Scopus İndeksli Yayınlar Koleksiyonu
Permanent URI for this collectionhttps://hdl.handle.net/20.500.12573/395
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Article Citation - WoS: 6Citation - Scopus: 5Photoluminescent and Superhydrophobic Nanocomposites of Perovskite Nanocrystals(Elsevier, 2024-03) Ocal, Sema Karabel; Celik, Nusret; Onses, M. Serdar; Mutlugun, Evren; Karabel Ocal, SemaPerovskite 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 - WoS: 5Citation - Scopus: 5Optimization of High Efficiency Blue Emissive N-, S-Doped Graphene Quantum Dots(Elsevier, 2025-02) Tiras, Kevser Sahin; Soheyli, Ehsan; Sharifirad, Zeynab; Mutlugun, EvrenGraphene quantum dots (GQDs) with bright emission at short wavelengths have attracted much attention due to their importance in various applications such as light-emitting diodes. During or after synthesis, several parameters can significantly improve the optical properties of GQDs. This study presents a facile solvothermal method with low-cost precursors using glutamic acid as the carbon source to realize blue emitting GQDs. The positive effects of urea and 1-octanethiol as nitrogen and sulfur dopants on the photoluminescence quantum yield (PLQY) of the prepared GQDs were demonstrated and optimized. The results confirmed the formation of 2.2 nm nanoparticles with a bright emission around 381 nm with a full width at half maximum of 58 nm and a PLQY approaching 70 %. The decay lifetime of the emission also showed a tri-exponential profile with an average lifetime of 2.4 ns. The simplicity of the preparation method without any post-treatment process, together with a high PLQY of 70 % at short wavelengths, nominates the prepared GQDs for optoelectronics and UV light-driven biological purposes.Article Citation - WoS: 3Citation - Scopus: 3Designed Optimization of Photoluminescence Emission for Carbon Dots With Bright Blue Emission at 416 NM and Mono-Exponential Decay Lifetime(Elsevier, 2025-09) Ruwaih, Mohammed Abbas; Soheyli, Ehsan; Naji, Jalil; Mutlugun, Evren; Kikhavani, Tavan; Sahraei, Reza; Abbas Ruwaih, MohammedThe presented study introduces optimized blue-emissive carbon dots (CDs) with high photoluminescence efficiency up to 65 % at 416 nm, large Stokes shift (69 nm), and full-width at half maximum (FWHM) of 73 nm. Xray photoelectron spectroscopy confirmed the formation of carbon-based bonds as the main component of CDs, with reliable amounts of O, S, and N as dopant components. These features, along with single-exponential time-decay profile at long average lifetime of 10.05 ns, supported the significant role of uniformly distributed mid-gap energy levels in the recombination process. The simplicity, low-cost, non-toxicity, and short reaction time of CDs, along with their excellent emission properties in the deep-blue region, make them suitable for use in environmental monitoring and high-contrast bioimaging.Article Citation - WoS: 138Citation - Scopus: 146Cesium-Lead Based Inorganic Perovskite Quantum-Dots as Interfacial Layer for Highly Stable Perovskite Solar Cells With Exceeding 21% Efficiency(Elsevier, 2019-06) Akin, Seckin; Altintas, Yemliha; Mutlugun, Evren; Sonmezoglu, SavasDespite the excellent photovoltaic performances of perovskite solar cells (PSCs), the instability of PSCs under severe environment (e.g. humidity, light-induced, etc.) limits further commercialization of such devices. Therefore, in recent years, research on the long-term stability improvement of PSCs has been actively carried out in perovskite field. To address these issues, we demonstrated the incorporation of ultra-thin interfacial layer of inorganic CsPbBr1.85I1.15 perovskite quantum-dots (PQDs) that can effectively passivate defects at or near to the perovskite/hole transport material (HTM) interface, significantly suppressing interfacial recombination. This passivation layer increased the open circuit voltage (V-oc) of triple-cation perovskite cells by as much as 50 mV, with champion cells achieving V-oc similar to 1.14 V. As a result, we obtained hysteresis-free cells with the efficiency beyond 21%. More importantly, devices based on such architecture are capable of resisting humidity and light-induced. Remarkably, the device employing CsPbBr1.85I1.15 demonstrated a superb shelf-stability aganist to humidity under ambient conditions (R.H. >= 40%), retaining nearly 91% of initial efficiency after 30 days, while the efficiency of control device rapidly dropped to 45% from its initial value under the same conditions. Besides benefiting from the high moisture resistivity as well as supressed ion migration, PSC5 based on PQDs showed better operational stability (retaining 94% of their initial performance) than that of the PQDs-free one under continuous light irradiation over 400 h. In addition, a faster PL decay time of 4.66 ns was attained for perovskite/PQDs structure (5.77 ns for only PQDs structure) due to the favorable energy transfer at the interface, indicating a Forster resonance energy transfer (FRET) mechanism. This work indicates that inorganic PQDs are important materials as interlayer in PSC5 to supremely enhance the device stability and efficiency.