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Nature Nanotechnology

Harmonizing single photons with a laser pulse

Liang Zhai, Alisa Javadi

Published Apr 26, 2022• 3 citations
Publisher
DOI
10.1038/s41565-022-01117-0

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We demonstrate a miniaturized, scalable high rate, pulsed single-photon source in the telecom band obtained by heralding a spontaneous parametric downconversion source pumped with a highly tunable GHz repetition rate pulsed laser in an all-guided wave scheme. For developing this source, we first perform second harmonic generation of ultrashort pump pulses varying with GHz rate at the telecom wavelength. Our investigation demonstrates a trade-off between the spectral brightness and the single-photon purity of the heralded single-photon source by controlling the repetition rate of pump pulses. For a 5 GHz repetition rate, a periodically poled lithium niobate waveguide in type-0 configuration produces the highest spectral brightness ∼8.5×106pairs/s/mW/GHz. We quantify the single-photon purity using the second-order autocorrelation function g(2), which reaches the lowest value of ∼(3.4 ± 0.038) × 10−4 for 20 GHz repetition rate pulses, generating heralded single photons at 45 kHz rate. Our all-guided wave configuration offers easy integration and alignment, paving the way for developing scalable, integrable, tunable purity single-photon sources for quantum technology applications, such as quantum communication and quantum networks.
We theoretically study multiphoton ionization of the Ca atom irradiated by the second (photon energy 3.13.13.1 eV) and third (photon energy 4.65 eV) harmonics of Ti:sapphire laser pulses (photon energy 1.551.551.55 eV). Because of the dense energy level structure the second and third harmonics of a Ti:sapphire laser are nearly single-photon resonant with the 4s4p4s4p4s4p 1Po{}^{1}{P}^{o}1Po and 4s5p4s5p4s5p 1Po{}^{1}{P}^{o}1Po states, respectively. Although two-photon ionization takes place through the near-resonant intermediate states with the same symmetry in both cases, it turns out that there are significant differences between them. The photoelectron energy spectra exhibit the absence or presence of substructures. More interestingly, the photoelectron angular distributions clearly show that the main contribution to the ionization processes by the third harmonic arises from the far-off-resonant 4s4p4s4p4s4p 1Po{}^{1}{P}^{o}1Po state rather than the near-resonant 4s5p4s5p4s5p 1Po{}^{1}{P}^{o}1Po state. These findings can be attributed to the fact that the dipole moment for the 4s24{s}^{2}4s2 ${}^{1}{S}^{e}\ensuremath{-}4s5p$ 1Po{}^{1}{P}^{o}1Po transition is much smaller than that for the 4s24{s}^{2}4s2 ${}^{1}{S}^{e}\ensuremath{-}4s4p$ 1Po{}^{1}{P}^{o}1Po transition.