Sulfur and potassium co-doped graphitic carbon nitride for highly enhanced photocatalytic hydrogen evolution

[Display omitted] •The S + K-codoped g-C3N4 presents excellent H2 production (8.78 mmol g−1 h−1) under visible light.•The S + K-codoped g-C3N4 inhibits the recombination of photogenerated carriers.•The S + K-codoped g-C3N4 photocatalyst shows apparent quantum efficiency of 70 % at 420 nm for H2 prod...

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Veröffentlicht in:Applied catalysis. B, Environmental Environmental, 2020-09, Vol.273, p.119050, Article 119050
Hauptverfasser: Chen, Lu, Zhu, Dongyan, Li, Jintao, Wang, Xuxu, Zhu, Jiefang, Francis, Paul S., Zheng, Yuanhui
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Sprache:eng
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Zusammenfassung:[Display omitted] •The S + K-codoped g-C3N4 presents excellent H2 production (8.78 mmol g−1 h−1) under visible light.•The S + K-codoped g-C3N4 inhibits the recombination of photogenerated carriers.•The S + K-codoped g-C3N4 photocatalyst shows apparent quantum efficiency of 70 % at 420 nm for H2 production. Modifying the structure of a photocatalyst to tailor its electronic and physicochemical properties is an effective approach for efficient photocatalysis. Herein, we demonstrate that co-doping non-metal (S) and metal (K) atoms into graphitic carbon nitride (g-C3N4) provides excellent visible-light photocatalytic hydrogen production activity of 8.78 mmol g−1 h−1, which is 98 times higher than that of pristine g-C3N4 (0.09 mmol g−1 h−1). The apparent quantum efficiency of the S+K-co-doped g-C3N4 reaches 70 % at 420 nm. This outstanding photocatalytic performance attributed to an increased specific surface area from 6.78 to 74.23 cm3 g−1, which reduced the recombination of photogenerated charge carriers and enhanced conductivity. Various characterizations are undertaken to elucidate the S+K-co-doped g-C3N4 photocatalytic mechanism. Our work not only demonstrates a facile, eco-friendly and scalable strategy for the synthesis of S+K-co-doped g-C3N4 photocatalysts, but also opens a new avenue for the design of co-doped photocatalysts.
ISSN:0926-3373
1873-3883
1873-3883
DOI:10.1016/j.apcatb.2020.119050