WoS İndeksli Yayınlar Koleksiyonu
Permanent URI for this collectionhttps://hdl.handle.net/20.500.12573/394
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Article Enhanced Photoluminescence and Stability of CsPbBr3 Perovskite Nanocrystals Through AuCl Doping(Springer, 2026-02) Khorasani, Azam; Mutlugun, EvrenThis study delves into the transformative effects of inorganic gold chloride (AuCl) doping on all-inorganic cesium lead bromide (CsPbBr3) colloidal perovskite quantum dots (PeQDs). Using a precise hot injection synthesis method, AuCl was introduced at concentrations ranging from 0 to 10%, enabling a comprehensive analysis of its impact on the structural, morphological, and optical characteristics of CsPbBr3 PeQDs. We systematically investigated how varying AuCl levels influence photoluminescence (PL), PL quantum yield (PLQY), and the stability of these quantum dots. Advanced characterization techniques, including X-ray diffraction (XRD), scanning transmission electron microscopy (STEM), energy dispersive X-ray analysis (EDX), Fourier-transform infrared spectroscopy (FTIR), UV-Vis absorption, steady-state PL, absolute PL measurement, and time-resolved PL (TRPL), provided a detailed insight into these changes. Our findings indicate that AuCl doping is successfully integrated into CsPbBr3 PeQDs, with 5% identified as the optimal concentration. At this level, the quantum dots show enhanced PLQY, superior crystallinity, and increased stability at 50 degrees C and in ethanol solvent compared to undoped samples. While higher doping levels reduce QY and PL slightly, they still outperform the undoped CsPbBr3 PeQDs. These results demonstrate that AuCl doping can fine-tune the structural and optical properties of CsPbBr3 PeQDs, marking a significant step forward in developing tailored materials for advanced optoelectronic applications.Article Performance Boost in QLEDs Using Octanethiol-Capped Core/Shell Quantum Dots(IOP Publishing Ltd, 2026-01-07) Yazici, Ahmet F.; Yuruc, Adnan M.; Kelestemur, Yusuf; Serin, Ramis Berkay; Kacar, Rifat; Ulku, Alper; Mutlugun, EvrenQuantum dots attract significant attention as one of the most promising colloidal nanocrystals with unique optical properties and potential applications for the next generation of display technology. In this paper, we evaluate the performance of CdZnSeS-based alloyed-shell quantum dots (QDs) for electroluminescence devices upon additional shell growth and ligand exchange. This includes core/shell (C/S) and core/shell/shell (C/S/S) QDs, whose latter includes an additional ZnS shell and octanethiol (OT) ligands. We present detailed characterizations of QDs using transmission electron microscopy, XRD, and various spectroscopic techniques and demonstrate their QD light emitting (QLEDs). We find the photoluminescence quantum yield of C/S/S QDs increased from 68.8% to 88.7% compared to C/S QDs whereas the emission linewidth narrows from 22.2 nm to 20.8 nm. QLEDs fabricated with C/S/S QDs exhibit a higher peak external quantum efficiency (EQE) of 4.1% and maximum luminance of 85 000 cd m-2, compared to 2.3% EQE and 67 000 cd m-2 for C/S QLEDs. In this respect, the OT-assisted shell growth significantly improves the optical property of QDs and performance of QLEDs, likely attributed to the enhanced charge balance and increased radiative recombination rate.Article Citation - WoS: 1Citation - Scopus: 1Ultra-Durable Information-Encoded Anti-Counterfeiting Self-Assembled Nanocrystal Labels(Wiley-VCH Verlag GmbH, 2025-11-28) Haddadifam, Taha; Shabani, Farzan; Kalay, Mustafa; Khaligh, Aisan; Mutlugun, Evren; Onses, Mustafa Serdar; Demir, Hilmi VolkanForgery, a serious universal problem, is causing huge economic losses every year. Against forgery, information-encoded labelling systems have attracted significant attention for a diverse range of anti-counterfeiting applications. Here, cost-effective and ultra-durable nanocrystal-based labels are proposed and demonstrated in which information can be encoded as physically unclonable functions (PUFs) of hardware-oriented security systems. The fabrication method of the PUFs is based on the self-assembly of colloidal quantum wells (CQWs) and generation of unclonable features within their pattern at a liquid-liquid interface. These CQW PUFs are analyzed with well-known statistical