Browsing by Author "Davids, Wafeeq"

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    Advanced Ti – based AB and AB2 hydride forming materials
    (University of the Western Cape, 2011) Davids, Wafeeq; Linkov, V.M; Lototsky, M.V
    Ti – based AB and AB₂ hydride forming materials have shown to be very promising hydrogen storage alloys due to their reasonable reversible hydrogen storage capacity at near ambient conditions, abundance and low cost. However, these materials are not used extensively due to their poor activation performances and poisoning tolerance, resulting insignificant impeding of hydrogen sorption. The overall goal of this project was to develop the knowledge base for solid-state hydrogen storage technology suitable for stationary and special vehicular applications focussing mainly on Ti – based metal hydrides. In order to accomplish this goal, the project had a dual focus which included the synthesis methodology of Ti – based AB and AB₂ materials and the development of new surface engineering solutions, based on electroless plating and chemical vapour deposition on the surface modification of Ti – based metal hydride forming materials using Pd-based catalytic layers. TiFe alloy was synthesised by sintering of the Ti and Fe powders and by arc-melting. Sintered samples revealed three phases: TiFe (major), Ti₄Fe₂O, and β-Ti. Hydrogen absorption showed that the sintered material was almost fully activated after the first vacuum heating (400 °C) when compared to the arc-melted sample requiring several activation cycles. The increase in the hydrogen absorption kinetics of the sintered sample was associated with the influence of the formed hydrogen transfer catalyst, viz. oxygen containing Ti₄Fe₂O₁₋ₓ and β-Ti, which was confirmed by the XRD data from the samples before and after hydrogenation. The introduction of oxygen impurity into TiFe alloy observed in the sintered sample significantly influenced on its PCT performances, due to formation of stable hydrides of the impurity phases, as well as destabilisation of both β-TiFeH and, especially, γ-TiFeH₂. This finally resulted in the decrease of the reversible hydrogen storage capacity of the oxygen-contaminated sample. TiFe alloy was also prepared via induction melting using graphite and alumo-silica crucibles. It was shown that the samples prepared via the graphite crucible produced TiFe alloy as the major phase, whereas the alumo-silica crucible produced Ti₄Fe₂O₁-x and TiFe₂ as the major phases, and TiFe alloy as the minor one. A new method for the production of TiFe – based materials by two-stage reduction of ilmenite (FeTiO₃) using H₂ and CaH₂ as reducing agents was developed. The reversible hydrogen absorption performance of the TiFe – based material prepared via reduction of ilmenite was 0.5 wt. % H, although hydrogen absorption capacity of TiFe reported in the literature should be about 1.8 wt. %. The main reason for this low hydrogen capacity is due to large amount of oxygen present in the as prepared TiFe alloy. Thus to improve the hydrogen absorption of the raw TiFe alloy, it was melted with Zr, Cr, Mn, Ni and Cu to yield an AB₂ alloy. For the as prepared AB₂ alloy, the reversible hydrogen sorption capacity was about 1.3 wt. % H at P=40 bar and >1.8 wt.% at P=150 bar, which is acceptable for stationary applications. Finally, the material was found to be superior as compared to known AB₂-type alloys, as regards to its poisoning tolerance: 10-minutes long exposure of the dehydrogenated material to air results in a slight decrease of the hydrogen absorption capacity, but almost does not reduce the rate of the hydrogenation. Hydrogen storage performance of the TiFe-based materials suffers from difficulties with hydrogenation and sensitivity towards impurities in hydrogen gas, reducing hydrogen uptake rates and decreasing the cycle stability. An efficient solution to this problem is in modification of the material surface by the deposition of metals (including Palladium) capable of catalysing the dissociative chemisorption of hydrogen molecules. In this work, the surface modification of TiFe alloy was performed using autocatalytic deposition using PdCl₂ as the Pd precursor and metal-organic chemical vapour deposition technique (MO CVD), by thermal decomposition of palladium (II) acetylacetonate (Pd[acac]₂) mixed with the powder of the parent alloy. After surface modification of TiFe – based metal hydride materials with Pd, the alloy activation performance improved resulting in the alloy absorbing hydrogen without any activation process. The material also showed to absorb hydrogen after exposure to air, which otherwise proved detrimental.
