ABSTRACT
Though Pr3+ doped LiYF4 (LiYF4:Pr3+) bulk crystals are a well-known laser gain material with several radiative transitions, their nanocrystal counterparts have not been investigated with regards to these. Through downsizing to the nanoscale, novel applications are expected, especially in composite photonic devices. For example, nanocrystals in stable colloidal form with narrow size distribution are highly desirable to reduce scattering in such composites. Herein, we synthesized monodispersed LiYF4:Pr3+ nanocrystals having a size of 10 nm resulting in colorless clear stable colloidal dispersions and conducted an extensive optical characterization for the first time. We observed unexpected yet intense emission with excited state lifetimes comparable to bulk crystals in the visible spectrum through excitation at 444 nm and 479 nm. In macroscopic bulk crystals, this emission is only exploitable through excitation of a different, subjacent energy level. A comprehensive comparison to the bulk crystals provides deeper insight into the excitation mechanism and performance of these nanocrystals. The presented results pave the way for developing application-oriented LiYF4:Pr3+ nanocrystals as emitters with tailored properties for quantum optics or biomedical applications.
ABSTRACT
In recent years, optical nanothermometers have seen huge improvements in terms of precision as well as versatility, and several research efforts have been directed at adapting novel active materials or further optimizing the temperature sensitivity. The signal-to-noise ratio of the emission lines is commonly seen as the only limitation regarding high precision measurements. The role of re-absorption caused by a population of lower energy levels, however, has so far been neglected as a potential bottleneck for both high resolution and material selection. In this work, we conduct a study of the time dependent evolution of population densities in different luminescence nanothermometer classes under the commonly used pulsed excitation scheme. It is shown that the population of lower energy levels varies when the pump source fluctuates in terms of power and pulse duration. This leads to a significant degradation in temperature resolution, with limiting values of 0.5 K for common systems. Our study on the error margin indicates that either short pulsed or continuous excitation should be preferred for high precision measurements. Additionally, we derive conversion factors, enabling the re-calibration of currently available intensity ratio measurements to the steady state regime, thus facilitating the transition from pulse regimes to continuous excitation.
ABSTRACT
We demonstrate the controllable generation of infrared dispersive waves (DWs) from customized, in-house fabricated silica microstructured optical fibers (MOFs) by manipulating the location of zero dispersion wavelength (ZDW) through the structure of the fibers. The highly enriched shaping mechanism of arrested soliton in the MOFs with two ZDWs provides a technique for efficient energy transfer into the targeted eye-safe wavelengths at 1.7 and 2.0 µm by the virtue of DW formation.
ABSTRACT
In recent years, lanthanide-doped nanothermometers have been mainly used in thin films or dispersed in organic solvents. However, both approaches have disadvantages such as the short interaction lengths of the active material with the pump beam or complicated handling, which can directly affect the achievable temperature resolution. We investigated the usability of a polymer fiber doped with upconversion nanocrystals as a thermometer. The fiber was excited with a wavelength stabilized diode laser at a wavelength of 976 nm. Emission spectra were recorded in a temperature range from 10 to 35 ∘C and the thermal emission changes were measured. Additionally, the pump power was varied to study the effect of self-induced heating on the thermometer specifications. Our fiber sensor shows a maximal thermal sensitivity of 1.45%/K and the minimal thermal resolution is below 20 mK. These results demonstrate that polymer fibers doped with nanocrystals constitute an attractive alternative to conventional fluorescence thermometers, as they add a long pump interaction length while also being insensitive to strong electrical fields or inert to bio-chemical environments.
ABSTRACT
Lab-on-a-Chip (LoC) devices combining microfluidic analyte provision with integrated optical analysis are highly desirable for several applications in biological or medical sciences. While the microfluidic approach is already broadly addressed, some work needs to be done regarding the integrated optics, especially provision of highly integrable laser sources. Polymer optical fiber (POF) lasers represent an alignment-free, rugged, and flexible technology platform. Additionally, POFs are intrinsically compatible to polymer microfluidic devices. Home-made Rhodamine B (RB)-doped POFs were characterized with experimental and numerical parameter studies on their lasing potential. High output energies of 1.65 mJ, high slope efficiencies of 56 % , and 50 % -lifetimes of ≥900 k shots were extracted from RB:POFs. Furthermore, RB:POFs show broad spectral tunability over several tens of nanometers. A route to optimize polymer fiber lasers is revealed, providing functionality for a broad range of LoC devices. Spectral tunability, high efficiencies, and output energies enable a broad field of LoC applications.
