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Superatom Paramagnetism in Au-102(SR)(44)(1-/0/1+/2+) Oxidation States

机译:AU-102(SR)(44)(1- / 0/1 + / 2 +)氧化态的超级副名导

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摘要

Gold nanoclusters show distinctive magnetic properties and electronic structure. Nanoclusters of sufficiently small size restructure geometrically to stabilize electronically (e.g., a Jahn-Teller effect), whereas geometric distortion may not be possible in larger nanoclusters. In this work, the charge-state-dependent magnetism of the Au-102(SR)(44)(1-/0/1+/2+) nanocluster is investigated through Evans method NMR measurements. The 2+ charge state is shown as paramagnetic. This suggests that the nanocluster does not distort geometrically to pair electrons. Because the nanocluster lies within the transition range of molecule-like to bulk-like properties, this suggests that the geometric stabilization that becomes important in larger "magic number clusters" may be resistant to electronically driven distortions observed in smaller nanoclusters.
机译:金纳米能器显示出独特的磁性和电子结构。 几何上的纳米能器几何上几何上稳定以电子(例如,jahn-erker效应),而在较大的纳米单元中可能不可能进行几何变形。 在这项工作中,通过EVANS方法NMR测量研究了AU-102(SR)(SR)(44)(44)(44)(1- / 0/1 + / 2 +)纳米聚簇的电荷 - 状态依赖性磁。 2+充电状态显示为顺磁性。 这表明纳米光泽颗粒不会扭曲几何上以对电子。 因为纳米簇位于分子样的转变范围内以散装样的性质,所以这表明在较大的“魔法数簇”中变得重要的几何稳定性可能是在较小纳米单元中观察到的电子驱动的畸变。

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