ICFO-Institut de Ciencies Fotoniques, The Barcelona Institute of Science and Technology, 08860 Castelldefels, Barcelona, Spain.
ICREA-Institució Catalana de Recerca i Estudis Avançats, 08010 Barcelona, Spain.
Nat Commun. 2016 May 11;7:11493. doi: 10.1038/ncomms11493.
Attosecond light pulses in the extreme ultraviolet have drawn a great deal of attention due to their ability to interrogate electronic dynamics in real time. Nevertheless, to follow charge dynamics and excitations in materials, element selectivity is a prerequisite, which demands such pulses in the soft X-ray region, above 200 eV, to simultaneously cover several fundamental absorption edges of the constituents of the materials. Here, we experimentally demonstrate the exploitation of a transient phase matching regime to generate carrier envelope controlled soft X-ray supercontinua with pulse energies up to 2.9±0.1 pJ and a flux of (7.3±0.1) × 10(7) photons per second across the entire water window and attosecond pulses with 13 as transform limit. Our results herald attosecond science at the fundamental absorption edges of matter by bridging the gap between ultrafast temporal resolution and element specific probing.
由于能够实时探测电子动力学,太赫兹光脉冲在极端紫外光领域引起了广泛关注。然而,为了跟踪材料中的电荷动力学和激发,元素选择性是一个前提条件,这就要求软 X 射线区域(200 eV 以上)的此类脉冲同时覆盖材料成分的几个基本吸收边缘。在这里,我们通过实验证明了利用瞬态相位匹配来产生载波包络控制的软 X 射线超连续谱,其脉冲能量高达 2.9±0.1 pJ,在整个水窗范围内的通量为(7.3±0.1)×10(7)个光子/秒,并且具有 13 个阿秒的变换极限。我们的结果通过在超快时间分辨率和元素特定探测之间架起桥梁,在物质的基本吸收边缘处实现了阿秒科学。