A Quaternion Based Quantum Chemical ab initio Treatment of Coherent and Non-Coherent Electron Transport in Molecules

Abstract

We present a quaternion inspired formalism specifically developed to evaluate the intensity of the electrical current that traverses a single molecule connected to two semi-infinite electrodes as the applied external bias is varied. The self-adjustment of the molecular levels is fully described at a density functional ab initio quantum chemical level. Use of a quaternion approach allows for an integrated treatment of both coherent (ballistic) and non-coherent (co-tunneling) contributions to the effective charge transport, where the latter involve the existence of transient charged states of the corresponding molecular species. An expression for the net current is calculated by using second-order perturbation theory to take into account all possible transitions between states localized at the two different electrodes that involve intermediary levels in the so-called "extended molecule" complex that comprises the system of interest attached to two small metallic clusters. We show that by a judicious choice of the relevant molecular parameters, the formalism can be extended to describe the electronic transport both in conjugated as in saturated molecules, where localized orbitals are more likely to be found. In this manner, the method can be applied to the full range of coupling regimes, not only to the weak or strong cases, but also in intermediate situations, where ballistic and co-tunneling processes may coexist.