Dynamics of Electron Transfers in Photosensitization Reactions of Zinc Porphyrin Derivatives

Photocatalytic systems for CO reduction operate via complicated multi-electron transfer (ET) processes. A complete understanding of these ET dynamics can be challenging but is key to improving the efficiency of CO conversion. Here, we report the ET dynamics of a series of zinc porphyrin derivatives ( ) in the photosensitization reactions where sequential ET reactions of occur with a sacrificial electron donor (SED) and then with TiO . We employed picosecond time-resolved fluorescence spectroscopy and femtosecond transient absorption (TA) measurement to investigate the fast ET dynamics concealed in the steady-state or slow time-resolved measurements. As a result, Stern-Volmer analysis of fluorescence lifetimes evidenced that the reaction of photoexcited with SED involves static and dynamic quenching. The global fits to the TA spectra identified much faster ET dynamics on a few nanosecond-time scales in the reactions of one-electron reduced species ( ) with TiO compared to previously measured minute-scale quenching dynamics and even diffusion rates. We propose that these dynamics report the ET dynamics of formed at adjacent TiO without involving diffusion. This study highlights the importance of ultrafast time-resolved spectroscopy for elucidating the detailed ET dynamics in photosensitization reactions.