Matching Items (2)
Description
The free-base tetra-tolyl-porphyrin and the corresponding cobalt and iron porphyrin complexes were synthesized and characterized to show that this class of compound can be promising, tunable catalysts for carbon dioxide reduction. During cyclic voltammetry experiments, the iron porphyrin showed an on-set of ‘catalytic current’ at an earlier potential than the cobalt porphyrin’s in organic solutions gassed with carbon dioxide. The cobalt porphyrin yielded larger catalytic currents, but at the same potential as the electrode. This difference, along with the significant changes in the porphyrin’s electronic, optical and redox properties, showed that its capabilities for carbon dioxide reduction can be controlled by metal ions, allotting it unique opportunities for applications in solar fuels catalysis and photochemical reactions.
ContributorsSkibo, Edward Kim (Author) / Moore, Gary (Thesis director) / Woodbury, Neal (Committee member) / School of Molecular Sciences (Contributor) / School of Sustainability (Contributor) / Barrett, The Honors College (Contributor)
Created2016-05
Description
The conversion of water to hydrogen and of carbon dioxide to industrially relevant chemical precursors are examples of reactions that can be used to store renewable energy as fuels or chemical building blocks for creating sustainable chemical manufacturing cycles. Unfortunately, current industrial catalysts for these transformations are reliant on relatively expensive and/or rare materials, such as platinum in the case of hydrogen generation, or lack selectivity towards producing a desired chemical product. Such drawbacks prevent global-scale applications. Although replacing such catalysts with more efficient and earth-abundant catalysts could improve this situation, the fundamental science required for this is lacking. In the first part of this dissertation, the synthesis and characterization of a novel binuclear iron fused porphyrin designed to break traditional scaling relationships in electrocatalysis is presented. Key features of the fused porphyrin include: 1) bimetallic sites, 2) a π-extended ligand that delocalizes electrons across the multimetallic scaffold, and 3) the ability to store up to six reducing equivalents. In the second part of this thesis, the electrochemical characterization of benzimidazole-phenols as “proton wires” is described. These bioinspired assemblies model the tyrosine-histidine pair of photosystem II, which serves as a redox mediator between the light-harvesting reaction center P680 and the oxygen evolution complex that enables production of molecular oxygen from water in cyanobacteria, algae, and higher plants. Results show that as the length of the hydrogen-bond network increases across a series of benzimidazole-phenols, the midpoint potential of the phenoxyl/phenol redox couple becomes less oxidizing. However, benzimidazole-phenols containing electron-withdrawing trifluoromethyl substituents enable access to potentials that are thermodynamically sufficient for oxidative processes relevant to artificial photosynthesis, including the oxidation of water, while translocating protons over ~11 Å.
ContributorsReyes Cruz, Edgar Alejandro (Author) / Moore, Gary F (Thesis advisor) / Trovitch, Ryan J (Committee member) / Sayres, Scott G (Committee member) / Arizona State University (Publisher)
Created2023