Adsorption mechanism of the N and NRR intermediates on oxygen modified MnN-graphene layers - a single atom catalysis perspective

• Published in: Physical chemistry chemical physics : PCCP 2023-07, Vol.25 (27), p.18465-1848
• Main Authors: Genç, A. E, Tranca, I. C
• Format: Article
• ISSN: 1463-9076; 1463-9084
• DOI: 10.1039/d2cp05491d

In the present work the adsorption of N 2 and the nitrogen reduction reaction (NRR) intermediates have been investigated on oxygen modified MnN x O y ( x + y = 4, x ≠ 0)/graphene layers through periodic density functional theory calculations. Various number of oxygen atoms substitute nitrogen atoms within the MnN x O y , with their effect on the layer stability, chemical bonding and N 2 adsorption being explored. As the oxygen amount increases in the porphyrin unit, Mn-O interactions weaken with reference to that of Mn-N, bonding orbitals become less populated while the antibonding orbitals between Mn-N-O atoms become partially occupied, as evidenced by the Crystal orbital Hamiltonian population (COHP) and integrated crystal orbital bond index (ICOBI) analyses. During N 2 adsorption on the different layers, the substitution of two and three nitrogen atoms by oxygen leads to the longest N&z.tbd;N molecular bond length. Two main orientations for the N 2 molecules sorption have been investigated: side-on and end-on which are perpendicular and parallel to the surface normal, respectively. When the interaction of N 2 with MnNO 3 layer is considered, d-band center variation of the Mn with reference to the pre-adsorbed state is more obvious after side-on adsorption configuration. For the selected layers based on initial N 2 adsorption energies, the adsorption energies of nitrogen reduction reaction intermediates follow a trend based on the number of oxygen atoms in the porphyrin units. Charge density difference (CDD) maps and partial density of states (PDOS) analysis reveal that the interaction of N 2 with oxygen modified layers takes place through electron acception-donation mechanism between the partially occupied Mn-d orbitals and the 2p orbitals of the N 2 molecule. DDEC6-derived bond orders and atomic charges support the PDOS and adsorption/formation energy trends, and further clarify the bonding strengths of the atoms in the porphyrin units, as well as the Mn-N 2 interactions in the adsorbed systems. In the present work the adsorption of N 2 and the nitrogen reduction reaction (NRR) intermediates have been investigated on oxygen modified MnN x O y ( x + y = 4, x ≠ 0)/graphene layers through periodic density functional theory calculations.