A theoretical descriptor for screening efficient NO reduction electrocatalysts from transition-metal atoms on N-doped BP monolayer

Abstract

An electrochemical nitric oxide (NO) reduction reaction (NORR) is proposed as an attractive method for simultaneous realization of NO removal and ammonia (NH3) synthesis. Here, the potentials of 29 transition-metal atoms anchored on the nitrogen-doped BP monolayer (MN3/BP) as efficient NORR catalysts are systematically examined using first-principles calculations. Combining the adsorption Gibbs free energies of the N and OH species, a simple descriptor is constructed and a volcano plot of the NORR limiting potentials on the single atom catalysts (SACs) is established. Consequently, the MoN3/BP and IrN3/BP SACs are picked out as promising NORR electrocatalysts for NH3 synthesis with the limiting potentials of −0.10 V and −0.06 V, respectively. Their corresponding rate constants are significantly larger than or close to that of the excellent Pt(111) surface. The electronic analysis shows that the Mo-4d or Ir-5d orbitals can be well hybridized with the NO-2p orbitals, sufficiently activating the adsorbed NO species. Particularly, the MoN3/BP and IrN3/BP SACs possess high thermal stabilities and can be easily synthesized by using MoCl3 and IrCl3 as precursors, respectively. This work not only offers a simple descriptor to efficiently design NORR electrocatalysts but also provides a comprehensive atomic understanding on the mechanism of NO-to-NH3 conversion.