Electrochemical determination of ammonia at low concentrations: detection of N2-electroreduction product in alkaline medium

A catalytic system based on CeO<sub>2</sub>-supported Pt nanoparticles has been utilized and optimized to pursue electrochemical determination of ammonia (NH<sub>3</sub>) at fairly low concentrations (detection limit down to 2-3 μmol dm<sup>-3</sup> level) through voltammetric oxidation of NH<sub>3</sub> in alkaline medium (0.5 mol dm<sup>-3</sup> NaOH). Dispersing and supporting of platinum nanoparticles on partially-defective and sub-stoichiometric ceria tends to increase the electrochemically active-surface-area and reproducibility of operation of the Pt-based catalyst. The approach has been found suitable to detect NH<sub>3</sub> generated during electroreduction of nitrogen at Fe<sub>3</sub>P catalyst in the N<sub>2</sub>-saturated alkaline solution. Here the Pt-based "analytical" electrode has been utilized as the additional working electrode placed in the vicinity of the Fe<sub>3</sub>P-modified electrode. The analytical measurement does not require medium transfer to another solution because both Fe<sub>3</sub>P and Pt-based electrodes are operating in the sealed N<sub>2</sub>-electrolysis cell. Under such conditions, uncontrolled leakage and contamination by ammonia existing in the atmosphere can be avoided. The Pt-based electrode permits to perform blank experiments to comment about purity of electrolytes and nitrogen gas with respect to the presence of residual ammonia and the absence of oxygen and nitrogen oxides. Consequently, reliable determination of ammonia as the N<sub>2</sub>-electroreduction product following 2 h electrolysis at Fe<sub>3</sub>P iron phosphide catalyst becomes feasible. The results have been verified against spectrophotometric data. Formation of hydrazine or hydroxylamine as side (to ammonia) electroreduction products can be addressed by performing voltammetric diagnostic experiments with use of electrodes modified with Pt and Rh nanoparticles. Conversion of N<sub>2</sub> to NH<sub>3</sub> at Fe<sub>3</sub>P catalyst in 0.5 mol dm<sup>-3</sup> NaOH is fairly selective because no appreciable amounts of hydrazine or hydroxylamine have been detected.

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Publication Details

Journal
Talanta
Published
2025-05-04
DOI
https://doi.org/10.1016/j.talanta.2025.128272
Citations
1
Primary Topic
Ammonia Synthesis and Nitrogen Reduction
Type
article
Field-Weighted Citation Impact
0.39
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article

Electrochemical determination of ammonia at low concentrations: detection of N2-electroreduction product in alkaline medium

Paweł J. Kulesza, Iwona A. Rutkowska, Takwa Chouki, Beata Rytelewska et al.
1 citations
Talanta
Ammonia Synthesis and Nitrogen Reduction
0.39
article

Electrochemical determination of ammonia at low concentrations: detection of N2-electroreduction product in alkaline medium

Paweł J. Kulesza, Iwona A. Rutkowska, Takwa Chouki, Beata Rytelewska, Anna Chmielnicka, Saim Emin
article en
1 citations

Abstract

A catalytic system based on CeO<sub>2</sub>-supported Pt nanoparticles has been utilized and optimized to pursue electrochemical determination of ammonia (NH<sub>3</sub>) at fairly low concentrations (detection limit down to 2-3 μmol dm<sup>-3</sup> level) through voltammetric oxidation of NH<sub>3</sub> in alkaline medium (0.5 mol dm<sup>-3</sup> NaOH). Dispersing and supporting of platinum nanoparticles on partially-defective and sub-stoichiometric ceria tends to increase the electrochemically active-surface-area and reproducibility of operation of the Pt-based catalyst. The approach has been found suitable to detect NH<sub>3</sub> generated during electroreduction of nitrogen at Fe<sub>3</sub>P catalyst in the N<sub>2</sub>-saturated alkaline solution. Here the Pt-based "analytical" electrode has been utilized as the additional working electrode placed in the vicinity of the Fe<sub>3</sub>P-modified electrode. The analytical measurement does not require medium transfer to another solution because both Fe<sub>3</sub>P and Pt-based electrodes are operating in the sealed N<sub>2</sub>-electrolysis cell. Under such conditions, uncontrolled leakage and contamination by ammonia existing in the atmosphere can be avoided. The Pt-based electrode permits to perform blank experiments to comment about purity of electrolytes and nitrogen gas with respect to the presence of residual ammonia and the absence of oxygen and nitrogen oxides. Consequently, reliable determination of ammonia as the N<sub>2</sub>-electroreduction product following 2 h electrolysis at Fe<sub>3</sub>P iron phosphide catalyst becomes feasible. The results have been verified against spectrophotometric data. Formation of hydrazine or hydroxylamine as side (to ammonia) electroreduction products can be addressed by performing voltammetric diagnostic experiments with use of electrodes modified with Pt and Rh nanoparticles. Conversion of N<sub>2</sub> to NH<sub>3</sub> at Fe<sub>3</sub>P catalyst in 0.5 mol dm<sup>-3</sup> NaOH is fairly selective because no appreciable amounts of hydrazine or hydroxylamine have been detected.

TalantaVol. 295
University of Nova Gorica (SI), University of Warsaw (PL)
Clean water and sanitation
Openalex Percentile: Top 45%
Ammonia Synthesis and Nitrogen Reduction
0.39
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