Issue 8, 2023

Building dual-phased Ni2P–Ni2P4O12 electrocatalysts for efficient urea oxidation reaction

Abstract

The development of highly efficient electrocatalysts for urea oxidation reaction (UOR) is crucial for reproducible and clean energy technologies. Herein, dual-phased nickel-based cost-effective catalyst nickel phosphide (Ni2P)-nickel metaphosphate (Ni2P4O12) microspheric nanoparticles were fabricated through a two-step hydrothermal-phosphorization process by preciously controlling the feeding ratios of the Ni precursor and the P source. It merely needs a potential of 1.35 V vs. RHE to deliver a current density of 10 mA cm−2 with a small Tafel slop of 55 mV dec−1 and maintains high catalytic activity for 10 h in 1.0 M KOH with 0.33 M urea solution. The synergy effect and modulation of the electronic structure between Ni2P and Ni2P4O12 could be the reason for the good UOR performance. This work provides a new perspective for the further design of high-performance electrocatalysts in diverse energy fields.

Graphical abstract: Building dual-phased Ni2P–Ni2P4O12 electrocatalysts for efficient urea oxidation reaction

Supplementary files

Article information

Article type
Paper
Submitted
26 Dec 2022
Accepted
17 Jan 2023
First published
17 Jan 2023

New J. Chem., 2023,47, 4009-4017

Building dual-phased Ni2P–Ni2P4O12 electrocatalysts for efficient urea oxidation reaction

J. Zhou, X. Sun, W. Tan, Q. Cao, Y. Zhao, R. Ding, Y. Zhang, E. Liu and P. Gao, New J. Chem., 2023, 47, 4009 DOI: 10.1039/D2NJ06299B

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