Visible-Light Photocatalytic Degradation Efficiency of Tetracycline and Rhodamine B Using a Double Z-Scheme Heterojunction Catalyst of UiO-66-NH2/BiOCl/Bi2S3

BiOCl is a promising photocatalyst, but due to its weak visible light absorption capacity and low photogenerated electron-hole pair separation rate, its practical application is limited to a certain extent. In this study, a novel double Z-scheme heterojunction UiO-66-NH2/BiOCl/Bi2S3 catalyst was constructed to broaden the visible light response range and promote high photogenerated hole-electron separation of BiOCl. Its photocatalytic performance is evaluated by dissociating tetracycline (TC) and rhodamine B (RhB) in visible light. The optimal proportion of UiO-66-NH2/BiOCl/Bi2S3 hybrids exhibits the best degradation efficiency of visible light illumination (similar to 93% in 120 min for TC and similar to 98% in 60 min for RhB). The synergistic effect of a large visible light response range and the Z-scheme charge transfer mechanism ensure the excellent visible photocatalytic activity of UiO-66-NH2/BiOCl/Bi2S3. It is proven that h(+) and center dot O-2(-) are the main active substances in the photocatalysis process by active substance capture experiments and electron spin resonance tests. The intermediates and degradation processes are analyzed by high-performance liquid chromatography-mass spectrometry. This study proves that the new UiO-66-NH2/BiOCl/Bi2S3 photocatalyst has great application potential in the field of water pollution degradation and will provide a new idea for the optimization of BiOCl.