Lead- and tin-vacancy centers in diamond could work as a solid-state source of single photons with addressable spins at more practical temperatures than other approaches, an essential step for practical quantum communication networks.
Many applications in quantum information processing require multiple, identical quantum emitters. Among various color centers in diamond, tin-vacancy centers draw attention because of their high quantum efficiency and long spin coherence. The authors study the shifts of optical-transition frequencies of these centers in an applied electric field, and importantly find that both the linear and quadratic coefficients are orders of magnitude smaller than those of non-inversion-symmetric defects such as nitrogen-vacancy centers. This low susceptibility allows the integration of tin-vacancy centers into photonic nanostructures, which is essential for efficient spin-photon interfaces.
Color centers in diamond have attracted much interest as candidates for optically active, solid-state quantum bits. Of particular interest are inversion-symmetric color centers based on group-IV impurities in diamond because they emit strongly into their zero-phonon lines and are insensitive to electric field noise to first order. Early studies of the negatively charged tin-vacancy (${\mathrm{SnV}}^{\ensuremath{-}}$) center in diamond have found the ${\mathrm{SnV}}^{\ensuremath{-}}$ to be a promising candidate: it has high quantum efficiency, emits strongly into its zero-phonon lines, and is expected to have a long T2 spin coherence time at 4 K. To develop the ${\mathrm{SnV}}^{\ensuremath{-}}$ into a spin qubit requires further characterization, especially of the spin and optical properties of individual ${\mathrm{SnV}}^{\ensuremath{-}}$ in nanofabricated structures. In this work, we isolate single ${\mathrm{SnV}}^{\ensuremath{-}}$ centers in diamond nanopillars and characterize their emission properties and their spin response to a magnetic field. We observe narrow emission linewidths <250 MHz, as well as a strong polarization dependence of each transition. We also find the Zeeman splitting under a magnetic field to be in good agreement with theoretical prediction. Our results pave the way toward future employment of single ${\mathrm{SnV}}^{\ensuremath{-}}$ centers as optically accessible quantum memories.
The development of reliable devices to generate single photons is crucial for applications in quantum cryptography, as well as for fundamental quantum optics experiments. Due to their extremely high photostability at room temperature, optically active defects in solids, the so called color centers, are among the most promising candidates. Single NV (nitrogen-vacancy) centers in diamond have been demonstrated to be able to generate single photons and have already shown advantages compared to attenuated laser pulses in a quantum cryptography experiment. The nitrogen-vacancy center (NV center) in diamond consists of a substitutional nitrogen atom and an adjacent vacancy. This complex exhibits an optical transition with a fluorescence lifetime of 11.6 ns. The room temperature spectrum of the NV center consists of the zero-phonon line at 637 nm and broad phononic sidebands with a FWHM of more than 100 nm. Due to the existence of a shelving level the efficiency of the NV center as a single photon source is limited. Additionally, the high diffraction index of bulk diamond restricts the efficiency to collect the fluorescence light.