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The SnO2 quantum dots (SnO2QDs)/ZnS nanosheets (ZnSNs) heterojunction was fabricated via an in-situ synthetic method at room temperature. Rhodamine B, potassium dichromate, and tetracycline were used to discuss the photocatalytic activities of the as-prepared samples under the visible light illumination. The photocatalytic mechanism of the as-prepared samples was also proposed. The experimental results indicate that the degradation efficiency of the as-prepared SnO2QDs/ZnSNs heterojunction first increases and then decreases with increasing the usage of ZnSNs. When the mass ratio of SnO2QDs to ZnSNs is 1: 2 in 180 min, the asprepared samples have the highest degradation efficiency of 89.1% for rhodamine B, 97.7% for potassium dichromate, and 83.8% for tetracycline, which are much higher than 51.7%, 26.8%, and 0.9% of pure SnO2QDs as well as 37.9%, 87.1%, and 19.1% of pure ZnSNs, respectively. After it is repeatedly degraded for 3 times, it possesses the degradation efficiency of 62.5% for rhodamine B, which increases by 200.5% in comparison with 20.8% of the pure SnO2QDs. Moreover, the enhanced photocatalytic performances of the as-prepared hybrids are attributed to the formation of heterojunction between the SnO2QDs and ZnSNs. In addition, hydroxyl radicals and superoxide anion radicals play major roles during the photocatalytic degradation process, while holes play a minor role.

The Zn0.5Cd0.5S/SnO2 composite photocatalyst was synthesized via a hydrothermal method. The crystal phase, micromorphology, optical and photoelectric property as well as surface elements valence were characterized using X-ray diffraction, field emission scanning electron microscope, transmission electrical microscope, UV–Vis diffuse reflectance spectrometer, electrochemical impedance spectroscopy and X-ray photoelectron spectroscopy, respectively. Tetracycline was used to discuss the photocatalytic properties of the samples under visible light irradiation. Research results indicate that the as-synthesized Zn0.5Cd0.5S/SnO2 composite photocatalysts show better photocatalytic performance than that of pure samples. Moreover, the photocatalytic activity of the as-synthesized composites presents first increased and then decreased with increasing the amount of SnO2 in the composites. When the quality ratio of SnO2 to Zn0.5Cd0.5S is 7%, in 60 min, the as-synthesized composites reveal the best photocatalytic degradation efficiency of 92.9%, which is high than 85% of Zn0.5Cd0.5S and 0% of SnO2. This is ascribed of the improvement of the separation efficiency of photo-generated electron–hole pairs and the transmission rate of electrons. Furthermore, the decomposition mechanism of as-synthesized composites for tetracycline was also provided. The holes and superoxide radicals play crucial species in the photocatalytic degradation process.

The Zn2+ doped In2.77S4 (Zn–In2.77S4) photocatalyst has been synthesized via a one-step hydrothermal method. The tetracycline was adopted to measure the photocatalytic performance of the as-fabricated Zn–In2.77S4 composites. The probable photocatalytic degradation mechanism of the as-prepared composites was also discussed. Experimental results reveal that doping Zn2+ into In2.77S4 can broaden the light absorption range and improve the recycle ability as well as the separation efficiency of photo-generated electron–hole pairs of pure In2.77S4. Moreover, as the doping amount of Zn2+ increased the photocatalytic efficiency of the as-obtained Zn–In2.77S4 composites appears the tendency of firstly increasing and then decreasing. When the molar ratio of Zn2+ to In3+ is 0.04:1 (4%), in 15 min, the photocatalytic efficiency of the as-developed Zn–In2.77S4 photocatalyst reaches to the maximum of 90.0%. It is higher than 31.8% of pure In2.77S4. Furthermore, superoxide radicals and holes play major roles in the process of photodegradation tetracycline. This research can supply a promising guide to solve antibiotics pollution in water under sunlight.