Center for Biosensors and Bioelectronics, Biodesign Institute, Arizona State University, Tempe, AZ 85287, USA.
Nat Nanotechnol. 2011 Apr;6(4):226-31. doi: 10.1038/nnano.2011.20. Epub 2011 Feb 20.
In recent years, various single-molecule electronic components have been demonstrated. However, it remains difficult to predict accurately the conductance of a single molecule and to control the lateral coupling between the π orbitals of the molecule and the orbitals of the electrodes attached to it. This lateral coupling is well known to cause broadening and shifting of the energy levels of the molecule; this, in turn, is expected to greatly modify the conductance of an electrode-molecule-electrode junction. Here, we demonstrate a new method, based on lateral coupling, to mechanically and reversibly control the conductance of a single-molecule junction by mechanically modulating the angle between a single pentaphenylene molecule bridged between two metal electrodes. Changing the angle of the molecule from a highly tilted state to an orientation nearly perpendicular to the electrodes changes the conductance by an order of magnitude, which is in qualitative agreement with theoretical models of molecular π-orbital coupling to a metal electrode. The lateral coupling is also directly measured by applying a fast mechanical perturbation in the horizontal plane, thus ruling out changes in the contact geometry or molecular conformation as the source for the conductance change.
近年来,已经展示了各种单分子电子元件。然而,仍然难以准确预测单分子的电导率,并且难以控制分子的π轨道与附着在其上的电极的轨道之间的横向耦合。众所周知,这种横向耦合会导致分子能级的展宽和移动;反过来,这预计会极大地改变电极-分子-电极结的电导率。在这里,我们展示了一种新的基于横向耦合的方法,通过机械地调制在两个金属电极之间桥接的单个五苯分子的角度来机械地和可逆地控制单分子结的电导率。将分子的角度从高度倾斜的状态改变为几乎垂直于电极的取向,电导率会发生数量级的变化,这与分子π轨道与金属电极耦合的理论模型定性一致。通过在水平平面上施加快速机械扰动也可以直接测量横向耦合,从而排除了接触几何形状或分子构象变化作为电导变化的来源。