期刊
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
卷 57, 期 30, 页码 9372-9376出版社
WILEY-V C H VERLAG GMBH
DOI: 10.1002/anie.201804702
关键词
copolymers; exciton splitting; hydrogen production; ionothermal synthesis; polymeric carbon nitride
资金
- Alexander vonHumboldt Foundation
- Max Planck Society
- National Key RAMP
- D Program of China [2018YFA0209301]
- National Natural Science Foundation of China [21425309, 21761132002]
- 111 Project
Polymeric carbon nitride (PCN), in either triazine or heptazine form, has been regarded as a promising metal-free, environmentally benign, and sustainable photocatalyst for solar hydrogen production. However, PCN in most cases only exhibits moderate activity owing to its inherent properties, such as rapid charge carrier recombination. Herein we present a triazine-heptazine copolymer synthesized by simple post-calcination of PCN in eutectic salts, that is, NaCl/KCl, to modulate the polymerization process and optimize the structure. The construction of an internal triazine-heptazine donor-acceptor (D-A) heterostructure was affirmed to significantly accelerate interface charge transfer (CT) and thus boost the photocatalytic activity (AQY=60% at 420nm). This study highlights the construction of intermolecular D-A copolymers in NaCl/KCl molten salts with higher melting points but in the absence of lithium to modulate the chemical structure and properties of PCN.
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