Issue 33, 2024

Bimetallic atom-improved Ni3S2 bifunctional electrocatalysts for efficient hydrogen evolution reaction and overall water splitting performance

Abstract

The hydrogen evolution reaction (HER), as a pivotal half-reaction, significantly hinders the advancement of energy conversion efficiency. Metal electrodeposition on catalysts has been demonstrated to effectively enhance the HER reactivity. Here, Ni3S2–Fe–Ni with a multilayer structure was obtained by the electrodeposition of Ni3S2 with dopants Fe/Ni, in which a number of active sites were achieved and the intrinsic conductivity of the catalyst was well improved. Elemental analyses revealed the multilayer structure consisting of Ni3S2, NiS, and Fe. The Ni3S2–Fe–Ni catalyst exhibited impressive electrochemical performance due to optimization of its structure with the overpotentials of the HER and OER of only 83 and 190 mV. Notably, at a higher current density of 100 mA cm−2, the overpotentials for the HER and OER are only 339 and 365 mV. As a bifunctional electrocatalyst, its total splitting voltage was only 1.55 V. The catalysis performance remained nearly unchanged even after 48 h of stability testing. Finally, density functional theory (DFT) calculations revealed that the potential barriers in each reaction step of the OER are evenly distributed, and optimizing the Ni3S2 structure with iron and nickel atoms reduced the reaction energy barriers during the electrochemical process, improving the OER/HER performance.

Graphical abstract: Bimetallic atom-improved Ni3S2 bifunctional electrocatalysts for efficient hydrogen evolution reaction and overall water splitting performance

Supplementary files

Article information

Article type
Paper
Submitted
06 Jun 2024
Accepted
07 Jul 2024
First published
11 Jul 2024

CrystEngComm, 2024,26, 4478-4488

Bimetallic atom-improved Ni3S2 bifunctional electrocatalysts for efficient hydrogen evolution reaction and overall water splitting performance

J. Huang, L. Mu, Y. Ou, G. Zhao, J. Huang, X. Wang and B. Zhang, CrystEngComm, 2024, 26, 4478 DOI: 10.1039/D4CE00569D

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