Issue 38, 2025

Electronic tailoring of Ni–NbB2 nanorods via molten salt synthesis for high-efficiency alkaline hydrogen evolution

Abstract

The design of efficient and durable electrocatalysts for enhancing the kinetics of the hydrogen evolution reaction (HER) in alkaline water electrolysis is a significant challenge. Borides have attracted extensive attention due to their excellent corrosion resistance and unique structures. In this study, NbB2 was synthesized by the molten salt method, and then a metal nickel source was incorporated into the synthesized NbB2 to prepare a nickel-doped NbB2 electrocatalyst (Ni–NbB2) with a nanorod structure. Notably, Ni–NbB2 exhibited an overpotential of only 239 mV at a current density of 10 mA cm−2, significantly lower than that of pure NbB2 (562 mV), and also demonstrated long-term stability. The doping of metal nickel regulated the electronic structure of the metal Nb on the catalyst surface, accelerating the kinetics of the HER reaction. Moreover, the doping of Ni increased the number of catalytic active sites, promoting the full contact between the electrolyte and the catalytic reaction sites and accelerating the charge transfer rate. These findings open up new possibilities for enhancing the HER catalytic activity of metal borides through the strategy of heterometal doping.

Graphical abstract: Electronic tailoring of Ni–NbB2 nanorods via molten salt synthesis for high-efficiency alkaline hydrogen evolution

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
22 Jul 2025
Accepted
08 Sep 2025
First published
12 Sep 2025

New J. Chem., 2025,49, 16828-16834

Electronic tailoring of Ni–NbB2 nanorods via molten salt synthesis for high-efficiency alkaline hydrogen evolution

Y. Sun, B. Li, J. Lang, G. Che, Y. Wu and M. Shang, New J. Chem., 2025, 49, 16828 DOI: 10.1039/D5NJ02968F

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