Materials Science and Engineering / Malzeme Bilimi ve Mühendisliği

Permanent URI for this collectionhttps://hdl.handle.net/11147/4719

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  • Article
    Citation - WoS: 3
    Citation - Scopus: 4
    Experimental and First-Principles Investigation of Cr-Driven Color Change in Cesium Lead Halide Perovskites
    (American Institute of Physics, 2019) Özen, Sercan; Güner, Tuğrul; Topçu, Gökhan; Özcan, Mehmet; Demir, Mustafa Muammer; Şahin, Hasan
    Herein, we report room temperature Cr-doping for all-inorganic perovskites that have attracted great attention in recent years due to their extraordinary optical properties, low cost, and ease of synthesis. Incorporation of Cr 3 + ions into the perovskite crystal lattices is achieved by following a facile route involving an antisolvent recrystallization method at room temperature. It is shown that both Cr-doping and formation of crystals in the CsPbBr x Cl 3 - x phase are provided by increasing the concentration of the CrCl 3 solution. It is also observed that the doping procedure leads to the emergence of three types of distinctive peaks in the PL spectrum originating from CsPbBr x Cl 3 - x domains (476-427nm), Cr-strained host lattices (515nm), and midgap states formed by Cr dopants (675-775nm). It is also found that the Cr-doped perovskites emitting a dark violaceous color change their color to white with a high color rendering index (88) in 30-day time intervals. Easy-tunable optical properties of all-inorganic Cs perovskites indicate their great potential for future optoelectronic device applications.
  • Article
    Citation - WoS: 4
    Citation - Scopus: 4
    Color-Tunable All-Inorganic Cspbbr3 Perovskites Nanoplatelet Films for Photovoltaic Devices
    (American Chemical Society, 2019) Özcan, Mehmet; Özen, Sercan; Topçu, Gökhan; Demir, Mustafa Muammer; Şahin, Hasan
    Herein, we demonstrate a novel coating approach to fabricate CsPbBr3 perovskite nanoplatelet film with heat-free process via electrospraying from precursor solution. A detailed study is carried out to determine the effect of various parameters such as ligand concentration, electric field, flow rate, etc. on the optical properties. By controlling the volume ratios of the oleylamine (OAm) and oleic acid (OA), the coalescing and thickness of the resulting nanoplatelets can be readily tuned that results in control over emission in the range of 100 nm without any antisolvent crystallization or heating processes. The varying electrical field and flow rate was found as inefficient on the emission characteristics of the films. In addition, the crystal films were obtained under ambient conditions on the ITO coated glass surfaces as in the desired pattern. As a result, we demonstrated a facile and reproducible way of synthesizing and coating of CsPbBr3 perovskite nanoplatelets which is suitable for large-scale production. In this method, the ability of tuning the degree of quantum confinement for perovskite nanoplatelets is promising approach for the one-step fabrication of crystal films that may enable the use in optoelectronics.
  • Article
    Citation - WoS: 6
    Citation - Scopus: 8
    Enhanced Spontaneous Emission Rate in a Low-Q Hybrid Photonic-Plasmonic Nanoresonator
    (American Chemical Society, 2019) Gökbulut, Belkıs; İnanç, Arda; Topçu, Gökhan; Ünlütürk, Seçil Sevim; Özçelik, Serdar; Demir, Mustafa Muammer; İnci, Mehmet Naci
    In this paper, CdTe quantum dots (QDs)-doped single electrospun polymer nanofibers are partially coated with gold nanoparticles to form distinct hybrid photonic-plasmonic nanoresonators to investigate the critical role of the cavity-confined hybrid mode on the modification of the spontaneous emission dynamics of the fluorescent emitters in low-Q photonic cavities. A total enhancement factor of 11.2 is measured via a time-resolved experimental technique, which shows that there is an increase of about three times in the spontaneous emission rate for the QDs-doped gold nanoparticle-decorated nanofibers as they are compared with those uncoated ones. The physical mechanism affecting the spontaneous emission rate of the encapsulated QDs in such a hybrid photonic-plasmonic nanoresonator is explained to be due to regeneration of the mode field in the nanofiber cavity upon the interaction of the dipoles with the surface plasmons of distinctive gold nanoparticles that surround the outer surface of the nanofiber.
