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吸附在金属表面上的单分子的键选择光解。

Bond-Selected Photodissociation of Single Molecules Adsorbed on Metal Surfaces.

机构信息

Department of Physics and Astronomy, University of California, Irvine, California 92697-4575, USA.

Department of Chemistry, University of California, Irvine, California 92697-2025, USA.

出版信息

Phys Rev Lett. 2019 Feb 22;122(7):077401. doi: 10.1103/PhysRevLett.122.077401.

Abstract

We report the photoassisted activation of selected C─H bonds in individual molecules adsorbed on metal surfaces within the junction of a scanning tunneling microscope. Photons can couple to the C─H bond activation of specific hydrocarbons through a resonant photoassisted tunneling process. The molecule to be activated can be selected by positioning the tip with subangstrom resolution. Furthermore, structural tomography of the molecule and its dissociation products are imaged at different heights by the inelastic tunneling probe. The demonstration of single bond dissociation induced by resonant photoassisted tunneling electrons implies the attainment of atomic scale spatial resolution for bond-selected photochemistry.

摘要

我们报告了在扫描隧道显微镜结内的金属表面上吸附的单个分子中,选择的 C─H 键在光辅助下的激活。通过共振光辅助隧穿过程,光子可以与特定碳氢化合物的 C─H 键激活耦合。通过亚埃分辨率定位针尖,可以选择要激活的分子。此外,通过非弹性隧道探针在不同高度对分子及其解离产物进行结构断层扫描成像。共振光辅助隧穿电子诱导单键解离的证明意味着实现了用于键选择光化学的原子级空间分辨率。

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