WoS İndeksli Yayınlar Koleksiyonu
Permanent URI for this collectionhttps://hdl.handle.net/20.500.12573/394
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Article Citation - WoS: 2Citation - Scopus: 1Fully Inorganic Colloidal CsPbBr3 Perovskite Nanocrystals with Zn-Doping and Metal Oxide Encapsulation for Luminescent Display Panels(Amer Chemical Soc, 2025-11-07) Khorasani, Azam; Soheyli, Ehsan; Mutlugun, EvrenPerovskite nanocrystals (PeNCs) are emerging as exceptional materials due to their high photoluminescence quantum yield, tunable bandgap, and excellent charge carrier mobility, enabling a wide range of colors and promising applications in optoelectronics and photovoltaics. Despite their advantages, PeNCs face stability challenges caused by environmental factors. In the presented study, a facile and versatile colloidal hot-injection method was used to apply the beneficial aspects of Zn-doping in cesium lead bromide (CsPbBr3) PeNCs. The uniform platelet-shaped Zn-doped CsPbBr3 PeNCs were prepared by doping with a 0.1 molar ratio of zinc-oleate solution in the perovskite precursors during synthesis. Then, zinc-oxide (ZnO) and nickel-oxide (NiO) coating layers were utilized separately to effectively reduce surface defects, encapsulate PeNCs, and improve their stability issues. To fabricate the coated PeNCs with metal oxides, zinc acetate and nickel(II) acetate tetrahydrate solutions were prepared individually and added to the crude perovskite solutions. The quantum yield of Zn-doped CsPbBr3 (CsPb1-xZnxBr3) PeNCs coated with ZnO increased from 50% for bare CsPbBr3 to over 84%, while NiO-coated PeNCs exhibited a higher yield of 90% both of which remarkably enhanced the emission stability. Moreover, NiO coatings represented a proper protection against surface imperfections and improved resistance to external stimuli. The combination of facile/effective preparation method, excellent emission efficiency, and reliable emission stability nominates the prepared colloidal composite for display pixels, detectors, and lasers.Article Citation - WoS: 13Citation - Scopus: 13Tuning the Shades of Red Emission in InP/ZnSe Nanocrystals With Narrow Full Width for Fabrication of Light-Emitting Diodes(Amer Chemical Soc, 2023-10-13) Soheyli, Ehsan; Bicer, Aysenur; Ozel, Sultan Suleyman; Tiras, Kevser Sahin; Mutlugun, Evren; Sahin Tiras, KevserWhile Cd-based luminescent nanocrystals (NCs) are the most mature NCs for fabricating efficient red light-emitting diodes (LEDs), their toxicity related limitation is inevitable, making it necessary to find a promising alternative. From this point of view, multishell-coated, red-emissive InP-based NCs are excellent luminescent nanomaterials for use as an emissive layer in electroluminescent (EL) devices. However, due to the presence of oxidation states, they suffer from a wide emission spectrum, which limits their performance. This study uses tris-(dimethyl-amino)-phosphine (3DMA-P) as a low-cost aminophosphine precursor and a double HF treatment to suggest an upscaled, cost-effective, and one-pot hot-injection synthesis of purely red-emissive InP-based NCs. The InP core structures were coated with thick layers of ZnSe and ZnS shells to prevent charge delocalization and to create a narrow size distribution. The purified NCs showed an intense emission signal as narrow as 43 nm across the entire red wavelength range (626-670 nm) with an emission quantum efficiency of 74% at 632 nm. The purified samples also showed an emission quantum efficiency of 60% for far-red wavelengths of 670 nm with a narrow full width of 50 nm. The samples showed a relatively long average emission lifetime of 50-70 ns with a biexponential decay profile. To demonstrate the practical ability of the prepared NCs in optoelectronics, we fabricated a red-emissive InP-based LEDs. The best-performing device showed an external quantum efficiency (EQE) of 1.16%, a luminance of 1039 cd m(-2), and a current efficiency of 0.88 cd A(-1).Article Citation - WoS: 14Citation - Scopus: 13Spectrally Tunable White Light-Emitting Diodes Based on Carbon Quantum Dot-Doped Poly(N-Vinylcarbazole) Composites(Amer Chemical Soc, 2024-01-26) Sahin Tiras, Kevser; Bicer, Aysenur; Soheyli, Ehsan; Mutlugun, EvrenElectroluminescent white light-emitting diodes (WLEDs) are always of great interest for emerging display applications. Carbon-based quantum dots (CQDs) are the newest emerging nanoscale materials that can be employed for this purpose, owing to their broad and bright light emission properties. In the present work, highly luminescent CQDs with an emission quantum yield of 60% were prepared via a colloidal solvothermal method and subsequent silica gel column chromatography. The photoluminescence (PL) peak was located at 550 nm possessing yellow emission, with a full width at half-maximum of 98 nm and a relatively long lifetime of 10.23 ns through a single-exponential recombination