Abstract
Photocatalysis is attracting huge interest for addressing current energy and environmental issues by converting solar light into chemical energy. For this purpose, we investigated the effect of La3+ and Se4+ co-doping on the photocatalytic activity of BiFeO3. BiFeO3 and Bi0.92La0.08FeO3 nanoparticles containing different Se4+ doping content (BiFe(1−x)SexO3, x = 0.0, 0.02, 0.05, and Bi0.92La0.08Fe(1−x)SexO3, x = 0.0, 0.02, 0.05, 0.075, 0.1) were synthesized by a double solvent sol–gel route. The co-doped nanoparticles were characterized by X-ray diffractometry (XRD), field emission scanning electron microscopy (FESEM), high resolution transmission electron microscopy (HRTEM), and UV-vis diffuse reflectance spectroscopy (DRS), and their photocatalytic activity was studied by the photocatalytic degradation of Congo Red (CR) in aqueous solution under different wavelengths of light illumination. The band-gap of the pure BiFeO3 was significantly decreased from 2.06 eV to 1.94 eV. It was found that La3+ and Se4+ co-doping significantly affected the photocatalytic performance of pure BiFeO3. Moreover, with the increment of Se4+ doping into Bi0.92La0.08FeO3 up to an optimal value, the photocatalytic activity was maximized. In order to study the photosensitization process, photo-degradation of a colourless organic compound (acetophenone) was also observed. On the basis of these experimental results, the enhanced photocatalytic activities with La3+ and Se4+ co-doping could be attributed to the increased optical absorption, and efficient separation and migration of photo-generated charge carriers with the decreased recombination of electrons–holes resulting from co-doping effects. The possible photocatalytic mechanism of La3+ and Se4+ co-doped BiFeO3 was critically discussed.
Original language | English |
---|---|
Pages (from-to) | 11143-11151 |
Number of pages | 9 |
Journal | Journal of Materials Chemistry A |
Volume | 5 |
Issue number | 22 |
Early online date | 11 May 2017 |
DOIs | |
Publication status | Published - 2017 |
Externally published | Yes |
Funding
This work was supported by the National Natural Science Foundation of China (No. 11234005, No. 51332001) and National Key Research Program of China (Grant No. 2016YFA0201003).