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Yazar "Altin, Serdar" seçeneğine göre listele

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  • Küçük Resim Yok
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    Boron-doped porous carbon material derived from ZIF-11: Investigation of cotton fabric supercapacitor and Li-ion battery performances
    (Wiley, 2022) Bugday, Nesrin; Altin, Serdar; Bulut, Fatih; Altin, Emine; Yasar, Sedat
    Nitrogen-doped porous carbon (NPC@ZIF-11) and boron-NPC (BNPC@ZIF-11) materials were synthesized by pyrolysis methods, and structural characterization of the compounds was carried out by scanning electron microscopy, transmission electron microscopy, Fourier-transform infrared spectroscopy, X-ray diffraction, Brunauer-Elmet-Teller technique, Raman spectroscopy, and inductively coupled plasma-mass spectrometry techniques. The ZIF-11 was converted to the NPC@ZIF11 by pyrolysis. BNPC@ZIF-11 was fabricated from NPC@ZIF-11 by pyrolysis in the presence of phenylboronic acid. The fabric supercapacitor, sandwich-type supercapacitor, and Li-ion battery performances of NPC@ZIF-11 and BNPC@ZIF-11 were investigated. The capacity of the Li-ion cell was found as 720 mAh g(-1) for the first cycle, and it was decreased to 250 mAh g(-1) after 100 cycles. The capacitance values of the cylindrical devices were 92 F g(-1) and 115.6 F g(-1), for C1 and C4000 in KOH electrolytes. The BNPC@ZIF-11 was used as an electrode material on cotton fabric, and the highest obtained capacitance was 72.8 mF for 0.1 mA, which is a promising result for wearable energy storage materials.
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    Cationic versus anionic Pt complex: The performance analysis of a hybrid-capacitor, DFT calculation and electrochemical properties
    (Pergamon-Elsevier Science Ltd, 2019) Akkoc, Mitat; Demirel, Serkan; Oz, Erdinc; Altin, Serdar; Bayri, Ali; Dorcet, Vincent; Roisnel, Thierry
    The synthesis and characterization of cationic versus anionic platinum(II) complex of the type [PtCl3(DMSO)](-)[NHC](+) (NHC: N-heterocyclic carbene) is reported for the first time. The complex 3 was synthesized from silver(I)-NHC2, and K-2[PtCl4] in DMSO at 80 degrees C under exclusion of light. The ionic platinum(II) complex was obtained in high yield and fully characterized by H-1, C-13, Pt-195 NMR and HRMS spectroscopy, X-ray diffraction and elemental analysis. The structural properties of the complex were investigated by using Gaussian suit and the obtained parameters were crosschecked with the X-ray data. The HOMO-LUMO energies and electrostatic surface mapping of the complex were calculated and the results were discussed with the capacitive properties of the complex. Electrochemical analysis by cyclic voltammetry (CV) of the complex shows reversible redox peaks about platinum center. The complex was used as an electrode material for the capacitor device and result is promising that the highest performance of complex 3 was found as 10.22 F/g. (C) 2018 Elsevier Ltd. All rights reserved.
