Photonics / Fotonik
Permanent URI for this collectionhttps://hdl.handle.net/11147/2590
Browse
8 results
Search Results
Article Citation - WoS: 3Citation - Scopus: 3Influence of Cation Size and Polarity on Charge Transport in Ionic Liquid Based Electrolytes(Wiley, 2022) Aydın, Banu; Öner, Saliha; Zafer, Ceylan; Varlıklı, CananImidazolium-based ionic liquids (ILs) with allyl and ether side chains were synthesized and characterized. Comprehensive structural and photoelectrochemical characterizations were performed, transport properties of ILs were also examined as electrolyte components in dye sensitized solar cells (DSSCs). The properties of synthesized materials and DSSC performances were compared with 1-propyl-3-methyl imidazolium iodide (PMII) and 1-allyl-3-ethyl imidazolium iodide (AEII) as reference ILs. Ionic conductivities, diffusion coefficients and charge transfer resistances of synthesized ionic liquids were investigated on DSSCs by Electrochemical Impedance Spectroscopy (EIS). The diffusion coefficient values of triiodide ions in different ionic liquid-based electrolytes were measured by the means of diffusion limited current density method and found to be 1.75×10−7 cm2 s−1 and 2.05×10−7 cm2 s−1 with corresponding photocurrent densities of 10.38 mAcm−2 and 12.13 mAcm−2 for the reference AEII and PMII based electrolytes, respectively. However, for the electrolytes of 1-(2-methoxyethyl)-3-allyl imidazolium iodide and 1-allyl-3-methyl imidazolium iodide ionic liquids, these values were found to be 0.86×10−7 cm2 s−1 and 0.57×10−7 cm2 s−1 with photocurrent densities of 9.53 mAcm−2 and 8.98 mAcm−2, respectively. Allyl and ether substituted imidazolium ILs exhibited promising results as potential alternative electrolyte materials for DSSCs.Article Citation - WoS: 16Citation - Scopus: 16Silylethynyl substitution for preventing aggregate formation in perylene diimides(American Chemical Society, 2021) Aksoy, Erkan; Danos, Andrew; Li, Chunyong; Monkman, Andrew P.; Varlıklı, CananEthynylene-bridged perylene diimides (PDIs) with different sized silane groups have been synthesized as a steric blocking group to prevent the formation of non-radiative trap sites, for example, strong H-aggregates and other dimers or excimers. Excited singlet-state exciton dynamics were investigated by time-resolved photoluminescence and ultrafast pump-probe transient absorption spectroscopy. The spectra of the excimer or dimer aggregates formed by the PDIs at high concentrations were also determined. Although the photophysical properties of the bare and shielded PDIs are identical at micromolar concentrations, more shielded PDI2 and PDI3 exhibited resistance to aggregation, retaining higher photoluminescence quantum yield even at 10 mM concentration and in neat films. The PDIs also exhibited high photostability (1 h of continuous excitation), as well as electrochemical stability (multiple cycles with cyclic voltammetry). Prevention of dimer/aggregate formation in this manner will extend the uses of PDIs to a variety of high concentration photonics and optoelectronic applications, such as organic light-emitting diodes, organic photovoltaics, and luminescent solar concentrators.Article Citation - WoS: 2Citation - Scopus: 31-Octanol Is a Functional Impurity Modifying Particle Size and Photophysical Properties of Colloidal Zncdsse/Zns Nanocrystals(American Chemical Society, 2021) Sevim Ünlütürk, Seçil; Çağır, Ali; Varlıklı, Canan; Özçelik, SerdarImpurities in trioctylphophine (TOP) strongly affect nanocrystal synthesis. 