Chemical Photocatalysis with Rhodamine 6G: Investigation of Photoreduction by Simultaneous Fluorescence Correlation Spectroscopy and Fluorescence Lifetime Measurements.

Recent research has demonstrated that consecutive excitation of the radical anion state of commercially available dye molecules-generated by a photoinduced electron-transfer process-yields sufficient energy to stimulate challenging chemical reactions in photocatalysis. For this reason, an efficient transfer of dye molecules into their radical anion states upon photoexcitation is highly desirable, as is a long radical lifetime. However, the formation of these reactive states is strongly dependent on the redox agent, the local environment, for example, the solvents and additives, as well as on the properties of the excited states of the dye molecule.