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    Challenges and recent advancements in MXene-based high-capacity electrodes for future generation rechargeable batteries
    (Elsevier, 2025) Ashfaq, Rughianah Gohar; Arshad, Muhammad; Siddique, Sofia; Abrar, Areebah; Shah, Saqlain A.; Bulut, Fatih; Altin, Serdar
    An innovative family of 2-dimensional transition metal carbides, carbonitrides, and nitride multilayered materials, identified as MXenes, has attracted significant interest since the discovery of Ti3C2 in 2011. MXenes exhibit a broad surface area and excellent electronic conductivity and can be hydrophilic, hydrophobic, or a combination of both. It also possesses physical robustness, flexibility, and chemical and thermal resilience. Surface terminations such as hydroxyl (OH-), oxygen (O-), or fluorine (F-) groups impart hydrophilic properties to the surfaces of materials. Due to its outstanding conductive properties, large specific surface area, excellent mechanical characteristics, and distinctive multilayered structure, MXenes have extensive applications in energy storage devices, absorption processes, catalysis, and other fields. MXenes and related composite materials have gained significant traction in rechargeable batteries. While oxides, sulfides, and various other materials offer high capacities, they are also plagued by poor cyclability, limited conductivity, and volumetric expansion during reaction processes. Consequently, utilizing MXene-based composites can enhance the electronic conductivity, storage capacity, and overall electrochemical efficiency while mitigating volumetric expansion during charge/ discharge cycles. This comprehensive review article delves into the manufacturing process, structure, and characteristics of MXenes. We also explore the energy storage capabilities of these materials in future-generation rechargeable batteries, associated applications, and prospects for future research.
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    Cobalt-substituted P2-Na0.67MnO2 and purple basil-derived hard carbon for high-performance sodium-ion battery full cells: insight to ex situ structural analysis
    (Springer Heidelberg, 2025) Whba, Rawdah; Dogan, Ebru; Altin, Emine; Benzaid, Abdelali; Arshad, Muhammad; Altin, Serdar
    This study explores two energy storage materials: cobalt-doped P2-type Na0.67MnO2 (Na0.67Mn0.9Co0.1O2, NMCO) and hard carbon derived from purple basil (Ocimum basilicum L., HC-based PB) biomass. NMCO was synthesized via a solid-state method involving high-temperature quenching in liquid nitrogen (LN2). Analytical techniques confirmed a pure P2-type layered structure with reduced lattice volume due to Co3+ substitution. FTIR identified Na-O, Mn-O, and Co-O bonds, while XPS revealed reduced Mn3+ content, enhancing structural stability by mitigating the Jahn-Teller effect. Electrochemical tests of NMCO showed charge/discharge capacities of 184 mAhg(-1) and 185 mAhg(-1) with a coulombic efficiency of 99.5%. HC-based PB, exhibiting disordered graphitic structures, demonstrated higher charge and discharge capacities of 231 and 349 mAhg(-)(1), respectively, despite a relatively low efficiency of 66%. Long-term cycling demonstrated capacity fading for both materials after 100 cycles. Ex situ XRD confirmed NMCO's structural integrity, while HC's amorphous structure contributed to its stability. These findings provide valuable insights into these materials' electrochemical performance and durability for energy storage applications.
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    Current-Voltage Measurements and Vortex Dynamics in a Bi2Sr2CaCu2O x Whisker: Observation of the Peak Effect and Calculation of the Critical Current in the Flux Flow Regime with and Without Applied Field
    (Springer, 2013) Altin, Serdar; Bernstein, Pierre
    In this article, we report current-voltage measurements carried out on a Bi2Sr2CaCu2O (x) whisker in a large temperature range below the critical temperature with and without applied magnetic field. We examine the critical current peak effect and the vortex dynamics at low field. The critical current peak effect consists of the initial increase of the critical current that subsequently decreases as the applied field is increased. For current-voltage measurements, this effect is associated with a change in the current-voltage curves that are typical of the flux flow regime at low fields and resemble flux creep characteristics for higher fields. As a general rule, our observations are consistent with the models that link the peak effect to vortex phase transitions. We calculate the critical current in self-field in the flux flow regime taking into account intervortex forces. We suppose that most vortices are pinned by defects while mobile vortices move through plastic channels between the strongly pinned vortex regions. When an external field is applied, we suggest that the increase in the critical current that is observed is linked to oscillations of the pinned vortices.
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    Effect of carbon nanotubes/graphene nanoplates hybrid to ZnO matrix: production, electrical and optical properties of nanocomposite
    (Springer, 2020) Guler, Omer; Yavuz, Cagdas; Basgoz, Oykum; Altin, Serdar; Yahia, Ibrahim S.
