4.7 Article

Renewable biomass-derived carbon-supported g-C3N4 doped with Ag for enhanced photocatalytic reduction of CO2

Journal

JOURNAL OF COLLOID AND INTERFACE SCIENCE
Volume 606, Issue -, Pages 1311-1321

Publisher

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.jcis.2021.08.176

Keywords

g-C3N4; Ag nanoparticles; Biomass-derived carbon

Funding

  1. National Natural Science Foundation of China [21871124]
  2. Natural Science Foundation of Guangdong Province, China [2021A1515010071]
  3. start-up grant for talents of Shantou University [13009419024]
  4. Cross-Disciplinary Research Grant from Li Ka Shing Foundation [2020LKSFG01A]

Ask authors/readers for more resources

Constructing noble metal-doped g-C3N4/carbon composites is an effective approach to enhance the activity of CO2 photoreduction. This study introduces a novel Ag-doped gC(3)N(4)/biomass-derived carbon composite with unique features, such as highly dispersed Ag nanoparticles and a conductive quasi-spherical hollow structure of BN-C, which significantly improve the CO evolution rate without the need for sacrificial reagents or photosensitizers.
Constructing noble metal-doped g-C3N4/carbon composites is a feasible route to overcome the intrinsic drawbacks of pristine g-C3N4 for enhanced activity of CO2 photoreduction. Herein, a novel Ag-doped gC(3)N(4)/biomass-derived carbon composite with hollow bird's nest-like (Ag-g-C3N4/BN-C) is designed and prepared via a simple yet effective one-step pyrolysis method. In the Ag-g-C3N4/BN-C, the highlydispersed Ag nanoparticles (20-30 nm) with the surface plasmon resonance (SPR) effect act as a significant cocatalyst not only to efficiently trap the photogenerated electrons from g-C3N4 to boost the separation of photogenerated electron-hole pairs but also to produce additional active ``hot electrons, while the conductive quasi-spherical hollow structure of BN-C doubles the specific surface area with multiple reflections of light, providing abundant active sites and more utilization efficiency of light energy. As a result, the Ag-g-C3N4/BN-C exhibits a remarkably enhanced CO evolution rate of 33.3 lmol.g(-1.)h(-1Y) without addition of any sacrificial reagents and photosensitizers, superior to those of both the pristine g-C3N4 and many reported g-C3N4-based counterparts. The findings of this work demonstrate a good indication for integrating g-C3N4 with SPR-dependence noble metal and renewable biomass-derived carbon for enhanced CO2 photoreduction, which may be extended to modify other semiconductor materials for more photocatalytic applications with enhanced activity. (C) 2021 Elsevier Inc. All rights reserved.

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