Issue 19, 2016

Electrochemically synthesized freestanding 3D nanoporous silver electrode with high electrocatalytic activity

Abstract

Three-dimensional nanoporous metals of highly porous structure and interconnected ligaments are attractive for electrochemical reactions. Herein, freestanding 3D nanoporous silver (np-Ag) is prepared by a facile electrochemical approach, i.e., first electro-oxidizing silver to silver halides followed by electro-reduction of the silver halides by controlling the potential applied to the electrode. The np-Ag displays 130 and 11.5 times enhancement in catalytic activity for the oxygen reduction reaction and the formaldehyde electro-oxidation reaction, respectively, relative to the flat polycrystalline silver, and even outperforms the commercial nano-Pt catalyst. Detailed experimental and theoretical studies discover that both the facilitated mass transportation in the 3D interconnected porous structures and the favored kinetics contribute to the superior electro-catalytic activity of np-Ag.

Graphical abstract: Electrochemically synthesized freestanding 3D nanoporous silver electrode with high electrocatalytic activity

Supplementary files

Article information

Article type
Paper
Submitted
31 May 2016
Accepted
07 Jul 2016
First published
08 Jul 2016

Catal. Sci. Technol., 2016,6, 7163-7171

Electrochemically synthesized freestanding 3D nanoporous silver electrode with high electrocatalytic activity

L. Yuan, L. Jiang, T. Zhang, G. Wang, S. Wang, X. Bao and G. Sun, Catal. Sci. Technol., 2016, 6, 7163 DOI: 10.1039/C6CY01174H

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