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Magnetic instability and pair binding in aromatic hydrocarbon superconductors

机译:芳烃超导体中的磁不稳定和对结合

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摘要

Understanding magnetism and electron correlation in many unconventional superconductors is essential to explore mechanism of superconductivity. In this work, we perform a systematic numerical study of the magnetic and pair binding properties in recently discovered polycyclic aromatic hydrocarbon (PAH) superconductors including alkali-metal-doped picene, coronene, phenanthrene, and dibenzopentacene. The π-electrons on the carbon atoms of a single molecule are modelled by the one-orbital Hubbard model, and the energy difference between carbon atoms with and without hydrogen bonds is taking into account. We demonstrate that the spin polarized ground state is realized for charged molecules in the physical parameter regions, which provides a reasonable explanation of local spins observed in PAHs. In alkali-metal-doped dibenzopentacene, our results show that electron correlation may produce an effective attraction between electrons for the charged molecule with one or three added electrons.
机译:了解许多非常规超导体中的磁性和电子相关性对于探索超导机理至关重要。在这项工作中,我们对最近发现的多环芳烃(PAH)超导体(包括碱金属掺杂的pic烯,co,菲和二苯并五并烯)的磁性和成对结合特性进行了系统的数值研究。单分子碳原子上的π电子是通过单轨道Hubbard模型建模的,并且考虑了具有和不具有氢键的碳原子之间的能量差。我们证明,在物理参数区域中带电分子实现了自旋极化基态,这为PAHs中观察到的局部自旋提供了合理的解释。在掺杂碱金属的二苯并戊并烯中,我们的结果表明,电子相关性可能会在一个或三个添加电子的带电分子的电子之间产生有效的吸引。

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