Rapid charge transfer in TiO2/COF S-scheme heterojunction for boosting H2O2 photosynthesis and Rhodamine B degradation
Yanyan Zhao, Yong Zhang, Haiyan Tan, C.F. Ai, Jianjun Zhang
Abstract
Cooperative coupling of hydrogen peroxide (H 2 O 2 ) photosynthesis with organic pollutant degradation is promising strategy applied in chemical synthesis and environmental protection. Nonetheless, the photocatalytic performance is limited by sluggish photogenerated carrier separation and limited redox potentials. Herein, an S-scheme heterojunction was constructed by assembling the TiO 2 nanoparticles and a Schiff-base COF together. The formed S-scheme TiO 2 /COF heterojunction can efficiently produce H 2 O 2 and degrade Rhodamine B (RhB) synchronously. The S-scheme charge transfer mechanism in TiO 2 /COF composite is well unveiled by in situ irradiated X-ray photoelectron spectroscopy and DFT calculation. The femtosecond transient absorption spectra reveal the superior charge migration at interface between TiO 2 and COF. The designed TiO 2 /COF composite shows drastically enhanced H 2 O 2 yield of 1326 μmol·g −1 ·h −1 in RhB solution, and the AQY value of 4.11% under 420 nm monochromatic light irradiation is achieved. Meanwhile, 100% of RhB degraded under light irradiation for 40 min with TiO 2 /TD COF as photocatalyst. This work exemplifies a promising approach to design COF-based S-scheme heterojunction with ameliorative photocatalytic performance for simultaneous organic pollutants degradation and H 2 O 2 production. • TiO 2 /TD COF S-scheme heterojunction was constructed. • TiO 2 /TD COF shows enhanced H 2 O 2 yield coupling with highly RhB degradation. • S-scheme charge migration mechanism has been proved. • Fully utilization of hole-electron has been realized. • This work exemplifies a promising way to design TiO 2 based S type heterojunction.