Issue 8, 2015

A highly reactive and magnetic recyclable catalytic system based on AuPt nanoalloys supported on ellipsoidal Fe@SiO2

Abstract

A facile method has been developed for the synthesis of highly active and well-defined AuPt nanoalloys supported on the surface of ellipsoidal Fe@SiO2 nanoparticles. This method involves the loading of Pt NPs on the Fe2O3@SiO2 nanocapsules via Sn2+ linkage and reduction, then in situ fabrication of Au nanoparticles by the galvanic replacement reaction between Au and Pt, and finally calcination and reduction to convert the nonmagnetic Fe2O3 to Fe core with high saturation magnetization. XRD and XPS analysis demonstrates the alloy structure of AuPt nanoparticles in the final samples. The obtained Fe@SiO2/AuPt samples exhibit a remarkably higher catalytic activity in comparison with the supported monometallic counterparts toward the reduction of 4-nitrophenol to 4-aminophenol by NaBH4. The catalyst can be reused for several cycles with convenient magnetic separation.

Graphical abstract: A highly reactive and magnetic recyclable catalytic system based on AuPt nanoalloys supported on ellipsoidal Fe@SiO2

Supplementary files

Article information

Article type
Paper
Submitted
11 Nov 2014
Accepted
07 Jan 2015
First published
07 Jan 2015

J. Mater. Chem. A, 2015,3, 4642-4651

A highly reactive and magnetic recyclable catalytic system based on AuPt nanoalloys supported on ellipsoidal Fe@SiO2

Z. Zhang, Y. Zhou, Y. Zhang, S. Zhou, S. Xiang, X. Sheng and P. Jiang, J. Mater. Chem. A, 2015, 3, 4642 DOI: 10.1039/C4TA06085G

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