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在解离的H₂⁺中双表面布居动力学的阿秒频闪观测

Attosecond strobing of two-surface population dynamics in dissociating H2+.

作者信息

Staudte A, Pavicić D, Chelkowski S, Zeidler D, Meckel M, Niikura H, Schöffler M, Schössler S, Ulrich B, Rajeev P P, Weber Th, Jahnke T, Villeneuve D M, Bandrauk A D, Cocke C L, Corkum P B, Dörner R

机构信息

Institut für Kernphysik, J.W. Goethe Universität, D-60486 Frankfurt/Main, Germany.

出版信息

Phys Rev Lett. 2007 Feb 16;98(7):073003. doi: 10.1103/PhysRevLett.98.073003. Epub 2007 Feb 14.

DOI:10.1103/PhysRevLett.98.073003
PMID:17359022
Abstract

Using H2+ and D2+, we observe two-surface population dynamics by measuring the kinetic energy of the correlated ions that are created when H2+ (D2+) ionize in short (40-140 fs) and intense (10(14) W/cm2) infrared laser pulses. Experimentally, we find a modulation of the kinetic energy spectrum of the correlated fragments. The spectral progression arises from a hitherto unexpected spatial modulation on the excited state population, revealed by Coulomb explosion. By solving the two-level time-dependent Schrödinger equation, we show that an interference between the net-two-photon and the one-photon transition creates localized electrons which subsequently ionize.

摘要

利用H2+和D2+,我们通过测量当H2+(D2+)在短(40 - 140飞秒)且强(10^14瓦/平方厘米)的红外激光脉冲中电离时产生的关联离子的动能,来观测双表面布居动力学。在实验中,我们发现了关联碎片动能谱的调制现象。这种光谱进展源于库仑爆炸所揭示的、迄今未曾预料到的激发态布居的空间调制。通过求解含时二级薛定谔方程,我们表明净双光子跃迁与单光子跃迁之间的干涉产生了局域化电子,这些电子随后发生电离。

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Molecular vibrational trapping revisited: a case study with D2.重新审视分子振动俘获:以D2为例的案例研究。
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