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Overcoming Nitrogen Reduction to Ammonia Detection Challenges: The Case for Leapfrogging to Gas Diffusion Electrode Platforms

[Image: see text] The nitrogen reduction reaction (NRR) is a promising pathway toward the decarbonization of ammonia (NH(3)) production. However, unless practical challenges related to the detection of NH(3) are removed, confidence in published data and experimental throughput will remain low for ex...

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Detalles Bibliográficos
Autores principales: Kolen, Martin, Ripepi, Davide, Smith, Wilson A., Burdyny, Thomas, Mulder, Fokko M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2022
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9127788/
https://www.ncbi.nlm.nih.gov/pubmed/35633897
http://dx.doi.org/10.1021/acscatal.2c00888
Descripción
Sumario:[Image: see text] The nitrogen reduction reaction (NRR) is a promising pathway toward the decarbonization of ammonia (NH(3)) production. However, unless practical challenges related to the detection of NH(3) are removed, confidence in published data and experimental throughput will remain low for experiments in aqueous electrolyte. In this perspective, we analyze these challenges from a system and instrumentation perspective. Through our analysis we show that detection challenges can be strongly reduced by switching from an H-cell to a gas diffusion electrode (GDE) cell design as a catalyst testing platform. Specifically, a GDE cell design is anticipated to allow for a reduction in the cost of crucial (15)N(2) control experiments from €100–2000 to less than €10. A major driver is the possibility to reduce the (15)N(2) flow rate to less than 1 mL/min, which is prohibited by an inevitable drop in mass-transport at low flow rates in H-cells. Higher active surface areas and improved mass transport can further circumvent losses of NRR selectivity to competing reactions. Additionally, obstacles often encountered when trying to transfer activity and selectivity data recorded at low current density in H-cells to commercial device level can be avoided by testing catalysts under conditions close to those in commercial devices from the start.