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Vibrational spectroscopies offer great potential for standoff detection of chemical and biological warfare agents, avoiding contamination to the operator and equipment. Among them, particularly promising is Coherent anti-Stokes Raman scattering (CARS) spectroscopy, using synchronized pump/Stokes laser pulses to set up a vibrational coherence of target molecules at a laser focus, which is read by further interaction with a probe pulse, resulting in the emission of a coherent beam detectable at a distance. CARS has previously demonstrated the capability to detect bacterial spores based on the Raman spectrum of the characteristic molecule calcium dipicolinate (CaDPA); however, a complex and bulky laser technology, which is only suitable for a laboratory environment, was employed. Here we develop a broadband CARS setup based on a compact, industrial grade ytterbium laser system. We demonstrate high signal-to-noise ratio detection ofBacillus atrophaeusspores at a concentration of 105cfu/mm2, at a standoff distance of 1 m, and an acquisition time of 1 s. Our system, which combines chemical specificity and sensitivity along with improved ruggedness and portability, paves the way to a new generation of instruments for real-world standoff detection of chemical and biological threats.

The enhancement of nonlinear optical effects via nanoscale engineering is a hot topic of research. Optical nanoantennas increase light-matter interaction and provide, simultaneously, a high throughput of the generated harmonics in the scattered light. However, nanoscale nonlinear optics has dealt so far with static or quasi-static configurations, whereas advanced applications would strongly benefit from high-speed reconfigurable nonlinear nanophotonic devices. Here we propose and experimentally demonstrate ultrafast all-optical modulation of the second harmonic (SH) from a single nanoantenna. Our design is based on a subwavelength AlGaAs nanopillar driven by a control femtosecond light pulse in the visible range. The control pulse photoinjects free carriers in the nanostructure, which in turn induce dramatic permittivity changes at the band edge of the semiconductor. This results in an efficient modulation of the SH signal generated at 775 nm by a second femtosecond pulse at the 1.55 ?m telecommunications (telecom) wavelength. Our results can lead to the development of ultrafast, all optically reconfigurable, nonlinear nanophotonic devices for a broad class of telecom and sensing applications.

A laser system for standoff coherent anti-Stokes Raman scattering (CARS) spectroscopy of various materials under ambient light conditions is presented. The system is based on an ytterbium laser and an ultrafast optical parametric amplifier for the generation of a broadband pump tunable from 880 to 930 nm, a Stokes at 1025 nm, and a narrowband probe at 512.5 nm. High-resolution Raman spectra encompassing the fingerprint region (400-1800 cm−1) are obtained in 5 ms for toluene, and 100 ms for two types of sugars, glucose and fructose, at a distance of 1 m. As a demonstration of the potential of the setup, hyperspectral images of a 2×2-cm2 target area are collected for a toluene cuvette and a glucose/fructose pressed disk. Our approach is suitable for implementation of a portable system for standoff CARS imaging of chemical and biological materials.

We report on a compact and versatile time-domain spectrometer operating in the THz spectral region from 0.2 to 2.5 THz based on ultrafast Yb:CALGO laser and photo-conductive antennas. The spectrometer operates with the optical sampling by cavity tuning (OSCAT) method based on laser repetition rate tuning, which allows at the same time the implementation of a delay-time modulation scheme. The whole characterization of the instrument is presented and compared to the classical THz time-domain spectroscopy implementation. THz spectroscopic measurements on a 520-μm thick GaAs wafer substrate together with water vapor absorption measurements are also reported to further validate the instrument capabilities.

We report a comprehensive characterization of tunable continuous-wave (CW) and passive Q-switching laser performance of Dy-doped zirconium fluoride fiber emitting around 3 µm. The in-band pumped CW laser operation is investigated for pump wavelengths varying from 2.7 µm to 2.825 µm, for fiber lengths ranging from 0.4 m to 2 m, and for output coupling efficiency from 10% to 50%, leading to a maximum laser slope efficiency of 44% and a tuning range larger than 300 nm. With Findlay-Clay analysis and Rigrod analyses, optimal cavity parameters are retrieved, paving the way for further optimizations in performance. The passively Q-switched laser operation of Dy-doped fluoride fiber is achieved employing a semiconductor saturable absorber mirror for the first time, demonstrating a stable operation with a minimum pulse duration of 580 ns, a highest repetition frequency of 103 kHz and a pulse energy up to 300 nJ.

