Spin-Dependent Oxygen Reduction Electrocatalysis Is Suppressed by Electron-Withdrawing Substitution in Perfluorinated Iron Phthalocyanine

The oxygen reduction reaction (ORR) plays a key role in energy conversion systems. Perfluorinated iron phthalocyanine (16(F)FePc), a member of the MN 4 molecular catalyst family, has been reported to exhibit enhanced ORR activity compared to unsubstituted iron phthalocyanine (FePc). This is attributed to fluorine-induced electron-withdrawing effects that decrease the electron-density of the FeN 4 active site. On the other hand, because O 2 is paramagnetic, the electron spin is a relevant factor in ORR electrocatalysis through chirality-induced spin selectivity (CISS). In this work, the interplay between inductive electron-withdrawing effects and CISS-driven electrocatalysis was studied in self-assembled electrode systems based on FePc and 16(F)FePc. The molecular catalysts were immobilized on polycrystalline gold (Au _Poly ) and Au(111) substrates using l - and d -methionine as chiral linkers, which act as spin filters. Single-molecule conductance of l - and d -methionine was further evaluated by spin-polarized scanning tunneling microscope break-junction (SP-STM-BJ) measurements to assess chirality-dependent electron transport. ORR activity was examined using a rotating ring−disk electrode configuration to determine the total number of electrons transferred and H 2 O 2 yield. The ORR behavior of FePc and 16(F)FePc assembled on methionine reveals the interplay between CISS and inductive electron-withdrawing effects. FePc shows chirality-dependent electroactivity, favoring the four-electron pathway. In contrast, 16(F)FePc exhibits negligible chirality dependence for ORR, indicating that the strong electron-withdrawing effect of fluorine substituents on the Fe center dominates the reduction process. These results demonstrate that inductive substituent effects can override spin-dependent electrocatalysis, providing insight into the design of molecular catalysts in which CISS contributions are modulated or suppressed.

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Journal
ACS Catalysis
Published
2026-06-30
DOI
https://doi.org/10.1021/acscatal.6c02633
Primary Topic
Electrocatalysts for Energy Conversion
Type
article
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article

Spin-Dependent Oxygen Reduction Electrocatalysis Is Suppressed by Electron-Withdrawing Substitution in Perfluorinated Iron Phthalocyanine

Ingrid Ponce, Ana María Méndez‐Torres, José H. Zagal, Rubén Oñate et al.
ACS Catalysis
Electrocatalysts for Energy Conversion
article

Spin-Dependent Oxygen Reduction Electrocatalysis Is Suppressed by Electron-Withdrawing Substitution in Perfluorinated Iron Phthalocyanine

Ingrid Ponce, Ana María Méndez‐Torres, José H. Zagal, Rubén Oñate, Alexis Aspée, Nadim Darwish, Nayareth Vilches‐Labbé, Luis Acuña-Saavedra, Laura Scarpetta-Pizo, Manuel Esteban Díaz-Pérez, Natalia Yupanqui-Mondino, Javier Ponce-Vergara
article en

Abstract

The oxygen reduction reaction (ORR) plays a key role in energy conversion systems. Perfluorinated iron phthalocyanine (16(F)FePc), a member of the MN 4 molecular catalyst family, has been reported to exhibit enhanced ORR activity compared to unsubstituted iron phthalocyanine (FePc). This is attributed to fluorine-induced electron-withdrawing effects that decrease the electron-density of the FeN 4 active site. On the other hand, because O 2 is paramagnetic, the electron spin is a relevant factor in ORR electrocatalysis through chirality-induced spin selectivity (CISS). In this work, the interplay between inductive electron-withdrawing effects and CISS-driven electrocatalysis was studied in self-assembled electrode systems based on FePc and 16(F)FePc. The molecular catalysts were immobilized on polycrystalline gold (Au _Poly ) and Au(111) substrates using l - and d -methionine as chiral linkers, which act as spin filters. Single-molecule conductance of l - and d -methionine was further evaluated by spin-polarized scanning tunneling microscope break-junction (SP-STM-BJ) measurements to assess chirality-dependent electron transport. ORR activity was examined using a rotating ring−disk electrode configuration to determine the total number of electrons transferred and H 2 O 2 yield. The ORR behavior of FePc and 16(F)FePc assembled on methionine reveals the interplay between CISS and inductive electron-withdrawing effects. FePc shows chirality-dependent electroactivity, favoring the four-electron pathway. In contrast, 16(F)FePc exhibits negligible chirality dependence for ORR, indicating that the strong electron-withdrawing effect of fluorine substituents on the Fe center dominates the reduction process. These results demonstrate that inductive substituent effects can override spin-dependent electrocatalysis, providing insight into the design of molecular catalysts in which CISS contributions are modulated or suppressed.

ACS Catalysis
Universidad de Santiago de Chile (CL), Curtin University (AU), Universidad Bernardo O'Higgins (CL), Universidad Central de Chile (CL)
Agencia Nacional de Investigación y Desarrollo, Fondo Nacional de Desarrollo Científico y Tecnológico
Clean water and sanitation
Openalex Percentile: Top 21%
Electrocatalysts for Energy Conversion
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