RESUMO
Advances in optical spectroscopy and microscopy have had a profound impact throughout the physical, chemical and biological sciences. One example is coherent Raman spectroscopy, a versatile technique interrogating vibrational transitions in molecules. It offers high spatial resolution and three-dimensional sectioning capabilities that make it a label-free tool for the non-destructive and chemically selective probing of complex systems. Indeed, single-colour Raman bands have been imaged in biological tissue at video rates by using ultra-short-pulse lasers. However, identifying multiple, and possibly unknown, molecules requires broad spectral bandwidth and high resolution. Moderate spectral spans combined with high-speed acquisition are now within reach using multichannel detection or frequency-swept laser beams. Laser frequency combs are finding increasing use for broadband molecular linear absorption spectroscopy. Here we show, by exploring their potential for nonlinear spectroscopy, that they can be harnessed for coherent anti-Stokes Raman spectroscopy and spectro-imaging. The method uses two combs and can simultaneously measure, on the microsecond timescale, all spectral elements over a wide bandwidth and with high resolution on a single photodetector. Although the overall measurement time in our proof-of-principle experiments is limited by the waiting times between successive spectral acquisitions, this limitation can be overcome with further system development. We therefore expect that our approach of using laser frequency combs will not only enable new applications for nonlinear microscopy but also benefit other nonlinear spectroscopic techniques.
Assuntos
Lasers , Análise Espectral Raman/instrumentação , Análise Espectral Raman/métodos , Fatores de Tempo , VibraçãoRESUMO
Sub-Doppler broadband multi-heterodyne spectroscopy is proposed and experimentally demonstrated. Using two laser frequency combs of slightly different repetition frequencies, we have recorded Doppler-free two-photon dual-comb spectra of atomic rubidium resonances of a width of 6 MHz, while simultaneously interrogating a spectral span of 10 THz. The atomic transitions are uniquely identified via the intensity modulation of the observed fluorescence radiation. To the best of our knowledge, these results represent the first demonstration of Doppler-free Fourier transform spectroscopy and extend the range of applications of broadband spectroscopy towards precision nonlinear spectroscopy.
RESUMO
We demonstrate chirped-pulse operation of a Cr : YAG passively mode-locked laser. Different operation regimes of the laser are extensively investigated in the vicinity of zero dispersion both experimentally and numerically. It is shown that for a given laser configuration, transition to the positive dispersion regime allows a 5-fold increase in the output pulse energy, which is otherwise limited by the onset of the multipulsing or 'chaotic' mode-locking. The output pulses have 1.4 ps duration and are compressible down to 120 fs in a 3 m piece of silica fiber, enabling supercontinuum generation in a nonlinear fiber. The spectrum shape and operation stability of the chirped-pulse regime depend strongly on the amount and shape of the intracavity dispersion. The numerical model predicts the existence of the minimum amount of the positive dispersion, above which the chirped-pulse regime can be realized. Once located, the chirped-pulse regime can be reliably reproduced and is sufficiently stable for applications.
RESUMO
The spectral dynamics of a mid-infrared multimode Cr(2+):ZnSe laser located in a vacuum sealed chamber containing acetylene at low pressure is analyzed by a stepping-mode high-resolution time-resolved Fourier transform interferometer. Doppler-limited absorption spectra of C(2)H(2) in natural isotopic abundance are recorded around 4000 cm(-1) with kilometric absorption path lengths and sensitivities better than 3 10(-8) cm(-1). Two cold bands are newly identified and assigned to the ν(1)+ν(4) (1) and ν(3)+ν(5) (1) transitions of (12)C(13)CH(2). The ν(1)+ν(5) (1) band of (12)C(2)HD and fourteen (12)C(2)H(2) bands are observed, among which for the first time ν(2)+2ν(4) (2)+ν(5) (-1).
RESUMO
The spectrum of a laser frequency comb consists of several hundred thousand equally spaced lines over a broad spectral bandwidth. Such frequency combs have revolutionized optical frequency metrology and they now hold much promise for significant advances in a growing number of applications including molecular spectroscopy. Despite an intriguing potential for the measurement of molecular spectra spanning tens of nanometres within tens of microseconds at Doppler-limited resolution, the development of dual-comb spectroscopy is hindered by the demanding stability requirements of the laser combs. Here we overcome this difficulty and experimentally demonstrate a concept of real-time dual-comb spectroscopy, which compensates for laser instabilities by electronic signal processing. It only uses free-running mode-locked lasers without any phase-lock electronics. We record spectra spanning the full bandwidth of near-infrared fibre lasers with Doppler-limited line profiles highly suitable for measurements of concentrations or line intensities. Our new technique of adaptive dual-comb spectroscopy offers a powerful transdisciplinary instrument for analytical sciences.
