A user‐friendly, fiber‐coupled, single‐photon source operating at telecom wavelengths is a key component of photonic quantum networks providing long‐haul, ultra‐secure data exchange. To take full advantage of quantum‐mechanical data protection and to maximize the transmission rate and distance, a true quantum source providing single photons on demand is highly desirable. This great challenge is tackled by developing a ready‐to‐use semiconductor quantum‐dot‐based device that launches single photons at a wavelength of 1.3 µm directly into a single‐mode optical fiber. In the proposed approach, the quantum dot is deterministically integrated into a nanophotonic structure to ensure efficient on‐chip coupling into a fiber. The whole arrangement is integrated into a 19ʺ compatible housing to enable stand‐alone operation by cooling via a compact Stirling cryocooler. The realized source delivers single photons with a multiphoton events probability as low as 0.15 and a single‐photon emission rate of up to 73 kHz into a standard telecom single‐mode fiber.

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Energy transfer in the excited state of molecules including quenching, rotational and vibrational energy transfer, and polarization scrambling is one of the major factors which limit the accuracy of laser-induced fluorescence (LIF) measurements. In this contribution, we present time-, wavelength-, and polarization-resolved spectra of OH in a stoichiometric H2/air flame at atmospheric pressure. Emphasis is placed on the investigation of the role of polarization effects and of multi-quantum vibrational energy transfer on fluorescence spectra originating from the OH A2sigma+ state. Results are compared to simulations using a rate-equation model (LASKIN) developed in our group.