Generation of isolated attosecond pulses in the far field by spatial filtering with an intense few-cycle mid-infrared laser

We report theoretical calculations of high-order harmonic generation (HHG) of Xe with the inclusion of multi-electron effects and macroscopic propagation of the fundamental and harmonic fields in an ionizing medium. By using the time-frequency analysis we show that the reshaping of the fundamental laser field is responsible for the continuum structure in the HHG spectra. We further suggest a method for obtaining an isolated attosecond pulse (IAP) by using a filter centered on axis to select the harmonics in the far field with different divergence. We also discuss the carrier-envelope-phase dependence of an IAP and the possibility to optimize the yield of the IAP. With the intense few-cycle mid-infrared lasers, this offers a possible method for generating isolated attosecond pulses.Comment: 8 figure

N2 HOMO-1 orbital cross section revealed through high-order-harmonic generation

Citation: Troß, J., Ren, X., Makhija, V., Mondal, S., Kumarappan, V., & Trallero-Herrero, C. A. (2017). N2 HOMO-1 orbital cross section revealed through high-order-harmonic generation. Physical Review A - Atomic, Molecular, and Optical Physics, 95(3). doi:10.1103/PhysRevA.95.033419We measure multi-orbital contributions to high harmonic generation from aligned nitrogen. We show that the change in revival structure in the cutoff harmonics has a counterpart in the angular distribution when a lower-lying orbital contributes to the harmonic yield. This angular distribution is directly observed in the laboratory without any further deconvolution. Because of the high degree of alignment we are able to distinguish angular contributions of the highest occupied molecular orbital 1 (HOMO-1) orbital from angle-dependent spectroscopic features of the HOMO. In particular, we are able to make a direct comparison with the cross section of the HOMO-1 orbital in the extreme ultraviolet region. © 2017 American Physical Society

Generation and control of non-local quantum equivalent extreme ultraviolet photons

We present a high precision, self-referencing, common path XUV interferometer setup to produce pairs of spatially separated and independently controllable XUV pulses that are locked in phase and time. The spatial separation is created by introducing two equal but opposite wavefront tilts or using superpositions of orbital angular momentum. In our approach, we can independently control the relative phase/delay of the two optical beams with a resolution of 52 zs (zs = zeptoseconds). In order to explore the level of entanglement between the non-local photons, we compare three different beam modes: Bessel-like, and Gaussian with or without added orbital angular momentum. By reconstructing interference patterns one or two photons at a time we conclude that the beams are not entangled, yet each photon in the attosecond pulse train contains information about the entire spectrum. Our technique generates non-local, quantum equivalent XUV photons with a temporal jitter of 3 zs, just below the Compton unit of time of 8 zs. We argue that this new level of temporal precision will open the door for new dynamical QED tests. We also discuss the potential impact on other areas, such as imaging, measurements of non-locality, and molecular quantum tomography.Comment: 11 pages 5 figures and supplemental materials with 12 pages and 7 figure

Measuring the Angle-Dependent Photoionization Cross Section of Nitrogen using High-Harmonic Generation

We exploit the relationship between high harmonic generation (HHG) and the molecular photorecombination dipole to extract the molecular-frame differential photoionization cross section (PICS) in the extreme ultraviolet (XUV) for molecular nitrogen. A shape resonance and a Cooper-type minimum are reflected in the pump-probe time delay measurements of different harmonic orders, where high-order rotational revivals are observed in N₂. We observe the energy- and angle-dependent Cooper minimum and shape resonance directly in the laboratory-frame HHG yield by achieving a high degree of alignment, [SEE FORMULA IN ABSTRACT cos2 θ] 0.8. The interplay between PICS and rotational revivals is confirmed by simulations using the quantitative rescattering theory. Our method of extracting molecular-frame structural information points the way to similar measurements in more complex molecules

