Eur. Phys. J. Appl. Phys. 101, 9 (2026)
https://doi.org/10.1051/epjap/2026006

Original Article

The dual role of vacancies and dopants in hydrogen dissociation and diffusion On Mg(0001)

¹ Laboratory of Coatings, Materials, and Environments (LCME), Mhamed Bougara University of Boumerdes (UMBB), Boumerdes 35000, Algeria
² Atomic Energy Commission “COMENA”, Algiers 16000, Algeria

^* e-mail: This email address is being protected from spambots. You need JavaScript enabled to view it.

Received: 28 October 2025
Accepted: 11 May 2026
Published online: 16 June 2026

Abstract

Magnesium hydrides offer superior theoretical hydrogen storage capacities; however, their practical implementation is severely constrained by sluggish sorption kinetics. This study employs first-principles density functional theory (DFT) to elucidate the atomistic mechanisms governing hydrogen interaction with Mg(0001) surfaces, incorporating clean, vacancy-containing, Ti-doped, and Ti–M (M = Nb, V, Zr) co-doped configurations. Two-dimensional potential energy surface mapping reveals that H₂ dissociation on pristine Mg(0001) is kinetically hindered by a 0.95 eV activation barrier along the bridge site (90,150). Substitutional Ti-doping significantly enhances surface reactivity, reducing this barrier to 0.25 eV, thereby functioning as a potent catalyst for hydrogen activation. Despite this catalytic benefit, nudged elastic band calculations identify a critical “dual role” for transition metal dopants: while Ti facilitates surface dissociation, it introduces a substantial subsurface kinetic trap characterized by a secondary migration barrier of 0.897 eV. Conversely, surface vacancies act primarily as diffusion promoters; although they increase the surface dissociation barrier to 1.10 eV, they facilitate hydrogen entry by lowering the initial penetration barrier to 0.328 eV. Projected density-of-states analysis confirms that Ti d-states provide the requisite orbital flexibility for facile dissociation but simultaneously induce localized stabilization that arrests long-range mobility. We demonstrate that Ti–V co-doping optimizes the energetic landscape, effectively mitigating Ti-induced trapping by restoring the subsurface barrier to 0.220 eV. This investigation identifies a fundamental Sabatier-type trade-off between surface activation and bulk transport, providing a robust theoretical framework for the strategic design of Mg-based storage materials.