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In situ electrochemical quantification of active sites in Fe–N/C non-precious metal catalysts

Author

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  • Daniel Malko

    (Imperial College London, South Kensington Campus)

  • Anthony Kucernak

    (Imperial College London, South Kensington Campus)

  • Thiago Lopes

    (Fuel Cells and Hydrogen Centre, Nuclear and Energy Research Institute, IPEN-CNEN/SP, Sao Paulo 05508-000, Brazil)

Abstract

The economic viability of low temperature fuel cells as clean energy devices is enhanced by the development of inexpensive oxygen reduction reaction catalysts. Heat treated iron and nitrogen containing carbon based materials (Fe–N/C) have shown potential to replace expensive precious metals. Although significant improvements have recently been made, their activity and durability is still unsatisfactory. The further development and a rational design of these materials has stalled due to the lack of an in situ methodology to easily probe and quantify the active site. Here we demonstrate a protocol that allows the quantification of active centres, which operate under acidic conditions, by means of nitrite adsorption followed by reductive stripping, and show direct correlation to the catalytic activity. The method is demonstrated for two differently prepared materials. This approach may allow researchers to easily assess the active site density and turnover frequency of Fe–N/C catalysts.

Suggested Citation

  • Daniel Malko & Anthony Kucernak & Thiago Lopes, 2016. "In situ electrochemical quantification of active sites in Fe–N/C non-precious metal catalysts," Nature Communications, Nature, vol. 7(1), pages 1-7, December.
  • Handle: RePEc:nat:natcom:v:7:y:2016:i:1:d:10.1038_ncomms13285
    DOI: 10.1038/ncomms13285
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    Citations

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    Cited by:

    1. Lopes, Thiago & Beruski, Otavio & Manthanwar, Amit M. & Korkischko, Ivan & Pugliesi, Reynaldo & Stanojev, Marco Antonio & Andrade, Marcos Leandro Garcia & Pistikopoulos, Efstratios N. & Perez, Joelma , 2019. "Spatially resolved oxygen reaction, water, and temperature distribution: Experimental results as a function of flow field and implications for polymer electrolyte fuel cell operation," Applied Energy, Elsevier, vol. 252(C), pages 1-1.
    2. Beltrán, Diana E. & Ding, Shuo & Xu, Hui & Wu, Gang & Litster, Shawn, 2023. "Air Contamination of Platinum-Group Metal-free Fuel Cell Cathodes with Atomically Dispersed Iron Active Sites," Applied Energy, Elsevier, vol. 349(C).
    3. Zhe Jiang & Xuerui Liu & Xiao-Zhi Liu & Shuang Huang & Ying Liu & Ze-Cheng Yao & Yun Zhang & Qing-Hua Zhang & Lin Gu & Li-Rong Zheng & Li Li & Jianan Zhang & Youjun Fan & Tang Tang & Zhongbin Zhuang &, 2023. "Interfacial assembly of binary atomic metal-Nx sites for high-performance energy devices," Nature Communications, Nature, vol. 14(1), pages 1-12, December.
    4. Lin, P.Z. & Sun, J. & He, C.X. & Wu, M.C. & Zhao, T.S., 2024. "Modeling proton exchange membrane fuel cells with platinum-group-metal-free catalysts," Applied Energy, Elsevier, vol. 360(C).
    5. Xin Wan & Qingtao Liu & Jieyuan Liu & Shiyuan Liu & Xiaofang Liu & Lirong Zheng & Jiaxiang Shang & Ronghai Yu & Jianglan Shui, 2022. "Iron atom–cluster interactions increase activity and improve durability in Fe–N–C fuel cells," Nature Communications, Nature, vol. 13(1), pages 1-11, December.
    6. Shuhu Yin & Hongyuan Yi & Mengli Liu & Jian Yang & Shuangli Yang & Bin-Wei Zhang & Long Chen & Xiaoyang Cheng & Huan Huang & Rui Huang & Yanxia Jiang & Honggang Liao & Shigang Sun, 2024. "An in situ exploration of how Fe/N/C oxygen reduction catalysts evolve during synthesis under pyrolytic conditions," Nature Communications, Nature, vol. 15(1), pages 1-9, December.
    7. Jie-Wei Chen & Zisheng Zhang & Hui-Min Yan & Guang-Jie Xia & Hao Cao & Yang-Gang Wang, 2022. "Pseudo-adsorption and long-range redox coupling during oxygen reduction reaction on single atom electrocatalyst," Nature Communications, Nature, vol. 13(1), pages 1-13, December.

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