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Achieving higher brightness of a single-photon emitter (SPE) is central for advanced applications from quantum information processing to quantum sensing. However, most approaches of integrating quantum emitters and photonic resonators require accurately localizing the emitter into a photonic structure, which is a challenge. Here, we report using dielectric microspheres for laser focusing to create SPEs in hexagonal boron nitride and in situ enhance the emission via photonic coupling between the SPE and the dielectric microspheres. The photoluminescence intensity is increased by 2.4-fold, achieving a high brightness SPE with a saturation intensity of up to 19.6 Mcounts s−1. This approach provides a feasible way to generate a high-performance SPE while simultaneously enabling precise coupling of the quantum light source and optical resonators. [ABSTRACT FROM AUTHOR]

Low‐dimensional halide perovskites with broad emission are a hot topic for their promising application as white light sources. However, the physical origin of this broadband emission in the sub‐bandgap region is still controversial. This work investigates the broad Stokes‐shifted emission bands in mixed lead‐tin 2D perovskite films prepared by mixing precursor solutions of phenethylammonium lead iodide (PEA2PbI4, PEA = phenethylammonium) and phenethylammonium tin iodide (PEA2SnI4). The bandgap can be tuned by the lead‐tin ratio, whereas the photoluminescence is broad and significantly Stokes‐shifted and appears to be fairly insensitive to the relative amount of Pb and Sn. It is experimentally observed that these low‐dimensional systems show substantially less bandgap bowing than their 3D counterpart. Theoretically, this can be attributed to the smaller spin–orbit coupling effect on the 2D perovskites compared to that of 3D ones. The time‐resolved photoluminescence shows an ultrafast decay in the high‐energy range of the spectra that coincides with the emission range of PEA2SnI4, while the broadband emission decay is slower, up to the microsecond range. Sub‐gap photoexcitation experiments exclude exciton self‐trapping as the origin of the broadband emission, pointing to defects as the origin of the broadband emission in 2D Sn/Pb perovskite alloys. [ABSTRACT FROM AUTHOR]

This paper reports the two-photon absorption (TPA) and the spectral-narrowed light emission (SNLE) from the crystals of 9, 10-distyrylanthracene (DSA) derivatives. The results obtained by the Z-scan method show that the tested molecules possess high TPA cross sections. Upon near-IR excitation, strong two-photon-excited fluorescence could be observed in the crystals of four types of materials. Furthermore, SNLE with low threshold occurs in three of the four crystals under pumping with the second harmonic generated in the amplifier. Single crystals of the DSA derivatives exhibit unique photonic properties, including strong solid-state fluorescence, large TPA cross section, and stimulated emission. The results demonstrate that these are potential candidates for compact and practical solid-state laser applications. [ABSTRACT FROM PUBLISHER]