Publications by authors named "Adrian N Pfeiffer"

We demonstrate high-harmonic generation for the time-domain observation of the electric field (HHG-TOE) and use it to measure the waveform of ultrashort mid-infrared (MIR) laser pulses interacting with ZnO thin-films or WS monolayers. The working principle relies on perturbing HHG in solids with a weak replica of the pump pulse. We measure the duration of few-cycle pulses at 3200 nm, in reasonable agreement with the results of established pulse characterization techniques.

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Here, we introduce a miniature beamline for transient absorption and dispersion spectroscopy, using a tailored deep ultraviolet field immediately after the noncollinear generation without subsequent optical elements. We explore the near-band-gap region in diamond in the presence of a few-femtosecond pump pulse where the delayed dynamical Franz-Keldysh effect and the almost instantaneous optical Kerr effect coexist.

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We propose and study the manipulation of the macroscopic transient absorption of an ensemble of open two-level systems via temporal engineering. The key idea is to impose an ultrashort temporal gate on the polarization decay of the system by transient absorption spectroscopy, thus confining its free evolution and the natural reshaping of the excitation pulse. The numerical and analytical results demonstrate that even at moderate optical depths, the resonant absorption of light can be reduced or significantly enhanced by more than 5 orders of magnitude relative to that without laser manipulation.

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In the field of high-order harmonic generation from solids, the electron motion typically exceeds the edge of the first Brillouin zone. In conventional nonlinear optics, on the other hand, the excursion of band electrons is negligible. Here, we investigate the transition from conventional nonlinear optics to the regime where the crystal electrons begin to explore the first Brillouin zone.

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Temporal pulse characterization methods can often not be applied to deep ultraviolet (DUV) pulses due to the lack of suitable nonlinear crystals and very low pulse energies. Here, a method is introduced for the characterization of two unknown and independent laser pulses. The applicability is broad, but the method is especially useful for pulses in the DUV, because pulse energies on the picojoule scale suffice.

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Noncollinear pulse characterization methods can be applied to over-octave spanning waveforms, but geometrical effects in the nonlinear medium such as beam smearing and critical sensitivity to beam alignment hinder their accurate application. Here, a method is introduced for the temporal and spatial characterization of two pulses by interferometric, spectrally resolved imaging of self-diffraction. Geometrical effects are resolved by the method and, therefore, do not limit the accuracy.

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The response of a bulk dielectric to an intense few-cycle laser pulse is not solely determined by the pulse envelope, but also by ultrafast processes occurring during each optical cycle. Here, a method is presented for measuring the retardation of a probe pulse in a strong-field pumped, bulk dielectric with subcycle resolution in the pump-probe delay. Comparisons to model calculations show that the measurement is sensitive to the timing of the electronic Kerr response.

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Light-induced coupling of core-excited states of Xe atoms is investigated by femtosecond extreme ultraviolet (XUV) transient absorption spectroscopy with photon energies ranging from 50 eV to 72 eV. Coupling of the 4d(-1)((2)D(5/2))6p((2)P(3/2)) (65.1 eV) and 4d(-1)((2)D(3/2))6p((2)P(1/2)) (67.

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