Journal
APPLIED SURFACE SCIENCE
Volume 540, Issue -, Pages -Publisher
ELSEVIER
DOI: 10.1016/j.apsusc.2020.148411
Keywords
Porous carbon nitride; Nitrogen-doping carbon; Photocatalytic; CO2 reduction
Categories
Funding
- National Natural Science Foundation of China [51872081, 21606075]
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Compared to bulk g-C3N4 synthesized by direct thermopolymerization of urea, N-doping carbon/CN exhibits pronounced nanopores, larger surface area, and increased basic sites, leading to a high CO2 adsorption capacity of about 5.5 times that of bulk g-C3N4. XPS results indicate that N-doping carbon units have been grafted into the g-C3N4 matrix through chemical interactions, enhancing electron transport on N-doping carbon/CN, resulting in significant photocatalytic activity on CO2 reduction with water vapor under visible light. The average CO production rate reaches 15.4 μmol g-1 h-1, about 7.0 times that of bulk g-C3N4.
Bulk graphitic carbon nitride (g-C3N4) shows inferior photocatalytic performance on CO2 conversion due to low CO2 capture and severe charge carriers recombination. In this work, a porous nitrogen-doping carbon grafted carbon nitride (N-doping carbon/CN) has been fabricated via the temperature-programmed thermal polymerization of urea with carboxyl functionalized polystyrene (HOOC-PS) nanospheres as template and carbon source. A series of characterizations including XRD, XPS, FE-SEM, TEM, BET-BJH and CO2-TPD have been investigated. It is found that, in comparison of bulk g-C3N4 synthesized by direct thermopolymerization of urea, N-doping carbon/CN presents pronounced nanopores, larger surface area and increased basic sites, which result in a high CO2 adsorption of about 5.5 times that on bulk g-C3N4. In addition, XPS results uncover N-doping carbon units have been grafted into g-C3N4 matrix through chemical interactions, which accelerate electron transport on N doping carbon/CN. As a result, porous N-doping carbon/CN exhibits prominent photocatalytic activity on CO2 reduction with water vapor under visible light. The average CO production rate reaches 15.4 mu mol center dot g(1)center dot h(-1), about 7.0 times that on bulk g-C3N4 (2. 2 mu mol center dot g(1)center dot h(-1)).
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