Abstract
The photocatalytic activity for H-2 production from water, without presence of hole scavengers, of thermally reduced TiO2 nanoparticles (H-500, H-700) and neat anatase were followed by in-situ continuous-wave light-induced electron paramagnetic resonance technique (CW-LEPR), in order to correlate the H-2 evolution rates with the electronic fingerprints of the photoexcited systems. Under UV irradiation, photoexcited electrons moved from the deep lattice towards the superficially exposed Ti sites. These photogenerated redox sites mediated (e(-)+h(+)) recombination and were the crucial electronic factor affecting catalysis. In the best-performant system (H-500), a synergic combination of mobile electrons was observed, which dynamically created diverse types of Ti3+ sites, including interstitial Ti3+, and singly ionized electrons trapped in oxygen vacancies (V-O(.)). The interplay of these species fed successfully surface exposed Ti4+ sites, which became a catalytically active, fast reacting Ti4+reversible arrow Ti3+ state that was key for the H-2 evolution process.