We have located links that may give you full text access.
Preparation of Ag@AgCl-doped TiO2/sepiolite and its photocatalytic mechanism under visible light.
Journal of Environmental Sciences (China) 2017 October
A cube-like Ag@AgCl-doped TiO2/sepiolite (denoted Ag@AgCl-TiO2/sepiolite) was successfully synthesized via a novel method. X-ray diffraction, scanning electron microscopy, energy dispersion X-ray fluorescence, X-ray photoelectron spectroscopy, Fourier transform infrared spectroscopy, and diffuse reflectance ultraviolet-visible spectroscopy were performed to determine the structure and physicochemical properties of Ag@AgCl-TiO2/sepiolite. SEM micrographs revealed that Ag@AgCl nanoparticles and TiO2 film are well deposited on the surface of tube-like sepiolite. As a result, Ag@AgCl-TiO2/sepiolite exhibits a red shift relative to TiO2/sepiolite. Photocatalytic experiments demonstrated that the dosage of catalysts plays an important role during photocatalysis. The photoelectrochemical activities of Ag@AgCl-TiO2/sepiolite and TiO2/sepiolite were also investigated. Photocurrent responses confirmed that the ability of Ag@AgCl-TiO2/sepiolite to separate photo-generated electron-hole pairs is stronger than that of TiO2/sepiolite. Methylene Blue degradation is also improved under alkaline conditions and visible light irradiation because more OH is produced by visible light excitation. This excellent catalytic ability is mainly attributed to the formed Ag nanoparticles and the Schottky barrier at the Ag/TiO2 interface. Active species analysis indicated that O2(-) and h(+) are implicated as active species in photocatalysis. Therefore, catalysts are excited to produce abundant electron-hole pairs after they absorb photons in photocatalysis.
Full text links
Related Resources
Get seemless 1-tap access through your institution/university
For the best experience, use the Read mobile app
All material on this website is protected by copyright, Copyright © 1994-2024 by WebMD LLC.
This website also contains material copyrighted by 3rd parties.
By using this service, you agree to our terms of use and privacy policy.
Your Privacy Choices
You can now claim free CME credits for this literature searchClaim now
Get seemless 1-tap access through your institution/university
For the best experience, use the Read mobile app