Browsing by Author "Way, Ashley Jacqulyne"

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    Edge functionalisation of graphene nanoribbons with a boron dipyrrin complex : a thesis presented in partial fulfilment of the requirements for the degree of Doctor of Philosophy in Nanoscience at Massey University, Manawatū, New Zealand
    (Massey University, 2017) Way, Ashley Jacqulyne
    Chemical modification can be used to tune the properties of graphene and graphene nanoribbons, making them promising candidates for carbon-based electronics. The control of edge chemistry provides a route to controlling the properties of graphene nanoribbons, and their self-assembly into larger structures. Mechanically fractured graphene nanoribbons are assumed to contain oxygen functionalities, which enable chemical modification at the nanoribbon edge. The development of graphene nanoribbon edge chemistry is difficult using traditional techniques due to limitations on the characterisation of graphene materials. Through the use of a chromophore with well-defined chemistry, the reactivity of the edges has been investigated. Small aromatic systems were used to understand the reactivity of the boron dipyrrin Cl-BODIPY, and with the aid of spectroscopic and computational methods, the substitution mechanism and properties of the compounds have been investigated. The synthetic procedure was then applied to graphene nanoribbons. Results from infrared and Raman spectroscopy studies show that edge-functionalisation of graphene nanoribbons with BODIPY was successful, and no modifications to the basal plane have been observed.
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    A spectroscopic analysis of ionic liquid properties : a thesis presented in partial fulfilment of the requirements for the degree of Master of Science in Nanoscience at Massey University, Manawatū, New Zealand
    (Massey University, 2013) Way, Ashley Jacqulyne
    The use of ionic liquids in chemical processes is becoming of increasing interest, due to the low volatility of ionic liquids, and the wide range of properties which they possess. The ability to select properties based on anion and cation choice is also desirable. As such, the development of a solvent reorganization energy scale incorporating both common organic solvents and ionic liquids is useful, as it can be used to determine appropriate ionic liquid replacements of common organic solvents for use in applications. Raman spectroscopy studies have been performed on solutions of the solvatochromic Reichardt’s dye in a selection of common organic and ionic liquid solvents. Due to the solvatochromism of Reichardt’s dye, it behaves differently in solvents with differing properties. As such, the cross-sections of bands in Raman spectra associated with Reichardt’s dye differ between solvents also. Modelling of these cross-sections enables solvent properties to be determined. Absorption spectra were acquired of each sample, and resonance Raman spectra of each sample were recorded at a range of excitation wavelengths. After appropriate data treatment, the absorption and Raman cross-sections were determined, in order to enable the modelling of absorption and Raman crosssection profiles. The modelling of these profiles enabled the solvent reorganization energy of the organic solvents and ionic liquids to be determined, and a relative scale of solvent reorganization prepared. Computational studies were performed in order to better understand the dynamics of Reichardt’s dye in solution. The results from the studies were used to assign the vibrational modes of the Reichardt’s dye to bands in the resonance Raman spectra. From a solvent reorganization standpoint, it was found that common organic solvents may be replaced by ionic liquids of similar properties in applications where solvent volatility is an issue. In addition to this, the information obtained through the use of the solvent reorganization energy scale is able to be directly related to applications of ionic liquids involving electron transfer.