Issue 22, 2023, Issue in Progress

Constructing interface engineering and tailoring a nanoflower-like FeP/CoP heterostructure for enhanced oxygen evolution reaction

Abstract

The inexpensive and highly efficient electrocatalysts toward oxygen evolution reaction (OER) in water splitting electrolysis have displayed promising practical applications to relieve energy crisis. Herein, we prepared a high-yield and structurally regulated bimetallic cobalt-iron phosphide electrocatalyst by a facile one-pot hydrothermal reaction and subsequent low-temperature phosphating treatment. The tailoring of nanoscale morphology was achieved by varying the input ratio and phosphating temperature. Thus, an optimized FeP/CoP-1-350 sample with the ultra-thin nanosheets assembled into a nanoflower-like structure was obtained. FeP/CoP-1-350 heterostructure displayed remarkable activity toward the OER with a low overpotential of 276 mV at a current density of 10 mA cm−2, and a low Tafel slope of only 37.71 mV dec−1. Long-lasting durability and stability were maintained with the current with almost no obvious fluctuation. The enhanced OER activity was attributed to the presence of copious active sites from the ultra-thin nanosheets, the interface between CoP and FeP components, and the synergistic effect of Fe–Co elements in the FeP/CoP heterostructure. This study provides a feasible strategy to fabricate highly efficient and cost-effective bimetallic phosphide electrocatalysts.

Graphical abstract: Constructing interface engineering and tailoring a nanoflower-like FeP/CoP heterostructure for enhanced oxygen evolution reaction

Supplementary files

Article information

Article type
Paper
Submitted
17 Feb 2023
Accepted
02 May 2023
First published
16 May 2023
This article is Open Access
Creative Commons BY license

RSC Adv., 2023,13, 15031-15040

Constructing interface engineering and tailoring a nanoflower-like FeP/CoP heterostructure for enhanced oxygen evolution reaction

L. Wang, H. Yang, L. Wang, Y. Li, W. Yang, X. Sun, L. Gao, M. Dou, D. Li and J. Dou, RSC Adv., 2023, 13, 15031 DOI: 10.1039/D3RA01096A

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