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Despite the rapid development of high-efficiency perovskite light-emitting diodes (PeLEDs) via material design and morphology control, a comprehensive evaluation of the power loss among various optical modes has seldom been conducted for the precise design of device architectures. Here, a quantitative analysis of light outcoupling efficiency (η out ) of PeLEDs is presented with the theoretical simulations by taking into account the key factors of refractive index and film thickness of various functional layers, and the emitter dipole orientation. For a planar PeLED, a rational design to enhance the η out is predicted by constructing multilayer stack in series of transparent electrode/high-index transport layer/perovskite emitter/low-index transport layer/reflective electrode. Furthermore, the role of photonic structures on the outcoupling management is explored, and the potential of a substantial increase in η out is demonstrated with an enhancement factor of over 1.75 by implementing a moth-eye nanostructure into the emitter. We anticipate that the findings shown here will provide the design guidelines for the optical optimization of PeLEDs. [ABSTRACT FROM AUTHOR]

Abstract While metal halide hybrid perovskite solar cells (PeSCs) are remarkably efficient, the rapid and undesirable degradation limit their practical applications for renewable energy sources. Herein, the evolution of perovskite decomposition under white light illumination has been investigated under the ultrahigh vacuum conditions, which can effectively rule out the influence of other factors such as oxygen or moisture. The chemical composition, electronic structure, surface morphology, and crystal structure of CH 3 NH 3 PbI 3 perovskite films have been systematically characterized by X-ray and ultraviolet photoelectron spectroscopies (XPS and UPS), scanning electron microscopy, and X-ray diffraction techniques. The surface roughening with cracks and defects occurs in CH 3 NH 3 PbI 3 perovskite films after a short-time white-light illumination in ultrahigh vacuum. In situ compositional analysis reveals the decomposition of the perovskite films with the appearance of metallic Pb feature, which is accompanied with the energy level shift towards higher binding energy during the illumination process. However, the decomposition rate is decreased and becomes saturated after exposed to light illumination for 24 h. These findings provide a direct evidence that CH 3 NH 3 PbI 3 perovskite is photosensitive, and a light-induced degradation mechanism is proposed. Graphical abstract Image 1 Highlights • The perovskite decomposition under white light illumination is explored under ultrahigh vacuum conditions. • In-situ compositional analysis reveals the perovskite decomposition with the appearance of metallic Pb. • A light-induced degradation mechanism is proposed. [ABSTRACT FROM AUTHOR]

Perovskites light emitting diodes (PeLEDs) are promising candidates for next-generation display devices because of their attractive properties of low-cost, solution processability and excellent color purity. For metal halide perovskite materials, the emission tuning can be easily achieved by altering halide composition. However, blue PeLEDs with chlorine incorporation usually suffer from the severe phase segregation and ion migration, resulting in the red-shifted electroluminescence and the efficiency degradation. Here, the partial substitution of Pb2+ ions with non-toxic Sr2+ is adopted to enhance the formation energy of Sr-alloyed perovskite films, leading to the negligible electroluminescence in electrically driven blue PeLEDs. The maximum brightness and efficiency are optimized simultaneously. Further, such a substitution can greatly enhance the thermal and operational stabilities of PeLEDs. Image 1 • Nontoxic strontium was adopted to partly substitute Pb in perovskites for blue emission. • Spectral and thermal stabilities of PeLEDs are improved by inhibiting ion migrations. • The stability enhancement arises from the increase in the formation energy. [ABSTRACT FROM AUTHOR]