4.6 Article

Mass Transport Modifies the Interfacial Electrolyte to Influence Electrochemical Nitrate Reduction

Journal

ACS SUSTAINABLE CHEMISTRY & ENGINEERING
Volume 11, Issue 20, Pages 7882-7893

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acssuschemeng.3c01057

Keywords

diffusion-migration-reaction model; electrolyte effects; infrared absorption spectroscopy; reaction microenvironment; reactive nitrogen; sustainable ammonia manufacturing

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The electrochemical nitrate reduction reaction (NO3RR) can be used to clean nitrate-polluted wastewater and produce ammonia in a sustainable way. This study investigates the influence of interfacial electrolyte on NO3RR performance, specifically focusing on the effects of mass transport conditions. Through simulations and experiments, the researchers found that diffusion layer thickness and electrolyte concentration affect NO3RR activity, while interfacial pH determines NO3RR selectivity. By optimizing these factors, they successfully increased the ammonia-to-nitrite selectivity by three times.
The electrochemical nitrate reduction reaction (NO3RR) can facilitate remediation of nitrate-polluted wastewater and sustainable production of ammonia. As an important component of the reaction microenvironment, the interfacial electrolyte substantially influences NO3RR but remains underexplored. Mass transport modifies the interfacial electrolyte properties (e.g., pH, solute concentrations) and thus regulates NO3RR activity and selectivity. In a representative flow-cell configuration with a titanium NO3RR electrode, we systematically controlled mass transport conditions and demonstrated their impacts on NO3RR performance. With continuum model simulation and in situ infrared absorption spectroscopy, we characterized the interfacial electrolyte environment under varied mass transport conditions. Furthermore, we strategically tuned the interfacial electrolyte properties and experimentally deconvoluted their impacts on NO3RR activity and selectivity. We found that diffusion layer thickness and background electrolyte concentration govern NO3RR activity, while interfacial pH steers NO3RR selectivity. Inspired by these findings, we applied pulsed potential to periodically refresh the interfacial electrolyte environment and lower the local pH, successfully tripling the relative ammonia-to-nitrite selectivity. Distinct from NO3RR studies that focus on reaction kinetics, this study was conducted under commonly observed mass transport limitations to advance mechanistic understanding behind mass transport effects and to help identify engineering opportunities that optimize ammonia production.

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