Issue 5, 2017

Facile synthesis of Bi2MoO6–MIL-100(Fe) metal–organic framework composites with enhanced photocatalytic performance

Abstract

A novel Bi2MoO6–MIL-100(Fe) heterostructure photocatalyst was synthesized by a facile solvothermal method for the first time, and characterized by X-ray diffraction, scanning electron microscopy, X-ray photoelectron spectroscopy, UV-vis diffuse reflectance spectra, transmission electron microscopy, and photoluminescence spectra. The as-prepared Bi2MoO6–MIL-100(Fe) composites exhibited excellent photocatalytic activity and stability towards the degradation of Rhodamine B (RhB) under visible light irradiation. The introduction of MIL-100(Fe) into semiconductor Bi2MoO6 improved the photocatalytic performance remarkably, and the optimal composite with 9% MIL-100(Fe) content showed the highest photocatalytic activity. According to the active radical trapping experiments, the h+ and ˙O2 radicals were the two main active species in the photocatalytic reaction. The enhanced photocatalytic performance is mainly attributed to the formation of the Bi2MoO6–MIL-100(Fe) heterostructure, which is beneficial to the transfer and separation of photo-generated electron–hole pairs. The possible mechanism of the enhanced photocatalytic performance of the Bi2MoO6–MIL-100(Fe) composites was discussed.

Graphical abstract: Facile synthesis of Bi2MoO6–MIL-100(Fe) metal–organic framework composites with enhanced photocatalytic performance

Article information

Article type
Paper
Submitted
01 Nov 2016
Accepted
04 Dec 2016
First published
12 Jan 2017
This article is Open Access
Creative Commons BY license

RSC Adv., 2017,7, 2943-2952

Facile synthesis of Bi2MoO6–MIL-100(Fe) metal–organic framework composites with enhanced photocatalytic performance

J. Yang, X. Niu, S. An, W. Chen, J. Wang and W. Liu, RSC Adv., 2017, 7, 2943 DOI: 10.1039/C6RA26110H

This article is licensed under a Creative Commons Attribution 3.0 Unported Licence. You can use material from this article in other publications without requesting further permissions from the RSC, provided that the correct acknowledgement is given.

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