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The recombination mechanisms leading to amplified spontaneous emission at the true-green wavelength in CH3NH3PbBr3 perovskites

机译:重组机制导致CH3NH3PbBr3钙钛矿中真绿色波长处的自发发射放大

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摘要

We investigated the mechanisms of radiative recombination in a CH3NH3PbBr3 hybrid perovskite material using low-temperature, power-dependent (77K), and temperature-dependent photoluminescence (PL) measurements. Two bound-excitonic radiative transitions related to grain size inhomogeneity were identified. Both transitions led to PL spectra broadening as a result of concurrent blue and red shifts of these excitonic peaks. The red-shifted bound-excitonic peak dominated at high PL excitation led to a true-green wavelength of 553nm for CH3NH3PbBr3 powders that are encapsulated in polydimethylsiloxane. Amplified spontaneous emission was eventually achieved for an excitation threshold energy of approximately 350μJ/cm2. Our results provide a platform for potential extension towards a true-green light-emitting device for solid-state lighting and display applications.
机译:我们使用低温,功率相关(77K)和温度相关的光致发光(PL)测量研究了CH3NH3PbBr3杂化钙钛矿材料中的辐射重组机制。确定了两个与晶粒尺寸不均匀性有关的激振辐射跃迁。由于这些激子峰同时发生蓝移和红移,两个跃迁均导致PL光谱变宽。在高PL激发下占主导地位的红移束缚激子峰导致封装在聚二甲基硅氧烷中的CH3NH3PbBr3粉末的真绿色波长为553nm。最终实现了约350μJ/ cm2的激发阈值能量的放大自发发射。我们的结果为固态照明和显示应用的真正绿色发光器件提供了潜在扩展的平台。

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