1-Octanol among other contaminants in TOP is identified for the first time as a functional impurity by H-1 NMR. The deliberate addition of 1-octanol into trioctylphosphine reduced particle size and modified photophysical properties of ZnCdSSe/ZnS colloidal nanocrystals. NMR analysis furthermore revealed that 1-octanol is bonded to the nanocrystal surfaces. The ratio of integrals for the O-CH2 protons of 1-octanol, which is the lowest compared to the other ligands, suggests that 1-octanol plays a critical role to tune the particle size of nanocrystals. The increased amount of 1-octanol added into TOP reduces the particle size from 9.8 to 7.2 nm, causing a progressive blue shift in the UV-vis and PL spectra but leaving the alloy composition unaffected. The rate of nonradiative processes is enhanced with the amount of 1-octanol added into TOP, correlating with higher dislocation density observed in the nanocrystals. As a conclusion, 1-octanol is proposed as a functional impurity that varies particle size and nonradiative photophysical processes in the ZnCdSSe/ZnS colloidal nanocrystals.Article Citation - WoS: 3Citation - Scopus: 4Soluble Cytotoxic Ruthenium(ii) Complexes With 2-Hydrazinopyridine(Pleiades Publishing, 2019) Soliman, A. A.; Attaby, F. A.; Alajrawy, O., I; Majeed, S. R.; Şahin, C.; Varlıklı, CananNew water soluble Ru(II) binary complex [Ru(C5H7N3)(X)(H2O)(2)] with 2-hydrazinopyridine and its ternary complexes with X = dichloride, oxalate, malonate or pyrophosphate ligands have been synthesized. The complexes have been characterized using elemental analyses, mass, IR, and UV-Vis. spectroscopies, cyclic voltammetry, magnetic susceptibility, and thermal analysis. The complexes are diamagnetic and the electronic spectral data showed that peaks are due to low spin octahedral Ru(II) complexes. The optimized structures of the complexes 1-4 indicate distorted octahedral geometry with bond angles around the ruthenium atom ranged from 80.44 degrees to 99.64 degrees. The values of the electronic energies (-635 to -1145 a.u.), the highest occupied molecular orbital energies (-0.181 to 0.073 a.u.) and lowest unoccupied molecular orbital energies (-0.056 to 0.167 a.u.) indicate the stability of the complexes. The complexes are polarized as indicated from the dipole moment values (9.39-14.27 Debye). The complexes have noticeable cytotoxicity with IC50 (mu M): 0.011-0.062 (HepG-2), 0.015-0.080 (MCF-7), 0.015-0.116 (HCT-116), and PC-3 (0.034-0.125).Article Citation - WoS: 11Citation - Scopus: 11Structural Stability of Physisorbed Air-Oxidized Decanethiols on Au(111)(American Chemical Society, 2020) Kabanoy, Nikolai; Tsvetanova, Martina; Klaysyuk, Andrey L.; Zandvliet, Harold J. W.; Sotthewes, Kai; Kap, Özlem; Varlıklı, CananWe have studied the dynamic behavior of decanethiol and air-oxidized decanethiol self-assembled monolayers (SAMs) on Au(111) using time-resolved scanning tunneling microscopy at room temperature. The air-oxidized decanethiols arrange in a lamellae-like structure leaving the herringbone reconstruction of the Au(111) surface intact, indicating a rather weak interaction between the molecules and the surface. Successive STM images show that the air-oxidized molecules are structurally more stable as compared to the nonoxidized decanethiol molecules. This is further confirmed by performing current-time traces with the feedback loop disabled at different locations and at different molecular phases. Density function theory calculations reveal that the diffusion barrier of the physisorbed oxidized decanethiol molecule on Au(111) is about 100 meV higher than the diffusion barrier of a chemisorbed Au-decanethiol complex on Au(111). A two-dimensional activity map of individual current-time traces performed on the air-oxidized decanethiol phase reveals that all the dynamic events take place within the vacancy lines between the air-oxidized decanethiols. These results reveal that the oxidation of thiols provides a pathway to produce more robust and stable self-assembled monolayers at ambient conditions.Article Citation - WoS: 31Citation - Scopus: 34Highly Efficient Supercapacitor Using