4.8 Article

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

期刊

ACS CATALYSIS
卷 12, 期 10, 页码 5726-5735

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acscatal.2c00888

关键词

ammonia; detection; nitrogen reduction; gas diffusion electrode; catalyst

资金

  1. Direct Electrolytic Ammonia Production project [15234]
  2. Netherlands Organisation for Scientific Research (NWO)

向作者/读者索取更多资源

This article presents a potential solution to the detection challenges in ammonia production by proposing the use of a gas diffusion electrode (GDE) cell design as a catalyst testing platform. By switching to the GDE cell design, the cost of crucial experiments can be reduced and the loss of NRR selectivity due to the inevitable drop in mass transport at low flow rates can be avoided.
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 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 N-15(2) control experiments from (sic)100-2000 to less than (sic)10. A major driver is the possibility to reduce the N-15(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.

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