Ultrafast Ultraviolet C and Visible Laser Light with Broadly Tunable Spectrum

TL;DR

This paper presents a versatile, tunable laser source capable of generating ultrashort pulses in the ultraviolet C and visible ranges, with potential applications in ultrafast imaging and spectroscopy.

Contribution

The authors introduce a novel technique combining spectral broadening and self-compression to produce widely tunable, ultrashort laser pulses with high energy in UV and visible spectra.

Findings

Achieved wavelength tunability from 230-580 nm.

Generated pulses as short as a few femtoseconds.

Enabled potential for sub-200 attosecond pulse trains.

Abstract

We demonstrate a versatile technique for generating continuously wavelength-tunable laser waveforms, with mJ pulse energies and ultrashort pulse durations down to few-cycle in the ultraviolet C and visible spectral ranges. Using the processes of self-phase modulation or Raman-induced spectral broadening, we substantially expand the spectrum of a femtosecond 1030 nm Yb:CaF$_{2}$ laser, allowing for an extensive wavelength-tunability of the second and fourth harmonics of the laser within the visible and ultraviolet C spectral regions at 460-580 nm and 230-290 nm. In addition, our approach exploits nonlinearly assisted self-compression in the second harmonic upconversion of the spectrally broadened infrared pulses with high-order dispersion. This results in 8-30 femtosecond pulses in the visible with an intensity enhancement of up to 30 times. Such an ultrashort visible and ultraviolet C source is ideal for investigating ultrafast dynamics in molecules, solids, and bio and nano systems. Furthermore, this tunable light source enables the generation of bright, narrow-bandwidth, continuously wavelength-tunable, coherent light in the extreme ultraviolet to soft X-ray spectral region. Theoretically, the X-ray pulse structure can consist of sub-200 as pulse trains, making such a source highly suitable for dynamic multidimensional imaging. This includes coherent diffractive imaging of ferromagnetic nanostructures where resonant X-ray scattering is essential, as well as X-ray absorption spectroscopies of advanced quantum materials at pico-nanometer spatial and atto-femtosecond temporal scales.