Issue 22, 2024

A high-entropy FeCoMnCuNi diselenide self-standing electrode with outstanding water-electrolysis performance in alkaline medium

Abstract

Developing non-noble metal efficient electrocatalysts with high activity and stability is extremely essential for hydrogen generation by water electrolysis with low cost. Herein, we report a novel binder-free high-entropy self-standing electrode with a unique three-dimensional structure and petunia-, needle- and fork-like morphology prepared by the hydrothermal and selenization methods. Due to high entropy, lattice distortion and high-curvature tip-enhancement effects, the prepared FeCoMnCuNiSe2 with an ultralow overpotential of 71.6 mV at 100 mA cm−2 exhibited superior activity for the hydrogen evolution reaction (HER) in 1.0 M KOH solution, far outperforming almost all reported advanced non-noble metal HER catalysts. More impressively, the assembled FeCoMnCuNiSe2||FeCoMnCuNiSe2 overall-water splitting device with more than 45 h of continuous operational stability at 10, 20 and 50 mA cm−2 in 1.0 M KOH required a remarkably low cell voltage of 1.30 V at 10 mA cm−2 as well, demonstrating a promising practical application prospect in future water electrolysis.

Graphical abstract: A high-entropy FeCoMnCuNi diselenide self-standing electrode with outstanding water-electrolysis performance in alkaline medium

Supplementary files

Article information

Article type
Research Article
Submitted
23 Jul 2024
Accepted
26 Sep 2024
First published
27 Sep 2024

Inorg. Chem. Front., 2024,11, 7936-7946

A high-entropy FeCoMnCuNi diselenide self-standing electrode with outstanding water-electrolysis performance in alkaline medium

X. Guo, M. Zhou, Z. Liu, S. Mu, K. Wang, H. Shi, F. Wang, S. Lu, Z. Ni and G. Liu, Inorg. Chem. Front., 2024, 11, 7936 DOI: 10.1039/D4QI01835D

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