We combine hot-electron dynamical modelling and ultrafast transient absorption spectroscopy to investigate the onset of non-perturbative effects of optical nonlinearities in plasmonic nanostructures, breaking the correspondence between dynamics of optical signal and photoexcited hot carriers.

We report on a compact optical frequency comb, operating in the wavelength range from 670 to 1500 nm, based on diode-pumped low-noise femtosecond Yb:CALGO amplified laser system. Both the carrier-envelope offset and repetition rate are phase-locked to reference synthesizers. A full characterization of the frequency comb, in terms of frequency stability, phase noise analysis, and optical beating against a single-frequency non-planar ring oscillator Nd:YAG laser, is presented, showing the excellent properties of the Yb:CALGO comb.

Bending vibrational modes are responsible for a relevant fraction of molecular absorption spectra in the mid-infrared region at wavelengths beyond 12 μm. To date, the potential of this region for molecular fingerprinting, high-resolution spectroscopy and frequency metrology has been severely hampered by the lack of widely tunable single-mode lasers, with salt-diode lasers almost disappeared, nonlinear laser sources barely delivering optical powers in excess of few hundreds nanowatt [1] and commercial quantum-cascade-lasers (QCLs) hardly emitting beyond 12 μm in cw mode [2] . Recently, direct frequency comb spectroscopy has conquered such region and showed impressive capabilities to acquire ultrabroad high-resolution spectra till 16.7 μm [3] . Nevertheless, spectroscopic data of high metrological quality have not been reported yet, neither spectra with high quality factor in terms of signal-to-noise ratio per spectral point and number of spectral points per spectral feature.

We report on a compact laser system for detection of hazardous biological agents by standoff coherent anti-Stokes Raman spectroscopy (CARS). The system is based on ytterbium-laser technology featuring broad spectral coverage and high sensitivity. High-quality CARS spectra have been obtained for NaDPA powder, a substitute for CaDPA, which is the Raman marker of bacterial spores. In addition, endospores of B. atrophaeus deposited over a glass substrate have been detected by their CARS signature at a standoff distance of 1 m and an integration time of 1 s. The system will be further developed for imaging of bacterial spores deposited over wide surface areas at standoff distances.

The realization and complete characterization of a compact Optical Frequency Comb operating in the wavelength range from 670 to 1500 nm, based on diode-pumped low-noise femtosecond Yb:CALGO amplified laser system, is reported.

We exploit a widely tunable comb-locked frequency-swept synthesizer to test a new optical approach to primary gas thermometry based on a global fitting of multiple molecular absorption lines of the same band at different pressures.

A fiber laser system for standoff detection of chemical and biological species by coherent anti-Stokes Raman scattering is presented. The system is based on an ytterbium fiber laser and a hollow-core photonic crystal fiber for generation of broadband pump/Stokes pulses. High-resolution Raman spectra encompassing the fingerprint region ( 600 − 1600 c m − 1 ) are obtained for toluene, and two simulants of chemical and biological warfare agents, specifically dimethyl methylphosphonate and sodium dipicolinate. The system is operated at standoff distances of 2 m and integration times of 8 ms. The fiber technology makes the approach suitable for implementation as a compact standoff detection and identification system.

An amendment to this paper has been published and can be accessed via a link at the top of the paper.

Ultrafast nanophotonics is an emerging research field aimed at the development of nanodevices capable of light modulation with unprecedented speed1–4. A promising approach exploits the optical nonlinearity of nanostructured materials (either metallic or dielectric) to modulate their effective permittivity via interaction with intense ultrashort laser pulses. Although the ultrafast temporal dynamics of such nanostructures following photoexcitation has been studied in depth5, sub-picosecond transient spatial inhomogeneities taking place at the nanoscale have been overlooked so far. Here, we demonstrate that the inhomogeneous spacetime distribution of photogenerated hot carriers induces a transient symmetry breaking in a highly symmetric plasmonic metasurface. The process is fully reversible and results in a broadband transient dichroism with a recovery of the initial isotropic state in less than 1 ps, overcoming the speed bottleneck caused by slower (electron–phonon and phonon–phonon) relaxation processes. Our results pave the way to ultrafast dichroic devices for high-speed modulation of light polarization. Inhomogeneity of the photogenerated carrier spacetime distribution enables transient symmetry breaking in a metasurface. As a result, broadband transient dichroism is demonstrated.