    Electrical and optical properties of pure andcarbon nanotube (CNT)/graphene nanoplate (GNP) mixture-reinforced zinc oxide (ZnO)matrix at different temperatures were investigated. UV-Vis absorption andelectrical conductivity measurements were used in order to determine theproperties were mentioned above. Samples were divided two main groups based ontheir matrix: one of them commercially acquired ZnO and the other one wasproduced via sol-gel method. Both groups have the same four sub-groupsaccording to the percentage of the weight of the reinforcing. SEM imagesindicated that commercially obtained ZnO matrix has hexagonal structure whileZnO manufactured by sol-gel was mainly in sphere form. Raman spectroscopy and TEM analyses proved that graphene nanoplate structure was producedsuccessfully, and XRD characterization shows that ZnO was produced in asuitable way by sol-gel method. The results indicated that electricalconductivity of the samples which from pure to 0.4% reinforced was decreasedwith increasing in reinforcing percentage. However, samples with 0.8% CNT/GNPmixture reinforcing showed greatest electrical conductivity. The highest reflectionpercentages of the samples were obtained from the pure specimens while thelowest ratios were observed in the highest reinforced samples. Activationenergy and optical band gap values were calculated according to electrical andoptical graphs.
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    Effect of Vanadium-Titanium Co-doping on the BPSCCO Superconductor
    (Springer, 2011) Yazici, Duygu; Ozcelik, Bekir; Altin, Serdar; Yakinci, M. Eyyuphan
    We have produced the (BiPb)(2)V (x) Sr2Ca3Cu4-y Ti (y) O12+delta compounds for x=0.05 and y=0, 0.05, 0.10 and 0.20 by glass-ceramic method. The effects of vanadium adding and Ti doping on the structure have been investigated by electrical resistance, scanning electron micrographs (SEM), XRD patterns and magnetic hysteresis loop measurements. It has been found that the high-T (c) superconducting phase, (2223), is formed in the samples annealed at 845 degrees C for 185, with concentration x=y=0.05. However, with increasing Ti doping the (2223) phase transforms into the (2212) phase. We have observed no superconducting properties for x=0.05 and y=0.20 compound. It has completely transformed to semiconductor. In addition, the critical current densities (J (c)), calculated from the hysteresis loop measurements by using Bean's critical state model are obtained for the samples in the same doping range. Our data have indicated that J (c) decreases with increasing temperature and Ti concentration.
  • Küçük Resim Yok
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    Electrical Properites of Superconducting Cross - (nano) Whiskers Junction
    (Tubitak Scientific & Technological Research Council Turkey, 2005) Altin, Serdar; Yakinci, Eyuphan; Balci, Yakup; Aksan, M. Ali
    Bi-2212 superconducting single crystal (nano) whiskers have been fabricated by annealing a melt-quenched (glass) Bi3Sr2Ca2Cu3Ox precursor. A couple of (nano) Whiskers obtained were placed crosswise on a YSZ single crystal substrate and then heat treated at 830 C for 25 minute to form nano-scale junction. The T-c of each nano-whisker was found to be 85 K and the critical current density, J(c), of the whiskers was calculated to be 1177 Acm(-2) at zero field. The I - V characteristics of the nano-junction at 30 K were found to show a multiple-branch structure, which is the main behavior of the Josephson junction.