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    Consolidated nanomaterials synthesized using nickel micro-wires and carbon nanotubes
    (University of the Western Cape, 2007) Davids, Wafeeq; Linkov, Vladimir M.; Nechaev, Alexander; Ndungu, Patrick; Dept. of Chemistry; Faculty of Science
    Nano-devices are the next step in the application of nanomaterials in modern technology. One area of research that is receiving an increased amount of attention globally is the fabrication of new nano-devices for applications in hydrogen energy technologies. The current work focuses on the synthesis and characterization of nano-devices with potential application in alkaline electrolysis and secondary polymer lithium ion batteries. Previous work with Nickel micro-wires demonstrated the potential to use these nanomaterials as electrodes in alkaline electrolysis. Carbon nanotubes have been shown to posse excellent electrochemical properties. A new direction in research is explored by combining nickel micro-wires with CNT, a new consolidated composite carbon nanocomposite can be realized and the characterization of such a novel composite was the focus of this thesis. Novel composite carbon nanomaterials were synthesized using an electrochemical template technique and a hydrocarbon pyrolysis step. The first step involved the deposition of nickel within the pores of ion track etched Polyethylene terephthalate (PET) membrane; with pore diameters of 1μ, 0.4μ and 0.2 μ. Electrochemical deposition of nickel was carried out galvanostatically in a nickel hard bath between 35-40°C, and using a deposition current density of 75 mAcm2. Carbon nanotubes were then deposited directly onto the surface of the nickel micro-wires via a chemical vapour deposition (CVD) technique using liquid petroleum gas (LPG) as the carbon source. CVD was done at a temperature of 800°C and the deposition time was 5 minutes. The morphology and structural studies of these novel composite nanomaterials were studied by scanning electron microscopy (SEM), transmission electron microscopy (TEM) and X-ray diffraction (XRD). Electrochemical investigations were done using Cyclic Voltammetry (CV), Chronoamperometry (CA) and Electrochemical Impedance Spectroscopy (EIS). After removal of the template, before CNT CVD growth, SEM images revealed free standing arrays of nickel micro-wires, and after CNT growth via CVD the SEM micrographs showed that the morphology of the Ni micro-wires was moderately altered by the CVD process. From the XRD results it was shown that the crystallinity of the Nimicro-wires was persevered after the CVD process. The XRD of the nickel micro-wires with CNT grown directly on the surface revealed the characteristic CNT peak at 2θ =24.60. Cyclic Voltammetry (CV) was performed on the consolidated composite nanomaterial in an alkaline solution. The CV revealed that the novel composite carbon nanomaterial was the most active for hydrogen evolution when compared to unmodified Ni micro-wires and a flat nickel electrode. This was attributed to the increase in electrochemical accessible surface area. Electrochemical impedance spectroscopy (EIS) showed that the novel composite carbon nanomaterial had a much higher capacitance than the nickel micro-wires, a flat nickel electrode, a flat nickel substrate modified with CNT, and a graphite electrode. When a similar comparison was done using a commercially available anode for lithium ion battery applications, the novel consolidated composite carbon nanomaterial had double the capacitance of the commercial anode. The consolidated composite carbon nanomaterial was modified by depositing Pt on to the surface of the CNT via electroless deposition. The presence of Pt was determined by Energy dispersive spectrometry and the electrocatalytic activity of the Pt modified consolidated composite carbon nanomaterial was significantly improved. The work presented in this thesis provides a new and unique direction in the synthesis and application of novel consolidated carbon nanomaterials through true synergistic effect between nickel micro-wires and CNT. The exploration of the characteristics of the system and the ability to functionalize the CNT with different moieties allows for a wide range of application in energy conversion devices.