Amassian A, Desai T V, Kowarik S, Hong S, Woll A R, Malliaras G G, Schreiber F, Engstrom J R
Department of Materials Science and Engineering, Cornell University, Ithaca, New York 14853, USA.
J Chem Phys. 2009 Mar 28;130(12):124701. doi: 10.1063/1.3088835.
We have examined the dynamics of adsorption of diindenoperylene (DIP) on SiO(2) and SiO(2) modified with an interfacial organic layer using in situ real time synchrotron x-ray scattering, focusing on the effects of coverage. On both surfaces we observe a substantial increase in the probability of adsorption with increasing coverage, which is most dramatic at the highest incident kinetic energies. On the initially uncovered surfaces, we observe a smooth decrease in the probability of adsorption with increasing incident kinetic energy, indicative of trapping-mediated adsorption. Once both surfaces are covered by DIP, the effects of incident kinetic energy are greatly reduced, and trapping is very efficient over the range of kinetic energies examined. Possible reasons for efficient trapping at high coverage and at high incident kinetic energy include more efficient momentum transfer due to mass matching, and possibly direct molecular insertion. Comparison to results on another small-molecule, pentacene, suggests that this behavior should be common to hyperthermal growth of a variety of other small-molecule thin films.
我们使用原位实时同步加速器X射线散射研究了二茚并苝(DIP)在SiO₂以及用界面有机层修饰的SiO₂上的吸附动力学,重点关注覆盖度的影响。在这两种表面上,我们都观察到随着覆盖度增加,吸附概率大幅上升,这在最高入射动能时最为显著。在最初未覆盖的表面上,我们观察到随着入射动能增加,吸附概率平稳下降,这表明是俘获介导的吸附。一旦两个表面都被DIP覆盖,入射动能的影响就会大大降低,并且在研究的动能范围内俘获非常有效。在高覆盖度和高入射动能下有效俘获的可能原因包括由于质量匹配导致的更高效动量转移,以及可能的直接分子插入。与另一种小分子并五苯的结果比较表明,这种行为对于多种其他小分子薄膜的超热生长应该是常见的。