Fabrication of Na, Cl co-doped graphitic carbon nitride with enhanced photocatalytic activity for degradation of dyes and antibiotics
- 1. Shanghai Ocean University, Department of Chemistry, College of Food Science and Technology (China)
Description
Co-doping is a promising approach to change the electronic structure and increase the photocatalytic ability of graphitic carbon nitride (g-C3N4). Here, we reported a facile and green fabrication of Na, Cl co-doped g-C3N4 photocatalysts. In the fabrication, sodium and chlorine were incorporated into g-C3N4 synchronously. The bandgap of Na, Cl co-doped g-C3N4 decreased compared with pure g-C3N4 and the position of the valence band moved in the direction of enhanced oxidizing power. The co-doped photocatalysts exhibited the improved visible-light absorption and the reduced recombination rate of photogenerated electrons and holes. As a result, photocatalytic activity of Na, Cl co-doped g-C3N4 was remarkably improved for the photodegradation of rhodamine B and tetracycline hydrochloride under visible light irradiation. The photocatalysis mechanism of Na, Cl co-doped g-C3N4 was also discussed according to the results of active species trapping experiments.
Additional details
Identifiers
Publishing Information
- Journal Title
- Journal of Materials Science. Materials in Electronics
- Journal Volume
- 30
- Journal Issue
- 5
- Journal Page Range
- p. 4446-4454
- ISSN
- 0957-4522
- CODEN
- JSMEEV
INIS
- Country of Publication
- United Kingdom
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 52016456
- Subject category
- S36: MATERIALS SCIENCE;
- Descriptors DEI
- CARBON MONOXIDE; CARBON NITRIDES; CATALYSTS; DOPED MATERIALS; ELECTRONIC STRUCTURE; FABRICATION; GRAPHITE; PHOTOCATALYSIS; SYNTHESIS
- Descriptors DEC
- CARBON; CARBON COMPOUNDS; CARBON OXIDES; CATALYSIS; CHALCOGENIDES; ELEMENTS; MATERIALS; MINERALS; NITRIDES; NITROGEN COMPOUNDS; NONMETALS; OXIDES; OXYGEN COMPOUNDS; PNICTIDES
Optional Information
- Copyright
- Copyright (c) 2019 Springer Science+Business Media, LLC, part of Springer Nature