Abstract

Europium (III) and niobium (V) co-doped TiO2 nanopowders were synthesized in Ar/O2 radio-frequency thermal plasmas by pyrolyzing aqueous precursors that contained various concentrations of Eu3+/(Eu3++Nb5++Ti4+)=0–0.5at.% and Nb5+/(Eu3++Nb5++Ti4+)=0–1.0at.%. Phase identification was performed by X-ray diffraction (XRD), particle morphology was observed by transmission electron microscopy (TEM) and high-resolution transmission electron microscopy (HRTEM), and UV–vis absorption spectra were determined by UV–vis spectroscopy. The photocatalytic activities under UV and visible light irradiations were both evaluated by bleaching 20μM of a methyl orange aqueous solution. All the resulting powders had a phase composition of anatase (30–66nm crystalline size) (major phase: ∼80% mass proportion) and rutile (56–94nm crystalline size) polymorphs, with a relatively wide particle size distribution from several nanometers (faceted crystallites) to ∼100nm (spherical particles). The photocatalytic activities dominated by oxygen defects in the TiO2 host lattice for the powders prepared with identical doping concentrations of Eu3+ and Nb5+ were both superior under UV and visible light irradiations over those obtained with different doping amounts. More interestingly, the co-doped powder exhibited an improved photocatalytic performance under 600–700nm visible light illumination than the Eu3+-doped TiO2 and P25 commercial powders.

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