Issue 39, 2025

Low-temperature phosphidation synthesis of flower-like Ru-CoVO-P polymetallic catalyst for enhanced overall water splitting in alkaline seawater

Abstract

Developing efficient and stable bifunctional electrocatalysts for overall water splitting, especially in practical electrolytes such as seawater, remains a significant challenge in the field of energy conversion. Herein, we report the successful synthesis of a three-dimensional, flower-like polymetallic phosphide electrocatalyst (Ru-CoVO-P), constructed from self-assembled ultrathin nanosheets, via a facile hydrothermal method combined with a low-temperature phosphidation strategy. The catalyst exhibits excellent bifunctional activity in 1 M KOH, requiring overpotentials of only 88.7 mV (HER) and 248.3 mV (OER) to achieve 10 mA cm−2. After 240 hours of cycling in a two-electrode system, a cell voltage of only 1.753 V is required to achieve a current density of 50 mA cm−2. More importantly, the catalyst maintains excellent performance in 1 M KOH containing seawater, demonstrating outstanding stability and great application potential. The superior performance stems from the electronic structure modulation among the polymetallic components, as well as the abundant active sites and efficient mass transport capabilities provided by the hierarchical structure. This work provides a facile and effective synthesis strategy for developing advanced polymetallic phosphide catalysts suitable for practical seawater electrolysis.

Graphical abstract: Low-temperature phosphidation synthesis of flower-like Ru-CoVO-P polymetallic catalyst for enhanced overall water splitting in alkaline seawater

Supplementary files

Article information

Article type
Paper
Submitted
11 Jul 2025
Accepted
04 Sep 2025
First published
10 Sep 2025
This article is Open Access
Creative Commons BY-NC license

RSC Adv., 2025,15, 32732-32745

Low-temperature phosphidation synthesis of flower-like Ru-CoVO-P polymetallic catalyst for enhanced overall water splitting in alkaline seawater

Y. Tian, Y. Yang, D. Zhong, S. Zhang, B. Zhang, X. Li, H. Zhou, R. Zhao and L. Miao, RSC Adv., 2025, 15, 32732 DOI: 10.1039/D5RA04957A

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