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We present a system for extremely broadband terahertz (THz) generation based on an Ytterbium (Yb) amplified laser emitting 170-fs-long pulses centered at 1030 nm. The pulses are first spectrally broadened in an Ar-filled hollow-core capillary fiber (HCF) and then recompressed down to â¼18 fs with a chirped-mirror pair. Extreme broadband THz pulses of bandwidths up to 60 THz and peak electric field as high as 55 kV/cm are obtained via two-color plasma generation. The combination of high-power Yb laser systems with gas-filled HCF opens the path towards the realization of the next generation high-repetition-rate, extremely broadband, and intense-field THz time-domain spectroscopy systems.
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We introduce hydrofluorocarbon molecules as an alternative medium to noble gases with low ionization potential like krypton or xenon to compress ultrashort pulses of relatively low energy in a conventional hollow core fiber with subsequent dispersion compensation. Spectral broadening of pulses from two different laser systems exceeded those achieved with argon and krypton. Initially 40 fs, 800 nm, 120 µJ pulses were compressed to few optical cycles duration. With the same approach a compression factor of more than 10 was demonstrated for an ytterbium-based laser (1030 nm, 170 fs, 200 µJ) leading to 15.6 fs.
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We present the generation of high-peak-electric-field terahertz pulses via collinear optical rectification in a 2-(4-hydroxy-3-methoxystyryl)-1-methilquinolinium-2,4,6-trimethylbenzenesulfonate (HMQ-TMS) organic crystal. The crystal is pumped by an amplified ytterbium laser system, emitting 170-fs-long pulses centered at 1030 nm. A terahertz peak electric field greater than 200 kV/cm is obtained for 420 µJ of optical pump energy, with an energy conversion efficiency of 0.26% - about two orders of magnitude higher than in common inorganic crystals collinearly pumped by amplified femtosecond lasers. An open-aperture Z-scan measurement performed on an n-doped InGaAs thin film using such terahertz source shows a nonlinear increase in the terahertz transmission of about 2.2 times. Our findings demonstrate the potential of this terahertz generation scheme, based on ytterbium laser technology, as a simple and efficient alternative to the existing intense table-top terahertz sources. In particular, we show that it can be readily used to explore nonlinear effects at terahertz frequencies.
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Al-silicate fibers have excellent manufacturing quality. Unfortunately, high-Yb doping concentration may be limited by severe losses induced by photodarkening phenomenon. In this paper we demonstrate for the first time that Al-silicate Yb-doped fibers with high-inversion and doping concentration above 1 wt% can be successfully used by implementing a simple optical bleaching scheme. A co-injection into the active fiber of a few mW of light at around 550 nm wavelength successfully eliminates almost all photodarkening induced losses. We demonstrate operation at above 90% of the pristine output power level in several lasers with up to 30% Yb ions in the excited state. These results may allow using Yb-doped Al-silicate fibers with doping level increased by one order of magnitude. Finally, we provide a comprehensive picture of main parameters affecting photobleaching performance and, to the best of our knowledge, we report the first quantitative measurement of the Ytterbium excited state absorption cross-section in the visible range.
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We report on optical parametric generation in a mercury thiogallate (HgGa2S4) crystal pumped by 16 ps, 1064 nm pulses at 250 kHz. A broad tuning range extending from 1.19 to 1.47 µm (signal) and from 3.85 to 10 µm (idler) is achieved. Narrow bandwidth, quasi-Fourier limited operation with high beam quality for the signal/idler pulses and >14% pump depletion is obtained by continuous wave seed injection at 1.29 µm.
RESUMEN
In this Letter, the lifetime temporal reduction in ytterbium-doped aluminosilicate fibers due to pump-induced photodarkening (PD) has been reported. A linear correlation between lifetime reduction at equilibrium state and equilibrium losses due to the PD phenomenon was demonstrated. A squared-law dependence between lifetime reduction and dopant concentration (percent by weight) suggests a possible correction term for the rate equations system which allows improving its accuracy. Finally, a quenching effect was also observed for different pump power levels in order to find the corresponding lifetime value for different inversion levels. The quantitative analysis allows determination of the PD quenching term in the laser rate equations system to properly model a laser device that may be affected by this process.
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Low-threshold, efficient optical parametric generation at ~4.64 µm is demonstrated using CdSiP2 nonlinear crystal pumped by 150 ps Raman shifted pump pulses at 1198 nm in noncritical configuration at 1 kHz repetition rate. Maximum single pulse idler energy of 6 µJ and total conversion efficiency of 30% are achieved. Seeding at the signal wavelength with a distributed feedback laser diode enables ~25 fold narrowing of the bandwidths down to ~10 GHz, resulting in a Fourier product of ~1 for the ~100 ps long signal (1615 nm) and idler (4.64 µm) pulses.
