Solution-processable organometal halide perovskites have been emerging as very promising materials for light-emitting diodes (LEDs) because of their high color purity, low cost, and high photoluminescence quantum yield. However, their electroluminescent performance is still limited by incomplete surface coverage and inefficient charge injection into the perovskite. Here, we demonstrate highly efficient perovskite LEDs (PeLEDs) incorporating full film coverage and bipolar charge injection within the active layer by introducing perovskite precursor poly(9-vinylcarbazole):1,3,5-tris(1-phenyl-1H-benzimidazol-2-yl)benzene (PVK:TPBi) toluene solution into CHNHPbBr N,N-dimethylformamide solution. Both the film coverage and the charge injections were simultaneously improved by antisolvent of toluene and PVK:TPBi matrix, respectively. After the film morphology and weight ratio of PVK:TPBi were carefully adjusted, the optimal PeLEDs gave efficient emission with turn-on voltage of ∼2.8 V, maximum luminance of ∼7263 cd/m, maximum current efficiency of ∼9.45 cd/A, and maximum external quantum efficiency of ∼2.28%, which are among the best results based on MAPbBr reported to date.

Organic-inorganic hybrid perovskites have drawn considerable attention due to their great potentials in lighting and displaying. Despite great progress being demonstrated in perovskites light-emitting diodes (PeLEDs), the commercialization of PeLEDs was still limited by their low efficiencies and poor device stabilities. Utilizing the metallic nanoparticles was a feasible way to further improve the efficiencies of PeLEDs. Herein, substantially enhanced electroluminescent performance of CHNHPbBr-based PeLEDs were first demonstrated by incorporating plasmonic gold nanoparticles (Au NPs) into the hole injection layer of poly(3,4-ethylenedioxythiophene):poly(styrenesulfonate) (PEDOT:PSS). Compared to the reference device without Au NPs, 109% enhancement in maximum luminance and 97% enhancement in maximum EQE were achieved upon 9 vol % Au NPs doping. Such enhancements can be ascribed to the localized surface plasmon resonance between Au NPs and CHNHPbBr excitons, as well as the enhanced electrical conductivity of modified PEDOT:PSS. Our studies indicated great potential of Au NPs in developing highly efficient PeLEDs.

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Compared to organic-inorganic hybrid metal halide perovskites, all-inorganic cesium lead halides (e.g, CsPbBr) hold greater promise in being emissive materials for light-emitting diodes owing to their superior optoelectronic properties as well as their higher stabilities. However, there is still considerable potential for breakthroughs in the current efficiency of CsPbBr perovskite light-emitting diodes (PeLEDs). Electrode quenching is one of the main problems limiting the current efficiency of PeLEDs when poly(3,4-ethylenedioxythiophene): poly(styrenesulfonate) (PEDOT:PSS) is used as the hole injection layer. In this work, electrode quenching control was realized via incorporating Au NPs into PEDOT:PSS. As a result, the CsPbBr PeLEDs realized an improvement in maximum luminescence ranging from ∼2348 to ∼7660 cd m (∼226% enhancement) and current efficiency from 1.65 to 3.08 cd A (∼86% enhancement). Such substantial enhancement of the electroluminescent performance can be attributed to effective electrode quenching control at the PEDOT:PSS/CsPbBr perovskite interface via the combined effects of local surface plasma resonance coupling and enhanced hole transportation in the PEDOT:PSS layer by Au nanoparticles.

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