Abstract
Figuring out the specific pathway of semiconductor-mediated proton-coupled electron transfer (PCET) driven by light is essential to solar energy conversion systems. In this work, we reveal that the amount of adsorbed water molecules determines the photo-induced PCET pathway on the TiO(2) surface through systematic kinetic solvent isotope effect (KSIE) experiments. At low water content (<1.7 wt%), the photo-induced single-proton/single-electron transfer on TiO(2) nanoparticles follows a stepwise PT/ET pathway with the formation of high-energy H(+)/D(+)-O[double bond, length as m-dash]C or H(+)/D(+)-O-C intermediates, resulting in an inverse KSIE (H/D) ∼0.5 with (t) Bu(3)ArO· and KSIE (H/D) ∼1 with TEMPO in methanol-d (0)/d (4) systems. However, at high water content (>2 wt%), the PCET reaction follows a concerted pathway with a lower energy barrier, leading to normal KSIEs (H/D) ≥ 2 with both reagents. In situ ATR-FTIR observation and DFT calculations suggest that water molecules' existence significantly lowers the proton/electron transfer energy barrier, which coincides with our experimental observations.