Issue 43, 2024

Ce-doped nanorod-like NiFe-MOF with coordination substitution based on in situ co-doping method for boosting the oxygen evolution reaction

Abstract

Heteroatom-doped metal–organic frameworks (MOFs) have been widely used in OER catalysis. However, the effects of doping methods on these materials have rarely been reported. Herein, the structure and activity of Ce-doped nanorod-like MOFs (CeNi1.6Fe-MIL-53 and Ce@Ni1.6Fe-MIL-53) prepared by employing in situ co-doping and surface doping methods were analyzed. The structure of Ni1.6Fe-MIL-53 can be optimized at different levels by different Ce-introduction ways. In contrast, the in situ co-doping of Ce increases the number of active sites and better optimizes the band structure. Therefore, CeNi1.6Fe-MIL-53 exhibited good OER activity, which required an overpotential of only 277 mV at a current density of 10 mA cm−2, a Tafel slope of 31.03 mV dec−1 and a good stability maintained for 60 h. Moreover, when CeNi1.6Fe-MIL-53 was coupled as an electrolytic cell, the cell showed a low cell potential (1.54 V at 10 mA cm−2) and good stability (maintained for 33 h).

Graphical abstract: Ce-doped nanorod-like NiFe-MOF with coordination substitution based on in situ co-doping method for boosting the oxygen evolution reaction

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Article information

Article type
Paper
Submitted
06 Jun 2024
Accepted
29 Sep 2024
First published
30 Sep 2024

J. Mater. Chem. A, 2024,12, 29886-29897

Ce-doped nanorod-like NiFe-MOF with coordination substitution based on in situ co-doping method for boosting the oxygen evolution reaction

X. Wei, S. Yu, J. Li, T. Liu, S. Li, S. Hata, Z. Wu, Y. Shiraishi and Y. Du, J. Mater. Chem. A, 2024, 12, 29886 DOI: 10.1039/D4TA03929G

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