摘要
One of the feasible strategies to enhance the photocatalytic properties of TiO2 is to broaden the visible light response range and accelerate the separation rate of photo-induced electron–hole (e−–h+) pairs by designing and synthesizing heterostructures using narrow-band-gap semiconductors. In this study, a ternary heterostructure based on MOF-derived TiO2 was first fabricated via the self-sacrificing template method followed by a two-step chemical bath process. The as-obtained CdS/ZnIn2S4/TiO2 ternary heterostructures exhibited better visible-light photocatalytic properties for the degradation of Rhodamine B (RhB) and tetracycline (TC) than single-component and dual-component systems. Among the ternary heterostructures, it was found that the CdS/ZnIn2S4/TiO2-II showed the highest photoreactivity of 95.3% for RhB removal and 91.8% for TC removal within 40 min. In addition, CdS/ZnIn2S4/TiO2-II could maintain its photocatalytic properties during the stability test. The improvement in photocatalytic properties is attributed to the reasonable construction of a ternary heterostructure, which significantly accelerates the separation and transport of photogenerated e−–h+ pairs, improves the specific surface area, and broadens the visible light response range. This study demonstrates a promising strategy for developing ternary heterostructures as effective photocatalysts for the degradation of organic pollutants.
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