Issue 28, 2024

Modulating the electronic structure of Ru using a self-reconstructed MOF-NiFeOOH heterointerface for improved electrocatalytic water splitting

Abstract

Constructing efficient and stable electrocatalysts via electrochemical self-reconstruction is an effective strategy to achieve hydrogen evolution. Herein, as predicted by DFT, the construction of the MOF-NiFeOOH heterointerface can effectively regulate the electronic environment of Ru and the adsorption energy of hydrogen and water. Accordingly, a sandwich-like RuNiFe-MOF/NFF electrode was fabricated on a nickel–iron foam (NFF) using subsequent immersion and solvothermal methods. Through electrochemical self-reconstruction, the NiFe site underwent oxidation to a hypervalent state, forming a MOF-NiFeOOH heterojunction. The resulting Ru10NiFeOOH-MOF/NFF exhibited an overpotential of 15 mV@10 mA cm−2 for the hydrogen evolution reaction (HER) and could be stabilized for 100 h. Moreover, when combined with NiFeOOH-MOF/NFF as the anode, the constructed cell demonstrated a low voltage of 1.51 V@10 mA cm−2 and long-term durability. The outstanding efficiency of Ru10NiFeOOH-MOF/NFF can be credited to its intrinsic activity, the in situ reconstruction of the MOF, and the rearrangement of charges surrounding the active sites. This work makes a lot of sense for the design and understanding of the self-reconstruction and performance improvement mechanism of MOF-based electrodes.

Graphical abstract: Modulating the electronic structure of Ru using a self-reconstructed MOF-NiFeOOH heterointerface for improved electrocatalytic water splitting

Supplementary files

Article information

Article type
Paper
Submitted
14 Apr 2024
Accepted
04 Jun 2024
First published
04 Jun 2024

J. Mater. Chem. A, 2024,12, 17404-17412

Modulating the electronic structure of Ru using a self-reconstructed MOF-NiFeOOH heterointerface for improved electrocatalytic water splitting

Y. Guan, T. Liu, Y. Wu, C. Yang, B. Liu, B. Hu, W. Jiang, C. Liu and G. Che, J. Mater. Chem. A, 2024, 12, 17404 DOI: 10.1039/D4TA02569E

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