| Literature DB >> 33141452 |
Baogang Wu1, Liping Zhang2, Baojiang Jiang1, Qi Li1, Chungui Tian1, Ying Xie1, Weizuo Li1, Honggang Fu1.
Abstract
Actiniae-like carbon nitride (ACN) bundles were synthesized by the pyrolysis of an asymmetric supramolecular precursor prepared from L-arginine (L-Arg) and melamine. ACN has adjustable band gaps (2.25 eV-2.75 eV) and hollow microtubes with ultrathin pore walls, which enrich reaction sites, improve visible-light absorption and enhance charge separation. In the presence of phenylcarbinol, ACN exhibited excellent water-splitting ability (95.3 μmol h-1 ) and in the meanwhile phenylcarbinol was selectively oxidized to benzaldehyde (conversion of 90.9 %, selectivity of 99.7 %) under solar irradiation. For the concurrent reactions, 2 D isotope labeling, separation, and detection were conducted to confirm that the proton source of released hydrogen is water. The mechanism of water splitting and phenylcarbinol oxidation was also investigated.Entities:
Keywords: carbon nitride; phenylcarbinol oxidation; photocatalysis; supramolecular assembly; water splitting
Year: 2021 PMID: 33141452 DOI: 10.1002/anie.202013753
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336