tests, which show a uniqueness level of 0.5060 +/- 0.0323 and prove their randomness. In addition, a feature-matching algorithm is used to authenticate these information-encoded CQW PUFs. For the safety of the semiconductor chips, a CQW PUF is attached to the surface of the chip to protect against hardware cyber-attacks. Eventually, fabricated labels are examined against high temperatures and moisture environments. The fabricated CQW label is durable for a period of 150 days it is tested, demonstrating ultra-high stability of the label. High stability and durability, cost-effectiveness, and high encoding capacity make these proposed nanocrystal labels extremely attractive for large-scale commercialization.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 Enhanced Photoluminescence via Plasmonic Gold Nanoparticles and Improved Stability of Perovskite Nanocrystals in Macroporous (Polydimethylsiloxane) PDMS Matrices(Springer, 2025-10-09) Ocal, Sema Karabel; Tiras, Kevser Sahin; Onses, M. Serdar; Mutlugun, EvrenIn this work, we report a simple and cost-effective method for improving both the environmental stability and photoluminescence quantum efficiency (PLQY) of perovskite nanocrystals (PNCs). Through their embedding in a specially designed macroporous polydimethylsiloxane (MPDMS) matrix and incorporation of plasmonic gold nanoparticles (Au NPs), remarkable improvements are achieved. The resulting MPDMS@PNC composites are seen to retain near-unity quantum efficiency even after 24-h immersion in water and are observed to retain over 85% of the original efficiency even at 75 degrees C, displaying excellent thermal stability. More interestingly, by incorporating Au NPs and subjecting the material to mechanical pressure, the lifetime of the PNCs gets further increased. This is due to the more intimate spatial arrangement of Au NPs in the porous matrix, enhancing localized surface plasmon resonance (LSPR) coupling and thereby enhancing the photoluminescence (PL) of the PNCs. In general, this approach offers a scalable and robust route to designing stable, high-performance perovskite-based materials for next-generation optoelectronic applications.Article Zinc Chalcogenide Based Shell Layers for Colloidal Quantum Wells(Wiley, 2025-04-27) Aldemir, Cagatay Han; Yazici, Ahmet Faruk; Ergezer, Nehir; Korkmaz, Taha Can; Mutlugun, Evren; Kelestemur, YusufColloidal quantum wells, also known as colloidal nanoplatelets (NPLs), have emerged as a promising class of materials for light-emitting devices (LEDs). However, the most widely studied core/shell NPLs, which rely on cadmium-based shell layers, face challenges due to toxicity concerns and improper charge confinement. To address these limitations, a new synthetic approach is presented that enables the controlled growth of zinc chalcogenide-based shell layers on NPLs. The synthesized CdSe/ZnSe core/shell NPLs exhibit emission between 615 and 630 nm, with a moderate photoluminescence quantum yield (PL-QY) of 40-50%. It is also demonstrated that the lateral dimensions of the CdSe core NPLs significantly affect the optical properties of the core/shell heterostructures, with smaller lateral dimensions resulting in narrower emission linewidths as low as 20 nm. Further passivation of these core/shell NPLs with an additional ZnS shell layer significantly increases the PL-QY up to 80-90%. Finally, the device performance of these two core/shell NPLs is investigated by fabricating solution-processed LEDs. With LEDs incorporating CdSe/ZnSe/ZnS core/multi-shell NPLs as the active light-emitting layer, an external quantum efficiency (EQE) of 3.82% and a maximum brightness of 6477 cd m-2 is obtained. These findings underscore the significant potential of zinc chalcogenide-based shell layers in advancing colloidal NPLs toward high-performance light-emitting devices.