Journal
CHEMCATCHEM
Volume 9, Issue 9, Pages 1708-1715Publisher
WILEY-V C H VERLAG GMBH
DOI: 10.1002/cctc.201700492
Keywords
g-C3N4 nanosheets; H-2 evolution; in situ doping; iron doping; photocatalysis
Categories
Funding
- National Natural Science Foundations of China [21476108, 21276125]
- University Natural Science Research of Jiangsu Province [16KJB530003]
- Development of Jiangsu Higher Education Institutions (PAPD)
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A simple one-step pyrolysis process (compared with the routine method of liquid exfoliation and impregnation) was designed to synthesize Fe-doped graphitic carbon nitride (g-C3N4) nanosheets with NH4Cl as dynamic gas template and FeCl3 as the Fe source. Results of XPS and DRS indicated that the Fe species might exist at the state of Fe3+ and form Fe-N bonds with N atoms, thereby expanding visible light absorption regions and reducing the band gap of g-C3N4 nanosheets. Doping certain amounts of Fe could promote the exfoliation and further increase the specific surface area, while excessive Fe might break the sheet structure. The specific surface area of the optimized Fe-doped g-C3N4 nanosheets reached 236.52 m(2)g(-1), which was 2.5times higher than that of g-C3N4 nanosheets. Among various photocatalysts prepared, the sample (0.5wt% FeCl3) exhibited maximum photocatalytic performance in degradation of Methylene Blue and water splitting under visible light irradiation. The degradation rate of MB was about 1.4 and 1.7 times higher than that of pure g-C3N4 nanosheets and bulk g-C3N4, respectively. The H-2 production rate was 536 mu molh(-1)g(-1), which was 1.8 and 6 times higher than that of pure g-C3N4 nanosheets and bulk g-C3N4, separately.
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