Exploring Synergistic Effect on the Stability of Ni-, Pd-, Ir-Doped Ti_N (N = 1–15) Nanoparticles

Abstract

Bimetallic nanoclusters have attracted great interest due to their ability to enhance the catalytic properties of nanoclusters through synergetic effects that emerge from the combination of the metal nanocluster with different transition metal (TM) species. However, their indefinite composition and broad distribution hinder the insightful understanding of the interaction between these invasive metals in bimetallic doped nanoalloys. In this study, we report a density functional theory calculation with the PBEsol exchange-correlation functional for 16-atom TiN−1TM (TM = Ni, Ir, Pd) nanoalloys, which provides new insights into the synergetic effect of these invasive metals. The probe into the effect of these metal impurities revealed that the replacement of a Ti atom with Ni, Ir and Pd enhances the relative stability of the nanoalloys, and the maximum stability for a lower bimetallic composition is reached for Ti4Ir, Ti5Pd and Ti7Ni. The most stable nanoalloy is reached for the Ti12Ir cluster in comparison with the Ti12Pd and Ti12Ni clusters and pure Ti13 monoatomic nanocluster. This stability trend is as revealed well by both the binding energy and the dissociation energy. The average HOMO-LUMO gap for the bigger clusters revealed that the valence electrons in the HOMO can absorb lower energy, which is indicatory of a higher reactivity and lower stability. The quantum confinement is higher for the smaller clusters, which illustrates a higher stability and lower reactivity for those systems.

Keywords

• clusters
• doping
• binding energy
• relative stability
• HOMO-LUMO
• charge density difference