• Advanced Photonics
  • Vol. 2, Issue 3, 036004 (2020)
Jie Chen1、2, Kazuki Nitta2、3, Xin Zhao1, Takahiko Mizuno3、4、5, Takeo Minamikawa3、4、5、6, Francis Hindle7, Zheng Zheng1、8、*, and Takeshi Yasui3、4、5、6、*
Author Affiliations
  • 1Beihang University, School of Electronic and Information Engineering, Beijing, China
  • 2Tokushima University, Graduate School of Advanced Technology and Science, Tokushima, Japan
  • 3JST, ERATO MINOSHIMA Intelligent Optical Synthesizer, Tokushima, Japan
  • 4Tokushima University, Institute of Post-LED Photonics, Tokushima, Japan
  • 5Tokushima University, Graduate School of Technology, Industrial and Social Sciences, Tokushima, Japan
  • 6Tokushima University, Research Cluster on “Multi-scale Vibrational Microscopy for Comprehensive Diagnosis and Treatment of Cancer”, Tokushima, Japan
  • 7Université du Littoral Côte d’Opale, Laboratoire de Physico-Chimie de l’Atmosphère, Dunkerque, France
  • 8Beihang University, Beijing Advanced Innovation Center for Big Data-based Precision Medicine, Beijing, China
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    DOI: 10.1117/1.AP.2.3.036004 Cite this Article Set citation alerts
    Jie Chen, Kazuki Nitta, Xin Zhao, Takahiko Mizuno, Takeo Minamikawa, Francis Hindle, Zheng Zheng, Takeshi Yasui. Adaptive-sampling near-Doppler-limited terahertz dual-comb spectroscopy with a free-running single-cavity fiber laser[J]. Advanced Photonics, 2020, 2(3): 036004 Copy Citation Text show less

    Abstract

    Dual-comb spectroscopy (DCS) is an emerging spectroscopic tool with the potential to simultaneously achieve a broad spectral coverage and ultrahigh spectral resolution with rapid data acquisition. However, the need for two independently stabilized ultrafast lasers significantly hampers the potential application of DCS. We demonstrate mode-resolved DCS in the THz region based on a free-running single-cavity dual-comb fiber laser with the adaptive sampling method. While the use of a free-running single-cavity dual-comb fiber laser eliminates the need for two mode-locked lasers and their frequency control, the adaptive sampling method strongly prevents the degradation of spectroscopic performance caused by the residual timing jitter in the free-running dual-comb laser. Doppler-limit-approaching absorption features with linewidths down to 25 MHz are investigated for low-pressure acetonitrile/air mixed gas by comb-mode-resolved THz spectroscopy. The successful demonstration clearly indicates its great potential for the realization of low-complexity, Doppler-limited THz spectroscopy instrumentation.

    1 Introduction

    Coherent spectroscopic techniques in the terahertz (THz) or far-infrared region (frequencies of 0.1 to 10 THz and wavelengths of 30  μm to 3 mm) are the enabling technology for a wide variety of important applications.13 Among these techniques, photonic-based THz time-domain spectroscopy (THz-TDS)4,5 has been applied to the study of a diverse range of samples, such as the rotational transitions of polar gas molecules,6 the hydrogen bonding signature in aqueous systems,7 and self-assembly of proteins,8 because it takes advantage of the broad spectral bandwidth of THz emitters/receivers pumped by ultrafast lasers. This well-established THz-TDS scheme uses pump pulses and delayed probe pulses from a femtosecond mode-locked laser for THz radiation and THz detection, respectively. However, it has limited spectral resolution and accuracy due to constraints on the travel range, repeatability, and speed of the mechanical delay lines. Thus, the use of the photonic THz techniques for Doppler-limited spectral measurements and quantitative analysis of molecular rotational transitions, which are attractive for many applications including gas sensing, has not yet been well explored.

