Issue 7, 2013

Photocatalytic water oxidation with hematite electrodes

Abstract

Hematite's favorable 2.1 eV band gap, valence band position, stability, abundance, and light absorption properties make it a promising semiconductor material for solar-driven water oxidation. While a mechanism for water oxidation at the surface of hematite has not yet been experimentally established, it is widely agreed upon that surface-state mediated charge recombination at the electrode–electrolyte interface competes with water oxidation. This kinetic competition ultimately limits the water splitting efficiency. The identity and role of these surface states in the water oxidation reaction is still unclear. This perspective presents recent results in probing photocatalytic water oxidation with hematite electrodes and the role of surface states. In addition, the function of surface coatings on the hematite surface, and their role as catalysts or surface passivation materials, are discussed.

Graphical abstract: Photocatalytic water oxidation with hematite electrodes

Article information

Article type
Perspective
Submitted
02 May 2013
Accepted
29 May 2013
First published
30 May 2013

Catal. Sci. Technol., 2013,3, 1660-1671

Photocatalytic water oxidation with hematite electrodes

K. M. H. Young, B. M. Klahr, O. Zandi and T. W. Hamann, Catal. Sci. Technol., 2013, 3, 1660 DOI: 10.1039/C3CY00310H

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