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