Pulsed Electrolysis in Membrane Electrode Assembly Architecture for Enhanced Electrochemical Nitrate Reduction Reaction to Ammonia

电解 电化学 电极 无机化学 硝酸盐 催化作用 氨生产 化学 材料科学 化学工程 有机化学 电解质 物理化学 工程类 生物化学
作者
Ramireddy Boppella,Maryam Ahmadi,B Arndt,Danielle R. Lustig,Mohammadreza Nazemi
出处
期刊:ACS Catalysis [American Chemical Society]
卷期号:14 (23): 18223-18236 被引量:33
标识
DOI:10.1021/acscatal.4c05225
摘要

Electrochemical nitrate reduction reaction (NO3–RR) to ammonia offers a promising solution to environmental and energy challenges, converting a ubiquitous pollutant in aquatic environments into a carbon-free energy carrier and essential chemical feedstock. While considerable research has focused on electrocatalyst development, relatively less attention has been given to device engineering and electroanalytical techniques that play crucial roles in enhancing the performance of the electrocatalytic NO3–RR, especially at such low concentrations. Here, CuxRuy alloy catalysts were synthesized, and their electrocatalytic performance was investigated by using various electroanalytical techniques in H-type and membrane-electrode-assembly (MEA) configurations. The results revealed the poor performance of the electrocatalytic NO3–RR at low NO3– concentrations (0.01 M) in H cells due to the mass transfer loss, promoting the competing hydrogen evolution reaction. Pulsed electrolysis was leveraged as an effective strategy to enhance ammonia yield rate (3-fold) and Faradaic efficiency (FE) (2-fold) compared to the potentiostatic (i.e., constant voltage) condition at low nitrate concentrations, primarily by impacting the local microenvironment. Additionally, an MEA cell was constructed with anionic and bipolar membranes, and a comparative study was conducted by examining cell voltage, selectivity, and energy efficiency. The findings exhibited that membrane type significantly influences cell voltage and system efficiency. Notably, the CuRu alloy catalyst in an MEA system with an anion exchange membrane achieved a FE exceeding 90% at 200 mA cm–2 with the highest NH3 yield rate of 5.74 ± 0.27 mmol h–1 cm–2 and stability over 100 h assessed at 600 mA cm–2. The insights gained from this work could inform the rational design of the electrochemical NO3–RR to ammonia with enhanced catalytic performance at low nitrate concentrations.
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