Transition metal phosphides have been recognized as efficient co-catalysts to boost the activity of semiconductor photocatalysts. However, a rigorous and quantitative understanding is still to be developed about how transition metal phosphides influence photoexcited electron dynamics. Here, we present a nanosecond time-resolved transient absorption spectroscopy (TAS) study of the photoexcited electron dynamics in carbon nitrides (g-C3N4) before and after Co and/or P modifications. Our spectroscopic study showed that Co or P lowered the initial electron density, whereas they promoted the photoexcited electron relaxation of g-C3N4, with their half-life times (t50%) of 2.5 and 1.8 ns, respectively. The formation of a CoP co-catalyst compound promoted the electron relaxation (t50%=2.8 ns) without significantly lowering the charge separation efficiency. Density functional theory (DFT) calculations were undertaken to explore the underlying fundamental reasons and they further predicted that CoP, compared to Co or P modification, better facilitates photoexcited electron transfer from g-C3N4 to reactants.
All Science Journal Classification (ASJC) codes
- Analytical Chemistry
- Physical and Theoretical Chemistry
- Organic Chemistry