Issue 10, 2016

A robust iron oxyhydroxide water oxidation catalyst operating under near neutral and alkaline conditions

Abstract

Efficient electrochemical splitting of water to hydrogen and oxygen using cheap and abundant metal ion based catalysts is of fundamental significance to solar devices. For an efficient water splitting reaction, the development of a highly active, robust and cost-effective catalyst is desirable. Herein, we report iron oxyhydroxide thin films as an efficient water oxidation catalyst. The films have been electrochemically deposited applying anodic potential in the presence of a nonaqueous solvent, using ferrocene as the metal ion precursor and exclude interference from the problems of precipitation of iron hydroxide during the deposition process. The as-prepared films exhibit high catalytic activity towards the oxygen evolution reaction under alkaline as well as under near neutral conditions. Long term testing results showed that the films were able to oxidize water for almost 8 h of continuous operation with a current density of 10 mA cm−2 at an overpotential of 600 mV under near neutral conditions. The facile method of electrodeposition reported here with outstanding catalytic efficiency is of great significance for the large scale production of hydrogen.

Graphical abstract: A robust iron oxyhydroxide water oxidation catalyst operating under near neutral and alkaline conditions

Supplementary files

Article information

Article type
Communication
Submitted
12 Jan 2016
Accepted
22 Jan 2016
First published
25 Jan 2016

J. Mater. Chem. A, 2016,4, 3655-3660

A robust iron oxyhydroxide water oxidation catalyst operating under near neutral and alkaline conditions

D. R. Chowdhury, L. Spiccia, S. S. Amritphale, A. Paul and A. Singh, J. Mater. Chem. A, 2016, 4, 3655 DOI: 10.1039/C6TA00313C

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