  • Article
    Citation - WoS: 25
    Citation - Scopus: 28
    Colorimetric and Plasmonic Pressure Sensors Based on Polyacrylamide/Au Nanoparticles
    (Elsevier, 2019) Topçu, Gökhan; Güner, Tuğrul; İnci, Ezgi; Demir, Mustafa Muammer
    Colorimetric stimuli-responsive nanomaterials have emerged as an eminent tool for sensor applications. Among this class of sensing elements, gold nanoparticle-based (Au NP) nanostructures are promising materials due to their plasmonic features. In this study, free-standing flexible polymeric films having intense optical response upon application of mechanical pressure were fabricated based on polyacrylamide (PAAm) and Au NPs. Pressure may cause plasmonic shift most probably due to the disassembly of the clusters from blue to reddish individual particles depending on the extent of pressure. Temperature, time, and extent of pressure were examined in terms of spectral change of Au particles. The sensor films depict working range up to 160 MPa, which shows minor change at elevated temperatures probably due to the stress induced crystallization of PAAm. For practical applications, a simple red-green-blue (RGB) space-based algorithm was presented for smartphone-assisted detection of applied pressure. Moreover, the PAAm/Au composite structure shows self-healing without any additive under ambient conditions even after divided into pieces. (C) 2019 Elsevier B.V. All rights reserved.
  • Article
    Citation - WoS: 89
    Citation - Scopus: 85
    Cspbbr3 Perovskites: Theoretical and Experimental Investigation on Water-Assisted Transition From Nanowire Formation To Degradation
    (American Physical Society, 2018) Akbalı, Barış; Topçu, Gökhan; Güner, Tuğrul; Özcan, Mehmet; Demir, Mustafa Muammer; Şahin, Hasan
    Recent advances in colloidal synthesis methods have led to an increased research focus on halide perovskites. Due to the highly ionic crystal structure of perovskite materials, a stability issue pops up, especially against polar solvents such as water. In this study, we investigate water-driven structural evolution of CsPbBr3 by performing experiments and state-of-the-art first-principles calculations. It is seen that while an optical image shows the gradual degradation of the yellowish CsPbBr3 structure under daylight, UV illumination reveals that the degradation of crystals takes place in two steps: transition from a blue-emitting to green-emitting structure and and then a transition from a green-emitting phase to complete degradation. We found that as-synthesized CsPbBr3 nanowires (NWs) emit blue light under a 254 nm UV source. Before the degradation, first, CsPbBr3 NWs undergo a water-driven structural transition to form large bundles. It is also seen that formation of such bundles provides longer-term environmental stability. In addition theoretical calculations revealed the strength of the interaction of water molecules with ligands and surfaces of CsPbBr3 and provide an atomistic-level explanation to a transition from ligand-covered NWs to bundle formation. Further interaction of green-light-emitting bundles with water causes complete degradation of CsPbBr3 and the photoluminescence signal is entirely quenched. Moreover, Raman and x-ray-diffraction measurements revealed that completely degraded regions are decomposed to PbBr2 and CsBr precursors. We believe that the findings of this study may provide further insight into the degradation mechanism of CsPbBr3 perovskite by water.
  • Article
    Citation - WoS: 5
    Citation - Scopus: 5
    Enhancement of the Spontaneous Emission Rate of Perovskite Nanowires Coupled Into Cylindrical Hollow Nanocavities Formed on the Surface of Polystyrene Microfibers
    (American Chemical Society, 2019) Gökbulut, Belkis; İnanç, Arda; Topçu, Gökhan; Güner, Tuğrul; Demir, Mustafa Muammer; İnci, M. Naci
    Fluorescent CsPbBr3 nanowires are uniformly integrated into a porous polystyrene matrix in the form of microfibers to investigate the changes in their spontaneous emission rate. Cylindrical hollow nanocavities, ranging from 75 to 160 nm in diameter, are grown on the surface of the polymer microfibers during the fabrication process, which allow coupling light that is emitted from the excited CsPbBr3 nanowires. Time-resolved experiments elucidate that the spontaneous emission rate of the perovskite nanowires is observed to increase by a factor of 4.9, upon coupling of the excited optical modes into the nanocavities, which is demonstrated to be in good agreement with our theoretical calculations.
