An organometal halide perovskite supported Pt single-atom photocatalyst for H2 evolution

A supported single-atom catalyst provides an opportunity to make full use of noble metals with optimized efficiency and minimal amount. For photocatalytic applications, organometal halide perovskites are greatly ideal candidates as substrate materials for supporting single-atom catalysts because of their excellent properties and remarkable performance in the photoelectric area. However, atomically dispersing noble metals on organometal halide perovskites stably and firmly remains a challenge. Here, we realize the preparation of single-atom Pt immobilized on FAPbBr(3-x)I(x) (FA = CH(NH2)(2)) perovskite substrates through self-adsorption and photo-reduction, as a superb hydrogen evolution photocatalyst for hydrohalic acid splitting. Theoretical and experimental investigations show that Pt atoms are immobilized individually and coordinated with surface halide anions by replacing formamidinium groups. The developed Pt/FAPbBr(3-x)I(x) (FAPbBr(3-x)I(x) loaded with Pt single-atoms) sample shows an enhanced photocatalytic H-2 evolution activity of 682.6 mu mol h(-1) (100 mg) under simulated sunlight irradiation (AM1.5G, 100 mW cm(-2), irradiation area of pi cm(2)), with an exciting STH (solar-to-hydrogen efficiency) of 4.50%. This work provides a platform that facilitates the synthetic strategy for designing a halide ion coordinated single-atom catalyst, enhancing the photocatalytic performance of perovskite materials, and extending the boundary of the conventional supporting substrate and research fields for single-atom catalysts.

Automated summary

This study successfully immobilizes single Pt atoms onto FAPbBr(3-x)I(x) perovskite substrates, creating an efficient photocatalyst for the splitting of hydrohalic acid. Experimental and theoretical investigations demonstrate the individual immobilization of Pt atoms, coordinated with surface halide anions, resulting in enhanced photocatalytic H2 evolution activity and high solar-to-hydrogen efficiency.