Overcoming Nitrogen Reduction to Ammonia Detection Challenges

The Case for Leapfrogging to Gas Diffusion Electrode Platforms

Journal Article (2022)
Author(s)

M. Kolen (TU Delft - ChemE/Materials for Energy Conversion and Storage)

D. Ripepi (TU Delft - ChemE/Materials for Energy Conversion and Storage)

Wilson A. Smith (TU Delft - ChemE/Materials for Energy Conversion and Storage)

Thomas E. Burdyny (TU Delft - ChemE/Materials for Energy Conversion and Storage)

FM Mulder (TU Delft - ChemE/Materials for Energy Conversion and Storage)

Research Group
ChemE/Materials for Energy Conversion and Storage
Copyright
© 2022 M. Kolen, D. Ripepi, W.A. Smith, T.E. Burdyny, F.M. Mulder
DOI related publication
https://doi.org/10.1021/acscatal.2c00888
More Info
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Publication Year
2022
Language
English
Copyright
© 2022 M. Kolen, D. Ripepi, W.A. Smith, T.E. Burdyny, F.M. Mulder
Research Group
ChemE/Materials for Energy Conversion and Storage
Issue number
10
Volume number
12
Pages (from-to)
5726-5735
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Abstract

The nitrogen reduction reaction (NRR) is a promising pathway toward the decarbonization of ammonia (NH3) production. However, unless practical challenges related to the detection of NH3 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 Hcell 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 15N2 control experiments from €100−2000 to less than €10. A major driver is the possibility to reduce the 15N2 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 Hcells to commercial device level can be avoided by testing catalysts under conditions close to those in commercial devices from the start.