Covariant density functional theory (CDFT) is a modern theoretical tool for the description of nuclear structure phenomena. Different physical observables of the ground and excited states in even-even nuclei have been studied within the CDFT framework employing three major classes of the state-of-the-art covariant energy density functionals. The global assessment of the accuracy of the description of the ground state properties and systematic theoretical uncertainties of atomic nuclei have been investigated. Large-scale axial relativistic Hartree-Bogoliubov (RHB) calculations are performed for all Z < 106 even-even nuclei between the two-proton and two-neutron drip lines. The sources of theoretical uncertainties in the prediction of the two-neutron drip line are analyzed in the framework of CDFT. We concentrate on single-particle and pairing properties as potential sources of these uncertainties. The major source of these uncertainties can be traced back to the differences in the underlying single-particle structure of the various CEDFs. A systematic search for axial octupole deformation in the actinides and superheavy nuclei with proton numbers Z = 88 - 126 and neutron numbers from two-proton drip line up to N = 210 has been performed in CDFT. The nuclei in the Z ~ 96, N ~ 196 region of octupole deformation have been investigated in detail and their systematic uncertainties have been quantified. The structure of superheavy nuclei has been reanalyzed with inclusion of quadrupole deformation. Theoretical uncertainties in the predictions of inner fission barrier heights in superheavy elements have been investigated in a systematic way. The correlations between global description of the ground state properties and nuclear matter properties have been studied. It was concluded that the strict enforcement of the constraints on the nuclear matter properties (NMP) defined in Ref. [1] will not necessary lead to the functionals with good description of ground state properties. The different aspects of the existence and stability of hyperheavy nuclei have been investigated. For the first time, we demonstrate the existence of three regions of spherical hyperheavy nuclei centered around (Z ~ 138, N ~ 230), (Z ~ 156, N ~ 310) and (Z ~ 174, N ~ 410) which are expected to be reasonably stable against spontaneous fission.

The threat of the ongoing climate crisis requires the complete reduction of carbon emissions in the next two to three decades. Carbon dioxide electrochemical reduction (CO₂ER) poses a promising pathway to be able to maintain our current energy infrastructures in a carbon neutral fashion, by allowing the production of fuels and chemicals, such as CO, methanol and ethylene, with the use of carbon capture technologies and green energy. Thus far, Cu is the only metal that has demonstrated the ability to form hydrocarbon products. However, Cu is hindered by low selectivity. Improvements have been observed by coupling Cu with noble metals, such as Ag and Au. However, despite significant advancements, the technology has yet to achieve sufficient performance in activity, stability and selectivity for commercial viability. As such, this work pursued to further advance the activity of CO₂ER through the use of plasmonic Cu-based catalysts and the study of novel dinitrile-based electrolytes. It has recently been identified that CO₂ER can benefit from direct plasmonic effects induced by light illumination. In essence, certain light wavelengths can induce collective oscillations of the free electrons in the metallic particles, leading to an enhancement of their electrocatalytic performance. As such, the first project of this work involved the development and testing of plasmonic Cu-Ag bimetallic catalysts for the application of CO₂ER. Cu, Ag, as well as Cu-Ag bimetallic particles with variable morphologies were able to be synthesized through a facile one-pot sodium borohydride chemical reduction method. The synthesized catalyst performance was also compared to commercial catalysts. The synthesized particles were found to be active catalysts for CO₂ER, with improved electro-catalytic activities exhibited by Cu₈₅Ag₁₅, Cu₆₀Ag₄₀ and Cu syntheses in respective order. All nanoparticles demonstrated increases in the catalytic activity ranging between 15-26% under white light illumination, attributed to plasmonic promotion. The best plasmonic promotion of 26% was observed in the CuAg commercial alloy. Meanwhile, the best promotion of the synthesized bimetallic particles was of 18% found in the Cu₆₀Ag₄₀ catalyst. Additionally, improved electrochemical and plasmonic stability was observed with the use of the Cu-Ag bimetallic synthesized structures compared to monometallic Cu. In addition, most studies pertaining CO₂ER involve aqueous electrolytes due to their low cost and low toxicity. However, these systems are hindered by mass transfer limitations due to the low solubility of CO₂ in water. Organic-based electrolytes have been subjects of research as they possess higher CO₂ solubilities to water. As dinitriles pose a novelty in the role of CO₂ER, dinitrile-based electrolytes were studied and tested for the application. It was hypothesized that due to the decreased polarity in dinitrile solvents, CO₂ concentrations in the electrolyte would increase leading to improved catalytic activity. The testing was conducted by evaluating and comparing acetonitrile (ACN), adiponitrile (ADN) and sebaconitrile (SBN) solvent-based electrolytes. Increased CO₂ solubility was observed in the dinitriles with 582 mM and 503 mM of dissolved CO₂ in ADN and SBN respectively, compared to 270 mM in ACN. Results were corroborated through DFT modelling, indicating preference of CO₂ absorbance to nitrile groups on the molecules. However, despite increases in CO₂ concentration, the electrochemical activity decreased from ACN > ADN > SBN. The trend in activity was observed to be inversely proportional to the viscosity of the dinitrile solvents, which affected the ionic conductivity. Based on these developments, the present thesis opens a new perspective for the use of Cu-based nanoparticles for direct plasmonic enhancement with the use of a broad-range wavelength white light. Furthermore, the work also sheds light on the properties and resulting electrocatalytic activities of the use of dinitrile organic electrolytes for CO₂ER. The presented findings provide significant groundwork for further developments in the realm of CO₂ER.

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