ABSTRACT
We report on a compact mid-infrared laser architecture, comprising a chain of $ {\rm ZnGeP}_2 $ZnGeP2-based optical parametric amplifiers (OPAs), which afford a higher energy yield ($ \mathbin{\lower.3ex\hbox{$\buildrel \lt \over{\smash{\scriptstyle\sim}\vphantom{_x}}$}} 60\;\unicode{x00B5} {\rm J} $â¼x<60µJ at 1 kHz) compared to most conventional OPA gain media transparent in the 2-8-µm wavelength range. Specifically, our OPA scheme allows ready tunability in the molecular fingerprint regime and is tailored for strong-field excitation and coherent control of both stretch and bend (or torsional) vibrational modes in molecules. The OPAs are pumped and directly seeded (via supercontinuum generation) by a 2-µm, 3-ps Ho:YLF regenerative amplifier. The compressibility of the OPA output is demonstrated by a representative measurement of the near-Gaussian temporal profile of a dispersion-compensated 105-fs idler pulse at a central wavelength of 5.1 µm, corresponding to ${\sim}6 $â¼6 optical cycles. Detailed numerical simulations closely corroborate the experimental measurements, providing a benchmark and a platform to further explore the parameter space for future design, optimization, and implementation of high-energy, ultrafast, mid-infrared laser schemes.
ABSTRACT
We experimentally demonstrate in a difference-frequency generation mid-infrared frequency comb source the effect of temporal overlap between pump and signal pulses on the relative intensity noise (RIN) of the idler pulse. When scanning the temporal delay between our 130 fs long signal and pump pulses, we observe a RIN minimum with a 3 dB width of 20 fs delay and a RIN increase of 20 dB in 40 fs delay at the edges of this minimum. We also demonstrate active long-term stabilization of the mid-infrared frequency comb source to the temporal overlap setting corresponding to the lowest RIN operation point by an online RIN detector and active feedback control of the pump-signal pulse delay. This active stabilization setup allows us to dramatically increase the signal-to-noise ratio of mid-infrared absorption spectra.
ABSTRACT
High-energy, multi-octave supercontinuum (SC) generation in bulk media pumped with picosecond pulses in the mid-infrared, though pivotal in a myriad of applications, poses severe constraints due to wavelength scaling of the critical power criterion and the propensity to induce avalanche-ionization-seeded breakdown mechanisms. Here, we demonstrate a simple experimental geometry, relying on a very low numerical aperture for the pump pulse, and a crystal length commensurate with the Rayleigh length of the focusing geometry, generating a multi-octave, stable SC in yttrium aluminum garnet (YAG). The SC ranges from 500 nm to 3.5 µm (measured at -30 dB with spectral components at wavelengths up to 4.5 µm) when pumped by a 3 ps pulse centered at 2.05 µm in the anomalous dispersion regime. We also investigate the dynamics of filament formation in this interaction regime by monitoring the spectral and temporal evolution of the pulse during its propagation through the length of the crystal.
ABSTRACT
Synchronously pumped optical parametric oscillators (OPOs) are important tools for frequency comb (FC) generation in the mid-IR spectral range, where few suitable laser gain materials exist. For degenerate OPOs, self-phase-locking to the pump FC has been demonstrated. Here, we present a phase noise study of the carrier envelope offset frequency, revealing a -6 dB reduction compared to the pump FC over a wide Fourier frequency range. These results demonstrate that a degenerate OPO can be an ideal coherent frequency divider without any excess noise.
ABSTRACT
We present an experimental and numerical study on the spectrally resolved pump-to-output intensity noise coupling in soliton fiber oscillators. In our study, we observe a strong pump noise coupling to the Kelly sidebands, while the coupling to the soliton pulse is damped. This behavior is observed in erbium-doped as well as holmium-doped fiber oscillators and confirmed by numerical modeling. It can be seen as a general feature of laser oscillators in which soliton pulse formation is dominant. We show that spectral blocking of the Kelly sidebands outside the laser cavity can improve the intensity noise performance of the laser dramatically.
ABSTRACT
We demonstrate an experimental technique for both transverse and longitudinal characterization of bunched femtosecond free electron beams. The operation principle is based on monitoring of the current of electrons that obtained an energy gain during the interaction with the synchronized optical near-field wave excited by femtosecond laser pulses. The synchronous accelerating/decelerating fields confined to the surface of a silicon nanostructure are characterized using a highly focused sub-relativistic electron beam. Here the transverse spatial resolution of 450 nm and femtosecond temporal resolution of 480 fs (sub-optical-cycle temporal regime is briefly discussed) achievable by this technique are demonstrated.
ABSTRACT
We present a new chromatic numerical approach to simulate the amplification of laser pulses in multipass laser amplifiers. This enables studies on spectral effects such as gain narrowing and spectral shaping with optical elements expressed by a transmission transfer function. We observe good agreement between our simulations and measurements with a Ho:YLF regenerative amplifier (RA). To demonstrate the capabilities of our simulation model, we numerically integrate an intra-cavity etalon in this laser and find optimum etalon parameters that enhance the peak power of the output pulses up to 65%.
ABSTRACT
We demonstrate intracavity gain shaping inside a 2 µm Ho:YLF regenerative amplifier with a spectral bandwidth of 2.9 nm broadened to 5.4 nm, corresponding to Fourier-limited pulses of 1 ps duration. The intracavity gain shaping is achieved by using a simple etalon, which acts as a frequency-selective filter. The output of the regenerative amplifier is amplified by a single-pass amplifier, and we achieve total energy of 2.2 mJ and pulse duration of 2.4 ps at 1 kHz with pulse fluctuations <1%. The amplifier chain is seeded by a home-built mode-locked holmium-doped fiber oscillator.
