摘要
The efficient, stable, and selective photocatalytic conversion of nitric oxide (NO) into harmless products such as nitrate (NO3−) is greatly desired but remains an enormous challenge. In this work, a series of BiOI/SnO2heterojunctions (denoted asX%B-S, whereX% is the mass portion of BiOI compared with the mass of SnO2) were synthesized for the efficient transformation of NO into harmless NO3−. The best performance was achieved by the 30%B-S catalyst, whose NO removal efficiency was 96.3% and 47.2% higher than that of 15%B-S and 75%B-S, respectively. Moreover, 30%B-S also exhibited good stability and recyclability. This enhanced performance was mainly caused by the heterojunction structure, which facilitated charge transport and electron-hole separation. Under visible light irradiation, the electrons gathered in SnO2transformed O2to ·O2−and ·OH, while the holes generated in BiOI oxidized H2O to produce ·OH. The abundantly generated ·OH, ·O2−, and1O2species effectively converted NO to NO−and NO2−, thus promoting the oxidation of NO to NO3−. Overall, the heterojunction formation between p-type BiOI and n-type SnO2significantly reduced the recombination of photo-induced electron-hole pairs and promoted the photocatalytic activity. This work reveals the critical role of heterojunctions during photocatalytic degradation and provides some insight into NO removal.Keywords:NO removal;photocatalysis;BiOI/SnO2;heterojunction;enhanced mechanism
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