Constructing Cu1-Ti dual sites for highly efficient photocatalytic hydrogen evolution

Constructing dual sites is promising to break scaling relations between the adsorption energetics of reaction intermediates and ultimately improves the activity and selectivity due to the synergistic effect. However, it is a grand challenge to precisely form a dual-site configuration with one metal site adjacent to another active site. Loading single atoms onto oxides with pre-introduction of surface oxygen vacancies may be an alternative strategy to overcome such challenge. Motivated by our theoretical calculations that the dual sites formed by single Cu atoms and unsaturated Ti sites on TiO2 enables a higher activity towards hydrogen evolution from water splitting than corresponding single site, we successfully synthesized a Cu-1-Ti dual-site catalyst by depositing Cu single atoms on TiO2 nanoparticles with abundant surface oxygen vacancies. The designed target catalyst significantly outperforms the benchmark Pt nanoparticle decorated TiO2 with a high and stable activity towards photocatalytic hydrogen production.

Automated summary

Constructing dual-site catalysts has the potential to improve photocatalytic hydrogen production. Loading single atoms onto oxides with pre-introduction of surface oxygen vacancies offers an alternative strategy to overcome the challenge of forming a dual-site configuration. The Cu-1-Ti dual-site catalyst, formed by depositing Cu single atoms on TiO2 nanoparticles with abundant surface oxygen vacancies, demonstrates superior activity in photocatalytic hydrogen production.