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This study establishes a novel method for identifying carbon-based spin qubits in hexagonal boron nitride by decoding their atomic structures through electron-spin decoherence fingerprints. By leveraging first-principles calculations and isotope engineering, the research provides a critical pathway to characterize defects without relying solely on optical spectroscopy. This advancement directly addresses the challenge of scaling room-temperature quantum sensors and processors by enabling precise structural verification of qubit candidates.
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Coherence-Based Identification of Carbon-Based Spin Qubits in Hexagonal Boron Nitride from First Principles

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arXiv:2608.20833v1 Announce Type: new Abstract: Carbon-related defects in hexagonal boron nitride are promising room-temperature single-spin qubits and quantum sensors, but their atomic structures remain largely unidentified. Here we show, using first-principles calculations of electron-spin decoherence, that the atomic structure of each defect is imprinted in its spin coherence. Mapping the Hahn-echo dynamics of seven candidate carbon defects across magnetic field and four isotope-engineered nuclear-spin baths, we find that electron-spin-echo envelope modulation emerges at defect-specific magnetic fields, at which the nearest-neighbor nuclear spins satisfy a cancellation condition set by their hyperfine and quadrupole couplings. Both the fields and the modulation frequencies follow from an analytical model using computed hyperfine and quadrupole tensors alone, and they shift or vanish upon isotope substitution. At low fields, the field dependence of the coherence time separates the defects into two classes according to the sublattice occupied by carbon. These decoherence fingerprints, directly testable in isotope-engineered samples, establish a structural identification route complementary to optical spectroscopy.

Abstract:Carbon-related defects in hexagonal boron nitride are promising room-temperature single-spin qubits and quantum sensors, but their atomic structures remain largely unidentified. Here we show, using first-principles calculations of electron-spin decoherence, that the atomic structure of each defect is imprinted in its spin coherence. Mapping the Hahn-echo dynamics of seven candidate carbon defects across magnetic field and four isotope-engineered nuclear-spin baths, we find that electron-spin-echo envelope modulation emerges at defect-specific magnetic fields, at which the nearest-neighbor nuclear spins satisfy a cancellation condition set by their hyperfine and quadrupole couplings. Both the fields and the modulation frequencies follow from an analytical model using computed hyperfine and quadrupole tensors alone, and they shift or vanish upon isotope substitution. At low fields, the field dependence of the coherence time separates the defects into two classes according to the sublattice occupied by carbon. These decoherence fingerprints, directly testable in isotope-engineered samples, establish a structural identification route complementary to optical spectroscopy.

Quantum Physics (quant-ph); Mesoscale and Nanoscale Physics (cond-mat.mes-hall)

arXiv:2608.20833 [quant-ph]

(or arXiv:2608.20833v1 [quant-ph] for this version)

https://doi.org/10.48550/arXiv.2608.20833 Focus to learn more arXiv-issued DOI via DataCite (pending registration)

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