RESUMEN
An Nd:YVO4 amplifier consisting of two modules end pumped at 808 nm at 30 W total absorbed power has been designed for efficient, diffraction-limited amplification of ultrafast pulses from low-power seeders. We investigated amplification with a 50 mW, 7 ps Nd:YVO4 oscillator, a 2 mW, 15 ps Yb fiber laser, and a 30 mW, 300 fs Nd:glass laser. Output power as high as 9.5 W with 8 ps pulses was achieved with the 250 MHz vanadate seeder, whereas the 20 MHz fiber laser was amplified to 6 W. The femtosecond seeder allowed extracting Fourier-limited 4 ps pulses at 7 W output power. To our knowledge, these are the shortest pulses from any Nd:YVO4 laser device with at least 7 W output power. This suggests a novel approach to exploit the gain bandwidth of vanadate amplifiers with high output power levels. Such amplifier technology promises to offer an interesting alternative to high-power thin disk oscillators at few picoseconds duration, as well as to regenerative amplifiers with low-repetition-rate fiber seeders.
RESUMEN
Low-threshold, efficient optical parametric generation at ~6100 nm is demonstrated using CdSiP2 nonlinear crystal at 1 to 10 kHz repetition rates with relatively long 500 ps pump pulses at 1064 nm. Maximum single pulse energy of 8.7 µJ and average power of 79 mW are achieved for the idler. Seeding at the signal wavelength is employed using a distributed feedback laser diode, which enables approximately tenfold narrowing of the idler bandwidth down to less than 1 nm.
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We present an innovative implementation of the solid-state-biased coherent detection (SSBCD) technique, which we have recently introduced for the reconstruction of both amplitude and phase of ultra-broadband terahertz pulses. In our previous works, the SSBCD method has been operated via a heterodyne scheme, which involves demanding square-wave voltage amplifiers, phase-locked to the THz pulse train, as well as an electronic circuit for the demodulation of the readout signal. Here, we demonstrate that the SSBCD technique can be operated via a very simple homodyne scheme, exploiting plain static bias voltages. We show that the homodyne SSBCD signal turns into a bipolar transient when the static field overcomes the THz field strength, without the requirement of an additional demodulating circuit. Moreover, we introduce a differential configuration, which extends the applicability of the homodyne scheme to higher THz field strengths, also leading a two-fold improvement of the dynamic range compared to the heterodyne counterpart. Finally, we demonstrate that, by reversing the sign of the static voltage, it is possible to directly retrieve the absolute THz pulse polarity. The homodyne configuration makes the SSBCD technique of much easier access, leading to a vast range of field-resolved applications.
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In view of minimally-invasive clinical interventions, laser tissue soldering assisted by plasmonic nanoparticles is emerging as an appealing concept in surgical medicine, holding the promise of surgeries without sutures. Rigorous monitoring of the plasmonically-heated solder and the underlying tissue is crucial for optimizing the soldering bonding strength and minimizing the photothermal damage. To this end, we propose a non-invasive, non-contact, and non-ionizing modality for monitoring nanoparticle-assisted laser-tissue interaction and visualizing the localized photothermal damage, by taking advantage of the unique sensitivity of terahertz radiation to the hydration level of biological tissue. We demonstrate that terahertz radiation can be employed as a versatile tool to reveal the thermally-affected evolution in tissue, and to quantitatively characterize the photothermal damage induced by nanoparticle-assisted laser tissue soldering in three dimensions. Our approach can be easily extended and applied across a broad range of clinical applications involving laser-tissue interaction, such as laser ablation and photothermal therapies.
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We present a straightforward route for extreme pulse compression, which relies on moderately driving self-phase modulation (SPM) over an extended propagation distance. This avoids that other detrimental nonlinear mechanisms take over and deteriorate the SPM process. The long propagation is obtained by means of a hollow-core fiber (HCF), up to 6 m in length. This concept is potentially scalable to TW pulse peak powers at kW average power level. As a proof of concept, we demonstrate 33-fold pulse compression of a 1 mJ, 6 kHz, 170 fs Yb laser down to 5.1 fs (1.5 cycles at 1030 nm), by employing a single HCF and subsequent chirped mirrors with an overall transmission of 70%.
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Phonons (quanta of collective vibrations) are a major source of energy dissipation and drive some of the most relevant properties of materials. In nanotechnology, phonons severely affect light emission and charge transport of nanodevices. While the phonon response is conventionally considered an inherent property of a nanomaterial, here we show that the dipole-active phonon resonance of semiconducting (CdS) nanocrystals can be drastically reshaped inside a terahertz plasmonic nanocavity, via the phonon strong coupling with the cavity vacuum electric field. Such quantum zero-point field can indeed reach extreme values in a plasmonic nanocavity, thanks to a mode volume well below λ3/107. Through Raman measurements, we find that the nanocrystals within a nanocavity exhibit two new "hybridized" phonon peaks, whose spectral separation increases with the number of nanocrystals. Our findings open exciting perspectives for engineering the optical phonon response of functional nanomaterials and for implementing a novel platform for nanoscale quantum optomechanics.