    Because optical frequency combs9,10 provide unprecedented freedom and accuracy in manipulating optical frequencies, dual-comb spectroscopy (DCS)9,10 is a powerful tool for overcoming this limitation. The use of two optical combs with a small frequency spacing offset enables us to achieve greatly enhanced spectroscopic performance by avoiding the physical delay line. In the THz region, THz dual-comb spectroscopy (THz-DCS)1113 has become a promising pathway toward ultrahigh-resolution broadband THz spectroscopy. While two THz combs can be directly generated from a pair of THz quantum cascade lasers,1416 such compact THz sources have a relatively large repetition rate (frequency spacing) between comb modes and often poor mutual coherence between them, leading to coarse sampling spacing and limited spectral resolution. By contrast, if two stabilized optical combs with a highly mutual stability are used for the generation and detection of the THz comb, the mixing of dual THz combs with highly mutual coherence can be mapped to an RF comb with the temporal magnification factor (TMF), which is given by the ratio of the repetition rate frep1 to the repetition rate offset Δfrep (frep1/Δfrep). An RF comb is easily accessible with low-bandwidth electronics and further processed to yield high-bandwidth, high-resolution THz spectroscopic information. THz-DCS enables us to achieve the spectral resolution equal to the THz comb-mode linewidth, which is on the order of MHz or better.17,18 However, the practical use of mode-resolved THz-DCS is still hampered by the need for two repetition-rate-stabilized optical frequency comb sources because of their expensiveness and complexity in the same manner as optical DCS.

    Various schemes have been investigated to further reduce the complexity of THz-DCS and optical DCS systems. Recently, advances in the endeavor to generate a pair of frequency combs from a free-running single-cavity laser1928 have shown great potential toward this goal. By propagating through the same laser cavity, the dual-optical combs experience almost the same disturbances, and the common-mode fluctuations thereby prevent the decline of the mutual coherence between the dual combs. Such a single-cavity dual-comb laser (SCDCL) has been effectively applied to optical DCS25,2933 and THz-DCS34,35 with low complexity. The mode-resolved comb spectrum was obtained in optical and THz regions using SCDCL. However, their applications have been limited to pressure-broadening gas spectroscopy with absorption features of sub-GHz to GHz linewidth31,33 due to the limited spectral resolution resulting from the instability of the TMF caused by the residual timing jitter of the SCDCL. Recently, a computational phase correction method has been applied to the optical DCS. Depending on the noise characteristics and available signals, it could compensate for such timing jitters through a computational process after acquiring the interferogram in the time domain. A combination of frequency-stable combs and slow computation correction facilitated the realization of 1-Hz linewidth in the near-infrared region.36 The computational approach was also extended to the THz spectroscopy regime based on quantum cascaded lasers.37 It had been applied to the SCDCL for Doppler-limited gas spectroscopy in the near-infrared region,38 with a spectral linewidth of the observed absorption features around 600 MHz at a relatively high frep1 (142  MHz). Adaptive sampling is another attractive technique. By correcting the nonlinearity of the time scale caused by the TMF instability with the adaptive timing clock, the relative coherence between the two combs can be actively recovered for relatively long-time scales without any computational processing of interferograms. It has been demonstrated that a combination of the adaptive sampling method with two free-running lasers in DCS is more powerful than a combination of a constant sampling method with two stabilized lasers under no further postcorrection.39 Alternatively, the digital-domain adaptive sampling approach where the DCS signal is digitized but then resampled could be very effective as well and could deal with even faster noise.24,4044 These adaptive sampling approaches impose mutual coherence between the combs and therefore provide improved spectral resolution. A combination of such adaptive sampling methods with a lower-frep1 SCDCL will be the ultimate form of DCS for high spectroscopic performance and reduced system complexity.

    In this paper, we demonstrate an adaptive-sampling, near-Doppler-limited THz-DCS scheme based on a simple free-running SCDCL. Doppler-limit-approaching absorption features were investigated for low-pressure gas mixtures of acetonitrile and air.

    2 Materials and Methods

    2.1 Principle of Operation

    THz-DCS can be performed in the frequency domain11,12 or time domain.13 In the time-domain THz-DCS, the THz frequency comb spectrum is obtained by a combination of asynchronous optical sampling (ASOPS)4547 and Fourier transform (FT), as shown in Fig. 1(a). Using two mode-locked lasers with slightly mismatched repetition rates (frep1 and frep2, Δfrep=frep2frep1) for THz generation and detection, a THz pulse train (with a repetition rate of frep1, consecutive THz pulses of N, and a time window size of N/frep1) is slowed down to an RF pulse train (with a repetition rate of Δfrep, consecutive RF pulses of N, and a time window size of N/Δfrep) by the TMF (frep1/Δfrep) based on the temporal magnifying function of ASOPS; this enables a direct acquisition of the RF pulse train using a data acquisition board without the need for mechanical time-delay scanning. FT of the RF pulse train results in the mode-resolved RF comb spectrum with a frequency spacing of Δfrep. Finally, the mode-resolved THz comb spectrum is obtained by calibrating the frequency scale of the RF comb spectrum with the inverse of the TMF. The mode-resolved THz comb spectrum contains a series of successive narrow lines with a frequency spacing equal to the repetition rate (frep1) and a spectral sampling step equal to the inverse of the time window (frep1/N). The linewidth of each comb mode is equal to the spectral sampling step.

