Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1788122 | Current Applied Physics | 2012 | 5 Pages |
Photocatalytic degradation of methylene blue (MB) in water was examined using Er3+-doped TiO2 (Er–TiO2) nanorods prepared by a sol–gel derived electrospinning, calcination, and subsequent mechanical grinding. Different concentrations of Er dopant in the range of 0–1.0 mol% were synthesized to evaluate the effect of Er content on the photocatalytic activity of TiO2. Among Er3+–TiO2 catalysts, the 0.7 mol% Er3+–TiO2 catalyst showed the highest MB degradation rate. The degradation kinetic constant (k) increased from 1.0 × 10−3 min−1 to 5.1 × 10−3 min−1 with the increase of Er3+ doping from 0 to 0.7 mol%, but decreased down to 2.1 × 10−3 min−1 when Er3+ content was 1.0 mol%. It can be concluded that the degradation of MB under UV radiation was more efficient with Er3+–TiO2 catalyst than with pure TiO2. The higher activity might be attributed to the transition of 4f electrons of Er3+ and red shifts of the optical absorption edge of TiO2 by erbium ion doping.
► Photocatalytic degradation of methylene blue was examined using Er3+–TiO2 nanorods. ► Nanorods were prepared by electrospinning, calcinations and mechanical grinding. ► The 0.7 mol% Er3+–TiO2 catalyst showed the highest MB degradation rate. ► The degradation is attributed to the transition of 4f electrons of Er3+. ► And red shifts of the optical absorption edge of TiO2 by erbium ion doping.