pathway. CQDs were employed in an electroluminescent device architecture of an ITO/PEDOT:PSS/TFB/CQD:PVK/TPBi/LiF/Al structure and blended with poly(N-vinylcarbazole) (PVK) to evaluate their ability to reach white electroluminescent emission. Results confirmed a high external quantum efficiency (EQE) of 0.76% and a maximum luminescence of 774.3 cd<middle dot>m(-2). Tuning the ratio between CQDs and PVK from 1:10.25 to 1:5.75 resulted in a systematic shift in CIE x-y coordinates from 0.23-0.26 to 0.21-0.24, located close to the cool white region. The results of the present study can be considered a step forward in fabricating efficient WLEDs based on low-cost CQDs.Article Citation - WoS: 11Citation - Scopus: 13Solution-Processable Indenofluorenes on Polymer Brush Interlayer: Remarkable N-Channel Field-Effect Transistor Characteristics Under Ambient Conditions(Amer Chemical Soc, 2023-08-15) Can, Ayse; Deneme, Ibrahim; Demirel, Gokhan; Usta, HakanThe development of solution-processable n-type molecularsemiconductorsthat exhibit high electron mobility (& mu;(e) & GE;0.5 cm(2)/(V & BULL;s)) under ambient conditions, along withhigh current modulation (I (on)/I (off) & GE; 10(6)-10(7)) andnear-zero turn on voltage (V (on)) characteristics,has lagged behind that of other semiconductors in organic field-effecttransistors (OFETs). Here, we report the design, synthesis, physicochemicaland optoelectronic characterizations, and OFET performances of a libraryof solution-processable, low-LUMO (-4.20 eV) 2,2 & PRIME;-(2,8-bis(3-alkylthiophen-2-yl)indeno[1,2-b]fluorene-6,12-diylidene)dimalononitrile small molecules, & beta;,& beta;& PRIME;-C (n) -TIFDMTs, having varied alkyl chain lengths (n = 8, 12, 16). An intriguing correlation is identifiedbetween the solid-isotropic liquid transition enthalpies andthe solubilities, indicating that cohesive energetics, which are tunedby alkyl chains, play a pivotal role in determining solubility. Thesemiconductors were spin-coated under ambient conditions on denselypacked (grafting densities of 0.19-0.45 chains/nm(2)) ultrathin (& SIM;3.6-6.6 nm) polystyrene-brush surfaces.It is demonstrated that, on this polymer interlayer, thermally induceddispersive interactions occurring over a large number of methyleneunits between flexible alkyl chains (i.e., zipper effect) are criticalto achieve a favorable thin-film crystallization with a proper microstructureand morphology for efficient charge transport. While C-8 and C-16 chains show a minimal zipper effect upon thermalannealing, C-12 chains undergo an extended interdigitationinvolving & SIM;6 methylene units. This results in the formationof large crystallites having lamellar stacking ((100) coherence length & SIM;30 nm) in the out-of-plane direction and highly favorablein-plane & pi;-interactions in a slipped-stacked arrangement. Uninterruptedmicrostructural integrity (i.e., no face-on (010)-oriented crystallites)was found to be critical to achieving high mobilities. The excellentcrystallinity of the C-12-substituted semiconductor thinfilm was also evident in the observed crystal lattice vibrations (phonons)at 58 cm(-1) in low-frequency Raman scattering. Two-dimensionalmicrometer-sized (& SIM;1-3 & mu;m), sharp-edged plate-likegrains lying parallel with the substrate plane were observed. OFETsfabricated by the current small molecules showed excellent n-channelbehavior in ambient with & mu;(e) values reaching & SIM;0.9cm(2)/(V & BULL;s), I (on)/I (off) & SIM; 10(7)-10(8), and V (on) & AP; 0 V. Our study notonly demonstrates one of the highest performing n-channel OFET devicesreported under ambient conditions via solution processing but alsoelucidates significant relationships among chemical structures, molecularproperties, self-assembly from solution into a thin film, and semiconductingthin-film properties. The design rationales presented herein may openup new avenues for the development of high-electron-mobility novelelectron-deficient indenofluorene and short-axis substituted donor-acceptor & pi;-architectures via alkyl chain engineering and interface engineering.Article Citation - WoS: 51Citation - Scopus: 56Machine Learning-Aided Inverse Design and Discovery of Novel Polymeric Materials for Membrane Separation(Amer Chemical Soc, 2024-12-16) Dangayach, Raghav; Jeong, Nohyeong; Demirel, Elif; Uzal, Nigmet; Fung, Victor; Chen, YongshengPolymeric membranes have been widely used for liquid and gas separation in various industrial applications over the past few decades because of their exceptional versatility and high tunability. Traditional trial-and-error methods for material synthesis are inadequate to meet the growing demands for high-performance membranes. Machine learning (ML) has demonstrated huge potential to accelerate design and discovery of membrane materials. In this review, we cover strengths and weaknesses of the traditional methods, followed by a discussion on the emergence