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Ultrathin Porous Carbon Nitride Bundles with an Adjustable Energy Band Structure toward Simultaneous Solar Photocatalytic Water Splitting and Selective Phenylcarbinol Oxidation
Author(s) -
Wu Baogang,
Zhang Liping,
Jiang Baojiang,
Li Qi,
Tian Chungui,
Xie Ying,
Li Weizuo,
Fu Honggang
Publication year - 2021
Publication title -
angewandte chemie international edition
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.831
H-Index - 550
eISSN - 1521-3773
pISSN - 1433-7851
DOI - 10.1002/anie.202013753
Subject(s) - photocatalysis , graphitic carbon nitride , water splitting , selectivity , melamine , carbon nitride , materials science , photochemistry , benzaldehyde , photocatalytic water splitting , pyrolysis , absorption (acoustics) , nitride , carbon fibers , irradiation , chemical engineering , chemistry , catalysis , nanotechnology , organic chemistry , layer (electronics) , composite number , engineering , composite material , physics , nuclear physics
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.