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The ground exciton state of formamidinium lead bromide perovskite nanocrystals is a singlet dark state

机译:甲脒铅溴化溴化物钙钛矿纳米晶体的地基激子状态是单态暗状态

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摘要

Lead halide perovskites have emerged as promising new semiconductor materials for high-efficiency photovoltaics, light-emitting applications and quantum optical technologies. Their luminescence properties are governed by the formation and radiative recombination of bound electron-hole pairs known as excitons, whose bright or dark character of the ground state remains unknown and debated. While symmetry analysis predicts a singlet non-emissive ground exciton topped with a bright exciton triplet, it has been predicted that the Rashba effect may reverse the bright and dark level ordering. Here, we provide the direct spectroscopic signature of the dark exciton emission in the low-temperature photoluminescence of single formamidinium lead bromide perovskite nanocrystals under magnetic fields. The dark singlet is located several millielectronvolts below the bright triplet, in fair agreement with an estimation of the long-range electron-hole exchange interaction. Nevertheless, these perovskites display an intense luminescence because of an extremely reduced bright-to-dark phonon-assisted relaxation.
机译:铅卤化物佩洛夫斯基斯已成为高效光伏,发光应用和量子光学技术的新半导体材料。它们的发光性质由被称为激子的结合电子孔对的形成和辐射重组来控制,其基地的明​​亮或暗方特征仍然是未知的并且辩论。虽然对称性分析预测出圆形非发光地基激子,但是呈明亮的激子三联网,预测Rashba效应可能会扭转明亮和深度的排序。这里,我们在磁场下的单甲脒铅溴溴化锌钙钛矿纳米晶体的低温光致发光中提供了深色激子发射的直接光谱特征。暗态单位位于明亮三态度下方的几毫升,公平同步,估计远程电子空穴交换相互作用。然而,这些Perovskites由于亮度至黑暗的声子辅助放松而显示出强烈的发光。

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  • 来源
    《Nature Materials》 |2019年第7期|717-724|共8页
  • 作者单位

    Univ Bordeaux LP2N Talence France|Inst Opt Talence France|CNRS LP2N Talence France;

    Empa Swiss Fed Labs Mat Sci & Technol Dubendorf Switzerland;

    Univ Bordeaux LP2N Talence France|Inst Opt Talence France|CNRS LP2N Talence France;

    Empa Swiss Fed Labs Mat Sci & Technol Dubendorf Switzerland;

    Empa Swiss Fed Labs Mat Sci & Technol Dubendorf Switzerland|Swiss Fed Inst Technol Inst Inorgan Chem Dept Chem & Appl Biosci Zurich Switzerland;

    Univ Rennes CNRS UMR 6082 INSA Rennes Inst FOTON Rennes France;

    Univ Bordeaux LP2N Talence France|Inst Opt Talence France|CNRS LP2N Talence France;

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