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Long-term continuous ammonia electrosynthesis

Author

Listed:
  • Shaofeng Li

    (Technical University of Denmark)

  • Yuanyuan Zhou

    (Technical University of Denmark)

  • Xianbiao Fu

    (Technical University of Denmark)

  • Jakob B. Pedersen

    (Technical University of Denmark)

  • Mattia Saccoccio

    (Technical University of Denmark)

  • Suzanne Z. Andersen

    (Technical University of Denmark)

  • Kasper Enemark-Rasmussen

    (Technical University of Denmark)

  • Paul J. Kempen

    (Technical University of Denmark)

  • Christian Danvad Damsgaard

    (Technical University of Denmark
    Technical University of Denmark)

  • Aoni Xu

    (Technical University of Denmark)

  • Rokas Sažinas

    (Technical University of Denmark)

  • Jon Bjarke Valbæk Mygind

    (Technical University of Denmark)

  • Niklas H. Deissler

    (Technical University of Denmark)

  • Jakob Kibsgaard

    (Technical University of Denmark)

  • Peter C. K. Vesborg

    (Technical University of Denmark)

  • Jens K. Nørskov

    (Technical University of Denmark)

  • Ib Chorkendorff

    (Technical University of Denmark)

Abstract

Ammonia is crucial as a fertilizer and in the chemical industry and is considered to be a carbon-free fuel1. Ammonia electrosynthesis from nitrogen under ambient conditions offers an attractive alternative to the Haber–Bosch process2,3, and lithium-mediated nitrogen reduction represents a promising approach to continuous-flow ammonia electrosynthesis, coupling nitrogen reduction with hydrogen oxidation4. However, tetrahydrofuran, which is commonly used as a solvent, impedes long-term ammonia production owing to polymerization and volatility problems. Here we show that a chain-ether-based electrolyte enables long-term continuous ammonia synthesis. We find that a chain-ether-based solvent exhibits non-polymerization properties and a high boiling point (162 °C) and forms a compact solid-electrolyte interphase layer on the gas diffusion electrode, facilitating ammonia release in the gas phase and ensuring electrolyte stability. We demonstrate 300 h of continuous operation in a flow electrolyser with a 25 cm2 electrode at 1 bar pressure and room temperature, and achieve a current-to-ammonia efficiency of 64 ± 1% with a gas-phase ammonia content of approximately 98%. Our results highlight the crucial role of the solvent in long-term continuous ammonia synthesis.

Suggested Citation

  • Shaofeng Li & Yuanyuan Zhou & Xianbiao Fu & Jakob B. Pedersen & Mattia Saccoccio & Suzanne Z. Andersen & Kasper Enemark-Rasmussen & Paul J. Kempen & Christian Danvad Damsgaard & Aoni Xu & Rokas Sažina, 2024. "Long-term continuous ammonia electrosynthesis," Nature, Nature, vol. 629(8010), pages 92-97, May.
  • Handle: RePEc:nat:nature:v:629:y:2024:i:8010:d:10.1038_s41586-024-07276-5
    DOI: 10.1038/s41586-024-07276-5
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