Theoretical design toward highly efficient single-atom catalysts for nitrogen reduction by regulating the “acceptance-donation” mechanism

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Detail(s)

Original languageEnglish
Article number156827
Journal / PublicationApplied Surface Science
Volume623
Online published23 Feb 2023
Publication statusPublished - 30 Jun 2023

Abstract

Single-atom catalysts (SACs) show great potential for driving electrochemical nitrogen reduction reaction (NRR). However, the lack of physico-chemical understanding of the ambiguous activation mechanism impedes the development of electrocatalysts. In this work, using first principles calculations, we tuned NRR activity and elucidated regulation mechanism of N2 activation by constructing SACs based on defective Ti2CO2 and Ti2NO2 MXenes. Interestingly, Mo@Ti2CO2-v and W@Ti2CO2-v show excellent NRR activity and selectivity with low limiting potentials of –0.27 and –0.27 V at the first hydrogenation (*N2→*NNH) and the last hydrogenation (*NH2→*NH3) steps via distal pathway, respectively. The intrinsic activity tendency can be related to adsorption energy of intermediate *NNH (ΔE(*NNH)). Furthermore, electronic structure analysis demonstrates that number of unpaired electrons in d orbitals (Nun-d) determines occupation of d orbitals, thus regulating the “acceptance-donation” mechanism. Particularly, transition metals with Nun-d of 5 and 4 show moderate “acceptance-donation” interaction, thus achieving encouraging NRR performance. Moreover, ΔE(*NNH) and Nun-d can be considered as promising descriptors for screening and designing effective SACs. Finally, our investigation not only contributes to discovery of novel SACs toward NRR, but also provides insightful guidance for other electrochemical reactions with high bond-order molecules and multi-electron steps, such as ORR and CO2RR. © 2023 Elsevier B.V.

Research Area(s)

  • Ammonia, d orbital, DFT, Donation-acceptance, Nitrogen reduction, Single-atom catalysts

Citation Format(s)