Issue 68, 2016, Issue in Progress

Direct conversion mechanism from BiOCl nanosheets to BiOF, Bi7F11O5 and BiF3 in the presence of a fluorine resource

Abstract

In this work, we report the facile conversion from BiOCl nanosheets to BiOF, Bi7F11O5 and BiF3 by a novel ion exchange approach, in which the effects of fluorine source, F/Bi molar ratio and reaction medium (ethanol/water) on the products are mainly investigated. A plausible conversion mechanism is proposed to illustrate the formation of BiOF, Bi7F11O5 and BiF3. Furthermore, the photocatalytic activities of the samples are also investigated. It is amazing that under ultraviolet light irradiation (λ ≤ 420 nm), the activity of the as-formed Bi7F11O5/BiOCl sample is 3.28 times higher than that of BiOCl for the degradation of methyl orange (MO). It is demonstrated that the improved activity is mainly attributed to the formation of Bi7F11O5/BiOCl heterojunction, which has significantly improved the separation and transfer efficiency of charges. It is important that this study provides an initiative post-synthesis strategy to develop new, efficient photocatalysts.

Graphical abstract: Direct conversion mechanism from BiOCl nanosheets to BiOF, Bi7F11O5 and BiF3 in the presence of a fluorine resource

Supplementary files

Article information

Article type
Paper
Submitted
07 May 2016
Accepted
27 Jun 2016
First published
28 Jun 2016

RSC Adv., 2016,6, 63347-63357

Direct conversion mechanism from BiOCl nanosheets to BiOF, Bi7F11O5 and BiF3 in the presence of a fluorine resource

Y. Kan, F. Teng, Y. Yang, J. Xu and L. Yang, RSC Adv., 2016, 6, 63347 DOI: 10.1039/C6RA11877A

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements