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金属态纳米团簇的金原子临界数量:解决一个长达数十年的问题。

The Critical Number of Gold Atoms for a Metallic State Nanocluster: Resolving a Decades-Long Question.

作者信息

Zhou Meng, Du Xiangsha, Wang He, Jin Rongchao

机构信息

Department of Chemistry, Carnegie Mellon University, Pittsburgh, Pennsylvania 15213, United States.

Department of Physics, University of Miami, Coral Gables, Florida 33146, United States.

出版信息

ACS Nano. 2021 Sep 28;15(9):13980-13992. doi: 10.1021/acsnano.1c04705. Epub 2021 Sep 7.

DOI:10.1021/acsnano.1c04705
PMID:34490772
Abstract

Probing the transition from a metallic state to a molecular state in gold nanoparticles is fundamentally important for understanding the origin of surface plasmon resonance and the nature of the metallic bond. Atomically precise gold nanoclusters are desired for probing such a transition based upon a series of precise sizes with X-ray structures. While the definition of the metallic state in nanoclusters is simple, that is, when the HOMO-LUMO gap () becomes negligibly small ( < , where is the Boltzmann constant and the temperature), the experimental determination of ultrasmall (, of level) is difficult, and the thermal excitation of valence electrons apparently comes into play in ultrasmall nanoclusters. Although a sharp transition from nonmetallic Au(SR) to metallic Au(SR) (SR: thiolate) has been observed, there is still uncertainty about the transition region. Here, we summarize several criteria on determining the metallic state the molecular (or nonmetallic) state in gold nanoclusters, including (1) determined by optical and electrochemical methods, (2) steady-state absorption spectra, (3) cryogenic optical spectra, (4) transient absorption spectra, (5) excited-state lifetime and power dependence, and (6) coherent oscillations in ultrafast electron dynamics. We emphasize that multiple analyses should be performed and cross-checked in practice because no single criterion is definitive. We also review the photophysics of several gold nanoclusters with nascent surface plasmon resonance. These criteria are expected to deepen the understanding of the metallic to molecular state transition of gold and other metal nanoclusters and also promote the design of functional nanomaterials and their applications.

摘要

探究金纳米颗粒从金属态到分子态的转变对于理解表面等离子体共振的起源和金属键的本质至关重要。基于一系列具有X射线结构的精确尺寸,需要原子精确的金纳米团簇来探究这种转变。虽然纳米团簇中金属态的定义很简单,即当最高占据分子轨道-最低未占据分子轨道间隙()变得小到可以忽略不计(<,其中是玻尔兹曼常数,是温度)时,但超小(,数量级)的实验测定很困难,并且价电子的热激发显然在超小金纳米团簇中起作用。尽管已经观察到从非金属Au(SR)到金属Au(SR)(SR:硫醇盐)的急剧转变,但转变区域仍存在不确定性。在这里,我们总结了几种确定金纳米团簇中金属态与分子(或非金属)态的标准,包括(1)通过光学和电化学方法测定的,(2)稳态吸收光谱,(3)低温光谱,(4)瞬态吸收光谱,(5)激发态寿命和功率依赖性,以及(6)超快电子动力学中的相干振荡。我们强调,在实践中应进行多种分析并相互核对,因为没有单一标准是确定无疑的。我们还回顾了几种具有新生表面等离子体共振的金纳米团簇的光物理性质。这些标准有望加深对金和其他金属纳米团簇从金属态到分子态转变的理解,并促进功能纳米材料的设计及其应用。

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