Atomic photoionization experiment by harmonic-generation spectroscopy

Citation: Frolov, M. V., Sarantseva, T. S., Manakov, N. L., Fulfer, K. D., Wilson, B. P., Tross, J., . . . Trallero-Herrero, C. A. (2016). Atomic photoionization experiment by harmonic-generation spectroscopy. Physical Review A, 93(3), 5. doi:10.1103/PhysRevA.93.031403Measurements of the high-order-harmonic generation yield of the argon (Ar) atom driven by a strong elliptically polarized laser field are shown to completely determine the field-free differential photoionization cross section of Ar, i.e., the energy dependence of both the angle-integrated photoionization cross section and the angular distribution asymmetry parameter

Self referencing attosecond interferometer with zeptosecond precision

In this work we demonstrate the generation of two intense, ultrafast laser pulses that allow a controlled interferometric measurement of higher harmonic generation pulses with 12.8 attoseconds in resolution (half the atomic unit of time) and a precision as low as 680 zeptoseconds (10−21 seconds). We create two replicas of a driving femtosecond pulse which share the same optical path except at the focus where they converge to two foci. An attosecond pulse train emerges from each focus through the process of high harmonic generation. The two attosecond pulse trains from each focus interfere in the far field producing a clear interference pattern in the extreme ultraviolet region. By controlling the relative optical phase (carrier envelope phase for pulsed fields) between the two driving laser pulses we are able to actively influence the delay between the pulses and are able to perform very stable and precise pump-probe experiments. Because of the phase shaping operation occurs homogeneously across the entire spatial profile, we effectively create two indistinguishable intense laser pulses or a common path interferometer for attosecond pulses. Commonality across the two beams means that they are extremely stable to environmental and mechanical fluctuations up to a Rayleigh range from the focus. In our opinion this represents an ideal source for homodyne and heterodyne spectroscopic measurements with sub-attosecond precision

THREE-DIMENSIONAL MODIFICATION IN SILICON WITH INFRARED NANOSECOND LASER

11th ASME International Manufacturing Science and Engineering Conference (MSEC 2016), Blacksburg, VA, JUN 27-JUL 01, 2016International audienceMotivated by previous work on three-dimensional (3D) fabrication inside dielectrics, we report experimental results of 3D modification inside intrinsic silicon wafers using laser pulses with 1.55 gm wavelength and 3.5 ns pulse duration. Permanent modification in the form of lines is generated inside silicon by tightly focusing and continuously scanning the laser beam inside samples, without introducing surface damage. Cross sections of these lines are observed after cleaving the samples, and are further analyzed after mechanical polishing followed by chemical etching. With the objective lens corrected for spherical aberration, tight focusing inside silicon is achieved and the optimal focal depth is identified. The laser-induced modification has a triangular shape and appears in front of the geometrical focus, suggesting significant absorption in those regions and resulting in reduced energy density. The morphology of modified regions is found to be dependent on the laser polarization

THREE-DIMENSIONAL MODIFICATION IN SILICON WITH INFRARED NANOSECOND LASER

11th ASME International Manufacturing Science and Engineering Conference (MSEC 2016), Blacksburg, VA, JUN 27-JUL 01, 2016International audienceMotivated by previous work on three-dimensional (3D) fabrication inside dielectrics, we report experimental results of 3D modification inside intrinsic silicon wafers using laser pulses with 1.55 gm wavelength and 3.5 ns pulse duration. Permanent modification in the form of lines is generated inside silicon by tightly focusing and continuously scanning the laser beam inside samples, without introducing surface damage. Cross sections of these lines are observed after cleaving the samples, and are further analyzed after mechanical polishing followed by chemical etching. With the objective lens corrected for spherical aberration, tight focusing inside silicon is achieved and the optimal focal depth is identified. The laser-induced modification has a triangular shape and appears in front of the geometrical focus, suggesting significant absorption in those regions and resulting in reduced energy density. The morphology of modified regions is found to be dependent on the laser polarization