TY - JOUR
T1 - Enhanced photocatalytic activity of La3+ and Se4+ co-doped bismuth ferrite nanostructures
AU - IRFAN, Syed
AU - LI, Liangliang
AU - SALEEMI, Awais Siddique
AU - NAN, Ce-Wen
N1 - 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).
PY - 2017
Y1 - 2017
N2 - 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.
AB - 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.
UR - http://www.scopus.com/inward/record.url?scp=85021735320&partnerID=8YFLogxK
U2 - 10.1039/c7ta01847a
DO - 10.1039/c7ta01847a
M3 - Journal Article (refereed)
AN - SCOPUS:85021735320
SN - 2050-7488
VL - 5
SP - 11143
EP - 11151
JO - Journal of Materials Chemistry A
JF - Journal of Materials Chemistry A
IS - 22
ER -