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Ultrafast electron dynamics in an amino acid measured by attosecond pulses

机译:通过阿秒脉冲测量的氨基酸中超快电子动力学

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Electron transfer within a single molecule is the fundamental step of many biological processes and chemical reactions. It plays a crucial role in catalysis, DNA damage by ionizing radiation, photosynthesis, photovoltaics, and for switches based on molecular nano-junctions. The investigation of this process has been the subject of considerable research effort [1-2]. In this work we present the first direct measurement of ultrafast charge migration in a biomolecular building block, the amino acid phenylalanine, using attosecond pulses [3]. Clean plumes of isolated, neutral molecules were produced by laser induced acoustic desorption (LIAD] technique [4]. Phenylalanine molecules were irradiated by a short train of attosecond pulses produced by high-order harmonic generation in Xenon (the train was composed by two attosecond pulses], with a photon energy in the range 16–40 eV, followed at a variable temporal delay by a 6-fs visible/near infrared (500–950 nm, VIS/NIR} probe pulse. The parent and fragment ions produced were then extracted into a linear time of flight device for mass analysis. Figures l(a]-(b] showthe mass spectra obtained individually from the XUV and VIS/NIR pulses.
机译:单个分子内的电子转移是许多生物学过程和化学反应的基本步骤。它在催化,电离辐射引起的DNA损伤,光合作用,光伏发电以及基于分子纳米结的开关方面起着至关重要的作用。对这一过程的研究一直是大量研究工作的主题[1-2]。在这项工作中,我们提出了使用阿秒脉冲[3]首次直接测量生物分子构件氨基酸苯丙氨酸中超快电荷迁移的方法。激光诱导的声学解吸(LIAD)技术产生了干净的孤立的中性分子羽流[4]。苯丙氨酸分子受到氙中高次谐波产生所产生的一小串阿秒脉冲的照射(该串由两个阿秒组成脉冲],光子能量在16–40 eV的范围内,然后在可变的时间延迟后加上6-fs可见/近红外(500–950 nm,VIS / NIR}探测脉冲。产生的母离子和碎片离子分别是图1(a)-(b)分别显示了从XUV和VIS / NIR脉冲获得的质谱图。

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