Single-Walled Carbon Nanotube Electrodes and Ionic Liquid Incorporated Solid Gel Electrolyte(SAGE Publications, 2018) Siyahjani, Shirin; Öner, Saliha; Singh, Pramod K.; Varlıklı, CananGel polymer electrolyte (GPE) comprising a low viscosity ionic liquid, that is, 1-propyl-3-methyl imidazolium bis(trifluoromethyl sulfonyl)imide (PMI-TFSI, viscosity 38 cP at 20°C) and a polymer, that is, polyvinyl alcohol (PVA) have been prepared using solution cast technique and characterized by impedance spectroscopy, X-ray diffraction, differential scanning calorimetry, optical microscopy, and Fourier transform infrared spectroscopy. Blending PMI-TFSI with PVA matrix hindered the crystallinity of polymer matrix and presented remarkable enhancement in electrical conductivity with a conductivity maxima at 250 wt% PMI-TFSI. The prepared electric double-layer capacitor using single-walled carbon nanotube as symmetric electrodes and PVA:250 wt% PMI-TFSI as GPE presented a capacitance value of about 28 F g−Conference Object Citation - WoS: 9Citation - Scopus: 11White Led Light Production Using Dibromoperylene Derivatives in Down Conversion of Energy(Canadian Science Publishing, 2018) Aksoy, Erkan; Demir, Nuriye; Varlıklı, CananPerylene derivatives of N,N′-bis(2,6-diisopropylphenyl)-1,6(7)-dibromoperylene-3,4,9,10-tetracarboxylic diimide (DBrPDI) and 1,7-dibromo perylene-3,4,9,10-tetracarboxylic acid butyl ester (DBrPTE) were synthesized, and their structural and optical characterizations were explored. Both DBrPDI and DBrPTE, which were utilized as wavelength converters on a GaN/InGaN based blue LED, were singlet sensitizers and had molar absorptivity constants around 104 Lmol-1cm-1. The blue LED that was used had Commission internationale de l'eclairage (CIE) coordinates of x, y = 0.13, 0.06; power and luminous efficiencies of 2.7 lm/W and 6.6 cd/A @5 mA, respectively. Because the fluorescence quantum yield of DBrPDI was much higher than that of DBrPTE, a meaningful white light efficiency was obtained with the diimide derivative. The use of DBrPDI resulted in white light with CIE coordinates of x, y = 0.34, 0.29 and luminous efficiency of 6.35 cd/A @5 mA, respectively. Using DBrPDI in a resin matrix resulted in more than three orders of magnitude increase in the luminous efficiency value (23.0 cd/A @5 mA) while the CIE coordinates remained the same. Whenever the applied current reached 20 mA, a CRI value of Ra = 90 was obtained.Article Citation - WoS: 15Citation - Scopus: 21Triboluminescent Electrospun Mats With Blue-Green Emission Under Mechanical Force(American Chemical Society, 2017) İncel, Anıl; Varlıklı, Canan; McMillen, Colin D.; Demir, Mustafa MuammerFibrous mechanosensing elements can provide information about the direction of crack propagation and the mechanism of material failure when they are homogeneously dispersed into the bulk volume of materials. A fabrication strategy of fibrous systems showing triboluminescent (TL) responses is in high demand for such applications. In this work, micrometer-sized Cu(NCS)(py)2(PPh3) crystals were synthesized, and polymeric fibrous mats containing the TL crystals were obtained via electrospinning as a stress probe for the determination of mechanical impact. Four different polymeric systems have been employed (PMMA, PS, PU, and PVDF), and the mechano-optical sensing performance of electrospun mats of the polymer-crystal composites was measured. Photophysical properties (quantum yield, band gap, and broadness of the emission) of the TL crystal/electrospun mat composites were also studied. TL and PL emission maxima of the PU-based composite mat show identical behavior due to the chemical affinity between the two structures and the smallest fiber diameter. Moreover, the PU fiber mats exhibit long-lived bluish-green emission persisting over a large number of drops.
