Issue 15, 2025

Interface electronic coupling in NiCo2S4 nanorod-amorphous FeOOH nanosheets with enhanced catalytic activity in the oxygen evolution reaction

Abstract

The oxygen evolution reaction (OER) involves a four-electron couple transfer step with slow reaction kinetics, which is considered a bottleneck in the water-splitting process. Therefore, exploiting earth-abundant and cost-effective OER electrocatalysts has become promising in large-scale industrial applications. Herein, a heterogeneous interface OER catalyst consisting of NiCo2S4@FeOOH-1 supported on foam nickel (NF) was synthesized through a two-step hydrothermal-chemical etching method. NiCo2S4@FeOOH-1 showed an excellent performance as an OER catalyst, requiring an overpotential of only 385.6 mV to reach 100 mA cm−2 and it exhibited a Tafel slope of 80.4 mV dec−1, indicating the rapid reaction kinetics. The NiCo2S4@FeOOH-1 catalyst also exhibited exceptional long-term stability, maintaining a consistent performance for more than 20 hours in an alkaline environment. The robust interfacial effect between NiCo2S4 and FeOOH effectively shortened the electron transport pathway, contributing to the enhancement in electrocatalytic performance. This study provides significant insights into the catalytic mechanisms and opens a pathway for the development of hierarchical structures aimed at creating highly efficient and durable OER electrocatalysts.

Graphical abstract: Interface electronic coupling in NiCo2S4 nanorod-amorphous FeOOH nanosheets with enhanced catalytic activity in the oxygen evolution reaction

Supplementary files

Transparent peer review

To support increased transparency, we offer authors the option to publish the peer review history alongside their article.

View this article’s peer review history

Article information

Article type
Paper
Submitted
14 Jan 2025
Accepted
10 Mar 2025
First published
12 Mar 2025

New J. Chem., 2025,49, 6269-6276

Interface electronic coupling in NiCo2S4 nanorod-amorphous FeOOH nanosheets with enhanced catalytic activity in the oxygen evolution reaction

J. Tian, Y. Ye, J. Zhou, S. Li, B. Duan, L. Shen and B. He, New J. Chem., 2025, 49, 6269 DOI: 10.1039/D5NJ00188A

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