Abstract

Spin defects in van der Waals materials offer a promising platform for advancing quantum technologies. Here, we propose and demonstrate a powerful technique based on isotope engineering of host materials to significantly enhance the coherence properties of embedded spin defects. Focusing on the recently-discovered negatively charged boron vacancy center (VB−\mathrm{V}_{\mathrm{B}}^-) in hexagonal boron nitride (hBN), we grow isotopically purified h10B15N\mathrm{h}{}^{10}\mathrm{B}{}^{15}\mathrm{N} crystals. Compared to VB−\mathrm{V}_{\mathrm{B}}^- in hBN with the natural distribution of isotopes, we observe substantially narrower and less crowded VB−\mathrm{V}_{\mathrm{B}}^- spin transitions as well as extended coherence time T2T_2 and relaxation time T1T_1. For quantum sensing, VB−\mathrm{V}_{\mathrm{B}}^- centers in our h10B15N\mathrm{h}{}^{10}\mathrm{B}{}^{15}\mathrm{N} samples exhibit a factor of 44 (22) enhancement in DC (AC) magnetic field sensitivity. For additional quantum resources, the individual addressability of the VB−\mathrm{V}_{\mathrm{B}}^- hyperfine levels enables the dynamical polarization and coherent control of the three nearest-neighbor 15N{}^{15}\mathrm{N} nuclear spins. Our results demonstrate the power of isotope engineering for enhancing the properties of quantum spin defects in hBN, and can be readily extended to improving spin qubits in a broad family of van der Waals materials.

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