4.7 Article

Hydroxyl/amino and Fe(III) co-grafted graphite carbon nitride for photocatalytic removal of volatile organic compounds

Journal

ENVIRONMENTAL RESEARCH
Volume 197, Issue -, Pages -

Publisher

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.envres.2021.111044

Keywords

Graphitic carbon nitride; Surficial group-cluster bifunctionalization; Interfacial charge transfer effect; VOCs mineralization

Funding

  1. International Science and Technology Cooperation Program [2017YFE0127800]
  2. Shenzhen Science and Technology Innovation Project [JCYJ20180307164633296]

Ask authors/readers for more resources

A dual-functionalized carbon nitride photocatalyst with hydroxyl/amino and Fe(III) co-grafted has been fabricated to efficiently remove VOCs by enhancing adsorption capacity and regulating molecular oxygen activation. The synergistic effect of grafted functional groups and Fe(III) clusters accelerates carriers' separation in photocatalysis.
Hydroxyl/amino and Fe(III) co-grafted graphite carbon nitride (CN) is fabricated via alkaline hydrothermal treatment and followed by an impregnation adsorption process. In this unique fabrication, hydroxyl and amino groups enriched on the surface play a vital role in improving the adsorption capacity for volatile organic compounds (VOCs), while the grafted amorphous Fe(III) clusters could dominantly regulate the path of molecular oxygen activation via photo-Fenton reaction, and change the selectivity of intermediate reactive oxygen species (ROS) with the assistant of the rich surficial hydroxyl groups. Meanwhile, both the grafted functional groups and Fe(III) clusters can serve as photogenerated charge acceptors for collaboratively accelerating carriers' separation. Besides, the Fe(III)-mediated interfacial charge transfer effect (IFCT) also could extend visible light absorption and boost carriers' generation. Benefiting from the virtues of the complementary and synergy of the grafted hydroxyl/amino and Fe(III), the dual-functionalized CN is qualified as an efficient photocatalyst for removal of VOCs, which exhibits 22 and 18 times isopropanol (IPA) adsorption capacity and CO2 production than of pristine CN during photocatalytic IPA removal, respectively. Moreover, this work provides a new strategy of surficial group-cluster bifunctionalization for systematically improving sustainable solar-to-chemical energy conversion towards VOCs mineralization.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.7
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available