Photocatalytic properties of Bi2MoO6 nanoparticles prepared by an amorphous complex precursor
Introduction
Throughout last decades, heterogeneous photocatalysis has been positioned as a promissory efficient technology to resolve environmental and energy problems. Since the discovery of photocatalytic activity of TiO2 by UV irradiation [1], many works have been written describing novel methods to synthesized photocatalysts with special characteristics to achieve a high catalytic activity in red–ox reactions. The major applications investigated for this technology are the colour removal and dyes destruction, reduction of chemical oxygen demand (COD), mineralization of hazardous organics and purification and disinfection of water [2]. Within the overall category of dyestuffs rhodamine B dye (RhB), see Fig. 1, is famous for the stability as dye laser material. It has become a common organic pollutant, so the photodegradation of RhB is important to the purification of dye effluents to avoid damage in aquatic organisms [3].
Recently, some binary oxides with perovskite and related structures have shown photocatalytic activity under irradiation with visible light [4], [5], [6]. In this sense, oxides with Aurivillius structure type have received special attention. Some authors have reported Bi2WO6 as an interesting photocatalyst for water splitting and photodegradation of organic compounds under visible light irradiation [7], [8]. Moreover photocatalytic activity for O2 evolution has been observed in the analogous phase Bi2MoO6 [9], [10]. Particularly, the binary system Bi2O3–MoO3 have received special attention due the capacity of several oxides belonging the system to act as catalysts in the partial oxidation of olefins to produce unsaturated aldehydes, unsaturated nitrides or dienes [11]. Bi2MoO6 is the most studied compound within this family due to its interesting properties such as ion conductive, dielectric capacity, and luminescent and catalytic properties.
Frequently the solid-state reaction method employed to obtain the photocatalyst leads to materials with poor photocatalytic activity due to the small surface area developed. The so-called soft chemistry methods have shown to be efficient to prepare better catalysts than those synthesized by classical methods. In this sense, Kudo and Hijii [8] have reported the synthesis of Bi2MoO6 by hydrothermal synthesis, additionally the mechanosynthesis has been also employed for this purpose [12]. Recently Zhang et al. [13] have reported the formation of Bi2WO6 nanoparticles through a complex organic precursor. In the present work, the procedure described by Zhang has been followed in order to obtain the analogous oxide Bi2MoO6 with small particle size. The successful synthesis of nanoparticles of Bi2MoO6 will be providing an interesting candidate for photocatalytic applications.
Section snippets
Preparation of samples Bi2MoO6
Bi2MoO6 was prepared via an amorphous complex precursor by means of a procedure that was described previously for the synthesis of Bi2WO6 [13]. The 0.034 mol of diethylenetriaminepentaacetic acid (H5DTPA) (Aldrich, 99%) and 20 mL stronger ammonia water were put into 300 mL of hot distilled water. After dissolution, the 0.00984 mol Bi2O3 (Aldrich, 99.9%+) were added under a continuous stirring for 40 min in order to dissolve all the bismuth oxide. Then, 0.00143 mol (NH4)6Mo7O24·4H2O (Productos
Results and discussions
The material used as precursor of Bi2MoO6 was heated at 200 °C by 1 h in order to improve its handling. The resulting material was a red fine powder that was subsequently heated at 350, 375, 400, 450, 500 and 900 °C by different time intervals until to reach constant weight. To know the process formation of Bi2MoO6, TGA/DTA analyses were employed to follow the decomposition of precursor. Fig. 2 shows the TGA/DTA plot of the precursor powder at the temperature range 30–600 °C. Taking into account
Conclusions
Nanoparticles of Bi2MoO6 were prepared successfully by a method that involves an amorphous complex precursor. This route provides the possibility to obtain Bi2MoO6 until 200 °C below of the temperature employed by solid state reaction. This situation leads to the preparation of materials with higher surface area and small particle size. These factors contribute to consider to Bi2MoO6 as photocatalyst on reactions of dye-organic degradation with visible light irradiation. The photocatalytic
Acknowledgements
We wish to thank to CONACYT for supporting the project 43800 and the Universidad Autónoma de Nuevo León (UANL) for its invaluable support through the project PAICYT-2006. We also thank Departamento de Ecomateriales y Energía of Facultad de Ingeniería Civil (UANL) for its assistance on the characterization of materials.
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