Surface selenation engineering on metal cocatalysts for highly efficient photoreduction of carbon dioxide to methanol

Solar-driven reduction of CO2 and H2O to methanol is highly desirable owing to multiple advantages of green and renewable liquid fuels, whose efficiency and selectivity are restricted by sluggish charge kinetics and unfavorable surface reaction dynamics in conversional semiconductor photocatalysts. This study proposes a surface selenation strategy on metal cocatalysts to improve the photocatalytic performance in CO2-to-CH3OH conversion. Electron microscopy observation shows the formation of a stacked structure with crystalline Rh core sandwiched between semiconductor substrate and amorphous selenated Rh (RhSe) shell after the treatment. The combination of experimental characterizations with theoretical simulations reveals that Rh core smoothens the migration of photoelectrons from light-harvesting semiconductor to RhSe shell, while the selenation of Rh shell not only reduces the rate-limiting barriers required for CH3OH production, but also inhibits the occurrence of side H2 evolution. Enabled by such a design, significantly enhanced photocatalytic activities (41.2 mu mol gcat -1 h-1) and selectivties (91.2%) in CH3OH generation are achieved by the Rh@RhSe semi-core-shell cocatalysts, 12.7 and 6.4 times as high as that of pristine Rh, respectively. Moreover, the generalized strategy can be extended to other metal cocatalysts for improved CO2-to-CH3OH transformation, which opens a new avenue for powering the future with liquid sunshine.

Automated summary

Solar-driven reduction of CO2 and H2O to methanol is improved by surface selenation strategy on metal cocatalysts. The formation of a stacked structure with a crystalline Rh core sandwiched between semiconductor substrate and amorphous selenated Rh (RhSe) shell is observed. The selenation of Rh shell reduces rate-limiting barriers for CH3OH production and inhibits side H2 evolution, leading to significantly enhanced photocatalytic activities and selectivities.