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利用隧道显微镜在绝缘体上进行电子转移时的轨道变化测绘。

Mapping orbital changes upon electron transfer with tunnelling microscopy on insulators.

机构信息

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

出版信息

Nature. 2019 Feb;566(7743):245-248. doi: 10.1038/s41586-019-0910-3. Epub 2019 Feb 13.

Abstract

Electron transfer plays a crucial part in many chemical reactions, including photosynthesis, combustion and corrosion. But even though redox-state transitions change the electronic structure of the molecules involved, mapping these changes at the single-molecule level is challenging. Scanning tunnelling microscopy provides insights into the orbital structure of single molecules and their interactions, but requires the use of a conductive substrate that keeps molecules in a given charge state and thereby suppresses redox-state transitions. Atomic force microscopy can be used on insulating substrates to obtain structural and electrostatic information but does not generally access electronic states. Here we show that when synchronizing voltage pulses that steer electron tunnelling between a conductive atomic force microscope tip and a substrate with the oscillation of the tip, we can perform tunnelling experiments on non-conductive substrates and thereby map the orbital structure of isolated molecules as a function of their redox state. This allows us to resolve previously inaccessible electronic transitions in space and energy and to visualize the effects of electron transfer and polaron formation on individual molecular orbitals. We anticipate that our approach will prove useful for the investigation of complex redox reactions and charging-related phenomena with sub-ångström resolution.

摘要

电子转移在许多化学反应中起着至关重要的作用,包括光合作用、燃烧和腐蚀。但是,即使氧化还原态的转变改变了所涉及分子的电子结构,在单分子水平上对这些变化进行映射也是具有挑战性的。扫描隧道显微镜可以提供对单个分子及其相互作用的轨道结构的深入了解,但需要使用导电衬底来保持分子处于给定的电荷状态,从而抑制氧化还原态的转变。原子力显微镜可以在绝缘衬底上使用,以获取结构和静电信息,但通常无法访问电子态。在这里,我们表明,当将引导电子隧穿的电压脉冲与针尖的振荡同步时,我们可以在非导电衬底上进行隧穿实验,从而可以根据氧化还原状态绘制分离分子的轨道结构。这使我们能够分辨出以前在空间和能量上无法访问的电子跃迁,并可视化电子转移和极化子形成对单个分子轨道的影响。我们预计,我们的方法将有助于以亚埃分辨率研究复杂的氧化还原反应和与充电相关的现象。

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