Abstract

Semiconductor photocatalysis as an alternative technology has received extensive attention for addressing the worldwide energy and environment issues. However, it is still a great challenge and imperative to profoundly understand the migration mechanisms for achieving the complete utilization of photoexcited charge carriers. In this paper, a series of g-C3N4/ZnIn2S4 heterojunction composites were fabricated by thermal polycondensation and solvothermal methods and then thoroughly characterized by a range of techniques. Photocatalytic selective oxidation of aromatic alcohols to corresponding aldehydes with O2 under visible light irradiation was introduced as a model reaction system to evaluate the photocatalytic performance of the as-prepared samples. The results exhibit that when the main constituent of photocatalyst is ZnIn2S4, the transfer of the photogenerated charge carriers adopts a band-band mechanism in g-C3N4/ZnIn2S4 heterojunction composite. However, when the main constituent of photocatalyst is g-C3N4, the transfer of the photogenerated charge carriers adopts a Z-scheme mechanism. Therefore, the different compositions of the composite samples lead to the different electronic conductivities and then affect the direction of the built-in electric field in the relative p-n junction, finally causing the different transfer mechanisms of the photogenerated charge carriers for g-C3N4/ZnIn2S4 composite samples.

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