  • Küçük Resim Yok
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    Elektrikli Araç Teknolojisinde Kullanılan Kurşun Asit ve Li-iyon Bataryaların Galvanostatik Test Sonuçlarının Karşılaştırılması
    (2023) Balci, Esra; Altin, Serdar; Altundağ, Sebahat; Gündüz, Gürkan
    Yenilenebilir enerji kaynaklarının sürekliliğini sağlamak ve içten yanmalı motorlar yerine elektrikli araçların kullanılması çevre ve yaşam kalitesini direk etkilemektedir. Farklı metaller katkılanarak geliştirilmesi amaçlanan bataryalar üzerinde çalışmalar hala sürmektedir. Yüksek performans sergileyen ve uzun hizmet ömrü sunabilen bataryalar günümüzde her alanda talep edilmektedir. Bu çalışmada Li-iyon bataryalar ve kurşun-asit aküler hakkında genel bilgilendirme sunulması hedeflenmiştir. Pillerin elektrokimyasal davranışlarının analizi galvanostatik yöntem kullanılarak (100 çevrimde; sabit akım altında) gerçekleştirilmiştir. Hazır üretim olan pillerin; kapasite-döngü sayıları ile şarj-deşarj eğrileri incelendiğinde; Li-iyon türü batarya grubunda yer alan pilin (Sony VTC5) daha yüksek kapasite sergileyerek daha uzun hizmet ömrü sunacağını göstermiştir.
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    Epoxy/block copolymer and nanocomposites: Advancements and applications in aerospace
    (Elsevier, 2025) Whba, Rawdah; Whba, Fathyah; Sahinbay, Sevda; Altin, Serdar
    The development of materials for aerospace applications has increasingly focused on epoxy resins, block copolymers (BCPs), and nanocomposites due to their excellent mechanical, thermal, and environmental properties. Epoxy resins are valued for their strength, stiffness, and chemical resistance, but their brittleness and cracking tendencies pose challenges. BCPs address these issues by improving toughness and flexibility. Nanocomposites, incorporating nanoparticles such as graphene, carbon nanotubes, and nanoclays, further enhance the thermomechanical properties and environmental resistance of epoxy/BCP systems. These advanced materials are ideal for aerospace components exposed to harsh conditions, offering improved durability, reduced weight, and enhanced performance. This chapter examines recent progress in integrating epoxy resins and BCPs, focusing on the role of nanocomposites in overcoming material limitations for aerospace applications. It also discusses the challenges of achieving uniform nanoparticle dispersion, ensuring long-term durability under extreme conditions, and overcoming manufacturing complexities. Despite these challenges, these materials have the potential to revolutionize the aerospace industry, improving performance, reducing weight, and increasing durability, thus driving future innovations in aircraft design and performance. © 2026 Elsevier Inc. All rights reserved..
  • Küçük Resim Yok
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    Fabrication and electrochemical performance of Ho-substituted C/LiFePO4: Improved battery performance
    (Springer, 2021) Altin, Serdar; Yolun, Abdurrahman
    Ho-substituted C/LiFePO4 samples were successfully fabricated, and their structural properties were examined by X-ray diffraction (XRD), Scanning Electron Microscopy (SEM), and Fourier transform infrared spectroscopy (FTIR) measurements. The magnetic structure of LiFePO4 correspondence to the high spin configuration of Fe2+ ions and Ho3+ causes the increase of the mu(eff) values and suppressed the antiferromagnetic transition. The XRD analysis showed an amorphous structure due to carbon, and peaks were matched by olivine-type LiFePO4. Furthermore, the lattice volume was increased with the addition of Ho. The Ho-substituted cells show similar cycling voltammetry (CV) graphs with the CV of the undoped LiFePO4 cells. According to charge/discharge cycling measurements for constant current at room temperature, the highest capacity was obtained for LiFe0.99Ho0.01PO4. The Ho-substituted LiFePO4 has a higher C-rate when compared with the undoped LiFePO4 and so it is found that a low concentration of Ho in LiFePO4 has better battery performance and may be used in commercial batteries.
