Ferré A, Boguslavskiy A E, Dagan M, Blanchet V, Bruner B D, Burgy F, Camper A, Descamps D, Fabre B, Fedorov N, Gaudin J, Geoffroy G, Mikosch J, Patchkovskii S, Petit S, Ruchon T, Soifer H, Staedter D, Wilkinson I, Stolow A, Dudovich N, Mairesse Y
Université de Bordeaux-CNRS-CEA, CELIA, UMR5107, F33405 Talence, France.
1] National Research Council Canada, 100 Sussex Drive, Ottawa, K1A 0R6 Ontario, Canada [2] Department of Physics, University of Ottawa, 150 Louis Pasteur, Ottawa, K1N 6N5 Ontario, Canada.
Nat Commun. 2015 Jan 22;6:5952. doi: 10.1038/ncomms6952.
High-order harmonic generation in polyatomic molecules generally involves multiple channels of ionization. Their relative contribution can be strongly influenced by the presence of resonances, whose assignment remains a major challenge for high-harmonic spectroscopy. Here we present a multi-modal approach for the investigation of unaligned polyatomic molecules, using SF6 as an example. We combine methods from extreme-ultraviolet spectroscopy, above-threshold ionization and attosecond metrology. Fragment-resolved above-threshold ionization measurements reveal that strong-field ionization opens at least three channels. A shape resonance in one of them is found to dominate the signal in the 20-26 eV range. This resonance induces a phase jump in the harmonic emission, a switch in the polarization state and different dynamical responses to molecular vibrations. This study demonstrates a method for extending high-harmonic spectroscopy to polyatomic molecules, where complex attosecond dynamics are expected.
多原子分子中的高次谐波产生通常涉及多个电离通道。它们的相对贡献会受到共振存在的强烈影响,而共振的归属仍然是高谐波光谱学面临的主要挑战。在此,我们以SF6为例,提出一种用于研究未取向多原子分子的多模态方法。我们结合了极紫外光谱、阈上电离和阿秒计量学的方法。碎片分辨阈上电离测量表明,强场电离至少打开了三个通道。发现其中一个通道中的形状共振在20 - 26 eV范围内主导信号。这种共振在谐波发射中引起相位跃变、极化状态的切换以及对分子振动的不同动力学响应。这项研究展示了一种将高谐波光谱学扩展到多原子分子的方法,在多原子分子中预计会出现复杂的阿秒动力学。