Bi-doped ruthenium oxide nanocrystal for water oxidation in acidic media

Abstract

There is an urgent need to develop a cost-effective and highly efficient acidic OER catalyst to support the progress of proton exchange membrane water electrolysis technology. Ruthenium-based catalysts, which possess high activity and significantly lower cost compared to iridium-based catalysts, emerge as competitive candidates. However, their suboptimal stability constrains the wide application of RuO2. Herein, we develop ultra-small Bi0.05Ru0.95O2 nanocrystal with diameter of approximately 6.5 ± 0.1 nm for acidic OER. The Bi0.05Ru0.95O2 nanocrystal electrocatalyst exhibits a low overpotential of 203.5 mV at 10 mA cm−2 and 300+ hour stability at a high water-splitting current density of 100 mA cm−2 in 0.5 M H2SO4 with a low decay rate of 0.44 mV h−1. Density functional theory (DFT) calculation results confirmed the adsorbate evolving mechanism (AEM) occurring on Bi0.05Ru0.95O2, which prevents lattice oxygen from participating in the reaction, thus avoiding the collapse of the structure. We proved that the Bi dopants could play a crucial role in not only reducing the energy barrier of the potential-determining step, but also delivering electrons to Ru sites, thereby alleviating the over-oxidation of Ru active sites and enhancing operation durability.

Graphical abstract: Bi-doped ruthenium oxide nanocrystal for water oxidation in acidic media

Supplementary files

Article information

Article type
Paper
Submitted
02 Jūl. 2024
Accepted
14 Okt. 2024
First published
14 Okt. 2024

Nanoscale, 2024, Advance Article

Bi-doped ruthenium oxide nanocrystal for water oxidation in acidic media

S. Chen, H. Liu, B. Yuan, W. Xu, A. Cao, M. G. Sendeku, Y. Li, X. Sun and F. Wang, Nanoscale, 2024, Advance Article , DOI: 10.1039/D4NR02745K

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