Issue 76, 2015

Synthesis, characterization and photocatalytic activity of magnetically separable γ-Fe2O3/N,Fe codoped TiO2 heterojunction for degradation of Reactive Blue 4 dye

Abstract

In the present work, nanocrystalline undoped, N-doped and N,Fe codoped TiO2 have been synthesized using a sol–gel method for the photocatalytic degradation of Reactive Blue 4 dye under visible light, with N,Fe codoped TiO2 exhibiting the best activity. Furthermore, to counter the problem of separation of the N,Fe codoped TiO2 photocatalyst, magnetically separable γ-Fe2O3/N,Fe codoped TiO2 heterojunctions were fabricated and found to exhibit enhanced photoactivity with 100% dye degradation, compared to 85% with N,Fe codoped TiO2. This behavior has been attributed to the facilitated electron–hole transfer in the γ-Fe2O3/N,Fe codoped TiO2 heterojunctions, low electron–hole recombination rate, existence of a pure anatase phase and narrow band gap of 1.5 eV. The recycled γ-Fe2O3/N,Fe codoped TiO2 also demonstrated good repeatability of photoactivity. The mechanism involved in the degradation of dye by γ-Fe2O3/N,Fe codoped TiO2 has also been discussed. In conclusion, the synthesis of magnetically separable and visible light active titania by the coupling of γ-Fe2O3 and N,Fe codoped TiO2 to overcome the limitations of a narrow band gap and non-recyclability, with the additional advantage of enhanced photocatalytic activity for the degradation of Reactive Blue 4 dye, has been achieved.

Graphical abstract: Synthesis, characterization and photocatalytic activity of magnetically separable γ-Fe2O3/N,Fe codoped TiO2 heterojunction for degradation of Reactive Blue 4 dye

Article information

Article type
Paper
Submitted
29 Apr 2015
Accepted
23 Jun 2015
First published
23 Jun 2015

RSC Adv., 2015,5, 61623-61630

Author version available

Synthesis, characterization and photocatalytic activity of magnetically separable γ-Fe2O3/N,Fe codoped TiO2 heterojunction for degradation of Reactive Blue 4 dye

N. Kaur, S. Kaur Shahi and V. Singh, RSC Adv., 2015, 5, 61623 DOI: 10.1039/C5RA07812A

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