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<p>The Li-mediated nitrogen reduction reaction (Li-NRR) has been proposed as one of the most promising ambient production routes for green ammonia. However, the effect of the applied potential (<i>E</i><sub>we</sub>) on the reaction performance and the properties of the solid electrolyte interphase (SEI) remain poorly understood. Herein, we combine potential controlled experiments using a reliable Li<sub>x</sub>FePO<sub>4</sub> based reference electrode with post-mortem SEI characterization techniques, wherein we observe both an increase in the LiF concentration in the SEI, originating from LiTFSI decomposition, and the Faradaic efficiency (FE<sub>NH3</sub>) with an increasing <i>E</i><sub>we</sub>. The transition from a predominantly organic SEI at low <i>E</i><sub>we</sub> (−3.2 V<sub>SHE</sub>) to a LiF-enriched layer at higher <i>E</i><sub>we</sub> indicates the existence of kinetic barriers for the SEI formation reactions. Moreover, thicker and denser SEI structures observed at a higher <i>E</i><sub>we</sub> enhance the Li-NRR by improving the mass transport regulation between reactant species. However, these thicker and denser SEI morphologies lead to current instabilities due to dynamic SEI thickening and breakdown.</p>

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The Effect of Applied Potential on the Li-mediated Nitrogen Reduction Reaction Performance

  • 期刊论文

  • 出版模式：

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  • 发表日期：

    2025年11月27日

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  • Boaz Izelaar,
  • Pranav Karanth,
  • Arash Toghraei,
  • Santosh K. Pal,
  • Nandalal Girichandran,
  • Mark Weijers,
  • Ruud W. A. Hendrikx,
  • Fokko M. Mulder,
  • Ruud Kortlever

摘要

The Li-mediated nitrogen reduction reaction (Li-NRR) has been proposed as one of the most promising ambient production routes for green ammonia. However, the effect of the applied potential (Ewe) on the reaction performance and the properties of the solid electrolyte interphase (SEI) remain poorly understood. Herein, we combine potential controlled experiments using a reliable LixFePO4 based reference electrode with post-mortem SEI characterization techniques, wherein we observe both an increase in the LiF concentration in the SEI, originating from LiTFSI decomposition, and the Faradaic efficiency (FENH3) with an increasing Ewe. The transition from a predominantly organic SEI at low Ewe (−3.2 VSHE) to a LiF-enriched layer at higher Ewe indicates the existence of kinetic barriers for the SEI formation reactions. Moreover, thicker and denser SEI structures observed at a higher Ewe enhance the Li-NRR by improving the mass transport regulation between reactant species. However, these thicker and denser SEI morphologies lead to current instabilities due to dynamic SEI thickening and breakdown.