Loading…

Three-dimensional coral-like cobalt selenide as an advanced electrocatalyst for highly efficient oxygen evolution reaction

Oxygen evolution reaction (OER) influences some important renewable energy technologies such as water splitting. Although many OER electrocatalysts have been studied to surmount this difficult problem, the development of a highly active, inexpensive and sustained OER electrocatalyst is still a great...

Full description

Saved in:
Bibliographic Details
Published in:Electrochimica acta 2016-03, Vol.194, p.59-66
Main Authors: Liao, Mei, Zeng, Guangfeng, Luo, Tingting, Jin, Zhaoyu, Wang, Yujue, Kou, Xingming, Xiao, Dan
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
Description
Summary:Oxygen evolution reaction (OER) influences some important renewable energy technologies such as water splitting. Although many OER electrocatalysts have been studied to surmount this difficult problem, the development of a highly active, inexpensive and sustained OER electrocatalyst is still a great challenge. In this study, we report a novel, cost-effective cobalt selenide (coral-like CoSe) electrocatalyst with high current density (∼97.5mAcm−2at 1.606V vs. RHE) and strong durability in alkaline media. The chronoamperometric response of coral-like CoSe electrocatalyst can remain 98% of its initial current density after 10000s at the overpotential of 350mV in 1M KOH. The prepared coral-like CoSe electrode exhibits a low overpotential of 295mV at a current density of 10mAcm−2 and a small Tafel slope of 40mVdec−1, which exceeds previously reported state-of-art RuO2 electrocatalyst and is much better than CoSe nanoparticles (CoSe NPs) and precursor Co(OH)2 electrocatalysts. This work affords us a 3D Co-based electrocatalyst with high performance and strong durability under alkaline conditions, which can be applied to energy conversion and storage processes.
ISSN:0013-4686
1873-3859
DOI:10.1016/j.electacta.2016.02.046