Ferrocene unit substitution in nickel(<scp>ii</scp>) porphyrin(2.1.2.1) induces an extremely low oxygen evolution reaction overpotential

This study reports the synthesis, characterization, structure and the oxygen evolution reaction (OER) performance of ferrocene-substituted nickel(II) porphyrin(2.1.2.1) complexes. The Ni-3 complex, functionalized with two ferrocene units, demonstrates exceptional OER activity, achieving an overpotential of 280 mV at 10 mA cm<sup>-2</sup> in alkaline media. This enhancement is ascribed to the electron-rich ferrocene moieties, which act as efficient electron-transfer mediators during catalysis. DFT calculations corroborate these findings, revealing a theoretical overpotential of 0.79 eV for the dual-ferrocene-substituted catalyst. These results underscore the critical role of ferrocene in lowering the overpotential of molecular OER catalysts.

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Publication Details

Journal
Dalton Transactions
Published
2025-01-01
DOI
https://doi.org/10.1039/d5dt00580a
Citations
7
Primary Topic
Electrocatalysts for Energy Conversion
Type
article
Field-Weighted Citation Impact
2.54
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article

Ferrocene unit substitution in nickel(ii) porphyrin(2.1.2.1) induces an extremely low oxygen evolution reaction overpotential

Liang Shen, Fengxian Qiu, Hongliang Huang, Songlin Xue et al.
7 citations
Dalton Transactions
Electrocatalysts for Energy Conversion
2.54
article

Ferrocene unit substitution in nickel(ii) porphyrin(2.1.2.1) induces an extremely low oxygen evolution reaction overpotential

Liang Shen, Fengxian Qiu, Hongliang Huang, Songlin Xue, Tao Jiang, Yiping Hu, Mingbo Zhou
article en
7 citations

Abstract

This study reports the synthesis, characterization, structure and the oxygen evolution reaction (OER) performance of ferrocene-substituted nickel(II) porphyrin(2.1.2.1) complexes. The Ni-3 complex, functionalized with two ferrocene units, demonstrates exceptional OER activity, achieving an overpotential of 280 mV at 10 mA cm<sup>-2</sup> in alkaline media. This enhancement is ascribed to the electron-rich ferrocene moieties, which act as efficient electron-transfer mediators during catalysis. DFT calculations corroborate these findings, revealing a theoretical overpotential of 0.79 eV for the dual-ferrocene-substituted catalyst. These results underscore the critical role of ferrocene in lowering the overpotential of molecular OER catalysts.

Dalton TransactionsVol. 54(21)
Jiangsu University (CN), Southwest Petroleum University (CN), Hunan Normal University (CN), Tiangong University (CN)
Openalex Percentile: Top 11%
Electrocatalysts for Energy Conversion
2.54
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