We report on efficient supercontinuum generation in tapered suspended-core $ {{\rm As}_{39}}{{\rm Se}_{61}} $As

Frequency combs have made optical metrology accessible to hundreds of laboratories worldwide and they have set new benchmarks in multi-species trace gas sensing for environmental, industrial and medical applications. However, current comb spectrometers privilege either frequency precision and sensitivity through interposition of a cw probe laser with limited tuning range, or spectral coverage and measurement time using the comb itself as an ultra-broadband probe. We overcome this restriction by introducing a comb-locked frequency-swept optical synthesizer that allows a continuous-wave laser to be swept in seconds over spectral ranges of several terahertz while remaining phase locked to an underlying frequency comb. This offers a unique degree of versatility, as the synthesizer can be either repeatedly scanned over a single absorption line to achieve ultimate precision and sensitivity, or swept in seconds over an entire rovibrational band to capture multiple species. The spectrometer enables us to determine line center frequencies with an absolute uncertainty of 30 kHz and at the same time to collect absorption spectra over more than 3 THz with state-of-the-art sensitivity of a few 10−10 cm−1. Beyond precision broadband spectroscopy, the proposed synthesizer is an extremely promising tool to force a breakthrough in terahertz metrology and coherent laser ranging.

Optical metrology and high-resolution spectroscopy, despite impressive progress across diverse regions of the electromagnetic spectrum from ultraviolet to terahertz frequencies, are still severely limited in the region of vibrational bending modes from 13 to 20 µm. This long-wavelength part of the mid-infrared range remains largely unexplored due to the lack of tunable single-mode lasers. Here, we demonstrate bending modes frequency metrology in this region by employing a continuous-wave nonlinear laser source with tunability from 12.1 to 14.8 µm, optical power up to 110 µW, MHz-level linewidth and comb calibration. We assess several CO2-based frequency benchmarks with uncertainties down to 30 kHz and we provide an extensive study of the v11 band of benzene, a significant testbed for the resolution of the spectrometer. These achievements pave the way for long-wavelength infrared metrology, rotationally-resolved studies and astronomic observations of large molecules such as aromatic hydrocarbons. The lack of widely tunable single-mode lasers in the long-wavelength part of the mid-infrared region has hindered optical metrology of bending vibrational modes. Here, a continuous-wave nonlinear laser source with tunability from 12.1 to 14.8 μm, coupled with a frequency comb, is used to measure bending modes frequencies of carbon dioxide and benzene with accuracy down to 30 kHz.

We present accurate measurements of the quadrupole S(3) and S(4) transitions of the ${\mathrm{D}}_{2}\phantom{\rule{4pt}{0ex}}2\ensuremath{-}0$ band. Self-perturbed spectra were collected in a wide pressure range with a cavity ring-down spectrometer linked to an optical frequency comb. The results of ab initio quantum scattering calculations were incorporated into the line-shape analysis which was performed using the Hartmann-Tran profile. This approach allowed us to mitigate the collisional systematics and to reach a 900-kHz accuracy of the transition frequencies, which represents a 30-fold improvement compared to previously available data. We also compare our findings with newly calculated transition frequencies that include relativistic and quantum electrodynamics corrections up to ${\ensuremath{\alpha}}^{7}$. The differences between theoretical and experimental values for the transition frequencies are 2.2 MHz and 3.3 MHz for the S(3) and S(4) transitions, respectively.

In this paper we propose multispectrum rotational states distribution thermometry as an optical method for primary thermometry. It relies on a global fitting of multiple absorption lines of the same band at different pressures. The approach allows leveraging both the temperature-dependent Doppler width and the temperature-dependent distribution of line intensities across the ro-vibrational band. We provide a proof-of-principle demonstration of the approach on the 3ν 1 + ν 3 band of CO2, for which several accurate line-strength models of both theoretical and experimental origin are available for the global fitting. Our experimental conditions do not allow to test the methodology beyond a combined uncertainty of 530 ppm, but the comparative analysis between different line-strength models shows promise to reduce the error budget to few tens of ppm. As compared to Doppler-broadening thermometry, the approach is advantageous to mitigate systematic errors induced by a wrong modelling of absorption line-shapes and to reduce, for a given experimental dataset, the statistical uncertainty by a factor of 2. When applied in a reverse way, i.e. using a gas of known temperature, the approach becomes a stringent testbed for the accuracy of the adopted line-strength model.

