Asai Yoshihiro
Research Institute for Computational Sciences, National Institute of Advanced Industrial Science and Technology, Umezono 1-1-1, Tsukuba Central 2, Tsukuba, Ibaraki 305-8568, Japan.
Phys Rev Lett. 2004 Dec 10;93(24):246102. doi: 10.1103/PhysRevLett.93.246102.
An electronic structure theory has been developed for an inelastic electric current of electron-intramolecular vibration coupling origin in terms of the Keldysh Green function method and the self-consistent Born approximation. Numerical calculations were made for the benzenedithiol molecule linking the two Au(111) electrodes. The calculations successfully reproduce typical features commonly observed in inelastic tunneling spectroscopy. The vibrational excitation energy due to the inelastic current was estimated. The inelastic electric current is quite important for the structural stability and the switching possibility of the molecular device.
基于凯尔迪什格林函数方法和自洽玻恩近似,已针对电子 - 分子内振动耦合起源的非弹性电流开发了一种电子结构理论。对连接两个Au(111)电极的苯二硫醇分子进行了数值计算。这些计算成功再现了非弹性隧穿光谱中常见的典型特征。估算了由非弹性电流引起的振动激发能。非弹性电流对于分子器件的结构稳定性和开关可能性非常重要。