Multivalent-effect immobilization of reduced-dimensional perovskites for efficient and spectrally stable deep-blue light-emitting diodes
Despite substantial advances in green and red metal halide perovskite light-emitting diodes (PeLEDs), blue PeLEDs, particularly deep-blue ones (defined as Commission International de l’Eclairage y coordinate (CIE y ) less than 0.06) that meet the latest Rec. 2020 colour gamut standard, lag dramatically behind owing to a severe phase segregation-induced electroluminescent spectral shift and low exciton utilization in broadened bandgap perovskite emitters. Here we propose a multivalent immobilization strategy to realize high-efficiency and spectrally stable deep-blue PeLEDs by introducing a polyfluorinated oxygen-containing molecule. Systematic experiments and extensive 5,000 fs ab initio molecular dynamics simulations reveal that a crucial role of the multivalent effect stemming from three kinds of interaction of hydrogen bond (F···H–N), ionic bond (F–Pb) and coordination bond (C=O:Pb) with perovskite is to synergistically stabilize the perovskite phase and enhance exciton radiative recombination. The resultant exciton concentration and exciton recombination rate of the deep-blue perovskite emitter are increased by factors of 1.66 and 1.64, respectively. In this context, our target PeLEDs demonstrate a peak external quantum efficiency of up to 15.36% at a deep-blue emission wavelength of 459 nm and a half-lifetime of 144 min at a constant current density of 0.45 mA cm − 2 . Moreover, the deep-blue PeLEDs maintain a constant spectrum peak with CIE chromaticity coordinates of (0.136, 0.051) under a steady driving current for 60 min.
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