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: 15Citation - Scopus: 14The Effect of Ligand Chain Length on the Optical Properties of Alloyed Core-Shell InPZnS/ZnS Quantum Dots(Elsevier Science SA, 2017-07) Altintas, Yemliha; Talpur, Mohammad Younis; Mutlugun, EvrenIn this work, we demonstrate the effect of organic ligands on the optical properties of alloyed core-shell InPZnS/ZnS quantum dots (QDs). We have systematically studied the synthesis and characterization of InPZnS/ZnS QDs using short and long chain length ligands i.e., butyric (C4), hexanoic (C6), octanoic (C8), dodecanoic (C12), myristic (C14), palmitic (C16) and stearic acids (C18), respectively. This study achieved more than 85% quantum yield with 43 nm full-width-half maximum value, using dodecanoic acid as the capping ligand. The properties of the QDs with short and long chain length ligands have been analyzed using UV Vis absorption spectrophotometer, steady state and time resolved photoluminescence spectrometer, X-ray diffraction, Zeta sizer, transmission electron microscopy and energy dispersive X-ray spectroscopy. (C) 2017 Published by Elsevier B.V.Article Citation - WoS: 1Citation - Scopus: 1Tailoring Quantum Dot Shell Thickness and Polyethylenimine Interlayers for Optimization of Inverted Quantum Dot Light-Emitting Diodes(MDPI, 2024-07-11) Yazici, Ahmet F.; Ocal, Sema Karabel; Bicer, Aysenur; Serin, Ramis B.; Kacar, Rifat; Ucar, Esin; Mutlugun, EvrenQuantum dot light-emitting diodes (QLEDs) hold great promise for next-generation display applications owing to their exceptional optical properties and versatile tunability. In this study, we investigate the effects of quantum dot (QD) shell thickness, polyethylenimine (PEI) concentration, and PEI layer position on the performance of inverted QLED devices. Two types of alloyed-core/shell QDs with varying shell thicknesses were synthesized using a one-pot method with mean particle sizes of 8.0 +/- 0.9 nm and 10.3 +/- 1.3 nm for thin- and thick-shelled QDs, respectively. Thick-shelled QDs exhibited a higher photoluminescence quantum yield (PLQY) and a narrower emission linewidth compared to their thin-shelled counterparts. Next, QLEDs employing these QDs were fabricated. The incorporation of PEI layers on either side of the QD emissive layer significantly enhanced device performance. Using PEI on the hole transport side resulted in greater improvement than on the electron injection side. Sandwiching the QD layer between two PEI layers led to the best performance, with a maximum external quantum efficiency (EQE) of 17% and a peak luminance of 91,174 cd/m2 achieved using an optimized PEI concentration of 0.025 wt% on both electron injection and hole injection sides. This study highlights the critical role of QD shell engineering and interfacial modification in achieving high-performance QLEDs for display applications.Article Citation - WoS: 3Citation - Scopus: 3Superior CdSe/ZnS@Fe2O3 Yolk-Shell Nanoparticles as Optically Active MRI Contrast Agents(Wiley-VCH Verlag GmbH, 2022-07) Ekici, Derya D.; Mutlugun, EvrenWe have developed a robust synthesis methodology for quantum dots (QDs) nanoparticles with magnetic properties designed for biomodal imaging. These nanocrsytlas consists of a semiconductor quantum dot core with engineered fluorescence, which is located in a paramagnetic iron oxide shell that acts as a magnetic resonance imaging (MRI) contrast agent. Yolk-shell CdSe/ZnS@Fe2O3 nanoparticles (NPs) are synthesized via sonochemical decomposition of iron pentacarbonyl (Fe(CO)(5)) using the oleylamine (OAm) as the ligand. The sonochemical synthesis method of magnetic fluorescent NPs that can be used as MRI contrast agents provided advantages such as improved quantum efficiency and homogeneous size distributions. It has been determined that the luminescence efficiency of quantum dots decreases in coatings that can be made at high temperatures by thermal decomposition. In order to eliminate the disadvantage of elevated temperatures, the sonochemical decomposition method, which allows coating at low temperatures, has been used. With this method, yolk-shell (CdSe/ZnS@Fe2O3) nanoparticles were produced with high photoluminescence quantum efficiency and homogeneous size distributions. The synthesis magnetic fluorescent NPs optimized was determined to have the injection temperature of Fe(CO)(5) at 60 degrees C, Fe(CO)(5)/CdSe@ZnS ratio 0.7, OAm/Fe(CO)(5) volume ratio 1.43 with an oxidation time 5 min. Under these conditions, the quantum efficiency was found to be 78 %, nanoparticle sizes between 11-14 nm and r(1) value was 0.199, r(2) value was 0.518 in MRI analysis. These optically active magnetic fluorescent nanoparticles as positive contrast agents (T1 weighted) are predicted to pave the way for the future of advanced bio-imaging systems.