The mechanism for low-temperature photoluminescence (PL) emissions in GaNAs epilayers and ${\mathrm{GaAs/GaN}}_x{\mathrm{As}}_{\text{1−x}}$ quantum well (QW) structures grown by molecular-beam epitaxy is studied in detail, employing PL, PL excitation, and time-resolved PL spectroscopies. It is shown that even though quantum confinement causes a strong blueshift of the GaNAs PL emission, its major characteristic properties are identical in both QW structures and epilayers. Based on the analysis of the PL line shape, its dependence on the excitation power and measurement temperature, as well as transient data, the PL emission is concluded to be caused by a recombination of excitons trapped by potential fluctuations in GaNAs.

Although perovskite light-emitting diodes (PeLEDs) have recently experienced significant progress, there are only scattered reports of PeLEDs with both high efficiency and long operational stability, calling for additional strategies to address this challenge. Here, we develop perovskite-molecule composite thin films for efficient and stable PeLEDs. The perovskite-molecule composite thin films consist of in-situ formed high-quality perovskite nanocrystals embedded in the electron-transport molecular matrix, which controls nucleation process of perovskites, leading to PeLEDs with a peak external quantum efficiency of 17.3% and half-lifetime of approximately 100 h. In addition, we find that the device degradation mechanism at high driving voltages is different from that at low driving voltages. This work provides an effective strategy and deep understanding for achieving efficient and stable PeLEDs from both material and device perspectives.

The optical signatures of Mg-related acceptors in GaN have been revisited in samples specifically grown on bulk GaN templates, to avoid strain broadening of the optical spectra. Bound-exciton spectra can be studied in these samples for Mg concentrations up to $[\mathrm{Mg}]\approx 2\times {10}^{19}{\mathrm{cm}}^{-3}$. Contrary to previous work it is found that instabilities in the photoluminescence spectra are not due to unstable shallow donors, but to unstable Mg-related acceptors. Our data show that there are two Mg-related acceptors simultaneously present: the regular (stable) substitutional Mg acceptor, and a complex acceptor which is unstable in $p$-GaN.

Single fractional monolayer (FM) CdSe/ZnSe structures have been grown by molecular beam epitaxy (MBE), employing both conventional MBE and migration-enhanced epitaxy (MEE). A precise calibration of the FM mean thickness in the range of 0.15–3.0 ML has been performed for both techniques, revealing more than a 3.5 times lower Cd incorporation ability for the MEE mode at the same Cd and Se incident fluxes. Steady-state and time-resolved photoluminescence spectroscopy is used to characterize the intrinsic morphology of the CdSe FMs, with a special emphasis on the submonolayer thickness range. Both MBE and MEE grown samples exhibit inhomogeneity of the excitonic system, which can be explained by coexistence of a homogeneous alloylike layer and relatively large CdSe 2D clusters. The MEE samples display smaller fluctuations of the layer thickness and island sizes.