Deterministic creation of strained color centers in nanostructures via high-stress thin films

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Abstract

Color centers have emerged as a leading qubit candidate for realizing hybrid spin-photon quantum information technology. One major limitation of the platform, however, is that the characteristics of individual color centers are often strain dependent. As an illustrative case, the silicon-vacancy center in diamond typically requires millikelvin temperatures in order to achieve long coherence properties, but strained silicon-vacancy centers have been shown to operate at temperatures beyond 1 K without phonon-mediated decoherence. In this work, we combine high-stress silicon-nitride thin films with diamond nanostructures to reproducibly create statically strained silicon-vacancy color centers (mean ground state splitting of 608 GHz) with strain magnitudes of ∼ 4 × 10 − 4 . Based on modeling, this strain should be sufficient to allow for operation of a majority silicon-vacancy centers within the measured sample at elevated temperatures (1.5 K) without any degradation of their spin properties. This method offers a scalable approach to fabricate high-temperature operation quantum memories. Beyond silicon-vacancy centers, this method is sufficiently general that it can be easily extended to other platforms as well.

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Assumpcao, D. R., Jin, C., Sutula, M., Ding, S. W., Pham, P., Knaut, C. M., … Loncar, M. (2023). Deterministic creation of strained color centers in nanostructures via high-stress thin films. Applied Physics Letters, 123(24). https://doi.org/10.1063/5.0171558

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