Electroreduction of N2 to NH3 catalyzed by a Mn/Re(111) single-atom alloy catalyst with high activity and selectivity: a new insight from a first-principles study

• Published in: Catalysis science & technology Vol. 12; no. 12; pp. 4074 - 4085
• Main Authors: Cao, Ning, Zhang, Nan, Yong-Qing Qiu, Chun-Guang Liu
• Format: Journal Article
• Language: English
• Published: Cambridge Royal Society of Chemistry 20.06.2022
• Subjects: Ammonia; Charge transfer; Chemical reduction; Chromium; Copper; Density functional theory; Electronic structure; First principles; Free energy; Gold; Hydrogenation; Iridium; Iron; Manganese; Mathematical analysis; Molybdenum; Palladium; Radicals; Rhenium; Selectivity; Silver; Single atom catalysts; Structural analysis; Transition metals
• ISSN: 2044-4753; 2044-4761
• DOI: 10.1039/d2cy00435f

First-principles calculations were employed to evaluate the doping effects on the activity and selectivity of various single-atom alloy (SAA) catalysts for the electrocatalytic nitrogen reduction reaction (eNRR). A series of SAA catalysts are formed by the introduction of different single transition metal (TM = Cr, Mn, Fe, Co, Ni, Cu, Mo, Tc, Ru, Rh, Pd, Ag, W, Os, Ir, Pt, and Au) atoms into a defective Re(111) surface. Our periodic density functional theory (DFT) calculations show that the Mn/Re(111) SAA has the ability to spontaneously adsorb N2 molecules rather than H atoms, and thus it can effectively improve the selectivity of the eNRR and inhibit that of the HER. Electronic structure analysis shows that hydrogenation of *N2 to *NNH on the surface of the Mn/Re(111) SAA catalyst results in the formation of a *N2−· radical via the charge transfer from the H atom to the adsorbed N2 molecule. Due to the very high reactivity of the *N2−· radical, the calculated free energy changes of the subsequent hydrogenation processes along the favorable distal pathway are close to 0 eV or even negative on the surface of the Mn/Re(111) SAA. All these results indicate that the Mn/Re(111) SAA may be an excellent catalyst with high activity and selectivity for the eNRR.