Issue 26, 2017

Bimetallic Ni–Mo nitride nanotubes as highly active and stable bifunctional electrocatalysts for full water splitting

Abstract

Designing low-cost, highly active and stable electrocatalysts is very important to various renewable energy storage and conversion devices. Herein we develop a facile method to fabricate bimetallic Ni–Mo nitride nanotubes, which can serve as highly active and stable bifunctional electrocatalysts for full water splitting. To drive a current density of 10 mA cm−2, the bimetallic Ni–Mo nitride nanotubes require an overpotential of 295 mV for the OER and 89 mV for the HER. The alkaline water electrolyzer with the nanotubes as cathode and anode catalysts requires a cell voltage of ca. 1.596 V to achieve a current density of 10 mA cm−2. Furthermore, the nanotubes for full water splitting show excellent stability even at a high current density of 370 mA cm−2, superior to the integrated performance of commercial Pt and IrO2. Our experimental results show that the NiOOH and NH groups formed at the catalyst surface during the OER process are active species for the OER, while the Ni(OH)2, NH and Mo species at the catalyst surface play a key role in the HER. The present strategy may open an avenue for fabrication of low-cost, highly active and stable electrocatalysts for large-scale water splitting.

Graphical abstract: Bimetallic Ni–Mo nitride nanotubes as highly active and stable bifunctional electrocatalysts for full water splitting

Supplementary files

Article information

Article type
Paper
Submitted
03 Apr 2017
Accepted
26 May 2017
First published
26 May 2017

J. Mater. Chem. A, 2017,5, 13648-13658

Bimetallic Ni–Mo nitride nanotubes as highly active and stable bifunctional electrocatalysts for full water splitting

Z. Yin, Y. Sun, C. Zhu, C. Li, X. Zhang and Y. Chen, J. Mater. Chem. A, 2017, 5, 13648 DOI: 10.1039/C7TA02876H

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