Issue 24, 2014

From Pt-rich dendrites to Ni-rich cuboctahedrons: structural evolution and electrocatalytic property studies

Abstract

In this paper, we report the evolution of the composition and morphology of PtxNi1−x (0 < x < 1) nanoalloys from Pt-rich dendrites to Ni-rich cuboctahedrons. However, the transformation processes were different under different temperatures. At 200 °C, the transformation was mainly completed through atomic addition, while there was a contribution from both atomic addition and oriented attachment at 220 °C. The electrocatalytic performance towards the methanol oxidation reaction (MOR) indicated the dendrites exhibited higher catalytic activity and better durability relative to the cuboctahedrons. For the cuboctahedrons with different compositions, the catalytic activity is mainly determined by the d-band position. This provides new insights into the controlled synthesis of Pt-based bimetallic nanoalloys and advances the understanding of their catalytic behaviour.

Graphical abstract: From Pt-rich dendrites to Ni-rich cuboctahedrons: structural evolution and electrocatalytic property studies

Supplementary files

Article information

Article type
Paper
Submitted
16 Jan 2014
Accepted
12 Mar 2014
First published
12 Mar 2014

CrystEngComm, 2014,16, 5331-5337

Author version available

From Pt-rich dendrites to Ni-rich cuboctahedrons: structural evolution and electrocatalytic property studies

D. Zhang, J. Li, J. Kang, T. Chen, Y. Zhang, L. Wang and L. Guo, CrystEngComm, 2014, 16, 5331 DOI: 10.1039/C4CE00099D

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