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胰岛素生长因子三肽吸附导致剧烈的 Au(111) 表面重构。

Drastic Au(111) surface reconstruction upon insulin growth factor tripeptide adsorption.

机构信息

Laboratoire de Réactivité de Surface, UMR CNRS 7197, Université Pierre et Marie Curie -UPMC Paris 6 case 178, 4 place Jussieu, 75005 Paris, France.

出版信息

J Am Chem Soc. 2012 Apr 18;134(15):6579-83. doi: 10.1021/ja302530q. Epub 2012 Apr 10.

Abstract

Adsorption of biomolecules at metal surfaces often creates two-dimensional ordering of the adlayers. However, metal substrate reconstruction is less commonly observed, unless upon annealing of the molecule-surface system. Here, we report on the drastic room-temperature reconstruction of the Au(111) surface, driven by the adsorption of insulin growth factor tripeptide molecules. Scanning tunneling microscopy images show that the surface reconstruction, which takes place without annealing the system, is dynamic and evolves over time. It is initiated at kinks and steps edges, but the reconstruction also takes place within defect-free terraces. Theoretical calculations are performed to explain the reconstruction at the molecular level.

摘要

生物分子在金属表面的吸附通常会导致吸附层的二维有序化。然而,除非对分子-表面体系进行退火,否则很少观察到金属衬底重构。在这里,我们报告了胰岛素生长因子三肽分子的吸附驱动下,金(111)表面的剧烈室温重构。扫描隧道显微镜图像表明,在不进行退火的情况下发生的表面重构是动态的,并随时间演变。它始于扭结和台阶边缘,但重构也发生在无缺陷的台面上。进行了理论计算以解释分子水平上的重构。

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