Lateral Intermolecular Self-Exchange Reactions for Hole and Energy Transport on Mesoporous Metal Oxide Thin Films.

Abstract

Intermolecular self-exchange energy and electron-transfer reactions occur without a loss of free energy. This behavior can be exploited for energy-transport applications when molecules that undergo self-exchange transfer reactions are immobilized on a solid support. This Article focuses upon lateral self-exchange reactions and the relevant interfacial chemistry that occurs on the mesoporous nanocrystalline (anatase) TiO2 thin films that are commonly used in dye-sensitized solar cells. It has been known for some time that all of the dye molecules (termed sensitizers) within such thin films can be reversibly oxidized and reduced by lateral self-exchange electron transfer provided that the sensitizer surface coverage exceeds a percolation threshold. Under conditions where excited-state electron injection into TiO2 is unfavored, lateral intermolecular energy-transfer reactions are also known to occur. The self-exchange rate constants have been quantified by electrochemical, absorption, and/or time-resolved anisotropy techniques and understood within the framework of Marcus theory. Such analysis reveals that the reorganization energy and the electronic coupling are sensitive to the identity of the molecular compound. Time-resolved anisotropy measurements have shown that lateral charge and energy-transfer reactions across the TiO2 surface occur in kinetic competition with charge recombination and excited-state relaxation, respectively. The extent to which lateral self-exchange reactions might be exploited for solar energy conversion applications is discussed, as are critical fundamental issues that remain unresolved.