Abstract

Carbon nitride has drawn numerous eyes in the past decade, whereas the photocatalytic performance is significantly limited by its wide band-gap (∼2.7 eV for C 3 N 4 ) simultaneously. Recently, C 3 N 5 with narrower band-gap has been reported, however, a systematically investigation on its photoactivity for H 2 production has not been reported. The present work demonstrates the synthesis of C 3 N 5 by thermal treatment of 3-amino-1,2,4-triazole, and the photocatalytic performance for H 2 production of C 3 N 5 is investigated comprehensively. Photocatalytic H 2 production rate of C 3 N 5 is ∼2.2 times higher than that of C 3 N 4 with 1.0 wt% Pt as co-catalyst, and series of experiments are carried out to explore the behind elements accounting for the high photoactivity. Combining the results of DRS, PL and photocurrent, it is found that C 3 N 5 possesses wider visible light absorption region, lower band-gap and quicker photogenerated e - /h + separation efficiency. Moreover, characterizations including in-situ DRIFTS are adopted to monitor the adsorption property of H 2 O on C 3 N 5 , which plays a significant role in surface water reduction reaction, and higher amount of adsorbed H 2 O molecules on C 3 N 5 is confirmed. The present work exhibits new insights into the high photocatalytic performance of N-rich carbon nitride catalysts. As a new type of carbon nitride, C 3 N 5 exhibits much higher photocatalytic H 2 production activity than conventional C 3 N 4 , which represents a new direction for designing materials for photocatalytic applications.

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