Assuntos
Lasers , Análise Espectral/instrumentação , Análise Espectral/métodos , Acetileno/análise , Acetileno/química , Técnicas de Química Analítica/instrumentação , Técnicas de Química Analítica/métodos , Desenho de Equipamento , Reprodutibilidade dos Testes , Fatores de TempoRESUMO
Supercontinua generated in highly nonlinear fibers by ultrashort-pulse lasers can be used for high-resolution Fourier transform absorption spectroscopy. The practical advantages of these bright ultrabroadband light sources for spectroscopy in the near-infrared region are reported. A Cr(4+):YAG femtosecond laser broadened by an extruded soft-glass photonic crystal fiber, emitting from 1200 to 2200 nm and from 675 to 950 nm, provides a spectral radiance 1 x 10(5) times higher than that of a 3000 K blackbody and 10(2) times higher than that of synchrotron radiation. The C(2)H(2) and NH(3) overtone spectra are recorded by using this source within a few seconds.
RESUMO
A new method, FM-FTS, combining frequency modulation heterodyne laser spectroscopy and Fourier transform spectroscopy is presented. It provides simultaneous sensitive measurement of absorption and dispersion profiles with broadband spectral coverage capabilities. Experimental demonstration of the overtone spectrum of C(2)H(2) in the 1.5 microm region is presented.
RESUMO
A femtosecond mode-locked laser is used for what is believed to be the first time as a broadband infrared source for high-resolution Fourier transform absorption spectroscopy. A demonstration is made with a Cr(4+):YAG laser. The entire nu(1)+nu(3) vibration-rotation band region of acetylene, observed after passing through a single-pass 80-cm-long cell, is simultaneously recorded between 1480 and 1600 nm, in 7.9 s with a signal-to-noise ratio equal to 1000. Two hot bands of the most abundant acetylene isotopologue and the nu(1)+nu(3) band of the (13)C(12)CH(2) are also present. Replacement of the usual conventional tungsten lamp by the bright laser source reduces by about a factor of 150 the recording time needed to get similar results. The noise equivalent absorption coefficient at 1 s averaging is equal to 7x10(-7) cm(-1)Hz(-1/2) per spectral element.
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Previously unobserved nitrous oxide transitions around 2.5 µm are measured by intracavity laser absorption spectroscopy (ICLAS) analyzed by time-resolved Fourier transform (TRFT) spectrometer. With an accuracy of the order of 10(-3) cm(-1), measured positions of 1637 assigned weak transitions are provided. They belong to 42 vibrational transitions, among which 33 are observed for the first time. These data are believed to be useful in particular to monitoring atmosphere purposes.
RESUMO
Intracavity laser absorption spectroscopy (ICLAS) with an evacuated Cr2+:ZnSe laser is performed with a high-resolution time-resolved Fourier transform interferometer with a minimum detectable absorption coefficient equal to 4 x 10(-9) cm(-1) Hz(-1/2) in the 2.5 microm region. This represents the extreme limit currently reached in the infrared by ICLAS with Doppler-limited resolution. The broad gain band of the crystal allows a spectral coverage at most equal to 125 nm, wide enough to see entire vibration bands. Weak CO2 bands observed up to now only in the Venusian atmosphere are recorded for the first time, to our knowledge, in a laboratory. An H2O detection limit down to 0.9 parts per billion by volume is also demonstrated.
RESUMO
Spectra composed of hundreds of time components for absorption path lengths of up to 130 km have been recorded near 1050 nm by combination of two recent techniques, intracavity laser spectroscopy with vertical external cavity surface-emitting multiple-quantum-well lasers and time-resolved Fourier transform spectroscopy. A sensitivity of 1 x 10(-10) cm(-1) Hz(-1/2) is achieved for 10(4) simultaneously acquired spectral elements, 3 orders of magnitude better than the sensitivity obtained in previous similar experiments. Specific advantages of the method, especially for frequency and intensity metrology of weak absorption transitions, are discussed.