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Gas-filled hollow core fibers allow the generation of single-cycle pulses at megahertz repetition rates. When coupled with difference frequency generation, they can be an ideal driver for the generation of carrier-envelope phase stable, octave-spanning pulses in the short-wavelength infrared. In this work, we investigate the dependence of the polarization state in gas-filled hollow-core fibers on the subsequent difference frequency generation stage. We show that by adjusting the input polarization state of light in geometrically symmetric systems, such as hollow-core fibers, one can achieve precise control over the polarization state of the output pulses. Importantly, this manipulation preserves the temporal characteristics of the ultrashort pulses generated, especially when operating near the single-cycle regime. We leverage this property to boost the down-conversion efficiency of these pulses in a type I difference frequency generation stage. Our technique overcomes the bandwidth and dispersion constraints of the previous methods that rely on broadband waveplates or adjustment of crystal axes relative to the laboratory frame. This advancement is crucial for experiments demanding pure polarization states in the eigenmodes of the laboratory frame.

Understanding the photodamage mechanism underlying the highly nonlinear dynamic of femtosecond laser pulses at the second transparent window of tissue is crucial for label-free microscopy. Here, we report the identification of two cavitation regimes from 1030 nm pulses when interacting with the central nervous system in zebrafish. We show that at low repetition rates, the damage is confined due to plasma-based ablation and sudden local temperature rise. At high repetition rates, the damage becomes collateral due to plasma-mediated photochemistry. Furthermore, we investigate the role of fluorescence labels with linear and nonlinear absorption pathways in optical breakdown. To verify our findings, we examined cell death and cellular responses to tissue damage, including the recruitment of fibroblasts and immune cells after irradiation. These findings contribute to advancing the emerging nonlinear optical microscopy techniques and provide a strategy for inducing precise, and localized injuries using near-infrared femtosecond laser pulses.

Ultrashort time-domain spectroscopy and field-resolved spectroscopy of molecular fingerprints are gold standards for detecting samples' constituents and internal dynamics. However, they are hindered by the Nyquist criterion, leading to prolonged data acquisition, processing times, and sizable data volumes. In this work, we present the first experimental demonstration of compressed sensing on field-resolved molecular fingerprinting by employing random scanning. Our measurements enable pinpointing the primary absorption peaks of atmospheric water vapor in response to terahertz light transients while sampling beyond the Nyquist limit. By drastically undersampling the electric field of the molecular response at a Nyquist frequency of 0.8 THz, we could successfully identify water absorption peaks up to 2.5 THz with a mean squared error of 12 * 10^-4. To our knowledge, this is the first experimental demonstration of time-domain compressed sensing, paving the path towards real-time field-resolved fingerprinting and acceleration of advanced spectroscopic techniques.