    Principle of operation. (a) Flowchart of time-domain THz-DCS. (b) Acquisition of the temporal waveform using the adaptive sampling method.

    Figure 1.Principle of operation. (a) Flowchart of time-domain THz-DCS. (b) Acquisition of the temporal waveform using the adaptive sampling method.

    Details of the adaptive sampling method have been discussed elsewhere,39 so only its brief description is given here. If the TMF is fluctuated by the residual timing jitter of the free-running SCDCL, linearity of the time scale of the RF pulse train is distorted as shown in the upper row of Fig. 1(b). Such temporal nonlinearity is transferred to the frequency scale of the RF comb and THz comb, which will seriously degrade the spectral resolution. If the RF pulse train is acquired by a sampling clock synchronized with the residual timing jitter, namely an adaptive clock, as shown in the middle row of Fig. 1(b), the time-scale linearity of the sampled signal can be recovered [see the lower row of Fig. 1(b)]. In this case, the time window size can be effectively extended without an accumulation of timing errors. It is also possible to acquire accumulated data over a longer period of time to realize an improved SNR.

    2.2 Single-Cavity Dual-Comb Laser

    The upper-left part of Fig. 2 shows a free-running SCDCL composed of an all-fiber ring-cavity oscillator, a band-pass filter, and erbium-doped fiber amplifiers (EDFAs). The dual-comb light beams with different center wavelengths and different frep were obtained from the fiber oscillator by multiplexing the mode-locking operation in the wavelength region.29,32,34 The fiber oscillator has an all-fiber ring cavity in which the dual-comb light beams propagate along a common-path route. The cavity consists of a hybrid wavelength division multiplexer and isolator (WDM/ISO), a piece of 0.46-m-long erbium-doped fiber (EDF) pumped by a 980-nm laser diode, a polarization controller (PC), a single-wall carbon nanotube saturable absorber (SA), an in-line polarizer (ILP) with polarization-maintained fiber (PMF) pigtails, and a 40% fiber output coupler (OC). In addition, a 65-cm-long dispersion compensation fiber was installed to optimize the intracavity dispersion at 4.0  fs/nm at 1560 nm. The total length of the cavity was 4.21  m. Due to the considerable birefringence of the PMF and the use of the ILP, spectral filtering and polarization-dependent loss tuning enable dual-comb lasing oscillation by adjusting the PC.29 Dual-comb light with different center wavelengths and different frep (λ1-comb with frep1 and λ2-comb with frep2) from the oscillator was separated into two independent combs with different center wavelengths and different frep by the bandpass filter, and the resulting two combs were further amplified by EDFAs. The difference in their center wavelengths is negligible for generation and detection of THz comb.

    Configuration of comb-mode-resolved adaptive sampling THz-DCS. SFG-X, sum-frequency-generation cross-correlator; BBO, beta-barium borate crystal; PC-THz comb, photocarrier THz comb; M, double-balanced mixer; FM, frequency multiplier (frequency multiplication factor N=40); PCA, photoconductive antenna; and AMP, current preamplifier.

    Figure 2.Configuration of comb-mode-resolved adaptive sampling THz-DCS. SFG-X, sum-frequency-generation cross-correlator; BBO, beta-barium borate crystal; PC-THz comb, photocarrier THz comb; M, double-balanced mixer; FM, frequency multiplier (frequency multiplication factor N=40); PCA, photoconductive antenna; and AMP, current preamplifier.

