Electrochemical nitrate reduction on boron-doped diamond cathodes in a single-compartment cell for selectivity control and nitrite suppression

Nitrate contamination in water sources poses significant environmental and public health concerns, motivating the development of selective electrochemical remediation strategies. Herein, a boron-doped diamond (BDD) cathode was evaluated for nitrate electroreduction in a single-compartment electrochemical cell and compared with a conventional Cu cathode under galvanostatic operation. Nitrate conversion, nitrogen product distribution, and specific energy consumption were assessed as a function of applied current density (6–30 mA cm-2). For both cathodes, nitrate conversion increased with current density; however, BDD consistently outperformed Cu at current densities ≥ 12 mA cm-2, reaching 50 ± 2% nitrate conversion at 30 mA cm-2, compared with 34.4 ± 5.0% for Cu under the same conditions. Notably, under the tested single-compartment conditions (NaCl as supporting electrolyte and a DSA® anode), BDD provided improved control of nitrogen speciation, with nitrite remaining below the detection limit (< 0.05 mg L-1 as NO₂⁻) across all operating conditions. At low current densities, BDD favored ammonium formation, reaching a maximum of 3.00 mg-N L-1 (as NH₄⁺-N) at 12 mA cm⁻², which was twofold higher than the maximum value obtained with Cu (1.50 mg-N L-1). In contrast, Cu promoted nitrite formation at high current densities, with detectable NO2--N concentrations appearing at ≥ 24 mA cm-2 and increasing up to 1.45 mg-N L-1 (as NO2--N) at 30 mA cm-2. Energy consumption increased markedly with current density for both electrodes, ranging from 195 to 4519 kWh kg-1 N–NO3- for BDD and 198 to 3546 kWh kg-1 N–NO3- for Cu. Although BDD does not compete with state-of-the-art catalysts in terms of ammonium productivity, its chemical stability and the observed low nitrite accumulation under single-compartment conditions make it a promising material for applications prioritizing selectivity control and operational robustness.

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Journal
Discover Catalysis.
Published
2026-09-12
DOI
https://doi.org/10.1007/s44344-026-00049-4
Primary Topic
Ammonia Synthesis and Nitrogen Reduction
Type
article
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article

Electrochemical nitrate reduction on boron-doped diamond cathodes in a single-compartment cell for selectivity control and nitrite suppression

Nicolás Alejandro Sacco, Andréa Moura Bernardes, Thiago Favarini Beltrame, Fernanda Miranda Zoppas et al.
Discover Catalysis.
Ammonia Synthesis and Nitrogen Reduction
article

Electrochemical nitrate reduction on boron-doped diamond cathodes in a single-compartment cell for selectivity control and nitrite suppression

Nicolás Alejandro Sacco, Andréa Moura Bernardes, Thiago Favarini Beltrame, Fernanda Miranda Zoppas, Débora Pedroso Righi Köhler
article en

Abstract

Nitrate contamination in water sources poses significant environmental and public health concerns, motivating the development of selective electrochemical remediation strategies. Herein, a boron-doped diamond (BDD) cathode was evaluated for nitrate electroreduction in a single-compartment electrochemical cell and compared with a conventional Cu cathode under galvanostatic operation. Nitrate conversion, nitrogen product distribution, and specific energy consumption were assessed as a function of applied current density (6–30 mA cm-2). For both cathodes, nitrate conversion increased with current density; however, BDD consistently outperformed Cu at current densities ≥ 12 mA cm-2, reaching 50 ± 2% nitrate conversion at 30 mA cm-2, compared with 34.4 ± 5.0% for Cu under the same conditions. Notably, under the tested single-compartment conditions (NaCl as supporting electrolyte and a DSA® anode), BDD provided improved control of nitrogen speciation, with nitrite remaining below the detection limit (< 0.05 mg L-1 as NO₂⁻) across all operating conditions. At low current densities, BDD favored ammonium formation, reaching a maximum of 3.00 mg-N L-1 (as NH₄⁺-N) at 12 mA cm⁻², which was twofold higher than the maximum value obtained with Cu (1.50 mg-N L-1). In contrast, Cu promoted nitrite formation at high current densities, with detectable NO2--N concentrations appearing at ≥ 24 mA cm-2 and increasing up to 1.45 mg-N L-1 (as NO2--N) at 30 mA cm-2. Energy consumption increased markedly with current density for both electrodes, ranging from 195 to 4519 kWh kg-1 N–NO3- for BDD and 198 to 3546 kWh kg-1 N–NO3- for Cu. Although BDD does not compete with state-of-the-art catalysts in terms of ammonium productivity, its chemical stability and the observed low nitrite accumulation under single-compartment conditions make it a promising material for applications prioritizing selectivity control and operational robustness.

Discover Catalysis.Vol. 3(1)
Consejo Nacional de Investigaciones Científicas y Técnicas (AR), Universidad Argentina de la Empresa (AR)
Conselho Nacional de Desenvolvimento Científico e Tecnológico, Universidad Nacional del Litoral, CYTED Ciencia y Tecnología para el Desarrollo, Agencia Nacional de Promoción Científica y Tecnológica
Affordable and clean energy
Openalex Percentile: Top 30%
Ammonia Synthesis and Nitrogen Reduction
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