  • Küçük Resim Yok
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    Fabrication, electrochemical performance, and in situ infrared thermal imaging of Na0.67(Mn0.5Fe0.5)1-xCuxO2 battery cells
    (Wiley, 2021) Altin, Serdar; Korkusuz, Keziban
    Na-0.67(Mn0.5Fe0.5)(1-x)CuxO2 powders (where x = 0, 0.05, 0.1, 0.2, and 0.3) were produced by quenching at 900 degrees C, and the structural features of the powders were studied in detail. It was found that the undoped and Cu-substituted for (x <= 0.2) powders had no impurity phases in the structure. Furthermore, the lattice volume calculated by the GSAS-II open-source program decreased with increasing Cu content, and it is suggested that Cu ions have a 3+ valence state in the samples. The cycling voltammetry of the cells is very similar to each other. The constant current charge/discharge cycling measurements were performed for up to 100 cycles, and the best performance was observed for x = 0.2 Cu substitution in Na-0.67(Mn0.5Fe0.5)(1-x)CuxO2. The best capacity value was obtained as 182.3 mAh/g at the C/10 rate for x = 0.2 Cu substitution. The cycling measurements at 50 degrees C exhibit worse capacity fade when compared to the measurements performed under ambient conditions. The in situ infrared thermal imaging measurements for the cell that had the highest performance in this study were performed for a constant voltage of 4.3 V for charging and 1.5 V for discharging of the cell. The ohmic heat was calculated from chronoamperometry measurements, and the heat generation was fitted with the quadratic term in the system.
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    High-performance electrodes for Li-ion cell: Heteroatom-doped porous carbon/CoS structure and investigation of their structural and electrochemical properties
    (Wiley, 2022) Bugday, Nesrin; Altin, Emine; Altin, Serdar; Yasar, Sedat
    As an essential class of anode materials, the synthesis and characterization of CoS@ZIF-12-C composite anode materials are reported. The two-step synthesis of CoS nanoparticles embedded in N-doped porous carbon by using a metal-organic framework (MOF) as the template. After structural characterization of CoS@ZIF-12-C composite materials, the main phase was found as CoS with symmetry of P63mmc. Benefiting from the CoS embedded in porous carbon structure, the half Li-ion battery cell tests of CoS@ZIF-12-C composite materials were performed by a 2-electrode method using CR2032 cells, and the capacities of the cells were measured for 200 cycles using 300 mAg(-1) and 500 cycles using 1000 mAg(-1). The first discharge capacities of the cells for 1000 mAg(-1) were found as 458, 1178, and 815 mAhg(-1) for CoS@ZIF-12-C-T, T = 700, 800, and 900 degrees C, respectively. An unexpected capacity increase was observed for the CoS@ZIF-12-C-700 and CoS@ZIF-12-C-900 half cells during the cycling. Ex-situ x-ray diffraction (XRD), Fourier Transform Infrared Spectroscopy (FTIR), and cyclic voltammetry (CV) analysis were performed after cycling of the cells for explanations of the capacity increase. Ex-situ XRD analysis of these cells showed phase transitions from crystalline to amorphous type structure, and ex-situ FTIR proves the preservation of the CoS phase during the cycling. A redox reaction mechanism was suggested to explain the cells' battery performance by ex-situ XRD analysis.
