Issue 9, 2014

Surface ligand mediated growth of CuPt nanorods

Abstract

CuPt alloy nanorods have been synthesized via one dimensional assembly of randomly orientated nanocrystallites in the presence of hexadecanoic acid and hexadecylamine as surface ligands. When hexadecanoic acid was added into the synthetic system first followed by a second step of adding hexadecylamine, strands of ultrathin CuPt nanowires were produced. The roles of the amine and organic acid are discussed. A novel ligand mediated mechanism is proposed, in which the formation of a stable monolayer structure of the ligands is the driving force to guide the 1D growth of the alloy nanorods without the influence of the crystal orientation. Photocatalytic hydrogen production from water has been performed using CuPt nanorods as a cocatalyst, which has a higher production rate (234.08 μmol h−1 g−1) than that of Pt nanorods under the same conditions (~66.35 μmol h−1 g−1). Our results suggest that polycrystalline CuPt nanorods with a large amount of defects are probably promising cocatalyst for photocatalysis.

Graphical abstract: Surface ligand mediated growth of CuPt nanorods

Supplementary files

Article information

Article type
Paper
Submitted
31 Jul 2013
Accepted
04 Dec 2013
First published
04 Dec 2013

CrystEngComm, 2014,16, 1714-1723

Surface ligand mediated growth of CuPt nanorods

F. Yu, X. Xu, C. J. Baddeley, R. M. Bellabarba, P. Lignier, R. P. Tooze, F. Fina, J. S. T. Irvine and W. Zhou, CrystEngComm, 2014, 16, 1714 DOI: 10.1039/C3CE41524D

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