Pulse compression in a short, normal dispersion photonic-crystal fiber is investigated with a Yb:CaGdAlO4 laser pumped by a low-power fiber-coupled single-mode diode that delivers 70-fs pulses at 1050 nm central wavelength, with 45-mW average power at 60 MHz repetition rate. A simple and power-efficient compressor based on a similar to 15-cm long, low-cost commercial nonlinear fiber, with normal dispersion at the laser wavelength, produces pulses as short as 14.9 fs, corresponding to similar to 4.25 optical cycles, with 29 mW average power after a prism-pair compressor in double pass configuration. Pulse quality was investigated with frequency resolved optical gating (FROG) analysis. Furthermore, a comparative analysis of noise properties of the oscillator, pump laser and compressed pulses has been performed. (C) 2020 Optical Society of America under the terms of the OSA Open Access Publishing Agreement

We theoretically predict and experimentally demonstrate by polarization-resolved ultrafast transient absorption that the inhomogeneous space-time distribution of photogenerated hot carriers induces a sub-picosecond symmetry breaking in a plasmonic metasurface made of highly symmetric metaatoms.

We demonstrate nonlinear compression of pulses at 1.03 µm and repetition rate of 200 kHz generated by a ytterbium fiber laser using two cascaded all-solid-state multipass cells. The pulse duration has been compressed from 460 to 22 fs, corresponding to a compression factor of ∼21. The compressed pulse energy is 15.6 µJ, corresponding to an average power of 3.1 W, and the overall transmission of the two compression stages is 76%. The output beam quality factor is M2 ∼1.2 and the excess intensity noise introduced by nonlinear broadening is below 0.05%. These results show that nonlinear pulse compression down to ultrashort durations can be achieved with an all-solid-state approach, at pulse energies much higher than previously reported, while preserving the spatial characteristics of the laser.

During the last decade, the photothermal properties of nanostructures have attracted an increasing interest for both fundamental and applied aspects, with potential impact on cancer therapy and solar devices [1]. In particular, metal nanoparticles have been widely exploited to absorb and concentrate light energy at the nanoscale, via plasmonic resonances. Most efforts in the field have dealt with the engineering of the individual nanoparticle configuration, from nanospheres to nanorods, nanoshells, nanocages, etc. (see e.g. Ref. 2 for an overview). Another route of research explored novel materials for plasmonics, including heavily doped semiconductors, and even all-dielectric materials with peculiar permittivity enabling quasi-static resonances without free carriers (see e.g. ref. 3 and references therein). However, the available degrees of freedom turned out to be relatively limited. A fresh new turn in the field is represented by plasmonic nanocrystal assemblies, i.e. so-called supraparticles or supracrystals of about 100 nm, consisting of few nm-sized metallic nanocrystals embedded in a matrix of organic ligands [4]. Thanks to their hybrid composition and their internal structure, these novel nanomaterials offer unprecedented possibilities for the engineering of both linear and nonlinear plasmonic phenomena.

Optical frequency comb sources provide thousands of precise and accurate optical lines in a single device enabling the broadband and high-speed detection required in many applications. A main challenge is to parallelize the detection over the widest possible band while bringing the resolution to the single comb-line level. Here we propose a solution based on the combination of a frequency comb source and a fibre spectrometer, exploiting all-fibre technology. Our system allows for simultaneous measurement of 500 isolated comb lines over a span of 0.12 THz in a single acquisition; arbitrarily larger span are demonstrated (3,500 comb lines over 0.85 THz) by doing sequential acquisitions. The potential for precision measurements is proved by spectroscopy of acetylene at 1.53 μm. Being based on all-fibre technology, our system is inherently low-cost, lightweight and may lead to the development of a new class of broadband high-resolution spectrometers., An ideal optical frequency-comb system should combine both single-line spectral resolution and a bandwidth broad enough to cover as many lines as possible. Here, the authors incorporate a fibre spectrometer to detect approximately 500 comb-lines with an instrument resolution of 120 megahertz.

Modulation transfer spectroscopy is used to demonstrate absolute frequency stabilization of an 8.6-µm-wavelength quantum cascade laser against a sub-Doppler absorption of the C H F 3 molecule. The obtained spectral emission properties are thoroughly characterized through a self-referenced optical frequency comb, stabilized against either a GPS-disciplined Rb clock or a 1.54-µm Er-fiber laser locked to a high-finesse ultra-low-expansion optical cavity. Fractional long-term stability and accuracy at a level of 4 × 10 − 12 (at 100 s) and 3 × 10 − 10 , respectively, are demonstrated, along with an emission linewidth as narrow as 10 kHz for observation times of 0.1 s.