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    High-performance Na-ion full-cells with P2-type Na0.67Mn0.5-xNixFe0.43Al0.07O2 cathodes: Cost analysis for stationary battery storage systems
    (Elsevier, 2024) Kalyoncuoglu, Burcu; Ozgul, Metin; Altundag, Sebahat; Bulut, Fatih; Oz, Erdinc; Sahinbay, Sevda; Altin, Serdar
    Na -ion batteries are viable alternatives to Li-ion batteries especially for stationary applications. Developing suitable electrode materials, half-cell and full-cell studies and cost analysis are major steps and challenges for their commercialization. In this study, we report the synthesis of a promising cathode material, Na0.67Mn0.5- xNixFe0.43Al0.07O2 (x = 0.02-0.10 with Delta x = 0.02), using a modified solid-state synthesis technique. The materials were heated at high temperature for 6 h in air and quenched in liquid N-2. We determined the solubility limit of Ni in Na0.67Mn0.5Fe0.43Al0.07O2 as x <= 0.06. The interlayer separation increases with increasing Ni content due to the ionic radii difference between Mn and Ni. X-ray photoelectron spectroscopy (XPS) measurements evidence the valance state of Ni in the x = 0.06 sample as 2+ and 3+. Cyclic voltammetry (CV) analysis of the half-cells were performed at 10 C-degrees, room temperature, and 50 degrees C to observe the effect of environmental temperature on redox mechanism. The highest half-cell capacity of the cells was determined as 181 mAh/g for x = 0.06 at C/3-rate. Artificial solid electrolyte interface (SEI) formation was performed on the hard carbon anode by presodiation technique and the full-cells of Na0.67Mn0.44Ni0.06- Fe0.43Al0.07O2/hard carbon were assembled in CR2032 coin cells. The capacity values of the cells at C/2, C, and 2C-rate were determined as 131.4 mAh/g, 116 mAh/g and 100.8 mAh/g for the 1 cycle and 33 mAh/g, 40.6 mAh/g and 49.9 mAh/g for the 500th cycle, respectively. The cost analysis for the commercial package for stationary energy storage system was performed by BatPac program and results are discussed.
  • Küçük Resim Yok
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    High-performance P2-Na0.67Mn0.85Cu0.15O2/Hard carbon full cell Na-ion battery: Pre-Sodiation of anode, p/n ratio optimizations, and Operando XAS studies
    (Pergamon-Elsevier Science Ltd, 2023) Altundag, Sebahat; Altin, Emine; Altin, Serdar; Ates, Mehmet Nurullah; Ji, Xiaobo; Sahinbay, Sevda
    Na-ion batteries have gained significant attention as a cost-effective and efficient energy storage option for large scale applications, serving as an alternative to the Li-ion batteries. However, commercialization of these batteries is still many steps away since most cathode materials suffer from significant capacity loss and more full-cell studies are required. In this work, we report the electrochemical properties of half-and full-cells of P2-type Na0.67Mn0.85Cu0.15O2 synthesized by solid state technique. X-ray diffraction, FT-IR, and Raman spectroscopy, scanning electron microscopy, and energy-dispersive X-ray spectroscopy techniques are used to determine the structural properties. Surface properties are studied by X-ray photoelectron spectroscopy and Bru-nauer-Emmett-Teller techniques. Half cells and full cells were constructed with Na-metal and hard carbon, respectively. Na-ion diffusion kinetics at 10 degrees C, room temperature, and 50 degrees C were determined experimentally. Galvanostatic cycling tests on half-cells show capacity values of 165/124 mAh/g for the 1./100. cycles with 24.8 % capacity fade. Operando x-ray absorption spectroscopy measurements were utilized to study local structural modification around transition metal ions during charge/discharge. In the full-cell studies, electrode mass ratio (p/n) and parameters for presodiation of hard carbon were optimized. Using 30 mA/g current density, the un-processed and the pre-sodiated full-cells reach capacity values of 48 mAh/g (p/n = 2.5) and 150 mAh/g (p/n = 0.75 and 1.15), respectively.
