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Details

Autor(en) / Beteiligte
Titel
RuS2@CN-x with exposed (200) facet as a high-performance photocatalyst for selective C–C bond cleavage of biomass coupling with H–O bond cleavage of water to co-produce chemicals and H2
Ist Teil von
  • Green chemistry : an international journal and green chemistry resource : GC, 2023-03, Vol.25 (8), p.3236-3246
Ort / Verlag
Cambridge: Royal Society of Chemistry
Erscheinungsjahr
2023
Link zum Volltext
Quelle
Alma/SFX Local Collection
Beschreibungen/Notizen
  • The selective photocatalytic C–C bond cleavage of biomass coupling with H–O bond cleavage of water for co-producing chemicals and H2 is of great significance, but limited successes have been reported. In this study, a RuS2@CN-x photocatalyst with only exposed crystal face (200) was prepared by anchoring RuS2 nanoparticles on carbon nitride (CN) nanosheets and successfully used in photocatalytic C–C bond cleavage of biomass-based sugars coupling with water splitting to co-generate lactic acid and hydrogen. Interestingly, the RuS2 (200) crystal face combined with the interfacial synergism between CN and RuS2 in RuS2@CN-x effectively improved visible light absorption and enhanced the transfer/separation efficiency of photo-generated carriers. The RuS2@CN-2 exhibited superior photocatalytic activity towards synchronous water splitting and biomass conversion to co-produce hydrogen (8698.3 μmol g−1 h−1) and lactic acid (91.5%). Furthermore, the experimental and DFT calculation results indicated that the exposed crystal face (200) of RuS2 significantly enhanced the photocatalytic activity of RuS2@CN-2. Moreover, this reaction system not only has excellent recyclability but also displays excellent universality for small molecule biomass-derived monosaccharides and macromolecular xylan. This work provides a novel route to efficiently co-produce hydrogen and fine chemicals from photocatalytic C–C bond cleavage of biomass coupling with H–O bond cleavage of water.
Sprache
Englisch
Identifikatoren
ISSN: 1463-9262
eISSN: 1463-9270
DOI: 10.1039/d3gc00367a
Titel-ID: cdi_proquest_journals_2804878612

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