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Exciton-polaritons in a crystalline anisotropic organic microcavity

机译:晶体各向异性有机微腔中的激子极化子

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Investigation of polaritons in organic microcavities with strong light-matter interaction is of fundamental and practical interest. In the paper we study for the first time the dispersion of exciton-polaritons in a microcavity utilizing anisotropic organic crystals with one and two molecules per unit cell as optically active material. It is known that in bulk anisotropic organic crystals (like anthracene, tetracene and similar ones) the energies of Coulomb excitons are non-analytical functions of their wave vector k at small k (i.e. the energy of the exciton is different for different directions of the wave vector in the limit k → 0). We show that this is not the case in a planar microcavity where Coulomb exciton states are two-dimensional and the energy of Coulomb excitons at small wave vectors is an analytical function. Also, in contrast to widely used inorganic microcavities, in an anisotropic organic microcavity the cavity photon modes with both possible polarizations mix with the exciton states in the formation of polariton states. We demonstrate that these two factors result for small wave vectors in an almost isotropic dispersion of polaritons in an anisotropic organic crystalline microcavity, which can be observed in reflection, transmission and photoluminescence spectra of organic microcavity.
机译:具有强烈的光-物质相互作用的有机微腔中的极化子的研究具有根本和实际意义。在本文中,我们首次研究了利用每单位晶胞一个和两个分子的各向异性有机晶体作为光学活性材料,在微腔中分散激子-极化子。众所周知,在块状各向异性有机晶体(如蒽,并四苯和类似晶体)中,库仑激子的能量是其波矢量k在小k时的非解析函数(即,激子的能量对于不同方向的激子是不同的)。波向量在极限k→0)。我们表明,在平面微腔中,库仑激子态是二维的,小波矢处的库仑激子能量是解析函数,情况并非如此。而且,与广泛使用的无机微腔相反,在各向异性有机微腔中,具有两种可能极化的腔光子模与激子态混合形成极化子态。我们证明这两个因素导致在各向异性有机晶体微腔中极化子几乎各向同性的分散中的小波矢量,这可以在有机微腔的反射,透射和光致发光光谱中观察到。

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