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Wave-packet excitation and quantum-beat spectroscopy of image-potential states

机译:图像势态的波包激发和量子拍谱

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Abstract: The ultrafast dynamics of electrons in image-potential states on a Cu(100) surface is studied by means of femtosecond time-resolved two-photon photoemission (2PPE). By coherently exciting several eigenstates of the Rydberg series we observe periodic oscillations of the 2PPE signal as a function of the delay time between pump and probe pulses. These quantum beats allow us to determine the spacing of high-order states (quantum number n $GREQ 4) that are difficult to resolve by conventional electron spectroscopy. The superposition of several states around n $EQ 7 creates an electron wave packet that describes the quasi-classical periodic motion of weakly bound electrons. Its distance from the surface is reflected in the strength of the photoemission signal. The electron is observed to move about 100 atomic distances away from the surface and oscillates back and forth with a period of 800 femtoseconds. The results demonstrate the power of coherent laser spectroscopy for surface studies.!25
机译:摘要:利用飞秒时间分辨双光子光发射(2PPE)研究了Cu(100)表面电子在图像电势状态下的超快动力学。通过相干地激发Rydberg序列的几个本征态,我们观察到2PPE信号的周期性振荡是泵浦脉冲和探针脉冲之间的延迟时间的函数。这些量子节拍使我们能够确定高阶态(量子数n $ GREQ 4)的间距,而传统电子光谱法很难解决这些间距。 n $ EQ 7周围几个状态的叠加会创建一个电子波包,该电子波包描述了弱束缚电子的准经典周期运动。它与表面的距离反映在光发射信号的强度中。观察到电子移动离开表面约100个原子距离,并以800飞秒的周期来回振荡。结果证明了相干激光光谱技术在表面研究中的强大实力!25

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