Suppr超能文献

原子力显微镜研究单分子中的电荷诱导结构变化。

Charge-Induced Structural Changes in a Single Molecule Investigated by Atomic Force Microscopy.

机构信息

Institute of Experimental and Applied Physics, University of Regensburg, 93053 Regensburg, Germany.

Debye Institute for Nanomaterials Science, Utrecht University, PO Box 80 000, 3508 TA Utrecht, Netherlands.

出版信息

Phys Rev Lett. 2019 Aug 9;123(6):066001. doi: 10.1103/PhysRevLett.123.066001.

Abstract

Intramolecular structural relaxations occurring upon electron transfer are crucial in determining the rate of redox reactions. Here, we demonstrate that subangstrom structural changes occurring upon single-electron charging can be quantified by means of atomically resolved atomic force microscopy (AFM) for the case of single copper(II)phthalocyanine (CuPc) molecules deposited on an ultrathin NaCl film. Imaging the molecule in distinct charge states (neutral and anionic) reveals characteristic differences in the AFM contrast. In comparison to density functional theory simulations these changes in contrast can be directly related to relaxations of the molecule's geometric structure upon charging. The dominant contribution arises from a nonhomogeneous vertical relaxation of the molecule, caused by a change in the electrostatic interaction with the surface.

摘要

分子内结构弛豫在电子转移过程中起着至关重要的作用,决定着氧化还原反应的速率。在这里,我们通过原子力显微镜(AFM)证明,在超薄 NaCl 膜上沉积的单个铜(II)酞菁(CuPc)分子的情况下,单电子充电时发生的亚埃级结构变化可以通过原子分辨的原子力显微镜(AFM)来定量。在不同的电荷状态(中性和阴离子)下成像分子,可以揭示出 AFM 对比度的特征差异。与密度泛函理论模拟相比,这种对比度的变化可以直接与分子在充电时的几何结构弛豫相关联。主要贡献来自于分子的非均匀垂直弛豫,这是由于与表面的静电相互作用发生变化引起的。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验