ABSTRACT
We demonstrate a Ho:YLF regenerative amplifier (RA) overcoming bifurcation instability and consequently achieving high extraction energies of 6.9 mJ at a repetition rate of 1 kHz with pulse-to-pulse fluctuations of 1.1%. Measurements of the output pulse energy, corroborated by numerical simulations, identify an operation point (OP) that allows high-energy pulse extraction at a minimum noise level. Complete suppression of the onset of bifurcation was achieved by gain saturation after each pumping cycle in the Ho:YLF crystal via lowering the repetition rate and cooling the crystal. Even for moderate cooling, a significant temperature dependence of the Ho:YLF RA performance was observed.
ABSTRACT
We demonstrate a simple and compact Holmium-doped fiber femtosecond oscillator, in-band pumped by a commercial Tm-doped fiber laser. The oscillator operates in the dispersion managed soliton regime at net zero intracavity dispersion and delivers >1 nJ pulse energy at 35 MHz repetition rate. The pulse duration directly at the oscillator output is 160 fs FWHM, close to the Fourier-limit of 145 fs FWHM. Using an additional nonlinear compressor stage, sub-100 fs FWHM pulse durations could be achieved. The nonlinear fiber compressor is implemented by a solid core highly nonlinear fiber for spectral broadening and a single mode fiber for pulse compression.
Subject(s)
Holmium , Lasers , Optical Fibers , Time FactorsABSTRACT
We report on a mid-IR frequency comb source of unprecedented tunability covering the entire 3-10 µm molecular fingerprint region. The system is based on difference frequency generation in a GaSe crystal pumped by a 151 MHz Yb:fiber frequency comb. The process was seeded with Raman-shifted solitons generated in a highly nonlinear suspended-core fiber with the same source. Average powers up to 1.5 mW were achieved at the 4.7 µm wavelength.
ABSTRACT
The development of the optical frequency comb (a spectrum consisting of a series of evenly spaced lines) has revolutionized metrology and precision spectroscopy owing to its ability to provide a precise and direct link between microwave and optical frequencies. A further advance in frequency comb technology is the generation of frequency combs in the extreme-ultraviolet spectral range by means of high-harmonic generation in a femtosecond enhancement cavity. Until now, combs produced by this method have lacked sufficient power for applications, a drawback that has also hampered efforts to observe phase coherence of the high-repetition-rate pulse train produced by high-harmonic generation, which is an extremely nonlinear process. Here we report the generation of extreme-ultraviolet frequency combs, reaching wavelengths of 40 nanometres, by coupling a high-power near-infrared frequency comb to a robust femtosecond enhancement cavity. These combs are powerful enough for us to observe single-photon spectroscopy signals for both an argon transition at 82 nanometres and a neon transition at 63 nanometres, thus confirming the combs' coherence in the extreme ultraviolet. The absolute frequency of the argon transition has been determined by direct frequency comb spectroscopy. The resolved ten-megahertz linewidth of the transition, which is limited by the temperature of the argon atoms, is unprecedented in this spectral region and places a stringent upper limit on the linewidth of individual comb teeth. Owing to the lack of continuous-wave lasers, extreme-ultraviolet frequency combs are at present the only promising route to extending ultrahigh-precision spectroscopy to the spectral region below 100 nanometres. At such wavelengths there is a wide range of applications, including the spectroscopy of electronic transitions in molecules, experimental tests of bound-state and many-body quantum electrodynamics in singly ionized helium and neutral helium, the development of next-generation 'nuclear' clocks and searches for variation of fundamental constants using the enhanced sensitivity of highly charged ions.
ABSTRACT
We report on a high-power fiber frequency comb exhibiting linear chirped-pulse amplification up to 80 W and generating 120 fs pulses. By proper matching of the group delay between the fiber stretcher and compressor, a compression ratio of 3100 could be achieved. Carrier envelope offset self-referencing and long-term phase locking to an rf reference is demonstrated, exemplifying the suitability of this system for generating vacuum and extreme-UV frequency combs via enhancement in passive cavities and high harmonic generation.
ABSTRACT
We report on stretched-pulse operation of a thulium-doped fiber laser. The laser generated pulses at a center wavelength of 1974 nm with an energy of 4 nJ that could externally be compressed to a duration of 173 fs.
Subject(s)
Computer-Aided Design , Lasers , Models, Theoretical , Optical Fibers , Thulium/chemistry , Computer Simulation , Equipment Design , Equipment Failure Analysis , Light , Scattering, RadiationABSTRACT
The properties of passively mode-locked laser oscillators based on Ytterbium doped gain media are studied theoretically along with experimental data. Based on the chirped-pulse approach limitations due to excessive non-linearities are avoided, opening up new routes for energy scaling of mode-locked solid-state oscillators. Predictions about potential future pulse energies are made and possible experimental problems are discussed.
