scholarly journals Sol-gel template synthesis of mesoporous carbon-doped TiO2 with photocatalytic activity under visible light

2018 ◽  
Vol 5 (9) ◽  
pp. 17422-17430 ◽  
Author(s):  
Evgeni Ovodok ◽  
Hanna Maltanava ◽  
Sergey Poznyak ◽  
Maria Ivanovskaya ◽  
Alexander Kudlash ◽  
...  
2014 ◽  
Vol 69 (5) ◽  
Author(s):  
Ooi Yee Khai ◽  
Leny Yuliati ◽  
Siew Ling Lee

New visible light driven photocatalysts of 1 mol% Cr doped TiO2 supported on TUD-1 have been successfully synthesized. The Cr-TiO2/xTUD-1 (x = 10, 20, 30, 40 and 50) photocatalysts were prepared via surfactant-free sol-gel method followed by wet impregnation procedures. XRD analysis revealed that both TiO2 and Cr were incorporated in the highly porous siliceous matrix. FTIR analysis showed the existence of Si-O-Ti in all the materials. As observed, tetrahedral-coordinated Ti species were dominant in Cr-TiO2/10TUD-1, Cr-TiO2/20TUD-1 and Cr-TiO2/30TUD-1. Meanwhile, octahedral- coordinated Ti species were the dominant species in Cr-TiO2/40TUD-1 and Cr-TiO2/50TUD-1. It has been demonstrated that the amount of TUD-1 as photocatalyst support affected the wavelength response and the bandgap energy of the resulting materials. All the materials have bandgap energy of ~2.9 eV. The photocatalytic performance of the synthesized materials was tested out in dye photodegradation under visible light irradiation at 298 K for 5 hours. Results showed that all Cr-TiO2/TUD-1 materials had higher photocatalytic activity than that of Cr-TiO2. This could be explained by the high surface area and porosity provided by TUD-1 in enhancing the adsorption and diffusivities of the dye molecules, hence leading to the promising photocatalytic activity. Among the materials prepared, Cr-TiO2/30TUD-1 appeared as the most superior photocatalyst which gave the highest dye photodegradation.


2009 ◽  
Vol 79-82 ◽  
pp. 2127-2130 ◽  
Author(s):  
Song Tao Gu ◽  
Xin Wang ◽  
Qiang Liu ◽  
Hao Quan Liu ◽  
Gui Jun Jiang ◽  
...  

A visible-light-active nitrogen and gadolinium codoped TiO2 catalyst was synthesized by the sol-gel route. For comparison, Gd-doped sample, N-doped sample, and pure titania were prepared through the same method, without adding the corresponding dopants. The as-prepared photocatalysts were characterized by X-ray diffraction (XRD) and Uv-vis spectra. The results showed that the codoped photocatalyst exhibited a smaller size than the undoped titania. The transformation from anatase to rutile was suppressed by doping with N and Gd atoms. Furthermore, the absorbance spectra of N, Gd-codoped TiO2 exhibited a significant red shift to the visible region. The photocatalytic activity of N, Gd-codoped TiO2 was evaluated by photodegradation of methyl orange under visible light irradiation. This codoped sample exhibited enhanced photocatalytic activity compared to N-doped TiO2, Gd-doped TiO2, and pure TiO2. The improvement of the photocatalytic activity was ascribed to the synergistic effects of the N and Gd co-doping.


2021 ◽  
Vol 17 (1) ◽  
pp. 103-112
Author(s):  
Diana Vanda Wellia ◽  
Dina Nofebriani ◽  
Nurul Pratiwi ◽  
Safni Safni

Porous N-doped TiO2 photocatalyst was successfully synthesized by an environmentally friendly peroxo sol-gel method using polyethylene glycol (PEG) as a templating agent. Here, the effect of PEG addition to the aqueous peroxotitanium solutions on the structure, pore properties and photocatalytic activity of the obtained photocatalysts was systematically studied. The prepared photocatalysts were characterized by X-ray diffraction (XRD), UV-Vis diffuse reflectance spectroscopy (DRS), and Brunauer-Emmett-Teller (BET). It was found that the doping of nitrogen narrows the band gap of TiO2 leading to enhance its visible-light response. The BET analysis shows that the prepared photocatalysts have a typical mesoporous structure with pore sizes of 3–6 nm. The photocatalytic activity of the prepared photocatalysts was evaluated by photocatalytic reduction of Cd(II) in an aqueous solution under visible light irradiation. The results show that porous N-doped TiO2 with the optimal PEG addition had the highest Cd(II) reduction of 85.1% after 2.5 h irradiation in neutral aqueous solution. This significant improvement in photocatalytic activity of the prepared photocatalysts was mainly attributed to the synergistic combination of N doping and porous structure, which could actively increase the catalytic active site of this photocatalysts. Copyright © 2021 by Authors, Published by BCREC Group. This is an open access article under the CC BY-SA License (https://creativecommons.org/licenses/by-sa/4.0). 


Materials ◽  
2019 ◽  
Vol 12 (23) ◽  
pp. 3874 ◽  
Author(s):  
Abderrahim El Mragui ◽  
Yuliya Logvina ◽  
Luís Pinto da Silva ◽  
Omar Zegaoui ◽  
Joaquim C.G. Esteves da Silva

Pure TiO2 and Fe- and Co-doped TiO2 nanoparticles (NPs) as photocatalysts were synthesized using wet chemical methods (sol-gel + precipitation). Their crystalline structure and optical properties were analyzed using X-ray diffraction (XRD), Raman spectroscopy and Fourier-transform infrared (FTIR) spectroscopy, ultraviolet-visible light (UV-Vis) diffuse reflectance spectroscopy (DRS), and photoluminescence (PL) spectroscopy. The photocatalytic activity of the synthesized nanoparticles was evaluated through degradation of carbamazepine (CBZ) under UV-A and visible-light irradiations. The XRD and Raman analyses revealed that all synthesized nanomaterials showed only the anatase phase. The DRS results showed that the absorption edge was blue-shifted for Fe-doped TiO2 NPs. The decrease in charge recombination was evidenced from the PL investigation for both Co-doped and Fe-doped TiO2 nanomaterials. An enhancement in photocatalytic degradation of carbamazepine in aqueous suspension under both UV-A light and visible-light irradiations was observed for Fe-doped Titania NPs by comparison with pure TiO2. These results suggest that the doping cations could suppress the electron/hole recombination. Therefore, the photocatalytic activity of TiO2-based nanomaterials was enhanced.


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