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    Highly Active Fe3O4@SBA-15@NHC-Pd Catalyst for Suzuki-Miyaura Cross-Coupling Reaction
    (Springer, 2022) Akkoc, Mitat; Bugday, Nesrin; Altin, Serdar; ozdemir, Ismail; Yasar, Sedat
    A novel Pd-NHC functionalized magnetic Fe3O4@SBA-15@NHC-Pd was synthesized and used as an efficient heterogeneous catalyst in the Suzuki-Miyaura C-C bond formation reactions. The Fe3O4@SBA-15@NHC-Pd characterized by X-Ray Diffraction (XRD), X-ray Photoelectron Spectroscopy (XPS), Fourier Transform Infrared (FTIR) spectroscopy, Scanning Electron Microscopy (SEM), Transmission Electron Microscopy (TEM), Energy Dispersive X-ray analysis (EDX), Thermogravimetric Analysis (TGA), Differential Thermal Analysis (DTA). The Inductively Coupled Plasma-Optical emission spectroscopy (ICP-OES) analysis was used to determine the exact amount of Pd (0.33 wt%) in Fe3O4@SBA-15@NHC-Pd. The TEM images of the catalyst showed the existence of palladium nanoparticles immobilized in the catalyst's structure, while no reducing agent was used. The NHC moieties in the catalyst structure could be stabilize Pd(0) nanoparticles prevents agglomeration. The magnetic catalyst was effectively used in the Suzuki-Miyaura cross-coupling reaction of substituted phenylboronic acid derivatives with (hetero)aryl bromides in the presence of a K2CO3 at room temperature in aqueous media and magnetic catalyst could be simply extracted from the reaction mixture by an external magnet. Different aryl bromides were converted to coupled-products in excellent yields with spectacular TOFs values (up to 1,960,339 h(-1)); in the presence of 1 mg of Fe3O4@SBA-15@NHC-Pd catalyst (contains 3.1 x 10(-6) mol% Pd) at room temperature in aqueous media. After reusability experiments, it is found that this catalyst was effectively used up to ten times in the reaction with almost consistent catalytic efficiency. A decrease in the activity of the 10th reused catalyst was found as 9%. Graphic Abstract
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    In vitro comparison of physical, chemical, and mechanical properties of graphene nanoplatelet added Angelus mineral trioxide aggregate to pure Angelus mineral trioxide aggregate and calcium hydroxide
    (Wiley, 2021) Kucukyildiz, Elif Nihan; Dayi, Burak; Altin, Serdar; Yigit, Oktay
    It is important to cover the pulp surface with a biocompatible material that is physically, mechanically, and chemically adequate. Graphene has the potential to form hard tissue, but at high doses, it shows toxic effects. It can be added to biocompatible materials at low doses to enhance their hard tissue forming potential. The aim of this study was to compare the physical, chemical, and mechanical properties of graphene nanoplatelet (GNP) added Angelus mineral trioxide aggregate (A-MTA) to pure A-MTA and calcium hydroxide. Homogeneous mixtures (created by adding +0.1 weight[wt]% and 0.3 wt% GNP to A-MTA), pure A-MTA, and Dycal were used. Three disc-shaped samples of each material were prepared using Teflon mold. Scanning electron microscope-energy dispersive X-ray (SEM-EDX), particle size, microhardness, and Fourier transform infrared spectroscopy (FTIR) analysis of the materials were performed in vitro. Data were analyzed using Kruskal-Wallis test followed by Conover test (p < .001). A-MTA and GNP added samples showed similar peaks in FTIR analysis. In the EDX analysis, the amount of carbon was observed with a higher increase at A-MTA + 0.3 wt% GNP than A-MTA + 0.1 wt% GNP. In the SEM image, hollow structure and particle size decreased as the amount of GNP increased; particle size was smaller at A-MTA + 0.3 wt% GNP than A-MTA + 0.1 wt% GNP (p < .001). A-MTA + 0.3 wt% GNP showed the highest microhardness while Dycal showed the lowest microhardness. The addition of GNP, a material with high potential for forming hard tissue, to the structure of capping materials can also positively contribute to the microhardness of the capping materials.
