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Authors

Lin Lin, State Key Laboratory of Precision and Intelligent Chemistry, University of Science and Technology of China, Hefei 230026, China; School of Chemistry and Materials Science, University of Science and Technology of China, Hefei 230026, China
Xiu-Xuan Hou, State Key Laboratory of Rare Earth Resource Utilization, Changchun Institute of Applied Chemistry Chinese Academy of Sciences, Changchun 130022, China
Zhe-Chen Fan, State Key Laboratory of Precision and Intelligent Chemistry, University of Science and Technology of China, Hefei 230026, China; School of Chemistry and Materials Science, University of Science and Technology of China, Hefei 230026, China
Yi-Xuan Yin, State Key Laboratory of Precision and Intelligent Chemistry, University of Science and Technology of China, Hefei 230026, China; School of Chemistry and Materials Science, University of Science and Technology of China, Hefei 230026, China
Wei-Yi Zhao, State Key Laboratory of Precision and Intelligent Chemistry, University of Science and Technology of China, Hefei 230026, China; School of Chemistry and Materials Science, University of Science and Technology of China, Hefei 230026, China
Kai Wei, State Key Laboratory of Precision and Intelligent Chemistry, University of Science and Technology of China, Hefei 230026, China; School of Chemistry and Materials Science, University of Science and Technology of China, Hefei 230026, China
Yu-Die Zhou, State Key Laboratory of Precision and Intelligent Chemistry, University of Science and Technology of China, Hefei 230026, China; School of Chemistry and Materials Science, University of Science and Technology of China, Hefei 230026, China
Li-Na Hou, State Key Laboratory of Precision and Intelligent Chemistry, University of Science and Technology of China, Hefei 230026, China; School of Chemistry and Materials Science, University of Science and Technology of China, Hefei 230026, China
Ying Wang, State Key Laboratory of Rare Earth Resource Utilization, Changchun Institute of Applied Chemistry Chinese Academy of Sciences, Changchun 130022, ChinaFollow
Hao Wan, State Key Laboratory of Precision and Intelligent Chemistry, University of Science and Technology of China, Hefei 230026, China; School of Chemistry and Materials Science, University of Science and Technology of China, Hefei 230026, ChinaFollow
Jun-Jie Ge, State Key Laboratory of Precision and Intelligent Chemistry, University of Science and Technology of China, Hefei 230026, China; School of Chemistry and Materials Science, University of Science and Technology of China, Hefei 230026, ChinaFollow

Corresponding Author

Ying Wang (ywang_2012@ciac.ac.cn);
Hao Wan (wh1992@mail.ustc.edu.cn);
Jun-Jie Ge (gejunjie@ustc.edu.cn)

Abstract

Fe-N-C catalysts have long suffered from kinetically sluggish oxygen reduction reaction (ORR) due to excessive adsorption strength toward oxygen intermediates and low site utilization. Heteroatom doping effectively accelerates ORR reaction kinetics through electronic structure modulation of metal sites for optimal intermediate adsorption, while chemical vapor deposition (CVD) enhances the turnover frequency (TOF) of active sites. Herein, we developed an FeSNC catalyst featuring abundant FeS1N4 sites via a dual-precursor CVD strategy. Experimental and theoretical analyses revealed that S incorporation disrupts the symmetric coordination of active sites, which optimizes OH* adsorption energies from 0.212 eV to 1.194 eV. Moreover, the TOF increased from 1.98 e–1·site–1·s–1 to 6.32 e–1·site–1·s–1, significantly enhancing the intrinsic activity of the catalyst. More notably, the hydrophilic character of S-containing species substantially improved hydrophilicity in the S-doped catalyst, thereby promoting mass transport of oxygen and proton delivery. As a result, the FeSNC catalyst exhibited an extremely high half-wave potential of 0.863 V in 0.1 mol·L–1 HClO4 and achieved a peak power density of 1.2 W·cm–2 in H2-O2 PEMFCs. This work highlights the critical role of coordination engineering.

Graphical Abstract

Keywords

Oxygen reduction reaction, Fe-N-C, Heteroatom doping, Electronic regulation, Mass transport

Creative Commons License

Creative Commons Attribution 4.0 International License
This work is licensed under a Creative Commons Attribution 4.0 International License.

Publication Date

2026-03-28

Online Available Date

2025-11-05

Revised Date

2025-10-27

Received Date

2025-09-28

JOE2509281- Supporting Information.pdf (1844 kB)
Axial Sulfur-Coordination Engineering Boosting Fe–N–C Catalysts for High-Performance Proton Exchange Membrane Fuel Cells - Supporting Information

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