    2.3 Adaptive Clock Generator

    The adaptive clock generator (ACG) provides the adaptive clock to suppress the residual long-term drift and timing jitter in the repetition rate difference Δfrep of the free-running SCDCL, enabling us to recover the temporal linearity of the acquired temporal waveform. To trace the timing fluctuation in real time, we used photoconductive heterodyning mixing between a reference CW-THz radiation and two photocarrier THz combs (PC-THz comb1 with frep1 and PC-THz comb2 with frep2) seeded by the SCDCL output,39 as shown in the middle part of Fig. 2. Two bowtie-shaped, low-temperature-grown GaAs photoconductive antennas (BT-PCA1 and BT-PCA2) were optically excited by the second-harmonic-generation light of the optical dual combs (not shown in Fig. 2). When the CW-THz radiation (fTHz=0.1  THz, linewidth<0.6  Hz, and average power=2.5  mW) from an active frequency multiplier (FM) chain sourced by a microwave frequency synthesizer was also incident on both BT-PCA1 and BT-PCA2, two RF beat signals were generated between the CW-THz and the nearest adjacent PC-THz comb modes. Their frequencies (fbeat1 and fbeat2) are given by |fTHzmfrep1| and |fTHzmfrep2|, respectively, assuming that the same m-order comb lines are involved. The fbeat2fbeat1 signal that carries the timing fluctuation information (=mfrep2mfrep1=mΔfrep) was obtained by electrical mixing in a double-balanced mixer (M). The resulting signal was further frequency-multiplied by an FM (frequency multiplication factor N=40), which serves as the adaptive sampling clock.

    2.4 THz Dual-Comb Spectroscopy

    The right part of Fig. 2 shows the experimental setup of THz-DCS. THz comb was radiated from a fiber-coupled, strip-line-shaped LT-InGaAs/InAlAs photoconductive antenna (PCA1, TERA 15-TX-FC, Menlo Systems, bias voltage=20  V, optical power of 20 mW) excited by λ1-comb pump light and then passed through a low-pressure gas cell (length=38  cm, diameter=17  mm). The THz comb was then detected by another fiber-coupled, dipole-shaped LT-InGaAs/InAlAs photoconductive antenna (PCA2, TERA 15-RX-FC, Menlo Systems, optical power=20  mW) that was pumped by the λ2-comb light. The electrical output of PCA2 was amplified by a current preamplifier (AMP, bandwidth=3.8  MHz, gain=1×106  V/A).

    A portion of the separated λ1-comb and λ2-comb lights was fed into a sum-frequency-generation cross-correlator (SFG-X), with a setup that was constructed based on a noncollinear configuration with a piece of β-BaB2O4 (BBO) crystal. The resulting SFG pulse that occurs every 1/Δfrep served as the trigger signal for the data acquisition board.

    The temporal waveform of the amplifier output was acquired with a data acquisition board. The mode-resolved THz comb spectrum was obtained by taking Fourier transform of the temporal waveform accumulated in the time domain. A rubidium frequency standard (Stanford Research FS725, accuracy=5×1011 and instability=2×1011 at 1 s) is used to provide the common time-base signal for the CW-THz source and the data acquisition board (not shown in Fig. 2).

    2.5 Sample

    Acetonitrile (CH3CN) is a symmetric top molecule with a rotational constant B of 9.194 GHz and a centrifugal distortion constant DJK of 17.74 MHz,48 and its gas phase has relatively complicated spectral absorption features in the THz domain. Frequencies of its rotational transitions are given as v=2B(J+1)2DJKK2(J+1),where J and K are rotational quantum numbers. There are two sets of characteristic features in the THz spectrum of CH3CN. From the first term in Eq. (1), there are multiple manifolds of rotational transitions that are equally spaced by 2B (18.388  GHz). From the second term in Eq. (1), each manifold further consists of a series of closely spaced absorption lines on the order of tens of MHz. The MHz-order absorption feature makes this gas a good candidate for the demonstration of Doppler-limited gas spectroscopy in the THz region.

    3 Results

    3.1 Basic Performance of SCDCL

    When the cavity EDF was pumped beyond its mode-locking threshold and the intracavity PC was properly adjusted, dual-comb mode-locking oscillation was achieved at two different center wavelengths with similar peak intensities, as shown in Fig. 3(a). Two spectral peaks at 1532.5 and 1557.7 nm have 3 dB bandwidths of 4.2 and 3.6 nm, respectively, corresponding to the λ1-comb light and λ2-comb light. Due to the finely adjusted, low intracavity anomalous dispersion, the λ1-comb light and λ2-comb light have slightly different repetition rates, frep1 (48.804486  MHz) and frep2 (48.804296  MHz), and their difference (Δfrep) is only 190  Hz, as shown in Fig. 3(b). After separate amplification by EDFAs, the dual-comb lights are spectrally broadened and temporally compressed to 110  fs at full-width-at-half-maximum (FWHM) by propagating through the standard single-mode fiber. The achieved pulse duration is sufficient to drive the broadband THz comb spectrum.

    Performance of the dual-comb fiber laser. (a) Output spectrum of the laser. (b) RF spectrum of the dual-comb pulses. (c) Fluctuations of frep1, frep2, and Δfrep. (d) Measured frequency instability of frep1 and Δfrep.

