Bi2S3@NH2-UiO-66-S composites modulated by covalent interfacial reactions boost photodegradation and the oxidative coupling of primary amines

Heterojunctions have attracted much attention due to the efficient separation and conduction of charge carriers in the photocatalytic reactions. However, the interfacial energy barrier between two components still limits the controllable assembly, separation, and conduction of photoexcited charge carriers, and further lower the photocatalytic activity. How to control the assembly of the heterojunction and accelerate the separation and conduction of photogenerated electron-holes by building a more intimate interfacial interaction is an important area of research. Herein, we report a series of Bi2S3@NH2-UiO-66-S heterostructures prepared by the covalent interfacial reaction. Novel composites exhibit excellent efficiencies for the photodegradation of methylene blue and the oxidative coupling of benzylamine and its derivatives. The turnover frequency is estimated to be about 8083 mu mol g(cat)(-1) h(-1). The super photocatalytic performance was attributed to the interfacial compactness by the covalent interfacial reaction. The expansion for the excellent performance was confirmed by UV-vis DRS, photocurrent measurement and EIS.

Automated summary

The study presents a series of Bi2S3@NH2-UiO-66-S heterostructures prepared by covalent interfacial reaction, which exhibit excellent performance in photocatalytic reactions with a turnover frequency of approximately 8083 mu mol g(cat)(-1) h(-1). The compactness of the interfacial interaction formed by the covalent reaction is crucial for the enhanced photocatalytic activity, as confirmed by UV-vis DRS, photocurrent measurement, and EIS.