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    Influence of precursor selection on the structural integrity and electrochemical performance of α-NaMnO2 cathode
    (Wiley, 2025) Dogan, Ebru; Whba, Rawdah; Canbay, Canan Aksu; Arshad, Muhammad; Sahinbay, Sevda; Altin, Serdar
    In this study, the alpha-NaMnO2 phase was successfully synthesized using three different combinations of starting materials: Na2O2/Mn2O3, Na2O2/MnO2, and Na2CO3/Mn2O3. A one-step heat treatment at 900 degrees C for 5 h under air with quenching was applied. X-ray diffraction analysis confirmed the formation of pure alpha-NaMnO2 phase in all three samples, with only slight variations in lattice parameters. Elemental and oxidation state analyses were conducted using X-ray photoelectron spectroscopy (XPS), scanning electron microscopy with energy-dispersive X-ray spectroscopy, and inductively coupled plasma measurements. XPS results revealed noticeable differences in Mn ion valence states, suggesting variations in oxygen stoichiometry and the presence of oxygen-excess structures. Electrochemical evaluations were performed in both half-cell and full-cell configurations. The samples exhibited distinct performance characteristics, with capacity fade over 100 cycles at C/3 between 1.5 and 4.3 V measured at 83.6%, 73.9%, and 83.1%, respectively. These differences correlated with the average oxidation state of Mn and O content. Full-cells, paired with presodiated commercial hard carbon anodes, showed the highest capacity for the Na2O2/MnO2 system and the best retention for the Na2CO3/Mn2O3 sample. Overall, this work demonstrates how even small variations in starting materials can significantly influence the structural and electrochemical behavior of alpha-NaMnO2.
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    Investigation of electrochemical performance of Na-ion batteries by hard carbon anodes produced by biomass of Prunusarmeniaca seeds
    (Springer, 2023) Oktay, Zeynep Melek; Onal, Yunus; Depci, Tolga; Altundag, Sebahat; Altin, Serdar; Yasar, Sedat; Altin, Emine
    Hard carbon is successfully fabricated using biomass of Prunusarmeniaca seed shells, and its structural properties are examined by different spectroscopic techniques. For using as an anode electrode in Na-ion batteries, the material is subjected to further pyrolysis at varying temperatures for achieving the necessary levels of conductivity and surface area which are important features for electrode materials. Distinguish properties of the hard carbon in the XRD study appeared as broad peaks at 2 & theta; = 23 & DEG; and 43 & DEG;. The purity of produced hard carbons was approved by EDX to analyze that the purity of hard carbon is greater than 99.9%, making it suitable for industrial use. It was found that the CV curves of the cells created in this work utilizing hard carbon were quite comparable to the CV curves of commercially produced hard carbon cells. According to charge/discharge cycling measurements for constant current at rt, the highest capacity of 210.2 mAh/g using 0.1 A/g is obtained for the material pyrolyzed at 1200 & DEG;C and the capacity fade was found as 0.11. From these promising results, it is thought that the produced hard carbon can be easily used in the production of anode electrodes in commercial Na-ion batteries and technological applications. So it is summarized that P. armeniaca seed shells is one of the main sources for the production of the hard carbon and it can be used as an anode materials in battery cells.
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    Investigation of hybrid-capacitor properties of ruthenium complexes
    (Wiley-Hindawi, 2019) Altin, Serdar; Oz, Erdinc; Altundag, Sebahat; Bayri, Ali; Roisnel, Thierty; Dorcet, Vincent; Bruneau, Christian
    Ru complexes were successfully produced, and their structural properties were investigated using FTIR, Raman, and single crystal XRD patterns. The HOMO, LUMO, Eg, and electronic surface potential (ESP) values of the molecules were calculated by a Gaussian program. The complexes were used for producing hybrid capacitor cells as electrode materials. According to electrochemical analysis, complex 2 showed the best CV graph between -1 V and +1 V and had the highest current value and hysteresis area when compared with the other complexes. The performance analysis and the capacity fade of the cells were investigated. The first capacity values of the complexes were 57.5, 22.1, 16.9, and 0.0021 F/g for complexes 1, 2, 3, and 4, respectively. The capacitive mechanism of the cells as relates to molecular interactions was also investigated. We suggested that the ESP values of the molecules were directly related to the capacitive performance of the cells. In addition to this, the best cycling performance was obtained for complex 2, which has the lowest Eg value among the complexes. We speculate that the charged regions on the complex materials have a crucial role in the increasing the capacitance of the cells.
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