Issue 4, 2016

Nanoscale cobalt metal–organic framework as a catalyst for visible light-driven and electrocatalytic water oxidation

Abstract

The Co-ZIF-67 metal–organic framework was investigated as a catalyst for visible light-driven and electrocatalytic water oxidation in basic and neutral media. Co-ZIF-67 exhibited efficient performance for visible light-driven water oxidation, with a turnover frequency of 0.035 s−1. Co-ZIF-67 also maintained a stable current density after electrolysis for over 24 h, and it electrocatalyzed the oxygen evolution reaction within a wide pH range. DFT calculations suggest that the catalyst activates water molecules while the dissociated proton is received by nearby 2-methylimidazole ligands. This process permits Co-ZIF-67 to effectively catalyze the photocatalytic and electrocatalytic oxidation of water.

Graphical abstract: Nanoscale cobalt metal–organic framework as a catalyst for visible light-driven and electrocatalytic water oxidation

Supplementary files

Article information

Article type
Letter
Submitted
06 Nov 2015
Accepted
15 Feb 2016
First published
16 Feb 2016

New J. Chem., 2016,40, 3032-3035

Author version available

Nanoscale cobalt metal–organic framework as a catalyst for visible light-driven and electrocatalytic water oxidation

Q. Xu, H. Li, F. Yue, L. Chi and J. Wang, New J. Chem., 2016, 40, 3032 DOI: 10.1039/C5NJ03113C

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