    Figure 3.Performance of the dual-comb fiber laser. (a) Output spectrum of the laser. (b) RF spectrum of the dual-comb pulses. (c) Fluctuations of frep1, frep2, and Δfrep. (d) Measured frequency instability of frep1 and Δfrep.

    The temporal drifts of frep1, frep2, and Δfrep under free-running conditions were monitored in time because they alter the TMF between the THz comb and RF comb. As shown in Fig. 3(c), the drifts of both repetition rates are 2.5  Hz in 120 s and follow the same trend owing to the identical fluctuations in the completely shared path for both pulses. The resulting fluctuation of Δfrep is merely 5.1 mHz in terms of standard deviation without active stabilization. The frequency instability of frep1 and Δfrep in the SCDCL was measured for different gate times as indicated by the red solid and hollow circles in Fig. 3(d). For comparison, we also evaluated the frequency instability of frep1 and Δfrep for two independently stabilized fiber-comb lasers [see the blue solid and hollow circles in Fig. 3(d)] and two independently free-running fiber-comb lasers [see the green solid and hollow circles in Fig. 3(d)]. When comparing the SCDCL with two independently free-running fiber-comb lasers, frep1 and Δfrep show similar trends. The fluctuation of frep1 for the SCDCL is nearly one order larger than that of free-running lasers when the gate time is more than 1 s, which might be due to the better outer packaging of the fiber-comb laser for environmental immunity. However, the frequency stability of Δfrep in the SCDCL was significantly better than that in the two free-running fiber-comb lasers over a short time. Next, when comparing the SCDCL with two independently stabilized fiber-comb lasers, the SCDCL shows better short-term stability in Δfrep than the two independently stabilized fiber-comb lasers. By contrast, the two independently stabilized fiber-comb lasers show better long-term stability in Δfrep and frep1 than the SCDCL. Importantly, even though the SCDCL is inferior to the two independently stabilized fiber-comb lasers in terms of the long-term stability of Δfrep and frep1 due to the lack of active laser stabilization, the adaptive sampling method allows us to overcome such inferiority significantly as demonstrated later, leading to a reduced system complexity and excellent spectroscopic performance.

    3.2 Performance of Adaptive Sampling THz-DCS

    To investigate the effectiveness of the proposed adaptive sampling THz-DCS method, 100,000 temporal waveforms of 10-consecutive THz pulse train were acquired and accumulated by the adaptive sampling method. For a comparison, similar temporal waveforms were acquired based on a constant sampling method, which is widely used for data acquisition of the previous DCS with SCDCL.31,33 In the case of the constant sampling method as shown in the upper part of Fig. 4(a), the THz pulses almost disappeared except for the first pulse because the residual timing jitter causes random walk-off of the temporal sampling positions in each time-delay scan, leading to a low efficiency in the signal accumulation. Obviously, when the number of signal accumulation is largely increased, the constant sampling method with the SCDCL is not suitable to extend the temporal window of the accumulated temporal waveform up to multiple pulse periods. Therefore, previous DCS with SCDCL was demonstrated in a short acquisition time of the temporal waveform (typically, <1  s).31,33 When the adaptive sampling method was used for THz-DCS with SCDCL, each THz pulse was clearly observed in the accumulated temporal waveform, as shown in the lower part of Fig. 4(a). Moreover, each THz pulse was the complete duplicate of each other, coincident with the behavior of THz comb in the time domain. As shown in the inset of Fig. 4(a), the asymmetric bipolar monocycle pulse shape is due to the dipole radiation from the photoconductive antenna, with its temporal waveform given by a time derivative of transient photocurrent induced by the pump light. These results imply that the adaptive sampling method has the capability to significantly suppress the instability of TMF over a long data acquisition time.

    (a) Comparison of the temporal waveforms averaged 100,000 times obtained using different sampling clocks. Inset: a zoomed-in plot of the main THz pulse. (b) Comb-mode-resolved THz spectrum through air at room pressure. Inset: a zoomed-in plot around 0.5672 THz.

    Figure 4.(a) Comparison of the temporal waveforms averaged 100,000 times obtained using different sampling clocks. Inset: a zoomed-in plot of the main THz pulse. (b) Comb-mode-resolved THz spectrum through air at room pressure. Inset: a zoomed-in plot around 0.5672 THz.

