Iron wheels on silicon: Wetting behavior and electronic structure of adsorbed organostannoxane clusters

被引:10
作者
Frehill, F [1 ]
Schulte, KHG
Martin, CP
Wang, L
Patel, S
Purton, JA
Vos, JG
Moriarty, P
机构
[1] Dublin City Univ, Natl Ctr Sensor Res, Dublin 9, Ireland
[2] Dublin City Univ, Sch Chem Sci, Dublin 9, Ireland
[3] Univ Nottingham, Sch Phys & Astron, Nottingham NG7 2RD, England
[4] Daresbury Lab, Daresbury WXX 4AD, Cheshire, England
关键词
D O I
10.1021/la036414y
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Atomic force microscopy and synchrotron radiation (SR) spectroscopy have been used to study the wetting behavior and electronic structure of thin films of a novel organometallic cluster - [BuSn(O)OC(O)Fc](6) ("Fc" = ferrocenyl) - on silicon substrates. This cluster comprises six ferrocene units connected to a stannoxane central core - "an iron wheel on a tin drum" (V. Chandrasekhar; et al. Angew. Chem., Int. Ed. 2000, 39, 1833). Thin films spin-cast onto native oxide-terminated silicon readily dewet the substrate. We have utilized advanced image analysis techniques based on Minkowski functionals to provide a detailed quantitative analysis of the morphology of the stannoxane overlayers. This analysis shows that the dewetting patterns are rather far removed from those expected to arise from a simple Poisson distribution of centers, and we discuss the implications of this finding in terms of nucleated and spinodal dewetting. Variations in both the surface roughness and the in-plane correlation length have been followed as a function of annealing time to probe the surface dewetting dynamics. SR valence band photoemission illustrates that the highest occupied molecular orbital (HOMO) of the cluster is found 2 eV below the Fermi level. Fe 2p --> 3d and Sn 3d --> 5p resonant photoemission spectroscopy have been used to enhance the cross sections of the partial density of states associated with the Fe and Sn atoms. Sn atoms make a large contribution to the HOMO of the cluster, whereas the Fe atoms are associated with an electronic environment seemingly very similar to that in the "parent" ferrocene molecule.
引用
收藏
页码:6421 / 6429
页数:9
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