We show theoretically that the photoionization process in a hollow-core photonic crystal fiber filled with a Raman-inactive noble gas leads to a constant acceleration of solitons in the time domain with a continuous shift to higher frequencies, limited only by ionization loss. This phenomenon is opposite to the well-known Raman self-frequency redshift of solitons in solid-core glass fibers. We also predict the existence of unconventional long-range nonlocal soliton interactions leading to spectral and temporal soliton clustering.
View Article and Find Full Text PDFBy using a gas-filled kagome-style photonic crystal fiber, nonlinear fiber optics is studied in the regime of optically induced ionization. The fiber offers low anomalous dispersion over a broad bandwidth and low loss. Sequences of blueshifted pulses are emitted when 65 fs, few-microjoule pulses, corresponding to high-order solitons, are launched into the fiber and undergo self-compression.
View Article and Find Full Text PDFWe numerically investigate the effect of ionization on ultrashort high-energy pulses propagating in gas-filled kagomé-lattice hollow-core photonic crystal fibers by solving an established uni-directional field equation. We consider the dynamics of two distinct regimes: ionization induced blue-shift and resonant dispersive wave emission in the deep-UV. We illustrate how the system evolves between these regimes and the changing influence of ionization.
View Article and Find Full Text PDFWe report on the spectral broadening of ~1 μJ 30 fs pulses propagating in an Ar-filled hollow-core photonic crystal fiber. In contrast with supercontinuum generation in a solid-core photonic crystal fiber, the absence of Raman and unique pressure-controlled dispersion results in efficient emission of dispersive waves in the deep-UV region. The UV light emerges in the single-lobed fundamental mode and is tunable from 200 to 320 nm by varying the pulse energy and gas pressure.
View Article and Find Full Text PDFA unique characteristic of transient stimulated Raman scattering, in which the spatiotemporal evolution of the fields and the molecular excitation follow a universal self-similarity law, is observed in gas-filled photonic crystal fibers. As the input laser power is increased, the coupled system "optical fields + molecular excitation" goes through the same phases of time evolution but at a higher rate. Using the self-similarity law we are able to completely reconstruct the evolution of the pump and Stokes fields from one measurement.
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