High yield ammonia production via glucose oxidation assisted electrochemical nitrate reduction

Abstract

Electrocatalytic nitrate (NO3-) reduction reaction (NO3RR) provides a potential route for the synthesis of value-added ammonia (NH3) and removal of nitrate pollutants. However, this reaction is limited by nitrate adsorption and slow kinetics involving multiple proton and electron transfer steps. The sluggish OER can hinder NO3RR performance, but replacing it with a more facile oxidation process enhances performance. Herein, we have demonstrated glucose oxidation assisted NO3RR, utilizing CuNi(1:2)S as a bifunctional catalyst demonstrating high NH3 Faradaic efficiency (F.E.) of 93.44% with a yield rate of 4.7 mg h-1 cm-2 or 280.47 mmol gcat-1 h-1 at -0.4 V vs. RHE along with achieving high current densities applicable at industrial levels and its high activity compared to monometallic variants was explained using the ultraviolet photoelectron spectra (UPS) technique. Further, a mechanistic study using in-situ electrochemical Raman spectroscopy, illustrates the hydrogenation of NO3- to NH3 via NO2- intermediate. Moreover, replacing OER with glucose oxidation reaction (GOR) in full cell system could decrease the total energy input by 200 mV and increase the NH3 yield from 120.95 µg h-1 cm-2 to 259.46 µg h-1 cm-2. Furthermore, the high value-added products were obtained at both anode and cathode at a low cell voltage. More interestingly, we demonstrate the practical extraction of high-purity NH4Cl (s) and NH3 aqueous product from electro-reduced NO3- after electrolysis at 100 mA cm-2 for 50 h, with a collection efficacy of 89.84% of condensed NH3 (aq) solution.

Supplementary files

Article information

Article type
Paper
Submitted
16 Oct 2024
Accepted
23 Feb 2025
First published
25 Feb 2025

J. Mater. Chem. A, 2025, Accepted Manuscript

High yield ammonia production via glucose oxidation assisted electrochemical nitrate reduction

A. Chaturvedi, S. Kaur, K. Garg and T. C. Nagaiah, J. Mater. Chem. A, 2025, Accepted Manuscript , DOI: 10.1039/D4TA07397E

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