Issue 46, 2011

Magnetically separable BiFeO3nanoparticles with a γ-Fe2O3 parasitic phase: controlled fabrication and enhanced visible-light photocatalytic activity

Abstract

A facile sol–gel approach with a fixed calcination temperature is developed to prepare BiFeO3 (BFO) nanoparticles, and the gel-drying temperature is adjusted to control the appearance of a γ-Fe2O3 parasitic phase. The room temperature ferromagnetism of the samples is strongly dependent on the gel-drying temperature. When the gel-drying temperature increases from 80 to 140 °C, the saturated magnetization of the corresponding samples jumps from 0.22 emu g−1 to 1.2 emu g−1, allowing the nanoparticles to be magnetically separated in solution. From examination by transmission electron microscopy and X-ray photoelectron spectroscopy, it is confirmed that the γ-Fe2O3 parasitic phase is nucleated during the gel-drying process under high temperatures above 120 °C, and remains in the subsequent annealing process, resulting in the anomalous enhanced magnetization. Comparing with pure BFO nanoparticles prepared under low gel-drying temperature, the BFO/γ-Fe2O3 samples exhibit significantly increased visible-light photocatalytic ability towards rhodamine B. The formation of a heterojunction structure between the BFO and γ-Fe2O3 phases is proposed to be responsible for the enhanced photocatalytic activity. Further enhanced photocatalytic activity is obtained in this study when adding a small amount of H2O2 during photocatalysis, indicating the samples have photo-Fenton-like catalytic activity.

Graphical abstract: Magnetically separable BiFeO3 nanoparticles with a γ-Fe2O3 parasitic phase: controlled fabrication and enhanced visible-light photocatalytic activity

Article information

Article type
Paper
Submitted
03 Jul 2011
Accepted
19 Sep 2011
First published
25 Oct 2011

J. Mater. Chem., 2011,21, 18645-18652

Magnetically separable BiFeO3 nanoparticles with a γ-Fe2O3 parasitic phase: controlled fabrication and enhanced visible-light photocatalytic activity

R. Guo, L. Fang, W. Dong, F. Zheng and M. Shen, J. Mater. Chem., 2011, 21, 18645 DOI: 10.1039/C1JM13072B

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