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Machine learning is a powerful tool in finding hidden data patterns for quantum information processing. Here, we introduce this method into the optical readout of electron-spin states in diamond via single-photon collection and demonstrate improved readout precision at room temperature. The traditional method of summing photon counts in a time gate loses all the timing information crudely. We find that changing the gate width can only optimize the contrast or the state variance, not both. In comparison, machine learning adaptively learns from time-resolved fluorescence data, and offers the optimal data processing model that elaborately weights each time bin to maximize the extracted information. It is shown that our method can repair the processing result from imperfect data, reducing 7% in spin readout error while optimizing the contrast. Note that these improvements only involve recording photon time traces and consume no additional experimental time, they are thus robust and free. Our machine learning method implies a wide range of applications in precision measurement and optical detection of states.
The diamond nitrogen-vacancy (NV) center is a leading platform for quantum information science due to its optical addressability and room-temperature spin coherence. However, measurements of the NV centers spin state typically require averaging over
We utilize nonlinear absorption to design all-optical protocols that improve both charge state initialization and spin readout for the nitrogen-vacancy (NV) center in diamond. Non-monotonic variations in the equilibrium charge state as a function of
Applications of negatively charged nitrogen-vacancy center in diamond exploit the centers unique optical and spin properties, which at ambient temperature, are predominately governed by electron-phonon interactions. Here, we investigate these interac
We theoretically propose a method to realize optical nonreciprocity in rotating nano-diamond with a nitrogen-vacancy (NV) center. Because of the relative motion of the NV center with respect to the propagating fields, the frequencies of the fields ar
We present systematic measurements of longitudinal relaxation rates ($1/T_1$) of spin polarization in the ground state of the nitrogen-vacancy (NV$^-$) color center in synthetic diamond as a function of NV$^-$ concentration and magnetic field $B$. NV