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Design and test of a rigid endomicroscopic system for multimodal imaging and femtosecond laser ablation.

Conventional diagnosis of laryngeal cancer is normally made by a combination of endoscopic examination, a subsequent biopsy, and histopathology, but this requires several days and unnecessary biopsies can increase pathologist workload. Nonlinear imaging implemented through endoscopy can shorten this diagnosis time, and localize the margin of the cancerous area with high resolution. Develop a rigid endomicroscope for the head and neck region, aiming for in-vivo multimodal imaging with a large field of view (FOV) and tissue ablation. Three nonlinear imaging modalities, which are coherent anti-Stokes Raman scattering, two-photon excitation fluorescence, and second harmonic generation, as well as the single photon fluorescence of indocyanine green, are applied for multimodal endomicroscopic imaging. High-energy femtosecond laser pulses are transmitted for tissue ablation. This endomicroscopic system consists of two major parts, one is the rigid endomicroscopic tube 250mm in length and 6mm in diameter, and the other is the scan-head ( in size) for quasi-static scanning imaging. The final multimodal image accomplishes a maximum FOV up to , and a resolution of is achieved over FOV. The optics can easily guide sub-picosecond pulses for ablation. The system exhibits large potential for helping real-time tissue diagnosis in surgery, by providing histological tissue information with a large FOV and high resolution, label-free. By guiding high-energy fs laser pulses, the system is even able to remove suspicious tissue areas, as has been shown for thin tissue sections in this study.

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Highly efficient, in-band pumped thulium-doped fibers for high-power ultrafast 2 µm wavelength laser systems

Ultrafast fiber laser sources emitting fs-pulses around 2 μm have many applications in medicine, metrology and sensing as well as in various frequency-conversion techniques. Thulium-doped fiber amplifiers are a promising platform for power scalable ultrafast amplification in this wavelength region. Usually, these ultrafast, high-power fiber laser systems were pumped at a wavelength around 790 nm and obtain slope efficiencies in the range of 50 % in the 100 W-class. Due to the high quantum defect obtained with this pump technique and the related high heat loads, considerable thermal challenges still must be overcome when scaling the power further. In this contribution we present a concept on highly efficient, high-power thulium-doped fiber amplifiers pumped at 1692 nm. This pump concept is suitable for high-power, high-energy, ultrafast Tm-doped fiber laser systems. In this proof of principle demonstration, we achieve a slope efficiency of 80% in a standard commercially available, thulium-doped photonic crystal fiber (PCF) with ~60 W of average power when pumping at 1692 nm compared to 47 % slope efficiency by pumping at 793 nm. In the simulation we investigated the heat load and core temperature evaluation along the fiber. These findings demonstrate an improvement in the amplification efficiency of large-mode area fiber amplifiers which are suitable for ultrafast operation on Yb-like efficiencies. The reduced heat load paves the way to even higher average powers from ultrafast Tm-doped fiber lasers with the potential to provide multi-mJ energy fs-pulses at kW-level average power from a single amplifier channel.

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Field-resolved spectroscopy approaching ultimate detection sensitivity

Abstract Electric-field oscillations are now experimentally accessible in the THz-to-PHz frequency range1–11. Their measurement delivers the most comprehensive information content attainable by optical spectroscopy – if performed with high sensitivity. Yet, the trade-off between bandwidth and efficiency associated with the nonlinear mixing necessary for field sampling has so far strongly restricted sensitivity in applications such as field-resolved spectroscopy of molecular vibrations12,13. Here, we demonstrate electric-field sampling of octave-spanning mid-infrared waves in the 18-to-39 THz (600-to-1300 cm-1) spectral region, with amplitudes ranging from the MV/cm level down to a few mV/cm. Employing powerful short-wave mid-infrared gate pulses14,15, the field-measurement sensitivity approaches within a factor of 4 the ultimate detection limit of capturing all photons in the temporal gate. This combination of detection sensitivity and dynamic range enables optimum use of newly-emerging high-power waveform-controlled infrared sources12,14,16–22 for molecular spectroscopy. In a proof-of concept experiment, we performed broadband quantitative linear spectroscopy of multiple gases over more than 8 orders of magnitude in concentration, at an interaction length of only 45 cm. Our technique brings fast, label-free, quantitative multivariate detection of volatile organic compounds over the entire known physiologically-relevant molecular landscape23,24 within reach.

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