Catalytic reduction of N <sub>2</sub>O by CO molecules using transition metal-phosphomolybdic acid (TM <sub>1</sub>/PMA) single-atom catalysts: A theoretical perspective

The efficient catalytic conversion of hazardous gases (e.g., N<sub>2</sub>O and CO) into non-harmful by products is important due to the severe environmental and health burdens posed by these gases. Here, quantum chemical studies have been carried out to investigate the catalytic reduction of N<sub>2</sub>O by CO over a phosphomolybdic acid (PMA) cluster anchored with 3d transition metal atoms under mild reaction conditions. For N<sub>2</sub>O reduction, all 3d-TM<sub>1</sub> adatoms on the PMA cluster have been systematically screened as single-atom catalysts (SACs). TM<sub>1</sub>/PMA systems possess significant adsorption energies towards N<sub>2</sub>O and CO, and co-adsorption energies of N<sub>2</sub>O+CO are a necessary prerequisite for the start of the catalytic cycle. The results indicate that N<sub>2</sub>O is decomposed first on the TM<sub>1</sub>/PMA surface, forming N<sub>2</sub> and O-TM<sub>1</sub>/PMA intermediate. The Ti<sub>1</sub>-(0.53 eV), V<sub>1</sub>-(0.40 eV), Cr<sub>1</sub>-(0.86 eV), and Fe<sub>1</sub>/PMA (0.94 eV) have low activation energy barriers that are comparable to those of the other catalysts that were chosen, making them active and selective catalysts for the N<sub>2</sub>O decomposition. However, the remaining O atom on the TM<sub>1</sub>/PMA was an active species for the oxidation of CO molecules. The Fe<sub>1</sub>/PMA catalyst has an activation energy barrier of 0.43 eV and is a promising catalyst for the oxidation of CO. CO occupying the TM<sub>1</sub> site with stronger adsorption energy than N<sub>2</sub>O will restrict the reaction’s effectiveness. A lower temperature can hinder the generation of the side products N<sub>2</sub> and O<sub>2</sub> generated due to the disproportionation of N<sub>2</sub>O molecules. A concerted reaction mechanism can also initiate the reaction by first adhering CO molecules to the TM<sub>1</sub>/PMA surface. The computed activation energy barriers of the rate-limiting step are (Ti<sub>1</sub>=0.52 eV, V<sub>1</sub>=0.76 eV, and Fe<sub>1</sub>=0.88 eV), respectively. Thus, 3d TM<sub>1</sub>/PMA is predicted to be an efficient catalyst for converting toxic gases N<sub>2</sub>O and CO into non-hazardous N<sub>2</sub> and CO<sub>2</sub> under normal conditions.

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Publication Details

Journal
Nano Research Energy
Published
2025-03-20
DOI
https://doi.org/10.26599/nre.2025.9120158
Citations
3
Primary Topic
Catalysis and Oxidation Reactions
Type
article
Field-Weighted Citation Impact
1.17
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article

Catalytic reduction of N 2O by CO molecules using transition metal-phosphomolybdic acid (TM 1/PMA) single-atom catalysts: A theoretical perspective

Babar Ali, Sharmarke Mohamed, Ahsanulhaq Qurashi, Shamraiz Hussain Talib et al.
3 citations
Nano Research Energy
Catalysis and Oxidation Reactions
1.17
article

Catalytic reduction of N 2O by CO molecules using transition metal-phosphomolybdic acid (TM 1/PMA) single-atom catalysts: A theoretical perspective

Babar Ali, Sharmarke Mohamed, Ahsanulhaq Qurashi, Shamraiz Hussain Talib, Arif Hassan Dar, Jun Li
article en
3 citations

Abstract

The efficient catalytic conversion of hazardous gases (e.g., N<sub>2</sub>O and CO) into non-harmful by products is important due to the severe environmental and health burdens posed by these gases. Here, quantum chemical studies have been carried out to investigate the catalytic reduction of N<sub>2</sub>O by CO over a phosphomolybdic acid (PMA) cluster anchored with 3d transition metal atoms under mild reaction conditions. For N<sub>2</sub>O reduction, all 3d-TM<sub>1</sub> adatoms on the PMA cluster have been systematically screened as single-atom catalysts (SACs). TM<sub>1</sub>/PMA systems possess significant adsorption energies towards N<sub>2</sub>O and CO, and co-adsorption energies of N<sub>2</sub>O+CO are a necessary prerequisite for the start of the catalytic cycle. The results indicate that N<sub>2</sub>O is decomposed first on the TM<sub>1</sub>/PMA surface, forming N<sub>2</sub> and O-TM<sub>1</sub>/PMA intermediate. The Ti<sub>1</sub>-(0.53 eV), V<sub>1</sub>-(0.40 eV), Cr<sub>1</sub>-(0.86 eV), and Fe<sub>1</sub>/PMA (0.94 eV) have low activation energy barriers that are comparable to those of the other catalysts that were chosen, making them active and selective catalysts for the N<sub>2</sub>O decomposition. However, the remaining O atom on the TM<sub>1</sub>/PMA was an active species for the oxidation of CO molecules. The Fe<sub>1</sub>/PMA catalyst has an activation energy barrier of 0.43 eV and is a promising catalyst for the oxidation of CO. CO occupying the TM<sub>1</sub> site with stronger adsorption energy than N<sub>2</sub>O will restrict the reaction’s effectiveness. A lower temperature can hinder the generation of the side products N<sub>2</sub> and O<sub>2</sub> generated due to the disproportionation of N<sub>2</sub>O molecules. A concerted reaction mechanism can also initiate the reaction by first adhering CO molecules to the TM<sub>1</sub>/PMA surface. The computed activation energy barriers of the rate-limiting step are (Ti<sub>1</sub>=0.52 eV, V<sub>1</sub>=0.76 eV, and Fe<sub>1</sub>=0.88 eV), respectively. Thus, 3d TM<sub>1</sub>/PMA is predicted to be an efficient catalyst for converting toxic gases N<sub>2</sub>O and CO into non-hazardous N<sub>2</sub> and CO<sub>2</sub> under normal conditions.

Nano Research EnergyVol. 4(2)
King Fahd University of Petroleum and Minerals (SA), Khalifa University of Science and Technology (AE), Southern University of Science and Technology (CN)
Openalex Percentile: Top 24%
Catalysis and Oxidation Reactions
1.17
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