Papers by Author: Edy Herianto Majlan

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Abstract: Catalysis is the major process involved in fuel cell technology to generate electricity which is known renewable. Generally, fuel cell electrodes utilize platinum supported carbon to catalyze the reactions at both cathode and anode. However, cheaper substitution materials such as nitrogen-doped carbon catalyst have attracted greater attention in recent year due to its significant catalytic activity at cathode in fuel cell. Nitrogen-doped CNT (N-CNT) is believed to allow oxygen reduction reaction (ORR) at cathode to take place which play a role as n-type dopant for electrical conductivity. The objective of this paper is to understand the mechanism of oxygen adsorption on N-CNT using the density-functional theory (DFT). N-CNT with two configurations involve sp2 and sp3 hybridized nitrogen are studied and compared in order to find the most thermodynamically stable N-CNT for sustainable ORR activity in fuel cell. The structural stability is studied through the binding energies of each configurations and the metallic behavior is examined through the energy gaps from the HOMO-LUMO studies. Finally, the adsorption energies and deformation energies of oxygen on N-CNT is discussed. Results revealed that sp3 hybridized N-CNT gives the most stable structure with compatible oxygen adsorption ability.
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Abstract: Metal and Metal oxide nanofibers have different potential to play an essential role in a series of application, among them copper and copper oxide nanostructures is a promising semiconductor material with potential applications in many field. In this paper, electrospinning method via sol-gel was used to fabricate copper and copper oxide nanofibers. Synthesize of copper and copper oxide nanofibers and also effect of calcinations temperature on morphology investigated by thermal gravimetric analysis, scanning electron microscopy (SEM), Transmission electron microscopy, x-ray diffraction(XRD), Fourier transform infrared spectroscopy (FTIR) and Brunauer Emmett and Teller (BET).
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Abstract: Flooding and membrane dehydration are phenomena that must be avoided in a proton exchange membrane fuel cell (PEMFC) operation. It needs a sufficient knowledge about water transport behaviors. Electro-osmotic drag and back diffusion are the dominant water transport mechanisms through the membrane in PEMFC. In this study, the relative humidity (RH) profile along the channel at both anode and cathode sides have been recorded. The experiment was conducted in a single cell PEMFC with single serpentine flow field design. The water content profile was strongly influenced by RH profile thus in turn influenced the electro-osmotic drag coefficient, water diffusion coefficient and back diffusion flux. The operating temperatures of cell also influence those water transport behavior. The temperature was varied at 25, 40, 50 and 60 oC, while the pressure at the anode and the cathode was fixed at 1 bar. The higher the temperature, the smaller the water contents but with higher electro-osmotic drag coefficient, water diffusion coefficient and back diffusion flux. After all, the strategy of using saturated hydrogen and dry air in this study successfully prevents flooding and membrane dehydrating in the system – that are the major problems in PEMFC operation.
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Abstract: The assembly of proton exchange membrane fuel cell (PEMFC) is the important factor for the performance. The achievement of proper design will improve the pressure distribution and the electrical contact resistance between fuel cell parts. The assembly pressure affects the contact behavior between of bipolar plate and gas diffusion layer (GDL). In this study, finite element analysis (FEA) was used to analyze the behavior of single cell fuel cell under the variation of assembly pressure. It shows 3D of deformation, and the compression pressure every part of the fuel cell components. The simulation varied the torque assembly from 1 Nm to 3 Nm with increment 0.5 Nm. The simulation using FEA shows that high assembly pressure also affects to the high deformation and stress in the components of fuel cell. This phenomenon affects to the performance of PEM fuel cell.
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Abstract: Composite anodes made of NiO and SDC-(Li/Na)2CO3 were investigated in relation to their structure, morphology, and porosity. As a first step, the anode powder was prepared by mixing the NiO with SDC-(Li/Na)2CO3 via solid state reaction in weight percentage of 60 : 40 wt% and in various compositions of carbonates (20 and 30wt%), namely NiO-SDC8020 and NiO-SDC7030, respectively. The powder mixtures were then calcined at 680oC. The resultant powder was fine with surface area of about 13.10-13.70 m2/g and an average particle size of 0.32-0.37µm. The powders consist of two phases i.e. the cubic NiO and face-centered cubic structure SDC-(Li/Na)2CO3 as confirmed with x-ray diffraction. The microstructures were observed under scanning electron microscopy (SEM). The anode pellets were later compacted at different pressures (27, 32 and 37 MPa) and sintered at 600oC. The optimum porosity (20.99-24.78%) was achieved for samples of NiO-SDC8020 and NiO-SDC7030 sintered at 600oC and cold pressed at 32 and 37 MPa.
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Abstract: Electrospun Poly (vinylidene fluoride) (PVdF) fine fiber of 100-300 nm in diameter in ribbon shape was synthesized through the electrospinning process via sol-gel. In order to synthesize infusible nanofibers all processing of dehydrofluorination and carbonization was investigated. Iron nanoparticles was doped with PVDF nanofibers in order to be effective in surface area, and porosity to increase the hydrogen storage. The composition, morphology, structure and surface area of PVDF/Iron Oxide nanofibers were investigated by thermo gravimetric analysis (TGA) to determinate the temperature of possible decomposition and crystallinity, scanning electron microscopy (SEM), transmission electron microscopy (TEM), Micromeritics (ASAP2020) used to study the textural properties of the sample, like surface area, total pore volume, and micro pore volume. The result shows that the PVDF without dehydrofluorination treatment for infusibility become melt at around 160 °C. By adding the iron oxide nanoparticles as a catalyst it can improve the characteristic of the carbon fiber for hydrogen storage. In best of our knowledge, PVDF doping with iron oxide investigated for first time.
