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MAX phases are layered hexagonal early transition metal carbides, sometimes nitrides, where M is an early transition metal, A is an A group element, most prominently groups 13 or 14, and X is either carbon or nitrogen.1 They are gaining a lot of attention because of their unusual properties. Particularly,

MAX phases are layered hexagonal early transition metal carbides, sometimes nitrides, where M is an early transition metal, A is an A group element, most prominently groups 13 or 14, and X is either carbon or nitrogen.1 They are gaining a lot of attention because of their unusual properties. Particularly, their hardness, chemical stability at room temperature, and high melting points. These properties provide a material that is viable for a wide range of demanding applications.2,3 MAX phases display a combination of both ceramic and metallic characteristics. Furthermore, they also serve as a precursor for two-dimensional MXenes.4,5<br/>Generally, bulk synthesis of MAX phases is done through traditional solid state synthesis techniques. For example, three solid state synthesis techniques include solid state method, hot pressing and arc melting and annealing. During solid state method, the powder precursors are preheated between 350 and 400°C, allowing for decomposition of starting reagents and removal of volatile products leaving only the oxides. At this point the germination phase has completed, and the crystal growth phase begins. Under the effect of a concentration gradient and very high temperatures, cations migrate, forming well-ordered layers. Slow cooling rates are used in order to ensure crystallinity of the product.6 The second method, hot pressing, involves the mixing of powder precursors thoroughly and then cold pressed into a green body – a ceramic body powder pre-sintering. They are then heated under vacuum and often high pressure in order to form the product. Two variants of hot-pressing exits: reactive hot pressing, where the pressure during the reaction will vary throughout the reaction, and isostatic hot pressing, where the pressure is held constant throughout the entire reaction.7 Another solid-state technique is arc melting and annealing. During arc melting, alternating current is applied to the electrode inside an inert reactor, which is arranged as to generate an arc discharge. The heat produced by arcing causes rapid melting of the samples.8 While these methods are most common, they are not always viable due to the specialized equipment required in order to achieve the high temperature and pressure conditions. Furthermore, these specific techniques don’t allow for high control over particle size and morphology. <br/>Because of this, alternative, non-conventional synthesis techniques have been developed involving more readily available tube furnaces and microwaves, which lack the extreme pressures instead opting for ambient conditions.9 Sol-gel techniques have been developed by the group of Christina Birkel, and have successfully produced MAX phases through calcination of homogeneous citric acid-based gel-precursors. Some advantages of using these gel-precursors include shorter diffusion paths, and faster mass transport, thus, resulting in lower reaction temperatures and shorter reaction times. Ultimately, this allows for control over particle morphology and size.10<br/>The focus of this work is to discover optimal synthesis conditions to create spherical Cr2GaC. Spherical MAX phases have been briefly explored in existing literature using polymer-based hollow microsphere templates.10 These polymer microspheres have been used to synthesize spherical metal oxides. This is achieved by heating the metal oxide precursors which adhere to the spheres, then by thermal treatment, the template is then removed.11 <br/>Two different microsphere templates will be explored to study the advantages and disadvantages of different size distributions and surface conditions of the spheres. Furthermore, reaction temperature, reaction time, citric acid equivalents, and gel to microsphere ratio will be altered to determine optimal synthesis parameters for depositing Cr2GaC onto spherical templates. Cr2GaC serves as a model compound because it has been successfully synthesized through sol-gel chemistry in the past.10 This phase will be prepared through non-conventional sol-gel chemistry, with various heating profiles, both furnace and microwave, and will be characterized through X-ray diffraction (XRD), and Rietveld refinement. Further, the morphology and atomic composition will be analyzed through scanning electron microscopy (SEM) and energy-dispersive X-ray spectroscopy (EDS).

ContributorsWasserbeck, Andrew (Author) / Birkel, Christina (Thesis director) / Siebert, Jan Paul (Committee member) / Materials Science and Engineering Program (Contributor) / Chemical Engineering Program (Contributor) / Barrett, The Honors College (Contributor)
Created2021-05
Description

MAX phases are ternary carbides or nitrides that possess unique material characteristics, often simplified as a mix of metallic and ceramic properties. Many aspects of MAX phases are still being researched, but they have exciting potential applications in high-temperature structural systems, the next generation of nuclear power plants, and concentrated

MAX phases are ternary carbides or nitrides that possess unique material characteristics, often simplified as a mix of metallic and ceramic properties. Many aspects of MAX phases are still being researched, but they have exciting potential applications in high-temperature structural systems, the next generation of nuclear power plants, and concentrated solar power. This project aims to benefit further research into these applications by validating a rapid unconventional synthesis method: microwave-assisted sol-gel synthesis. Three MAX phases (Cr2GaC, Cr2GeC, and V2GeC) were successfully synthesized via this route, which should open the door for more rapid prototyping and ultimately more efficient research.

