Semenov Institute of Chemical Physics, Russian Academy of Sciences, Ul. Kosygina 4, Moscow 119991, Russia.
J Chem Phys. 2017 May 21;146(19):194308. doi: 10.1063/1.4983486.
The tunneling spectra of the ordered monolayer films of decamolybdodicobaltate (DMDC) compounds deposited from aqueous solutions on HOPG were measured by scanning tunnel microscopy in air. The DMDC spectra, as well as the tunneling spectra of other polyoxometalates (POMs), exhibit well-defined negative differential resistances (NDRs). The mechanism of formation of these spectral features was established from the collection of revealed NDR dependences on the external varying parameters and found to be common to all systems exhibiting Wannier-Stark localization. A model of biresonance tunneling was developed to provide an explanation for the totality of experimental data, both the literature and original, on the tunneling POM probing. A variant of the tunneling electron-vibrational POM spectroscopy was proposed allowing the determination of the three basic energy parameters-energy gaps between the occupied and unoccupied states, frequencies of the vibrational transitions accompanying biresonance electron-tunneling processes, and electron-vibrational interaction constants on the monomolecular level.
通过扫描隧道显微镜在空气中测量了从水溶液沉积在 HOPG 上的有序十钼二钴酸盐 (DMDC) 化合物的隧道谱。DMDC 谱以及其他多金属氧酸盐 (POM) 的隧道谱都表现出明显的负微分电阻 (NDR)。通过收集揭示的 NDR 对外部变化参数的依赖关系,确定了形成这些光谱特征的机制,并发现它适用于所有表现出 Wanier-Stark 局域化的系统。提出了双共振隧道模型,以解释所有实验数据,包括文献和原始数据,关于隧道 POM 探测。提出了一种隧道电子-振动 POM 光谱学的变体,允许确定三个基本能量参数-占据和未占据态之间的能隙、伴随双共振电子隧道过程的振动跃迁频率以及单分子水平上的电子-振动相互作用常数。