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Ultrathin Ni–Fe MOF nanosheets: efficient and durable water oxidation at high current densities

journal contribution
posted on 2024-07-24, 14:51 authored by Xin Zhao, Yang Yang, Yue Liu, JunYu Shi, Qiaoxia Li, Qunjie Xu, Wen-Feng LinWen-Feng Lin

Efficient, durable, and economical electrocatalysts are crucial for advancing energy technology by facilitating the oxygen evolution reaction (OER). Here, ultrathin Ni-Fe metal-organic skeleton (MOF) nanosheets were in situ created on nickel foam (NiFe-UMNs/NF).
The catalyst exhibited excellent OER catalytical abilities, with only 269 mV overpotentials at
250 mA cm -2. Besides, when integrated with Pt/C/NF, NiFe-UMNs/NF held the potential for
application in industrial alkaline water electrolysis with initial voltage retention of approximately
86% following a continuous operation of 100 h at a current density of 250 mA cm -2 . The super
performance of the NiFe-UMNs/NF catalyst is attributed to ultra-thin morphology, super
hydrophilicity, and synergistic effects between Ni and Fe within the MOF. In situ Raman showed
that NiFe-UMNs were converted to NiFeOOH as the active species in the OER process. Density
Functional Theory (DFT) revealed that iron doping accelerated the rate-determining step and
reduced the OER reaction energy barrier. This work elucidated a promising electrocatalyst for
OER and enriched the practical implementation of MOF materials.

Funding

Sustainable Hydrogen Production from Seawater Electrolysis : EP/W03784X/1

History

School

  • Aeronautical, Automotive, Chemical and Materials Engineering

Published in

Langmuir

Volume

40

Issue

25

Pages

13122 - 13133

Publisher

American Chemical Society (ACS)

Version

  • AM (Accepted Manuscript)

Rights holder

© American Chemical Society

Publisher statement

This document is the Accepted Manuscript version of a Published Work that appeared in final form in Langmuir (© American Chemical Society) after peer review and technical editing by the publisher. To access the final edited and published work see: https://pubs.acs.org/doi/10.1021/acs.langmuir.4c01065.

Acceptance date

2024-06-04

Publication date

2024-06-13

Copyright date

2024

ISSN

0743-7463

eISSN

1520-5827

Language

  • en

Depositor

Prof Wen Feng Lin. Deposit date: 25 June 2024

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