ContributorsPatarakun, Keene Narin (Author) / Birkel, Christina (Thesis director) / Seo, Don (Committee member) / Petuskey, William (Committee member) / Mechanical and Aerospace Engineering Program (Contributor) / Barrett, The Honors College (Contributor)
Created2021-05
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Description
Due to the potential synergistic properties from combining inorganic and organic moieties, inorganic/organic hybrids materials have recently attracted great attention. These hybrids are critical components in coating and nanocomposite additive technologies and have potential for future application in catalysis, energy production or storage, environmental remediation, electronic, and sensing technologies.

Due to the potential synergistic properties from combining inorganic and organic moieties, inorganic/organic hybrids materials have recently attracted great attention. These hybrids are critical components in coating and nanocomposite additive technologies and have potential for future application in catalysis, energy production or storage, environmental remediation, electronic, and sensing technologies. Most of these hybrids utilize low dimensional metal oxides as a key ingredient for the inorganic part. Generally, clay materials are used as inorganic components, however, the use of low dimensional transition metal oxides may provide additional properties not possible with clays. Despite their potential, few methods are known for the use of low dimensional transition metal oxides in the construction of inorganic/organic hybrid materials.Herein, new synthetic routes to produce hybrid materials from low dimensional early transition metal oxides are presented. Included in this thesis is a report on a destructive, chemical exfoliation method designed specifically to exploit the Brønsted acidity of hydrated early transition metal oxides. The method takes advantage of (1) the simple acid-base reaction principle applied to strong two-dimensional Brønsted solid acids and mildly basic, high-polarity organic solvents, (2) the electrostatic repulsion among exfoliated nanosheets, and (3) the high polarity of the organic solvent to stabilize the macroanionic metal oxide nanosheets in the solvent medium. This exfoliation route was applied to tungstite (WO3∙H2O) and vanadium phosphate hydrate (VOPO4∙H2O) to produce stable dispersions of metal oxide nanosheets. The nanosheets were then functionalized by adduct formation or silane surface modification. Both functionalization methods resulted in materials with unique properties, which demonstrates the versatility of the new exfoliation methods in preparing novel hybrid materials. Further extension of the method to aqueous systems allowed discovery of a new synthetic method for electrically-conducting polyaniline-polyoxometalate hybrid materials. Namely, destructive dissolution of MoO2(HPO4)(H2O) in water produces protons and Strandberg-type phosphomolybdate clusters, and in the presence of aniline and an oxidizing agent, the clusters self-assemble with protonated anilines and selectively form polyaniline-phosphomolybdate hybrids on various types of surfaces through in situ oxidative chemical polymerization. New conductive nanocomposite materials were produced by selectively coating the surface of silica nanoparticles.
ContributorsCiota, David (Author) / Seo, Dong-Kyun (Thesis advisor) / Trovitch, Ryan (Committee member) / Birkel, Christina (Committee member) / Arizona State University (Publisher)
Created2022
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Description
MAX phases are an intriguing class of materials with exotic combinations of properties, essentially turning them into metallic ceramics. Despite this unique feature, no commercialization has been accomplished yet. Looking at the state of the art within the MAX phase community, almost all published studies can be summarized using the

MAX phases are an intriguing class of materials with exotic combinations of properties, essentially turning them into metallic ceramics. Despite this unique feature, no commercialization has been accomplished yet. Looking at the state of the art within the MAX phase community, almost all published studies can be summarized using the term “traditional high temperature synthesis”. Contrasting the scientific interest that has been on the rise especially since the discovery of MXenes, the synthetic spectrum has been largely the same as it has been over the past decades.Herein, the newly-emerging sol-gel chemistry is being explored as an alternative non-conventional synthetic approach. Building on the successful sol-gel synthesis of Cr2GaC, this study focuses around the expansion of sol-gel chemistry for MAX phases. Starting with a thorough mechanistic investigation into the reaction pathway of sol-gel synthesized Cr2GaC, the chemical understanding of this system is drastically deepened. It is shown how the preliminary nano-structured metal-oxide species develop into bulk oxides, before the amorphous and disordered graphite partakes in the reaction and reduces the metals into the MAX phase. Furthermore, the technique is extended to the two Ge- based MAX phases V2GeC and Cr2GeC, a critical step needed to prove the viability and applicability of the newly developed technique. Additionally, by introducing Mn into the Cr-Ga-C system, a Mn-doping was achieved, and for the first time for (Cr1–xMnx)2GaC, a unit cell increase could be recorded. Based on magnetometry measurements, the currently widely accepted assumption of statistically distributed Mn in the M-layer is challenged. The versatility of wet chemistry is explored using the model system Cr2GaC. Firstly, the MAX phase can be obtained in a microwire shape leveraging the branched biopolymer dextran, eliminating the need for any post-synthesis machining. Via halide intercalation, the electrical transport properties could be purposefully engineered. Secondly, leveraging the unique and linear biopolymer chitosan, Cr2GaC was obtained as thick films and dense microspheres, drastically opening potential areas of application for MAX phases. Lastly, hollow microspheres with diameters of tens of μm were synthesized via carboxymethylated dextran. This shape once more opens the door to very specific applications requiring sophisticated structures.
ContributorsSiebert, Jan (Author) / Birkel, Christina (Thesis advisor) / Gould, Ian (Committee member) / Kouvetakis, John (Committee member) / Arizona State University (Publisher)
Created2022