论文标题
通过原子力显微镜探测分子激发态
Probing molecular excited states by atomic force microscopy
论文作者
论文摘要
通过使用原子力显微镜进行单电荷注射,我们研究了分子在多层绝缘膜上的氧化还原反应。首先,我们通过连接一个孔来积极地为分子充电。然后,我们通过连接电子并观察到中和的三个通道来中和。我们合理地认为,这三个通道对应于向中性基态的过渡,最低的能量三重态激发态和最低的能量单线激发态。通过单电子隧道光谱法,我们测量了获得三重态和单线激发状态能量之间的能量差异。将实验值与激发态能量的密度功能理论计算进行比较。我们的结果表明,可以制备激发态中的分子,并且可以通过受控的单芯注射来量化光学间隙的能量。我们的工作证明了与激发态转变有关的无处不在的电子跟踪过程,并提供了对在电子传递和表面上分子光电的现象相关的无处不在的电子跟踪过程。
By employing single charge injections with an atomic force microscope, we investigated redox reactions of a molecule on a multilayer insulating film. First, we charged the molecule positively by attaching a single hole. Then we neutralized it by attaching an electron and observed three channels for the neutralization. We rationalize that the three channels correspond to transitions to the neutral ground state, to the lowest energy triplet excited states and to the lowest energy singlet excited states. By single-electron tunneling spectroscopy we measured the energy differences between the transitions obtaining triplet and singlet excited state energies. The experimental values are compared with density functional theory calculations of the excited state energies. Our results show that molecules in excited states can be prepared and that energies of optical gaps can be quantified by controlled single-charge injections. Our work demonstrates the access to, and provides insight into, ubiquitous electron-attachment processes related to excited-state transitions important in electron transfer and molecular optoelectronics phenomena on surfaces.