Graphitic CN/ultrathin MoS (MoS/g-CN) hybrids were synthesized via a facile bathing and ultrasound method. In this process, a well-bonded interface structure was formed between ultrathin MoS nanosheets and g-CN through adjusting the amount of MoS in the MoS/g-CN hybrids. The MoS/g-CN hybrids were characterized by X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FT-IR), Raman spectroscopy (Raman), transmission electron microscopy (TEM) and UV-vis spectroscopy (UV-vis). The MoS/g-CN photocatalyst showed excellent photocatalytic activity in the photodegradation of organic pollutants. In this work, methyl orange (MO) was used as the simulative pollutant; the highest photodegradation rate (92.4%) was obtained when the amount of MoS was 5 wt% in the MoS/g-CN hybrids (0.05-MC), with a kinetic constant of 0.0189 min after being irradiated under visible light for 2 h. Besides, 0.05-MC also showed excellent recyclability and chemical stability, and a photodegradation rate of 79.93% was reached after being reused 10 times. For practical pollutants, the photocatalytic degradation rates of ciprofloxacin (CIP) and tetracycline hydrochloride (TC) have been increased dramatically under the visible light irradiation. The excellent photocatalytic properties of MoS/g-CN hybrids can be ascribed to the enhanced separation rate and accelerated mobility of photogenerated charges through ultrathin MoS nanosheets' modification.
Immobilized TiO2 nanotube arrays (NTAs) co-modified with Pt and CdS nanoparticles were fabricated by using the combination of photoreduction and chemical bath deposition methods. XRD, SEM, TEM, XPS, UV-Vis and EDX methods were employed to characterize the microstructure and composition of samples, and the results showed that CdS and Pt NPs were uniformly deposited on the surface of TiO2 nanotubes. The CdS/Pt/TiO2 NTAs exhibited a much higher photocatalytic activity compared to pure TiO2 NTAs and binary CdS (or Pt)/TiO2 NTAs under visible light irradiation. A kinetic study showed that the rate constants of Pt/TiO2, CdS/TiO2 and CdS/Pt/TiO2 NTAs are 0.00736, 0.01717 and 0.02077 min(-1), respectively, revealing a remarkable kinetic enhancement in the ternary heteronanostructures due to the synergistic effect of the three components. Besides, the CdS/Pt/TiO2 NTAs exhibit high stability after being used 22 times. Thus we proposed that such ternary heteronanostructures show great promise as immobilized catalysts for high efficient visible-light-driven photocatalysis.
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