Co-catalyst design to control charge transfer and product composition for photocatalytic H2 production and biomass reforming†
Abstract
The exploration of co-catalyst effects in photocatalytic H2 production along with biomass reforming is still limited. This study employs S- and N-doped graphene oxide dots (SNGODs) along with Pt and Ag co-catalysts to investigate the photocatalytic reforming of xylose (C5) into its derivatives and gaseous H2. Our study shows that Pt-SNGODs effectively catalyze both the reduction and oxidation steps: water reduction for H2 evolution and oxidative reforming of xylose into C5–C1 species through successive alternation of hydrolysis and photocatalytic oxidation. Ag-SNGODs are less effective in the H2 evolution reaction and the accumulated photogenerated electrons facilitate cleavage of xylose, through the retro-aldol reaction, into C3- and C2-species, which are then reformed into C3–C1 species. In addition to xylose cleavage, Ag-SNGODs are effective in reducing xylose and formate into radicals, which would proceed with C–C coupling to produce a C6 compound. The present study demonstrates how the co-catalyst of photocatalysts can influence the charge transfer dynamics and the product composition in photocatalytic biomass reforming.
- This article is part of the themed collections: Recent Open Access Articles and Solar Fuels and Chemicals: Photocatalytic Water Splitting and CO2 Reduction