| Literature DB >> 30199226 |
Shuai Yuan1, Zhao-Kui Wang1, Ming-Peng Zhuo1, Qi-Sheng Tian1, Yan Jin1, Liang-Sheng Liao1,2.
Abstract
Full inorganic cesium lead halide perovskites (IOPs) are regarded as attractive candidates for light-emitting diodes (LEDs) by their excellent luminescent conversion. However, unsatisfactory efficiency and stability are still the main drawbacks that hinder the commercialization progress of perovskite LEDs (PeLEDs). Here, we report an extremely uniform and flat CsPbBr3 film composing of self-assembly core-shell structured quantum dots (SCQDs) based on one-step precursor coating. The QDs size in the CsPbBr3 film is around 4.5 nm (smaller than the Bohr radius), which significantly confines injected carriers and leads to a ultrahigh exciton binding energy ( Eb) of 198 meV. In addition, unfavorable surfacial defects are dramatically passivated by a thin surfacial-capping layer composed of long-chain ammonium groups (phenylalanine bromide, PPABr), resulting in an ultralow nonradiative recombination rate. Consequently, the CsPbBr3 SCQDs film presents a high photoluminescence quantum yield (PLQY) of 85%. It enables the resulting green PeLEDs to deliver a recorded external quantum efficiency (EQE) over 15% with ideal operational stability. Furthermore, the developed CsPbBr3 SCQDs film also demonstrates promising potential in multifunctional lighting sources such as flexible and smart devices.Entities:
Keywords: LED; excitonic binding energy; in situ grown; perovskite; quantum dots; trap passivation
Year: 2018 PMID: 30199226 DOI: 10.1021/acsnano.8b05185
Source DB: PubMed Journal: ACS Nano ISSN: 1936-0851 Impact factor: 15.881