of ML for developing advanced polymeric membranes. We describe methodologies for data collection, data preparation, the commonly used ML models, and the explainable artificial intelligence (XAI) tools implemented in membrane research. Furthermore, we explain the experimental and computational validation steps to verify the results provided by these ML models. Subsequently, we showcase successful case studies of polymeric membranes and emphasize inverse design methodology within a ML-driven structured framework. Finally, we conclude by highlighting the recent progress, challenges, and future research directions to advance ML research for next generation polymeric membranes. With this review, we aim to provide a comprehensive guideline to researchers, scientists, and engineers assisting in the implementation of ML to membrane research and to accelerate the membrane design and material discovery process.Article Citation - WoS: 2Citation - Scopus: 2Light-Controlled Electrostatic Self-Assembly of Quantum Dots(Amer Chemical Soc, 2025-04-11) Akrema; Phul, Ruby; Yazici, Ahmet Faruk; Senel, Zeynep; Erdem, TalhaElectrostatic self-assembly is one of the important self-assembly mechanisms that found use in optoelectronics. Although this method enables realizing unconventional architectures, producing complicated architectures in large areas requires local control over the self-assembly process. One of the ways to achieve this control is to provide enough kinetic energy to the self-assembling nanoparticles so that they can escape electrostatic attraction. We hypothesize that this energy can be delivered to the nanoparticles by treating them with light that can be absorbed by the particles. Here, we test this idea to tailor the electrostatic self-assembly of semiconductor quantum dots (QDs) using a laser. Employing fluorescence and atomic force microscopy, we demonstrate that the QDs are not attached to the substrate in regions where they are exposed to light while they are coated in the absence of optical excitation. We further conduct theoretical analysis to show that elevated temperatures indeed allow the QDs to escape the electrostatic attraction of the charged polymers on the surface. We also demonstrate that increasing the temperature during the coating process without irradiating the sample gives similar results as the case when the sample was irradiated. Finally, we fabricate an uncoated region on the self-assembled QD film with dimensions of similar to 200 mu m x 0.5 cm to demonstrate the feasibility of our approach to control the bottom-up self-assembly. We believe that our results may pave the way for a cost-effective and sustainable approach for the fabrication of nanoelectronic and optoelectronic devices.Article Citation - WoS: 5Citation - Scopus: 5Inkjet Printing of Aqueous Silver Inks on Water-Soluble Fabrics for Transient Electronics Applications(Amer Chemical Soc, 2024-07-29) Onses, Zehra Gozutok; Kiremitler, N. Burak; Ozbasaran, Aleyna; Huang, Xian; Onses, Mustafa Serdar; Usta, Hakan; Gozutok Onses, ZehraThere is an urgent need to develop practical routes for manufacturing transient electronic devices to tackle the emerging issue of electronic waste and enable next-generation devices. This study reports additive patterning of conductive layers on industrially available water-soluble nonwoven fabrics composed of poly(vinyl alcohol) (PVA). Aqueous inks composed of reactive silver precursors can be practically patterned over water-soluble fabrics by inkjet printing. The efficient deposition of materials with droplet volumes on the order of picoliters ensures the generation of conductive patterns on a water-soluble fabric using a solution-processable fabrication with aqueous inks. The fabrication of conductive electrodes and transience behavior are studied on PVA fabrics with two different degrees of hydrolysis, providing tunability in the temperature-dependent degradation of the substrate. The application of the printed conductive pads is demonstrated in resistive heaters. The temperature of the fabric can exceed 100 degrees C in less than 15 s at a safe voltage of 3 V. The heater exhibits stable operation under cyclic heating and cooling. The presented approach presents key opportunities in additive patterning of aqueous solutions and colloidal dispersions over water-soluble substrates for transient device applications.Article Citation - WoS: 35Citation - Scopus: 36In Situ Synthesis of Horseradish Peroxidase Nanoflower@Carbon Nanotube Hybrid Nanobiocatalysts With Greatly Enhanced Catalytic Activity(Amer Chemical Soc, 2023-03-21) Dadi, Seyma; Temur, Nimet; Gul, O. Tolga; Yilmaz, Vedat; Ocsoy, IsmailOrganic-inorganic hybrid nanoflowers (NFs) consisting of horseradish peroxidase (HRP) and copper II (Cu2+) are successfully synthesized with the involvement of carbon nanotubes (CNTs) by in situ and post-modification methods. Catalytic activities of in situ synthesized HRP-NF@CNT (HRP-NF@CNT-Is) and post-modification-synthesized HRP-NF@CNTs (HRP-NF@CNT-Pm) are systematically examined. The 30 mg CNTs incorporated HRP-NF@CNT-Is (HRP-NF@ CNT-30Is) exhibits greatly increased catalytic activity and stability toward 3,3 ',5,5 '-tetramethylbenzidine (TMB), thanks to the synergistic effect between HRP-NF and CNTs and the peroxidase-like activity of CNTs in the presence of hydrogen peroxide (H2O2). While HRP-NF@CNT-30Is retains almost 85% of its initial activity even after 10 cycles, HRP-NF (without CNTs) loses half of its initial activity at the same experimental conditions. We study how two experimental parameters, the pH values and temperatures, influence the catalytic activity of HRP-NF@CNT-30Is, in addition to the fact that HRP-NF@CNT-30Is is employed to detect the presence of H2O2 and glutathione (GSH) with colorimetric and spectrophotometric readouts. For instance, HRP-NF@CNT-30Is is used to sensitively detect H2O2 in the range of 20 to 300 mu M with an LOD of 2.26 mu M. The catalytic activity of HRP-NF@CNT-30Is is suppressed in the presence of GSH, and then an obvious color change from blue to nearly colorless is observed. Using this strategy, GSH is also sensitively determined in the range of 20-200 mu M with an LOD of 11.2 mu M. We expect that HRP-NF@CNTs can be used as a promising and novel nanobiocatalyst for various biomedical and industrial applications in the near future.Article Citation - WoS: 6Citation - Scopus: 8Histone Deacetylase Inhibition and Autophagy Modulation Induces a Synergistic Antiproliferative Effect and Cell Death in Cholangiocarcinoma Cells(Amer Chemical Soc, 2023-06-08) Yenigul, Munevver; Akcok, Emel Basak Gencer; Gencer Akçok, Emel BaşakCholangiocarcinoma, also known as biliary tract cancer,is an aggressiveadenocarcinoma arising from epithelial cells lining the intra- andextrahepatic biliary system. The effects of autophagy modulators andhistone deacetylase (HDAC) inhibitors in cholangiocarcinoma are notfully known. It is essential to understand the molecular mechanismsand the effects of HDAC inhibitors in the context of cholangiocarcinoma.The antiproliferative effect of different HDAC inhibitors and autophagymodulation was investigated by the MTT cell viability assay in TFK-1and EGI-1 cholangiocarcinoma cell lines. Combination indexes werecalculated using CompuSyn software. Consequently, apoptosis was detectedby Annexin V/PI staining. The effect of the drugs on the cell cyclewas measured by the propidium iodide staining. The HDAC inhibitionwas confirmed via acetylated histone protein levels by western blotting.HDAC inhibitors, MS-275 and romidepsin, showed a better synergisticeffect with the nocodazole combination. The combination treatmentexerted its growth inhibitory effect by cell cycle arrest and inductionof apoptosis. The cell cycle analysis of the combination treatmentshowed that the S phase and G2/M phase were achieved. Moreover, thenecrotic and apoptotic cell population increased after single HDACinhibitors and combination treatment. The anti-cancer effect of HDACinhibitors is revealed by acetylation levels of histones. While acetylationlevels were increased in response to HDAC inhibitors and autophagymodulator combinations, the HDAC expression decreased. This studyhighlights the importance of the combination of HDAC inhibition andautophagy modulators and demonstrates a synergistic effect, whichcould be a promising therapy and novel treatment approach for cholangiocarcinoma.Article Citation - WoS: 7Citation - Scopus: 7Giant Negative Linear Compressibility, Isosymmetric Phase Transition, and Breathing Effect in a 3D Covalent Organic Framework(Amer Chemical Soc, 2023-12-26) Erkartal, MustafaA set of remarkable piezo-mechanical properties, including isosymmetric phase transition, negative linear compressibility (NLC), and a breathing effect in a three-dimensional covalent organic framework (NPN-3), was uncovered using density functional theory. The pressure-induced first-order phase transition observed between 0.9 and 1 GPa is isosymmetric and irreversible. NPN-3 shows giant NLC along the c-axis (K-c = 42.04 TPa-1) prior to the phase transition. The high-density NPN-3-hd obtained as a result of the phase transition shows an exciting phase transition from a closed pore to an open pore under hydrostatic tensile pressure, similar to the breathing effect. These extraordinary piezo-mechanical attributes within NPN-3 can be attributed to the diamondoid (dia) topology, which is commonly found within flexible MOFs and COFs. Additionally, the remarkable adaptability of the tetraphenyl adamantane monomer to distinct conformations under pressure can be seen in these properties. These findings underscore the potential utility of COFs as materials for piezo-mechanical sensors and serve as a source of inspiration for further exploration into the intricate mechanical behaviors of COFs.