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Abstract: The need and development of cleaner and greener alternative technologies using the heterogeneous catalytic system in the synthesis of fuel is very important. In this work hydrogen production via steam reforming of glycerol (C3H8O3) was carried out over nickel supported on hydroxyapatite [Ca5(PO4)3(OH)] as a biomaterial catalyst. The time reaction is carried out for 240 minutes in a fixed-bed reactor fixed at 600 oC and atmospheric pressure with the water-to-glycerol feed ratio of 8:1. Catalysts were prepared by mean of impregnation and sol-gel method with varied nickel loadings (3, 6, 9, 12 %) on hydroxyapatite. The catalysts were characterized by BET surface area, X-ray diffraction, and SEM-EDX techniques. It is found that 3 wt% of nickel loading prepared via sol-gel method exhibit the higher hydrogen production rates (63.62 % - 74.16 %) in comparison to the other nickel loadings.
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Abstract: In recent years, one dimensional nanostructure, nanowires, nanofibers with unique properties have been a subject of intense research due to reduction of devise dimension, potential properties from the re-arrangement at the molecular level and high surface area. There are many methods for synthesize such as laser ablation, chemical vapour deposition, solution method micro pulling down method but all these method faced to the major disadvantages of being complicated with long wasting time and relatively high expense . The electrospinning recently used for producing ceramic, metal, and carbon nanofibers. In this report, we incorporate palladium into silica nanofibers for the first time, and the effect of doping of palladium into the silica nanofibers is investigated. The different ratio of palladium to silica and comparing with silica nanofibers is also reported. The composition, morphology, structure and surface area of silica, and silica palladium nanofibers were investigated by thermo gravimetric analysis (TGA), x-ray diffraction (XRD), scanning electron microscopy (SEM),Fourier transform infrared spectroscopy (FT-IR), and Micromeriics. To the best of our knowledge, investigation on characteristic on Silica palladium nanofibers has not been reported up to now. The result reveal that the silica nanofibers compare to silica doped with palladium have lower diameter, and also by increasing the temperature above 600 °C, the reduction in length of nanofibers happened. High surface area of silica palladium nanofibers can be one of the promising materials for hydrogen storage.
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Abstract: One-dimensional nanostructures, like nanofibers, nanobelts, nanotubes, nanorods have been regarded as a new class of nanomaterials that have been attracted as the most promising building blocks for verity applications in the last few years. As one type of important structures with intensive research efforts have been devoted to the production and investigation of the metal oxides. Metal oxide nanofibers have different potential to play an essential role in a series of application such as optics, nanoelectronics, catalysts, sensors, storage, optoelectonics, and full cell. Copper oxide nanostructures is a promising semiconductor material with potential applications in photochemical, electrochemical, electrochromic especially in water splitting, catalysts, and fabrication of photovoltaic devices. In this paper electrospinning method via sol-gel was used to fabricate copper oxide nanofibers. Copper oxide nanofibers with different morphology were synthesized by different calcinations temperature. In this paper, effective parameters such as voltage, concentration of precursor and different calcinations temperature were characterized by thermal gravimetric analysis, scanning electron microscopy (SEM), Transmission electron microscopy, x-ray diffraction(XRD), Fourier transform infrared spectroscopy (FTIR) and Brunauer Emmett and Teller (BET).
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Abstract: Composite cathodes made of perovskite La0.6Sr0.4Co0.2Fe0.8O3 (LSCF) and SDC carbonates (SDC-(Li/Na)2CO3) were investigated in relation to their structure, morphology, thermal expansion coefficient and porosity. As a first step, the LSCF powder was prepared by sol-gel technique. This was followed by the preparation of the LSCF-SDC carbonates composite cathode by mixing the LSCF with SDC-(Li/Na)2CO3 electrolyte via solid state reaction in various compositions, i.e. 30, 40 and 50 wt.%, namely 70LSCF-30SDC7030, 60LSCF-40SDC7030 and 50LSCF-50SDC7030, respectively. The powder mixtures were then calcined at 680oC. The resultant powder was fine with surface area of about 3.39-7.42 m2/g and particle size of 0.56-0.66µm. The powder consists of two distinct phases, i.e. LSCF and SDC-(Li/Na)2CO3 as confirmed with x-ray diffraction. The microstructures were observed under scanning electron microscopy (SEM). Increasing the amount of the SDC-(Li/Na)2CO3 electrolyte in the composite cathode was found to bring the thermal expansion of the cathode closer to that of the electrolyte. The cathode pellets were later compacted at different pressures (27, 32 and 37 MPa) and sintered at 600oC. The optimum porosity (20.99-24.98%) was achieved for samples with SDC-(Li/Na)2CO3 content of 30-50% sintered at 600oC and cold pressed at 37 MPa.
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