Citation - Scopus: 46Highly Efficient Cd-Free Alloyed Core/Shell Quantum Dots With Optimized Precursor Concentrations(Amer Chemical Soc, 2016) Altintas, Yemliha; Talpur, Mohammad Younis; Unlu, Miray; Mutlugun, EvrenThe chemical composition, the emission spectral bandwidth, and photoluminescence quantum yield of a semiconductor quantum dot (QD) play an important role in the assessment of the performance of the applications related to the quantum dots. Quantum dots based on environmentally friendly compositions with high optical performance have been in demand for high-end technological applications. In this work, we propose and demonstrate a detailed synthesis approach for environmentally friendly and highly efficient InPZnS alloy/ZnS shell quantum dots. Following a systematic study of the ratio and type of the precursors involved, we achieved alloyed core shell InPZnS/ZnS QDs with tunable emission across the visible spectrum, having a record quantum efficiency up to 78% along with a full width at half-maximum as narrow as 45 nm. The effect of the systematic shell growth has been further investigated using time-resolved photoluminescence characterizations along with the observation of the suppression of the nonradiative decay channels, with the photoluminescence lifetime prolonged from 20.3 to 50.4 ns. The development of highly efficient and environmentally friendly QDs will pave the way for robust, sustainable optoelectronic applications.