New W doped TiO2 Photocatalysts by the Sol-Gel Method

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In the 1930s, the term photocatalysis was introduced as a new branch of catalysis [1]. Among photocatalytic applications, photocatalytic oxidation and the reduction of organic compounds in water, have become important and have received considerable attention during the last few years [1, 2]. Owing to its excellent catalytic and oxidative properties; titanium dioxide, TiO2, has been frequently employed to degrade most kinds of organic pollutants. Including detergents, dyes, pesticides and herbicides under UV-light irradiation in order to transform them in water, carbon dioxide and some simple mineral acids [3-6]. However, titanium dioxide was used also for other catalytic applications [7, 8]. Among the three common phases of crystalline TiO2, it is widely known that anatase (band gap = 3.2 eV, absorption ≤385 nm) is the most photocatalytically active. Therefore, only a small fraction (~ 5%) of the solar energy can be utilized in practical application [9,10]. Moreover, a low rate of electron transfer to oxygen and a high rate of recombination between excited electron/hole pairs lead to a low quantum yield rate and also a limited photooxidation rate [11,12]. Modification of TiO2 is thus, an active and important field of research. Efforts have been made using chemical or physical methods to enhance the photocatalytic activity of TiO2 through modification with different metal groups such as alkaline metals [13], earth alkaline metals [14], transition metals [15], rare earth metals [16], and noble metals [17], but with varying degree of results.

Transition metal doping have been widely used to extend TiO2’s light absorption in the visible-light region. In particular, tungsten (W) was reported as the best for the photodegradation under ...

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..., we have successfully prepared new W doped TiO2 photocatalysts by the sol-gel method. The new photocatalysts are characterized by different techniques such as DRS, BET, DRX, SEM, and TEM. Photocatalytic experiments are carried out using the CR as a photodegratable organic compound. The obtained results show the formation of nanoparticles with an average size of 10 nm. Moreover, the new photocatalysts have high surface areas and their light absorption extends to the visible region which can promote their photocatalytic activity. Thus it is found that W0.5-TiO2 calcined at 350°C for 2h shows much higher activity for the degradation of CR under visible light irradiation compared to the non-doped or to the highly W-doped TiO2.

References

[1] I.Fechete, Y.Wang, J.C.Vedrine, Catal.Today. 189 (2012) 2-27.

[2] M.A. Pena, J.L.G. Fierro, Chem.Rev.101 (2001) 1981.

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