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Information on quantum states pervades the visible spectrum of the ubiquitous Au-144(SR)(60) gold nanocluster

机译:量子态信息遍及无处不在的Au-144(SR)(60)金纳米团簇的可见光谱

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摘要

Absorption spectra of very small metal clusters exhibit individual peaks that reflect the discreteness of their localized electronic states. With increasing size, these states develop into bands and the discrete absorption peaks give way to smooth spectra with, at most, a broad localized surface-plasmon resonance band. The widely accepted view over the last decades has been that clusters of more than a few dozen atoms are large enough to have necessarily smooth spectra. Here we show through theory and experiment that for the ubiquitous thiolate cluster compound Au-144(SR)(60) this view has to be revised: clearly visible individual peaks pervade the full near-IR, VIS and near-UV ranges of low-temperature spectra, conveying information on quantum states in the cluster. The peaks develop well reproducibly with decreasing temperature, thereby highlighting the importance of temperature effects. Calculations using time-dependent density-functional theory indicate the contributions of different parts of the cluster-ligand compound to the spectra.
机译:非常小的金属簇的吸收光谱显示出各个峰,这些峰反映了其局部电子态的不连续性。随着尺寸的增加,这些状态发展成能带,离散的吸收峰让位于最大局部表面等离子体共振带宽的平滑光谱。在过去的几十年中,广泛接受的观点是几十个以上原子的簇足够大,足以具有必不可少的光谱。在这里,我们通过理论和实验表明,对于无处不在的硫醇盐簇化合物Au-144(SR)(60),必须修改此视图:清晰可见的各个峰遍布低光谱的完整近红外,可见光和近紫外范围温度光谱,传达有关簇中量子态的信息。随着温度降低,峰的再现性良好,从而突出了温度效应的重要性。使用随时间变化的密度泛函理论的计算表明了簇-配体化合物不同部分对光谱的贡献。

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