The use of energy is going to continue to increase rapidly due to population and economic advances occurring throughout the world. The most widely used energies produce carbon dioxide during their combustion and have finite limits on how much of these resources are available. A strong push to utilizing renewable energy is necessary to keep up with the demand. The only renewable energy that has unlimited supply is solar. Our goal is to find cost-effective alternatives to historically the most extensively used materials in dye-sensitized solar cells. In order to rely on efficiency changes coinciding with the introduction of a new component, a standard baseline of performance is necessary to establish. A reproducible fabrication procedure composed of standard materials was instituted; the efficiency parameters exhibited a less than 10% standard deviation for any set of solar cells. Any modifications to the cell components would be apparent in the change in efficiency. Our cell modifications focused on economical alternatives to the electrolyte, the counter electrode and the chromophore. Solution-based electrolytes were replaced with a non-volatile ionic liquid, 1-methyl-3-propylimidazolium iodide, and then a poly(imidazole-functionalized) silica nanoparticle. Solid-state electrolytes reduce or prevent leakage and could ease manufacturing in large-scale devices. Platinum has been the counter electrode catalyst primarily used with the iodide/triiodide redox couple, but is a rare metal making it rather costly. We reduce platinum loading by introducing a novel counter electrode that employs platinum nanoparticles embedded on a graphene nanoplatelet paper. The highly conductive carbon base also negates the use of the expensive conductive substrate necessary for the platinum catalyst, further reducing cost. We also study the differences in transitioning from ruthenium polypyridyls to iron-based chromophores in dye-sensitized solar cells. Iron introduces low-lying ligand field states which the charge-transfer transitions necessary for electron injection deactivate to. We study a series of molecules that converts from a historically well-known ruthenium dye stepwise to an iron-based chromophore that has exhibited photocurrent previously. Converting to iron proves to be complicated and we aim to continue our investigation in order to gain a better understanding of the complexity.
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