Issue 20, 2017

Colloidal synthesis of urchin-like Fe doped NiSe2 for efficient oxygen evolution

Abstract

The search for highly efficient non-precious metal electrocatalysts toward the oxygen evolution reaction (OER) is extremely essential for renewable energy systems. Here, we report the colloidal synthesis of Fe doped NiSe2, which functions as a high-performance electrocatalyst for the OER in alkaline solution. The NiFeSe catalysts are composed of urchin-like dendrites with a high number of active sites, which could provide fast transportation of electrons and electrolytes, and facile release of the evolved O2 bubbles during the OER catalysis. Benefitting from this unique urchin-like structure and strong electron interaction between Fe, Ni, and Se, the Ni1.12Fe0.49Se2 catalyst exhibits excellent electrocatalytic activity and high durability toward the OER in alkaline solution, with an overpotential of 227 mV at a current density of 10 mA cm−2, which is, to the best of our knowledge, higher than most of the reported selenide-based electrocatalysts.

Graphical abstract: Colloidal synthesis of urchin-like Fe doped NiSe2 for efficient oxygen evolution

Supplementary files

Article information

Article type
Paper
Submitted
26 Feb 2017
Accepted
15 Apr 2017
First published
19 Apr 2017

Nanoscale, 2017,9, 6821-6825

Colloidal synthesis of urchin-like Fe doped NiSe2 for efficient oxygen evolution

Y. Du, G. Cheng and W. Luo, Nanoscale, 2017, 9, 6821 DOI: 10.1039/C7NR01413A

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