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This study demonstrates that nitrogen-vacancy centers in hexagonal diamond (lonsdaleite) can achieve significantly longer spin coherence times than those found in standard cubic diamond, specifically through symmetry-broken configurations. By leveraging first-principles calculations to identify distinct defect structures with enhanced zero-field splitting, the research provides a theoretical pathway for superior quantum sensing and information processing hardware. These findings highlight lonsdaleite as a promising material platform that could overcome current coherence limitations inherent in conventional diamond-based qubits.
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Nitrogen Vacancy Centers in Hexagonal Diamond Exhibit Long Coherence Times

arXiv2 min read

arXiv:2608.05320v1 Announce Type: cross Abstract: We show that negatively charged nitrogen-vacancy (NV) centers in the hexagonal diamond polymorph lonsdaleite offer a route to spin qubits with enhanced coherence relative to their cubic-diamond counterparts. Using first-principles calculations, we examine two distinct defect configurations, AA, with the same symmetry as in cubic diamond and AB, with reduced symmetry. We find that the AB configuration of the NV center exhibits a finite transverse zero-field splitting, giving rise to an approximate fourfold enhancement of the Hahn-echo coherence time $T_2$ at zero magnetic field. The AA configuration, by contrast, closely reproduces the electronic structure and coherence properties of the cubic NV center. We further characterize the many-body electronic structure, vertical excitation energies, and photoluminescence spectra of both configurations, providing spectral fingerprints for their experimental identification. Our results establish symmetry-broken NV centers in lonsdaleite as promising candidates for quantum sensing and information science applications.

Abstract:We show that negatively charged nitrogen-vacancy (NV) centers in the hexagonal diamond polymorph lonsdaleite offer a route to spin qubits with enhanced coherence relative to their cubic-diamond counterparts. Using first-principles calculations, we examine two distinct defect configurations, AA, with the same symmetry as in cubic diamond and AB, with reduced symmetry. We find that the AB configuration of the NV center exhibits a finite transverse zero-field splitting, giving rise to an approximate fourfold enhancement of the Hahn-echo coherence time $T_2$ at zero magnetic field. The AA configuration, by contrast, closely reproduces the electronic structure and coherence properties of the cubic NV center. We further characterize the many-body electronic structure, vertical excitation energies, and photoluminescence spectra of both configurations, providing spectral fingerprints for their experimental identification. Our results establish symmetry-broken NV centers in lonsdaleite as promising candidates for quantum sensing and information science applications.

Materials Science (cond-mat.mtrl-sci); Computational Physics (physics.comp-ph); Quantum Physics (quant-ph)

arXiv:2608.05320 [cond-mat.mtrl-sci]

(or arXiv:2608.05320v1 [cond-mat.mtrl-sci] for this version)

https://doi.org/10.48550/arXiv.2608.05320 Focus to learn more arXiv-issued DOI via DataCite (pending registration)

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Full text under the publisher's open licence · 243 words

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