摘要
It is always difficult to control the growth of crystals during the formation of multiple quantum wells (MQWs) in the quasi-2D perovskite light emitting diodes (PeLEDs). In this study, we introduce the 1, 4, 7, 10-tetraoxacyclododecane ether into the quasi-2D perovskite of PEA 2 Cs n-1 Pb n Br 3n+1 to reduce the coordination rate between the phenethylamine bromide and the perovskite framework. As a result, Crown-ether assisted in-situ grown (CAIG) perovskite crystals (PCs) is grown with thick PbBr 4 layers (n > 55) during the spin-coating. For the CAIG PCs, the generation of small n phases (n = 1, 2 and 3) are significantly suppressed, resulting in almost flat energy structure with the phases of n ≥ 4. The generation rate of the excited states of the n ≥ 4 remains ultra-fast within ~0.77 ps even without the MQWs structures; however the decay of excited states becomes much slower. The CAIG PCs film has lower trap density , therefore promoting the carrier mobility , carrier diffusion length and the photoluminescence quantum yield . The PeLEDs based on the CAIG PCs film achieves the maximum luminescence of ~27562 cd m −2 and the maximum external quantum efficiency (EQE) of ~16.1%. The half-lifetime of the luminescence and the EQE measured in the atmosphere (a relative humidity of ~52% at 27 ℃) are exceeding ~17 and 43 h, respectively. Hence, it can be recognized as the most ambient stable device based on the PEA 2 Cs n-1 Pb n Br 3n+1 perovskite.
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