Issue 94, 2023

Nitrogen-doped Fe7S8 as highly efficient electrocatalysts for the hydrogen evolution reaction

Abstract

The high unoccupied d band energy of FeS2 basically results in weak orbital coupling with water molecules, consequently leading to sluggish water dissociation kinetics. Herein, we demonstrate that the N-induced doping effect and phase transition engineering (FeS2 to N-Fe7S8) can downshift the unoccupied d orbitals and strengthen the interfacial orbital coupling to boost the water dissociation kinetics. The fabricated N-Fe7S8/carbon cloth (CC) displays superb hydrogen evolution reaction performance with a low overpotential (89 mV at 10 mA cm−2) and small Tafel slope (105 mV dec−1) under alkaline conditions. It is revealed that the electronic structure of Fe is modulated by N doping and phase transition. The downshifted d band energy can strengthen water adsorption and reduce the energy barrier of water dissociation. Our work provides a new strategy to modify metal sulfide electrocatalysts for electrochemical energy conversion.

Graphical abstract: Nitrogen-doped Fe7S8 as highly efficient electrocatalysts for the hydrogen evolution reaction

Supplementary files

Article information

Article type
Communication
Submitted
13 Jul 2023
Accepted
10 Oct 2023
First published
10 Oct 2023

Chem. Commun., 2023,59, 14013-14016

Nitrogen-doped Fe7S8 as highly efficient electrocatalysts for the hydrogen evolution reaction

J. Ye, S. Niu, L. Zhang, G. Wang and J. Zhu, Chem. Commun., 2023, 59, 14013 DOI: 10.1039/D3CC03376G

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