4.8 Article

A Multifunctional Halide-Equivalent Anion Enabling Efficient CsPb(Br/I)3 Nanocrystals Pure-Red Light-Emitting Diodes with External Quantum Efficiency Exceeding 23%

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ADVANCED MATERIALS
卷 35, 期 8, 页码 -

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WILEY-V C H VERLAG GMBH
DOI: 10.1002/adma.202209002

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CsPb(Br; I)(3) nanocrystals; halide vacancies; phase separation; pure-red light-emitting diodes; self-doping effect

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In this study, a multifunctional additive of benzenesulfonate (BS-) is introduced into CsPb(Br/I)(3) nanocrystals to improve the efficiency and stability of pure-red perovskite LEDs (PeLEDs). The BS- can passivate defects on the surface of nanocrystals and increase the formation energy of halide vacancies. The electron-withdrawing property of sulfonate group can reduce the self-doping effect and alter the behavior of CsPb(Br/I)(3) nanocrystals. With this strategy, the pure-red PeLEDs achieve a synergistic boost in device performance with CIE coordinates of (0.70, 0.30) and a champion external quantum efficiency of 23.5%, approaching the Rec. 2020 red primary color.
Pure-red perovskite LEDs (PeLEDs) based on CsPb(Br/I)(3) nanocrystals (NCs) usually suffer from a compromise in emission efficiency and spectral stability on account of the surface halide vacancies-induced nonradiative recombination loss, halide phase segregation, and self-doping effect. Herein, a halide-equivalent anion of benzenesulfonate (BS-) is introduced into CsPb(Br/I)(3) NCs as multifunctional additive to simultaneously address the above challenging issues. Joint experiment-theory characterizations reveal that the BS- can not only passivate the uncoordinated Pb2+-related defects at the surface of NCs, but also increase the formation energy of halide vacancies. Moreover, because of the strong electron-withdrawing property of sulfonate group, electrons are expected to transfer from the CsPb(Br/I)(3) NC to BS- for reducing the self-doping effect and altering the n-type behavior of CsPb(Br/I)(3) NCs to near ambipolarity. Eventually, synergistic boost in device performance is achieved for pure-red PeLEDs with CIE coordinates of (0.70, 0.30) and a champion external quantum efficiency of 23.5%, which is one of the best value among the ever-reported red PeLEDs approaching to the Rec. 2020 red primary color. Moreover, the BS--modified PeLED exhibits negligible wavelength shift under different operating voltages. This strategy paves an efficient way for improving the efficiency and stability of pure-red PeLEDs.

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