  • Article
    Citation - WoS: 5
    Citation - Scopus: 5
    Effect of Chain Topology on Plasmonic Properties of Pressure Sensor Films Based on Poly(acrylamide) and Au Nanoparticles
    (Elsevier Ltd., 2019) Topçu, Gökhan; Demir, Mustafa Muammer
    Au nanoparticles have been recognized as a colorimetric sensing element in polymeric systems because clustering shifts the red color of individual particles into saturated blue due to distinct plasmonic variation. The mechanism of pressure sensing is based on the disintegration of the particle clusters into the individual particles in polymers upon application of pressure. Polymers are usually composed of linear chains that provide a viscoelastic medium for their diffusion. Changing topology of polymer chains from linear to crosslinked under fixed pressure makes a clear change in spectral features of the particles probably due to the hindrance of particle diffusion by the crosslinking points. Therefore, the working range of the sensor films can be increased to higher-pressure values. In this work, polyacrylamide/Au nanoparticle films were prepared by various concentrations of formaldehyde as a crosslinking agent from 0.5 to 5.0 wt %. The initial absorption signal gradually shifts from 690 to 545 nm for linear chains upon application of pressure while shifting goes down to 571 nm for crosslinked ones. The colorimetric change is also examined under humid environments. Contrary to the crosslinking process, humid environment facilitates the diffusion of particles since the chains swell with water molecules that provide a convenient medium for particle diffusion.
  • Article
    Citation - WoS: 17
    Citation - Scopus: 17
    Monitoring the Doping and Diffusion Characteristics of Mn Dopants in Cesium Lead Halide Perovskites
    (American Chemical Society, 2018) Güner, Tuğrul; Akbalı, Barış; Özcan, Mehmet; Topçu, Gökhan; Demir, Mustafa Muammer; Şahin, Hasan
    Cesium lead perovskites, in the form of CsPbX3 or Cs4PbX6, have been widely used for various optoelectronic applications due to their exceptionally good optical properties. In this study, the effect of Mn doping on the structural and optical properties of cesium lead halide perovskite crystals are investigated from both experimental and theoretical points of view. It is found that adding MnCl2 during the synthesis not only leads to a Mn-driven structural phase transition from Cs4PbBr6 to CsPbCl3 but also triggers the Br- to Cl- halide exchange. On the other hand, it is observed that, under UV illumination, the color of Mn-doped crystals changes from orange to blue in approximately 195 h. While the intensity of Mn-originated photoluminescence emission exponentially decays in time, the intensity of CsPbCl3-originated emission remains unchanged. In addition, diffusive motion of Mn ions results in both a growing population of MnO2 at the surface and transition of the host into a cesium-rich Cs4PbCl6 phase.
  • Article
    Citation - WoS: 21
    Citation - Scopus: 28
    Non-Iridescent Structural Colors From Uniform-Sized Sio2 Colloids
    (Elsevier Ltd., 2018) Topçu, Gökhan; Güner, Tuğrul; Demir, Mustafa Muammer
    Structural colors have recently attracted interest from diverse fields of research due to their ease of fabrication and eco-friendliness. These types of colors are, in principle, achieved by periodically arranged submicron-diameter colloidal particles. The interaction of light with a structure containing long-range ordered colloidal particles leads to coloration; this usually varies depending on the angle of observation (iridescence). However, the majority of the applications demand constant color that is independent of the viewing angle (non-iridescence). In this work, silica colloids were obtained using the Stöber method at different sizes from 150 to 300 nm in an alcoholic dispersion. The casting of the dispersion on a substrate leaves behind a photonic crystal showing a colorful iridescent film. However, centrifugation and redispersion of the SiO2 particles into fresh solvent may cause the formation of small, aggregated silica domains in the new dispersion. The casting of this dispersion allows for the development of photonic glass, presumably due to the accumulation of aggregates showing stable colloidal film independent of viewing angle. Moreover, depending on the size of the silica colloids, non-iridescent photonic glasses with various colors (violet, blue, green, and orange) are obtained.
  • Article
    Citation - WoS: 13
    Citation - Scopus: 16
    The Injection of Co2 To Hypersaline Geothermal Brine: a Case Study for Tuzla Region
    (Elsevier Ltd., 2019) Topçu, Gökhan; Koç, Gonca A.; Baba, Alper; Demir, Mustafa Muammer
    Scaling is a serious issue for geothermal power plants since it remarkably decreases the harvesting of energy. The reduction of pH by organic acids whose structure is close to CO2 for instance formic acid has been an effective solution for the minimization of scaling. Herein, the effect of CO2 injection on the formation of scaling particularly metal-silicates was investigated for the model case of Tuzla Geothermal Field (TGF) located in the northwest of Turkey. CO2 has an acidic character in aqueous systems because it leads to the formation of carbonic acid. The injection of 20.6 m3/s CO2 (approximately 88 ppm) to hypersaline brine of TGF is a promising green approach for both mitigation of scaling by reducing pH from 7.2 to 6.2 at the well-head and the minimization of potential corrosion compared to the use of formic acid (55 ppm).