摘要
Heterostructured photocatalysts Ag 3 VO 4 /g-C 3 N 4 were prepared by deposition-precipitation method in order to anchor Ag 3 VO 4 on the surface of N-vacancy g-C 3 N 4 (g-C 3 N 4 -VN). The photocatalytic activity of the samples was evaluated by degrading rhodamine B (RhB) in aqueous solution. Compared with the pure Ag 3 VO 4 and g-C 3 N 4 -VN, the heterojuncted photocatalyst 65 wt% Ag 3 VO 4 /g-C 3 N 4 -VN exhibits the best activity under visible light irradiation. The photodegradation rate constant of 65 wt% Ag 3 VO 4 /g-C 3 N 4 -VN is 0.0556 min −1 , which is 23.4, 5.8 and 6.4 times of that of pure Ag 3 VO 4 , pure g-C 3 N 4 -VN and P25, respectively. The excellent photocatalytic performance of the Ag 3 VO 4 /g-C 3 N 4 -VN catalysts can be ascribed to the matched band structures of Ag 3 VO 4 and g-C 3 N 4 , which strengthened the formation of the heterojuncted photocatalyst. The unique heterostructured photocatalyst is favorable for retarding the recombination of photogenerated electrons and holes, thus the photocatalytic activity is significantly increased. Further experiment also reveals that the •O 2 − and h + are the major active species in the degradation of RhB.
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