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Updated: Oct 4, 2026

Electrochemically and Bioelectrochemically Induced Ammonium Recovery
Published on: January 22, 2015
Electrolyte and gas flow rate balance in flow cells for lithium-mediated ammonia electrosynthesis
Anna Mangini1, Giulia Zagatti1, Julia Amici1
1Department of Applied Science and Technology, Politecnico di Torino, Corso Duca degli Abruzzi 24, Turin 10129, Italy. sara.garcia@polito.it.
Abstract:
The electrochemical lithium-mediated nitrogen reduction reaction (Li-NRR) has emerged as a leading approach for ammonia electrosynthesis under mild conditions, particularly in continuous flow-cell configurations. Despite the rapid progress of this strategy, as well as the remarkable efforts in electrolyte composition engineering and solid-electrolyte-interphase layer understanding, the impact of architecture-level parameters remains unclear and is often entangled with the intrinsic process reactivity and selectivity. Here, we systematically investigate the influence of electrolyte and nitrogen-gas flow rates on Li-NRR performance in a flow cell, attempting to decouple the effect of device-level parameters from reaction chemistry in determining activity, selectivity, and stability of the system. By balancing liquid and gas flows, we demonstrate stable device operation even at high electrolyte flow rates (18 mL min-1), allowing for a complete exchange of the electrolyte in the liquid chamber twice per minute. This electrolyte flow rate results in a simultaneous improvement of Faradaic efficiency, productivity, and ammonia recovery in the gas phase. Overall, our results highlight the critical influence of cell-architecture-related parameters on Li-NRR and emphasize the need to disentangle device engineering from electrolyte tailoring and electrochemical performance optimisation to enable a rational understanding of the mechanism understanding towards the translation of Li-NRR to a scalable process.
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