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Geometric and electronic properties of size-selected metal clusters on surfaces

机译:表面上尺寸选择的金属团簇的几何和电子性质

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摘要

Within this thesis, we present a project regarding metallic clusters on surfaces. We use scanning tunneling microscopy to investigate their geometric structure and scanning tunneling spectroscopy and ultraviolet photoelectron spectroscopy to study their electronic properties. A new cluster deposition machine built within a priority program of the German Research Foundation (DFG) [1] allows the investigation of size-selected clusters on surfaces.In a first set of experiments, we produced clusters by metal island growth on rare-gas multi-layers and investigated several combinations of different cluster materials on vari-ous rare gases on miscellaneous substrates. On a rare gas film of 60-monolayer thickness, the clusters are electronically decoupled from the substrate. This leads to a change of the reference energy, which is no longer the FERMI energy but the vacuum energy of the substrate. In this sense, we use the term free clusters on substrate.In a second part, after the successful setup and initial operation of the cluster deposition machine, we use a magnetron sputter gas aggregation cluster source [2] and a semi-continuous time-of-flight mass selector [3] to deposit mass-selected silver clusters (number of atoms n = 40, 55, 80, ...,923, and 2130) onto different substrates.In particular, mass-selected silver clusters with closed icosahedral shells deposited on a gold surface functionalized with a C60 monolayer show very interesting results. Despite of using five different silver cluster sizes between 55 and 923 atoms, we observed for all samples clusters with almost the same average cluster height of 1.7 nm. In addition, for Ag561 and Ag923 clusters we observed also larger clusters that roughly agree with the expected cluster sizes. Our present hypothesis is that the clusters deposited at room temperature, exhibit rather a metastable than an equilibrium shape.[1] DFG priority program SPP 1153: Clusters in Contact with Surfaces - Electronic Structure and Magnetism, website: http://www.ieap.uni-kiel.de/surface/ag-berndt/spp/index.html.[2] H. HABERLAND, M. MALL, M. MOSELER, Y. QIANG, Th. REINERS, and Y. THURNER: Filling of micron-sized contact holes with copper by energetic cluster impact, J. Vac. Sci. Technol. A 12, 2925 (1994).[3] B. v. ISSENDORFF and R. E. PALMER: A new high transmission infinite range mass selector for cluster and nanoparticle beams, Review of Scientific Instruments 70, 4497 (1999).
机译:在本文中,我们提出了一个有关表面金属簇的项目。我们使用扫描隧道显微镜研究其几何结构,并使用扫描隧道光谱和紫外光电子光谱研究其电子性质。在德国研究基金会(DFG)的优先计划中建造的新型团簇沉积机[1]允许研究表面上尺寸选定的团簇。在第一组实验中,我们通过在稀有气体中通过金属岛生长来生产团簇。并研究了各种簇状材料在多种基质上的各种稀有气体上的几种组合。在单层厚度为60的稀有气体膜上,簇从基板上电子解耦。这导致参考能量的变化,该参考能量不再是FERMI能量,而是基板的真空能量。从这个意义上讲,我们在衬底上使用自由簇。在第二部分中,在成功完成簇沉积机的设置和初始操作之后,我们使用了磁控溅射气体聚集簇源[2]和半连续时间-飞行质量选择器[3]将质量选择的银团簇(原子数n = 40、55、80,...,923和2130)沉积到不同的衬底上。特别是,质量选择的银团簇是封闭的沉积在用C60单层功能化的金表面上的二十面体壳显示出非常有趣的结果。尽管使用了55个和923个原子之间的五个不同的银簇尺寸,但我们观察到所有样品簇的平均簇高度几乎相同,为1.7 nm。此外,对于Ag561和Ag923群集,我们还观察到了较大的群集,这些群集大致与预期的群集大小一致。我们目前的假设是,在室温下沉积的团簇呈现出亚稳态而不是平衡的形状。[1] DFG优先计划SPP 1153:与表面接触的簇-电子结构和磁性,网站:http://www.ieap.uni-kiel.de/surface/ag-berndt/spp/index.html。[2] H. HABERLAND,M。MALL,M。MOSELER,Y。QIANG,Th。 REINERS和Y. THURNER:通过高能团簇冲击用铜填充微米级的接触孔,J。Vac。科学技术。 A 12,2925(1994)。[3] B.诉ISSENDORFF和R. E. PALMER:一种用于簇和纳米粒子束的新型高透射率无限范围质量选择器,《科学仪器》第70期,第4497页(1999年)。

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