Max-Planck-Institut für Kernphysik, Saupfercheckweg 1, 69117 Heidelberg, Germany.
Theoretische Chemie, Physikalisch-Chemisches Institut, Universität Heidelberg, Im Neuenheimer Feld 229, 69120 Heidelberg, Germany.
J Chem Phys. 2017 Mar 14;146(10):104305. doi: 10.1063/1.4978233.
The ultrafast transfer of excitation energy from one atom to its neighbor is observed in singly charged argon dimers in a time-resolved extreme ultraviolet (XUV)-pump IR-probe experiment. In the pump step, bound 3s-hole states in the dimer are populated by single XUV-photon ionization. The excitation-energy transfer at avoided crossings of the potential-energy curves leads to dissociation of the dimer, which is experimentally observed by further ionization with a time-delayed IR-probe pulse. From the measured pump-probe delay-dependent kinetic-energy release of coincident Ar + Ar ions, we conclude that the transfer of energy occurs on a time scale of about 800fs. This mechanism represents a fast relaxation process below the energy threshold for interatomic Coulombic decay.
在时间分辨的极端紫外(XUV)-光泵红外探测实验中,观察到从一个原子到其相邻原子的超快激发能量转移。在泵浦步骤中,通过单个 XUV 光子电离填充二聚体中的束缚 3s 空穴态。在势能曲线的 avoided crossing 处的激发能量转移导致二聚体的离解,这可以通过用时间延迟的 IR 探测脉冲进一步电离来实验观察到。从测量的泵浦-探测延迟相关的 Ar+Ar 离子的动能释放中,我们得出结论,能量转移发生在大约 800fs 的时间尺度上。该机制代表了原子间库仑衰变能量阈值以下的快速弛豫过程。