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Preparation and functionalization of free-standing nitrogen-doped carbon-based catalyst electrodes for electrocatalytic N2 fixation

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Qin,  Qing
Martin Oschatz, Kolloidchemie, Max Planck Institute of Colloids and Interfaces, Max Planck Society;

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Brandi,  Francesco
Majd Al-Naji, Kolloidchemie, Max Planck Institute of Colloids and Interfaces, Max Planck Society;

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Badamdorj,  Bolortuya
Nadezda V. Tarakina, Kolloidchemie, Max Planck Institute of Colloids and Interfaces, Max Planck Society;

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Oschatz,  Martin
Martin Oschatz, Kolloidchemie, Max Planck Institute of Colloids and Interfaces, Max Planck Society;

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Al-Naji,  Majd
Majd Al-Naji, Kolloidchemie, Max Planck Institute of Colloids and Interfaces, Max Planck Society;

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Citation

Qin, Q., Brandi, F., Badamdorj, B., Oschatz, M., & Al-Naji, M. (2021). Preparation and functionalization of free-standing nitrogen-doped carbon-based catalyst electrodes for electrocatalytic N2 fixation. Molecular Catalysis, 515: 111935. doi:10.1016/j.mcat.2021.111935.


Cite as: https://hdl.handle.net/21.11116/0000-0009-6237-B
Abstract
Nitrogen-doped carbon-based materials have been recently explored as promising electrocatalysts for N2 fixation. Herein, a nitrogen-doped carbon film as a self-standing electrode is synthesized through a novel and scalable strategy. After the film synthesis, a thin layer of Au nanoparticles is deposited, significantly enhancing the performance of such films in electrocatalytic N2 reduction. Owing to the exposed active sites and unique free-standing structure, it shows desirable performance towards electrochemical N2 fixation with a high Faradaic efficiency of 6.4 %, and a NH3 production rate of 18.3 μg h−1 cm−2 at a low given potential of -0.05 V vs. reversible hydrogen electrode. Such performance is superior in comparison with Au-nanoparticles-modified nitrogen-doped carbon powder. Further comparison of nitrogen-doped carbon film and nitrogen-doped carbon powder also demonstrates the benefits of the free-standing structure in comparison to film-based materials in terms of charge transfer and active sites per electrode surface area.