Co-catalyst design to control charge transfer and product composition for photocatalytic H2 production and biomass reforming

被引:3
作者
Nguyen, Van-Can [1 ]
Sanoe, Meyta [1 ]
Putri, Novy Pralisa [1 ]
Lee, Yuh-Lang [1 ,2 ]
Teng, Hsisheng [1 ,2 ]
机构
[1] Natl Cheng Kung Univ, Dept Chem Engn, Tainan 70101, Taiwan
[2] Natl Cheng Kung Univ, Hierarch Green Energy Mat Hi GEM Res Ctr, Tainan 70101, Taiwan
来源
SUSTAINABLE ENERGY & FUELS | 2024年 / 8卷 / 07期
关键词
GRAPHITIC CARBON NITRIDE; REDUCED GRAPHENE OXIDE; QUANTUM DOTS; SELECTIVE OXIDATION; HYDROGEN EVOLUTION; CATALYSTS; GLUCOSE; CONFINEMENT; REDUCTION; ALDEHYDES;
D O I
10.1039/d3se01544k
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The exploration of co-catalyst effects in photocatalytic H-2 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 (C-5) into its derivatives and gaseous H-2. Our study shows that Pt-SNGODs effectively catalyze both the reduction and oxidation steps: water reduction for H-2 evolution and oxidative reforming of xylose into C-5-C-1 species through successive alternation of hydrolysis and photocatalytic oxidation. Ag-SNGODs are less effective in the H-2 evolution reaction and the accumulated photogenerated electrons facilitate cleavage of xylose, through the retro-aldol reaction, into C-3- and C-2-species, which are then reformed into C-3-C-1 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 C-6 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.
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页数:13
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