Issue 2, 2024

In situ growth of copper oxide on MXene by combustion method for electrochemical ammonia production from nitrate

Abstract

The elimination of the nitrogen pollutant nitrate ions through the electrochemical synthesis of ammonia is an important and environment friendly strategy. Electrochemical nitrate reduction requires highly efficient, selective, and stable catalysts to convert nitrate to ammonia. In this work, a composite of copper oxide and MXene was synthesized using a combustion technique. As reported, nitrate ions are effectively adsorbed by CuxO (CuO & Cu2O) nanoparticles. Herein, MXene is an excellent assembly for anchoring CuxO on its layered surface because it has a strong support structure. Powder X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), scanning electron microscopy (SEM), and transmission electron microscopy (TEM) analyses show the presence of oxidation states of metal ions and the formation of CuxO nanofoam anchors on the surface of MXene (Ti3C2Tx). The optimized CuxO/Ti3C2Tx composite exhibits an improved nitrate reduction reaction. The electrochemical studies of CuxO/Ti3C2Tx show an interesting nitrate reduction reaction (NO3RR) with a current density of 162 mA cm−2. Further, CuxO/Ti3C2Tx shows an electrocatalytic activity with an ammonia production of 41 982 μg h−1 mcat−1 and its faradaic efficiency is 48% at −0.7 V vs. RHE. Thus, such performance by CuxO/Ti3C2Tx indicates a well-suitable candidate for nitrate ion conversion to ammonia.

Graphical abstract: In situ growth of copper oxide on MXene by combustion method for electrochemical ammonia production from nitrate

Supplementary files

Article information

Article type
Paper
Submitted
07 Aug 2023
Accepted
23 Nov 2023
First published
24 Nov 2023
This article is Open Access
Creative Commons BY-NC license

Nanoscale Adv., 2024,6, 481-488

In situ growth of copper oxide on MXene by combustion method for electrochemical ammonia production from nitrate

S. Ingavale, P. Marbaniang, M. Palabathuni and N. Mishra, Nanoscale Adv., 2024, 6, 481 DOI: 10.1039/D3NA00609C

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