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

磷钼酸 催化作用 过渡金属 Atom(片上系统) 分子 还原(数学) 透视图(图形) 化学 金属 无机化学 物理化学 材料科学 有机化学 计算机科学 嵌入式系统 人工智能 数学 几何学
作者
Shamraiz Hussain Talib,Babar Ali,Arif Hassan Dar,Ahsanulhaq Qurashi,Jun Li,Sharmarke Mohamed
出处
期刊: [Tsinghua University Press]
卷期号:4 (2): e9120158-e9120158 被引量:3
标识
DOI:10.26599/nre.2025.9120158
摘要

The efficient catalytic conversion of hazardous gases (e.g., N2O 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 N2O by CO over a phosphomolybdic acid (PMA) cluster anchored with 3d transition metal atoms under mild reaction conditions. For N2O reduction, all 3d-TM1 adatoms on the PMA cluster have been systematically screened as single-atom catalysts (SACs). TM1/PMA systems possess significant adsorption energies towards N2O and CO, and co-adsorption energies of N2O+CO are a necessary prerequisite for the start of the catalytic cycle. The results indicate that N2O is decomposed first on the TM1/PMA surface, forming N2 and O-TM1/PMA intermediate. The Ti1-(0.53 eV), V1-(0.40 eV), Cr1-(0.86 eV), and Fe1/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 N2O decomposition. However, the remaining O atom on the TM1/PMA was an active species for the oxidation of CO molecules. The Fe1/PMA catalyst has an activation energy barrier of 0.43 eV and is a promising catalyst for the oxidation of CO. CO occupying the TM1 site with stronger adsorption energy than N2O will restrict the reaction’s effectiveness. A lower temperature can hinder the generation of the side products N2 and O2 generated due to the disproportionation of N2O molecules. A concerted reaction mechanism can also initiate the reaction by first adhering CO molecules to the TM1/PMA surface. The computed activation energy barriers of the rate-limiting step are (Ti1=0.52 eV, V1=0.76 eV, and Fe1=0.88 eV), respectively. Thus, 3d TM1/PMA is predicted to be an efficient catalyst for converting toxic gases N2O and CO into non-hazardous N2 and CO2 under normal conditions.
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