Chinese Journal of Catalysis ›› 2026, Vol. 85: 182-192.DOI: 10.1016/S1872-2067(26)65010-3

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Nickel-based catalyst supported on porous carbon carrier with hydrophilic domains enables high-performance anion exchange membrane fuel cells

Pin Meng,1, Peichen Wang,1, Jiahe Yang,1, Yunlong Zhang, Hongda Shi, Xingyan Chen, Dingge Fan, Siyan Chen, Xi Lin, Dongdong Wang, Yang Yang(), Qianwang Chen()   

  1. Hefei National Research Center for Physical Sciences at the Microscale, Department of Materials Science and Engineering, University of Science and Technology of China, Hefei 230026, Anhui, China
  • Received:2025-09-06 Accepted:2025-10-30 Online:2026-06-18 Published:2026-05-18
  • Contact: *E-mail: cqw@ustc.edu.cn (Q. Chen),
    yangyang1991@ustc.edu.cn (Y. Yang).
  • About author:

    1Contributed equally to this work.

  • Supported by:
    National Key R&D Program of China(2021YFA1600202);National Natural Science Foundation(22272155);National Natural Science Foundation(22479135);Fundamental Research Funds for the Central Universities(WK9990000168)

Abstract:

Nickel (Ni)-based catalysts are the most promising platinum (Pt)-free anode hydrogen oxidation reaction (HOR) catalysts in anion exchange membrane fuel cells (AEMFCs). However, the limited reactivity of Ni in alkaline HOR presents a significant barrier to the commercialization of AEMFCs, due to both thermodynamic and kinetic constraints. Here, we employ zinc single atoms (Zn-SAs) modified porous carbon support to create microscopic hydrophilic domains aimed at optimizing electrode kinetics. We found that the doping of Zn-N species could manipulate the electron transfer between Ni and carbon support, which causes a drastically diminished adsorption of hydrogen on Ni, thus boosting the alkaline HOR activity from a thermodynamic perspective. Spectral and electrochemical data reveal that Zn sites facilitate hydroxide transfer at the Ni/Zn1-NC interface by improving hydrogen bond network connectivity. These enhancement enables the Ni/Zn1-NC AEMFC to deliver a peak power density of 678 mW cm-2, surpassing even a low loading of commercial Pt/C. This work illustrates the potential for high efficiency in platinum-group metal-free AEMFCs.

Key words: Hydroxide transfer, Hydrogen binding energy, Anion exchange membrane fuel cells, Hydrogen oxidation reaction