Enhanced photocatalytic performance and mechanism of Ag-decorated LaFeO3 nanoparticles
Spherical LaFeO 3 nanoparticles with an average size of 35 nm were synthesized by a polyacrylamide gel route. Ag nanoparticles of 8–18 nm in size were decorated onto LaFeO 3 particle surface by a chemical reduction method to yield Ag–LaFeO 3 composites. The samples were characterized by X-ray powder...
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Veröffentlicht in: | Journal of sol-gel science and technology 2017-05, Vol.82 (2), p.509-518 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Spherical LaFeO
3
nanoparticles with an average size of 35 nm were synthesized by a polyacrylamide gel route. Ag nanoparticles of 8–18 nm in size were decorated onto LaFeO
3
particle surface by a chemical reduction method to yield Ag–LaFeO
3
composites. The samples were characterized by X-ray powder diffraction, scanning electron microscopy, transmission electron microscopy, ultraviolet–visible diffuse reflectance spectroscopy, and photoluminescence spectroscopy. It is found that LaFeO
3
particles have two bandgap energies of 2.59 and 2.24 eV, which undergo almost no change when decorated with Ag nanoparticles. photoluminescence spectra demonstrate that the decoration of LaFeO
3
particles with Ag nanoparticles leads to a decreased recombination rate of photogenerated electrons and holes. The photocatalytic activity of the samples was evaluated by degrading Rhodamine B under simulated-sunlight irradiation. Compared to bare LaFeO
3
particles, Ag–LaFeO
3
composites exhibit an obviously enhanced photocatalytic activity. The formed •OH was examined by photoluminescence spectroscopy using terephthalic acid as the •OH scavenger, revealing an enhanced yield on the irradiated Ag–LaFeO
3
composites. To clarify the role of active species in the photocatalysis, the effect of ammonium oxalate (h
+
scavenger), ethanol (•OH scavenger), benzoquinone (•O
2
−
scavenger), and N
2
on the Rhodamine B degradation as well as the •OH yield was investigated. Based on the experimental results, •OH and •O
2
−
are suggested to be the main active species causing the dye degradation.
Graphical Abstract |
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ISSN: | 0928-0707 1573-4846 |
DOI: | 10.1007/s10971-017-4332-0 |