An optical-frequency-comb-referenced quantum cascade laser is used to perform wavelength-modulation Lamb-dip spectroscopy on a large number of ro-vibrational transitions falling in the CHF3 upsilon(5) fundamental band at 8.6 mu m. The combined (statistical + systematic) fractional uncertainty in the absolute determination of the line-center frequencies ranges from 9 x 10(-11) down to 2 x 10(-11). This represents an improvement by more than two orders of magnitude, as compared to a recent and extensive study performed with a high-resolution FTIR spectrometer [1]. Our investigation realizes a sharpened knowledge of the CHF3 spectrum over a wide interval, also managing to accurately determine the positions of very close, previously unresolved multiple ro-vibrational components. (C) 2020 Elsevier Ltd. All rights reserved.

We report a passively mode-locked Dy

Quantum cascade lasers (QCLs) are becoming a key tool in several advanced experiments in the field of precision molecular spectroscopy and absolute frequency metrology. In view of this, a thorough control of their emission properties must be achieved, including a narrow linewidth as well as a high frequency-stability combined with referencing to a primary standard. Here, we give a review on recent developments and next perspectives in this scope, with particular regard to the use of QCLs in fundamental physics spectroscopic searches.

We report a passively mode-locked Dy3+:fluoride fiber laser emitting around 3.1 μm based on the nonlinear polarization evolution technique in a ring configuration, using in-band pumping at 2.8 μm. Transform-limited and self-starting mode-locked pulses as short as 828 fs with a center wavelength around 3.1 μm and repetition rates up to 60 MHz are obtained. In the single-pulse regime, a maximum average output power of 204 mW is measured, corresponding to a peak power of 4.2 kW and a pulse energy of 4.8 nJ. This first demonstration, to the best of our knowledge, of a femtosecond mode-locked fiber laser emitting directly beyond 3 μm paves the way for frequency comb synthesis in the molecular fingerprint region.

The need of a fs-scale pulsed, high repetition rate, X-ray source for time-resolved fine analysis of matter (spectroscopy and photon scattering) in the linear response regime is addressed by the conceptual design of a facility called MariX (Multi-disciplinary Advanced Research Infrastructure for the generation and application of X-rays) outperforming current X-ray sources for the declared scope. MariX is based on the original design of a two-pass two-way superconducting linear electron accelerator , equipped with an arc compressor, to be operated in CW mode (1 MHz). MariX provides FEL emission in the range 0.2–8 keV with 1 0 8 photons per pulse ideally suited for photoelectric effect and inelastic X-ray scattering experiments. The accelerator complex includes an early stage that supports an advanced inverse Compton source of very high-flux hard X-rays of energies up to 180 keV that is well adapted for large area radiological imaging, realizing a broad science programme and serving a multidisciplinary user community, covering fundamental science of matter and application to life sciences, including health at preclinical and clinical level.

We report on efficient supercontinuum generation in tapered suspended-core A s 39 S e 61 fibers pumped by a femtosecond mode-locked Cr:ZnSe laser. The supercontinuum spectrum spans the mid-infrared spectral region from 1.4 to 4.2 µm, and its spectral coherence is proved by heterodyning with a single-frequency narrow-linewidth Er-fiber laser at 1.55 µm, measuring a beat note with 27-dB signal-to-noise ratio in a resolution bandwidth of 100 kHz. The intensity stability of the supercontinuum radiation is also characterized by relative intensity noise measurements.

A step forward in Doppler-broadening thermometry is demonstrated using a comb-assisted cavity-ring-down spectroscopic approach applied to an isolated near-infrared line of carbon dioxide at thermodynamic equilibrium. Specifically, the line-shape of the ${P}_{\mathrm{e}}(12)$ line of the $(30012)\ensuremath{\leftarrow}(00001)$ band of $\mathrm{C}{\mathrm{O}}_{2}$ at 1.578 \textmu{}m is accurately measured and its Doppler width extracted from a refined multispectrum fitting procedure accounting for the speed dependence of the relaxation rates, which were found to play a role even at the very low pressures explored, from 1 to 7 Pa. The thermodynamic gas temperature is retrieved with relative uncertainties of $8\ifmmode\times\else\texttimes\fi{}{10}^{\ensuremath{-}6}$ (type A) and $11\ifmmode\times\else\texttimes\fi{}{10}^{\ensuremath{-}6}$ (type B), which ranks the system at the first place among optical methods. Thanks to a measurement time of only $\ensuremath{\approx}5\phantom{\rule{0.16em}{0ex}}\mathrm{h}$, the technique represents a promising pathway toward the optical determination of the thermodynamic temperature with a global uncertainty at the ${10}^{\ensuremath{-}6}$ level.

