Department of Physics, Washington State University, 2710 University Drive, Richland, Washington 99354, USA.
ACS Nano. 2009 May 26;3(5):1225-30. doi: 10.1021/nn900232d.
How nanoclusters transform from one structural type to another as a function of size is a critical issue in cluster science. Here we report a study of the structural transition from the golden cage Au(16)(-) to the pyramidal Au(20)(-). We obtained distinct experimental evidence that the cage-to-pyramid crossover occurs at Au(18)(-), for which the cage and pyramidal isomers are nearly degenerate and coexist experimentally. The two isomers are observed and identified by their different interactions with O(2) and Ar. The cage isomer is observed to be more reactive with O(2) and can be preferentially "titrated" from the cluster beam, whereas the pyramidal isomer has slightly stronger interactions with Ar and is favored in the Au(18)Ar(x)(-) van der Waals complexes. The current study allows the detailed structural evolution and growth routes from the hollow cage to the compact pyramid to be understood and provides information about the structure-function relationship of the Au(18)(-) cluster.
纳米团簇如何随尺寸变化从一种结构类型转变为另一种结构类型是团簇科学中的一个关键问题。在这里,我们报告了对从金笼 Au(16)(-)到金字塔 Au(20)(-)的结构转变的研究。我们获得了明确的实验证据,表明笼到金字塔的交叉发生在 Au(18)(-),对于该结构,笼和金字塔异构体几乎是简并的,并在实验中共存。通过它们与 O(2)和 Ar 的不同相互作用观察到并识别出这两种异构体。观察到笼异构体与 O(2)的反应性更强,并且可以优先从团簇束中“滴定”,而金字塔异构体与 Ar 的相互作用略强,并且在 Au(18)Ar(x)(-)范德华复合物中更有利。目前的研究允许理解从空心笼到紧密金字塔的详细结构演变和生长途径,并提供有关 Au(18)(-)团簇的结构-功能关系的信息。