Early View e202504869
Research Article

Ferromagnetic Ordering Outperforms Coordination Effects in Governing Oxygen Reduction Catalysis on High-Index Nickel Single Crystals

Menglong Sun

Menglong Sun

Key Laboratory of Photochemistry, Institute of Chemistry, Chinese Academy of Sciences, Beijing, 100190 P.R. China

University of Chinese Academy of Sciences, Beijing, 100049 P.R. China

Both authors contributed equally to this work.

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Jiabin Chen

Jiabin Chen

Institute of Molecular Engineering Plus, College of Chemistry, Fuzhou University, Fuzhou, 350108 P.R. China

Both authors contributed equally to this work.

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Zhibin Zhang

Zhibin Zhang

State Key Laboratory for Mesoscopic Physics, Frontiers Science Center for Nano-optoelectronics, School of Physics, Peking University, Beijing, P.R. China

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Yuan Jing

Yuan Jing

Key Laboratory of Photochemistry, Institute of Chemistry, Chinese Academy of Sciences, Beijing, 100190 P.R. China

University of Chinese Academy of Sciences, Beijing, 100049 P.R. China

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Mengze Zhao

Mengze Zhao

State Key Laboratory for Mesoscopic Physics, Frontiers Science Center for Nano-optoelectronics, School of Physics, Peking University, Beijing, P.R. China

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Lili Chen

Lili Chen

Key Laboratory of Photochemistry, Institute of Chemistry, Chinese Academy of Sciences, Beijing, 100190 P.R. China

University of Chinese Academy of Sciences, Beijing, 100049 P.R. China

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Prof. Kaihui Liu

Prof. Kaihui Liu

State Key Laboratory for Mesoscopic Physics, Frontiers Science Center for Nano-optoelectronics, School of Physics, Peking University, Beijing, P.R. China

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Prof. Chuang Zhang

Corresponding Author

Prof. Chuang Zhang

Key Laboratory of Photochemistry, Institute of Chemistry, Chinese Academy of Sciences, Beijing, 100190 P.R. China

University of Chinese Academy of Sciences, Beijing, 100049 P.R. China

E-mail: [email protected]; [email protected]; [email protected]

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Prof. Xi Wang

Corresponding Author

Prof. Xi Wang

Key Laboratory of Luminescence and Optical Information, Ministry of Education, School of Physical Science and Engineering, Beijing Jiaotong University, No. 3 Shangyuancun Haidian District, Beijing, 100044 China

E-mail: [email protected]; [email protected]; [email protected]

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Prof. Jiannian Yao

Corresponding Author

Prof. Jiannian Yao

Key Laboratory of Photochemistry, Institute of Chemistry, Chinese Academy of Sciences, Beijing, 100190 P.R. China

University of Chinese Academy of Sciences, Beijing, 100049 P.R. China

Institute of Molecular Engineering Plus, College of Chemistry, Fuzhou University, Fuzhou, 350108 P.R. China

E-mail: [email protected]; [email protected]; [email protected]

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First published: 23 April 2025

Graphical Abstract

Our study explored the link between ferromagnetic ordering, coordination number, and ORR activity in nickel single-crystal foils. We found that Ni (210) facets outperform Ni (310) and Ni (520) due to higher saturation magnetization and optimized d-band positioning. DFT calculations confirmed that ferromagnetic ordering, not surface coordination, drives catalytic performance by enhancing spin polarization and lowering energy barriers. External magnetic fields further boosted the activity of Ni foils.

Abstract

The role of surface spin configuration in spin-dependent catalytic reactions remains contentious, particularly when compared to the established dominance of coordination environments. Here, we resolve this debate by systematically probing oxygen reduction reaction (ORR) mechanisms on high-index Ni single-crystal facets ([210], [310], [520]) through integrated density functional theory (DFT) and experimental studies. Contrary to conventional d-band center predictions, we demonstrate that ferromagnetic ordering fundamentally dictates catalytic activity by stabilizing triplet O2 adsorption and lowering spin-forbidden transition barriers. The Ni (210) facet exhibits superior ORR performance (half-wave potential: 0.842 V vs. RHE), outperforming Ni (310) and Ni (520) due to its optimized d-band center and enhanced saturation magnetization. External magnetic fields amplify this effect, yielding a 28% current density enhancement for Ni (210)—nearly triple that of Ni (520). Spin-polarized DFT calculations reveal that ferromagnetic ordering reduces the potential-determining step energy barrier for *OH desorption by 7.0%, overriding coordination-number effects. These findings establish ferromagnetic alignment as a critical design criterion for spin-engineered electrocatalysts, offering a paradigm shift from coordination-centric optimization to spin-polarized interface engineering.

Conflict of Interests

The authors declare no conflict of interest.

Data Availability Statement

The data that support the findings of this study are available in the supplementary material of this article.

The full text of this article hosted at iucr.org is unavailable due to technical difficulties.