Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection
Permanent URI for this collectionhttps://hdl.handle.net/11147/7148
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Article Synthesis, Characterization, Crystal Structure, Electrochemical and Photoluminescence Properties, Dft and Molecular Docking Studies, and Antimicrobial Activities of Two Mononuclear Nickel (II) Complexes With Pyrazole-Derived Ligands(Elsevier, 2025) Amin, Mina A.; Diker, Halide; Sahin, Onur; Varlikli, Canan; Soliman, Ahmed A.Two octahedral nickel complexes; [Ni(fdtp)2(DMF)2] (1) and [Ni(dcdtp)2(DMF)2] (2), based on 4-((3-fluorophenyl)diazenyl)-3-(trifluoromethyl)-1H-pyrazol-5-ol (fdtp) and 4-((2,4-dichlorophenyl)diazenyl)-3-(trifluoromethyl)-1H-pyrazol-5-ol (dcdtp) were synthesized. The complexes were characterized spectroscopically (FTIR, UV-Vis, Photoluminescence), Mass spectrometry, elemental analyses, electrochemically, thermally, and through Single-crystal X-ray investigations. The formation of the complexes was confirmed by the existence of Ni-O and Ni-N vibrations at bonds were observed as weak bands at 526-497 and 470-438 cm-1. According to the thermogravimetric analyses, the complexes were thermally stable and had relatively high activation energies (585.81 and 730.07 kJ mol-1 for 1, and 2, respectively). Cyclic voltammograms showed that the anodic potential region of 1 and 2 exhibited two irreversible oxidation peaks at 1.34 V &1.55 V and 1.41 V & 1.63 V, respectively, attributed to metal-localized oxidation. The complexes showed enhanced antibacterial activities compared to free ligands and comparable to the standard. The inhibition zones exhibited via 1 were about 21.7, 19.3, and 26.7 mm versus Escherichia coli (E. coli), Staphylococcus aureus (S. Aureus), and Bacillus Subtits (B. Subtits), respectively. Docking studies supported the antibacterial investigations; the binding energies of the complexes were -8.81 and -9.69 kcal/mol for 1 and 2 respectively, against E. coli (PDB ID: 6F86).Article Citation - WoS: 14Citation - Scopus: 14Dispersion Stability of Amine Modified Graphene Oxides and Their Utilization in Solution Processed Blue Oled(Elsevier Ltd., 2020) Diker, Halide; Bozkurt, Hakan; Varlıklı, CananGraphene oxide (GO) was modified with amine derivatives which contain short (SACA) and long (LACA) alkyl chains. SACAs were n-propylamine, dipropylamine, propanolamine and LACAs were 2-ethylhexylamine, di-hexylamine, dioctylamine, and 1,12-diaminododecane and modified GOs (mGOs) were named as nPRYLA-GO, DPRYLA-GO, PRPOHA-GO, 2EHA-GO, DHA-GO, DOA-GO, and DADOD-GO, respectively. Amine modification resulted in approximately 2-folds of decrement in d-spacing of GO (8.36 angstrom). The C:O ratio, N% and d-spacing values were increased as the alkyl chain length of amine source increased. Except for PRPOHA-GO, all of the mGOs were thermally stable until 100 degrees C. All mGOs were dispersed in dimethylformamide (DMF), ethylene glycol (EG) and isopropyl alcohol (iPA). Regardless of their structural differences, all of the mGOs formed stable dispersions in DMF, whereas SACA-mGOs and LACA-mGOs were compatible with EG and iPA, respectively. DMF, EG and iPA dispersions of DOA-GO, 2EHA-GO, nPRYLA-GO and PRPOHA-GO were doped in Al4083 and prepared composites were utilized as hole transport layer in solution processed blue OLEDs. Ground state energy levels of Al4083:DOA-GO, Al4083:EG, Al4083:PRPOHA-GO, Al4083:2EHA-GO and Al4083:nPRYLA-GO extracted from their X-ray photoelectron spectra were 0.49 eV, 0.67 eV, 0.91 eV, 0.98 eV and 1.00 eV below the work function of ITO, respectively. Among all Al4083:mGOs, the best device performance was obtained with the device that contains Al4083:DOA-GO (in EG), which presented 1.6, 1.7 and 1.5 fold enhancements in current, power and external quantum efficiencies, respectively, compared to those of Al4083:EG based device.Article Citation - WoS: 28Citation - Scopus: 29Enhancing the Efficiency of Mixed Halide Mesoporous Perovskite Solar Cells by Introducing Amine Modified Graphene Oxide Buffer Layer(Elsevier, 2020) Şahin, Çiğdem; Diker, Halide; Sygkridou, Dimitra; Varlıklı, Canan; Stathatos, EliasIn this study, graphene oxide (GO) was synthesized via Tour method and then modified with two different amine sources that contained different branched alkyl chains. The GO and modified GOs (mGOs) with dihexylamine (DHA) and 2-ethylhexylamine (2EHA) as amine sources were used respectively as buffer layers in mixed halide mesoporous perovskite solar cells (PSCs) in order to examine whether they could improve their performance. GO and mGO samples were characterized by several techniques such as X-Ray Diffraction, X-Ray photoelectron spectroscopy (XPS), Raman analysis and thermal gravimetric analysis (TGA). The preparation of the CH3NH3PbI3-xClx perovskite solution was performed using standard Schlenk techniques under argon atmosphere to attain a homogeneous coverage of the perovskite film. The solar cells with the additional layer of mGO derivatives between perovskite and hole transporting layer showed an improved overall performance compared to the reference devices which was attributed to the enhanced charge carrier transport via the mGOs. In particular, 10% increase to the overall performance of the solar cells was monitored in devices where 2-ethylhexylamine (2EHA) modified GO was used, compared to standard cell without buffer layer. (C) 2019 Elsevier Ltd. All rights reserved.Article Citation - WoS: 29Citation - Scopus: 32Enhanced Capacitive Behaviour of Graphene Based Electrochemical Double Layer Capacitors by Etheric Substitution on Ionic Liquids(Elsevier, 2020) Siyahjani, Shirin; Öner, Saliha; Diker, Halide; Gültekin, Burak; Varlıklı, CananIn this study, we report the effect of etheric substituents in imidazolium and ammonium based ionic liquids (IL) on the performance of electrochemical double layer capacitors (EDLC) consisted of gel polymer electrolyte (GPE) and reduced graphene oxide (RGO) electrode. GPEs contain poly (vinylidene fluoride-hexafluompropylene) (PVDF-HFP) and the ILs. Ammonium and imidazolium based ionic liquids (ILs) differ by their length of etheric groups and etheric group contents, respectively. According to the cyclic voltammetry, galvanostatic chargedischarge and electrochemical impedance spectroscopy measurements, longer etheric group substituted {N-methyl-2- (2-methoxyethoxy)-N,N-bis [2- (2-methoxyethoxy)ethyl] ethan-1-aminium bis(tri-fluoromethanesulfonyl)imide (AMEt-TFSI) and ether substituted (3-allyl-1-[2-(2-methoxyethoxy)ethyl]-1H-imidazole-3-ium bis(trifluommethanesulfonyeimide (AL3IL-TFSI), tender specific capacitances of 250 Fg(-1) and 238 Fg(-1) and energy density values of 61.36 wh kg(-1) and 61.56 wh kg(-1), respectively.