Institut für Theoretische Physik und Interdisziplinäres Zentrum für Molekulare Materialien, Friedrich-Alexander-Universität Erlangen-Nürnberg, Staudtstr. 7/B2, D-91058 Erlangen, Germany.
J Chem Phys. 2010 Aug 28;133(8):081102. doi: 10.1063/1.3474464.
In a nanoscale molecular junction at finite bias voltage, the intramolecular distribution of vibrational energy can strongly deviate from the thermal equilibrium distribution and specific vibrational modes can be selectively excited in a controllable way, regardless of the corresponding mode frequency. This is demonstrated for generic models of asymmetric molecular junctions with localized electronic states, employing a master equation as well as a nonequilibrium Green's function approach. It is shown that the applied bias voltage controls the excitation of specific vibrational modes by tuning the efficiency of vibrational cooling processes due to energy exchange with the leads.
在有限偏压的纳米级分子结中,分子内振动能量的分布可以强烈偏离热平衡分布,并且可以以可控的方式选择性地激发特定的振动模式,而与相应的模式频率无关。这对于具有局域电子态的不对称分子结的通用模型进行了演示,采用了主方程和非平衡格林函数方法。结果表明,通过调节与引线进行能量交换的振动冷却过程的效率,施加的偏压控制着特定振动模式的激发。