We report the first experimental demonstration of frequency-locking of an extended-cavity quantum-cascade-laser (EC-QCL) to a near-infrared frequency comb. The locking scheme is applied to carry out absolute spectroscopy of N2O lines near 7.87 {\mu}m with an accuracy of ~60 kHz. Thanks to a single mode operation over more than 100 cm^{-1}, the comb-locked EC-QCL shows great potential for the accurate retrieval of line center frequencies in a spectral region that is currently outside the reach of broadly tunable cw sources, either based on difference frequency generation or optical parametric oscillation. The approach described here can be straightforwardly extended up to 12 {\mu}m, which is the current wavelength limit for commercial cw EC-QCLs., Comment: 4 pages, 3 figures

The ν1 fundamental band of N2O is examined by a novel spectrometer that relies on the frequency locking of an external-cavity quantum cascade laser around 7.8 µm to a near-infrared Tm:based frequency comb at 1.9 µm. Due to the large tunability, nearly 70 lines in the 1240–1310 cm−1 range of the ν1 band of N2O, from P(40) to R(31), are for the first time measured with an absolute frequency calibration and an uncertainty from 62 to 180 kHz, depending on the line. Accurate values of the spectroscopic constants of the upper state are derived from a fit of the line centers (rms ≈ 4.8 × 10−6 cm−1 or 144 kHz). The ν1 transitions presently measured in a Doppler regime validate high accuracy predictions based on sub-Doppler measurements of the ν3 and ν3-ν1 transitions.

We demonstrate a Fourier transform (FT) coherent anti-Stokes Raman scattering (CARS) spectroscopy system based on fiber technology with ultra-broad spectral coverage and high-sensitivity. A femtosecond ytterbium fiber oscillator is amplified and spectrally broadened in a photonic crystal fiber to synthesize pulses with energy of 14 nJ at 1040 nm, that are compressed to durations below 20 fs. The resulting pulse train is coupled to a FT-CARS interferometer enabling measurement of high-quality CARS spectra with Raman shifts of ~3000 cm−1 and signal to noise ratio up to 240 and 690 with acetonitrile and polystyrene samples, respectively, for observation times of 160 µs; a detection limit of one part per thousand is demonstrated with a cyanide/water solution. The system has the potential to detect trace contaminants in water as well as other broadband high-sensitivity CARS spectroscopy applications.

We present a mid-IR high-precision spectrometer capable of performing accurate Doppler-free measurements with absolute calibration of the optical axis and high signal-to-noise ratio. The system is based on a widely tunable mid-IR offset-free frequency comb and a Quantum-Cascade-Laser (QCL). The QCL emission frequency is offset locked to one of the comb teeth to provide absolute-frequency calibration, spectral-narrowing, and accurate fine frequency tuning. Both the comb repetition frequency and QCL-comb offset frequency can be modulated to provide, respectively, slow- and fast-frequency-calibrated scanning capabilities. The characterisation of the spectrometer is demonstrated by recording sub-Doppler saturated absorption features of the CHF3 molecule at around 8.6 μm with a maximum signal-to-noise ratio of ∼7 × 103 in 10 s integration time, frequency-resolution of 160 kHz, and accuracy of less than 10 kHz.

We investigated a set of nineteen 12C16O2 transitions of the 2?1 + ?3 ro-vibrational band in the spectral region from 5064 to 5126 cm 1 at different pressures, using frequency-comb Vernier spec- troscopy. Our spectrometer enabled the systematic acquisition of molecular absorption profiles with high precision. Spectroscopic parameters, namely, transition frequency, linestrength, and self-pressure broadening coefficient, have been accurately determined by using a global fit procedure. These data are in agreement with theoretical values contained in HITRAN2016 database [I. E. Gordon et al., J. Quant. Spectrosc. Radiat. Transfer 203, 3-69 (2017)] at the same precision level. A moderate improvement of the line intensity determinations, by a factor 1.5 in the best case [P(10) transition at 5091.6 cm 1], should be noticed, projecting direct-comb-Vernier-spectroscopy as an adequate tool for spectral intensity calibration.