In:
Physical Chemistry Chemical Physics, Royal Society of Chemistry (RSC), Vol. 25, No. 37 ( 2023), p. 25818-25827
Abstract:
The nitrogen-vacancy center doped with hydrogen (NVH) is one of the most common defects in diamonds, and the doping of hydrogen is known to enable mobility among three equivalent C-radicals in the defect, which noticeably affects the spin coupling among the radicals. Here, we for the first time uncover the dynamic nature of magnetic coupling induced by H-migration in the NVH center of nanodiamonds, using spin-polarized density functional theory calculations and enhanced sampling metadynamics simulations. The mobility of doping H enables the interior NVH region to become a variable magnetic space (antiferromagnetic/AFM versus ferromagnetic/FM). That is, the dynamic H has three frequently reachable binding C sites where H enables the center to exhibit variable AFM coupling (high up to J = −1282 cm −1 ) and that in other H-reachable regions including N sites, it enables the center to exhibit FM coupling (high up to J = 598 cm −1 ). The magnetic switching (AFM ↔ FM) and strength fluctuation strongly depend on the H-position which can adjust the ratio of the C radical orbitals in their mixing orbitals for a special three-electron three-center covalent C⋯H⋯C H-bonding and radical orbital distributions. Clearly, this work provides insights into the dynamic switching of magnetic coupling in such multi-radical centers of defect nanodiamonds.
Type of Medium:
Online Resource
ISSN:
1463-9076
,
1463-9084
Language:
English
Publisher:
Royal Society of Chemistry (RSC)
Publication Date:
2023
detail.hit.zdb_id:
1476283-3
detail.hit.zdb_id:
1476244-4
detail.hit.zdb_id:
1460656-2
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