    Next, the mode-resolved THz comb spectrum was obtained by calculating the FT of the temporal waveform of the adaptive sampling RF pulse train [see the lower part of Fig. 4(a)], as shown in Fig. 4(b). A 50-dB power dynamic range was achieved in the 0.1- to 1.5-THz frequency band. An expanded view of the spectral region around 0.567 THz is shown in the inset of Fig. 4(b), indicating multiple discrete lines with a constant frequency spacing of 48.8 MHz exactly equal to frep1. The spectral width of each comb line was 4.88 MHz, which is exactly equal to the theoretical FT spectral resolution given by an inverse of the time window size (frep1/10 in this case). Because we later investigate the pressure-broadening characteristics of the sample gas within the range of absorption linewidth from a few tens MHz to 100 MHz, the comb-mode linewidth was set to be frep1/10 (= 4.88 MHz) to acquire the spectrum with a minimum required resolution and data size. In the previous study, the constant sampling THz-DCS with dual stabilized lasers could be demonstrated with the time window size of 100/frep1,49,50 whereas the adaptive sampling THz-DCS with dual free-running lasers was more powerful than the constant sampling THz-DCS with dual stabilized lasers.39 We consider that there is a space to further decrease the comb-mode linewidth in the present system. In this way, the combination of the adaptive sampling method with the SCDCL has the potential to reach spectral resolution of MHz level or below without the influence of the residual timing jitter in SCDCL. In Fig. 4(b), two spectral dips appeared at 0.557 and 0.752 THz with an FWHM linewidth of 7 GHz in the mode-resolved THz comb spectrum, which was caused by atmospheric water vapor existing in the THz optical path outside the gas cell. This is a simple demonstration of pressure-broadening gas spectroscopy in the THz region.

    3.3 Near-Doppler-Limited Spectroscopy of Low-Pressure Acetonitrile/Air Gas

    To demonstrate the high-resolution spectroscopic capability of the proposed system, THz spectroscopy of mixed gas of acetonitrile (CH3CN) and air was performed at low pressures. CH3CN has a rotational constant B of 9.194 GHz and a centrifugal distortion constant DJK of 17.74 MHz48 and is a good candidate for the demonstration of Doppler-limited gas spectroscopy in the THz region because of the closely spaced rotational transitions on the order of tens of MHz in each manifold. The gas cell was filled with a mixture of CH3CN and air with a total pressure of 360 Pa. The absorption spectrum of this mixed gas was obtained by normalizing the mode-resolved THz comb spectrum measured in the CH3CN/air-filled gas cell with that measured in the vacuum gas cell. Figure 5(a) shows the broadband spectrum of absorbance coefficient within the frequency range of 0.2 to 0.7 THz. 29 manifolds were observed with a frequency separation of 18.388 GHz equal to 2B and were correctly assigned to J=10 to 38 by comparison with the Jet Propulsion Laboratory (JPL) spectral database.51Figure 5(b) shows a zoomed-in plot of Fig. 5(a) within the frequency range of 0.31 to 0.37 THz. In addition to J=16 to 19 at the ground state, the manifolds of the rotational transitions at the vibrationally excited states49 were clearly observed as marked by the red asterisks. These spectral features could be obtained by the enhanced spectral resolving power and sensitivity in the low-pressure gas condition, which constitutes a significant enhancement in the spectroscopic performance compared with the previous demonstration.34

    Comb-mode-resolved THz spectroscopy of a mixture gas sample of CH3CN and air with a total pressure of 360 Pa. Absorption spectra of CH3CN within the frequency range of (a) 0.2 to 0.72 THz and (b) 0.31 to 0.37 THz. The red stars indicate the manifolds of the rotational transitions for the vibrationally excited states. (c) Comparison of the absorption spectra between the database fitting and the experimental data and their residual and (d) the corresponding zoomed-in plot around 0.3310 and 0.3677 THz. (e) Absorption spectra around 0.3310 THz and (f) 0.3677 THz.

    Figure 5.Comb-mode-resolved THz spectroscopy of a mixture gas sample of CH3CN and air with a total pressure of 360 Pa. Absorption spectra of CH3CN within the frequency range of (a) 0.2 to 0.72 THz and (b) 0.31 to 0.37 THz. The red stars indicate the manifolds of the rotational transitions for the vibrationally excited states. (c) Comparison of the absorption spectra between the database fitting and the experimental data and their residual and (d) the corresponding zoomed-in plot around 0.3310 and 0.3677 THz. (e) Absorption spectra around 0.3310 THz and (f) 0.3677 THz.

    Each manifold is composed of a number of closely spaced rotational transitions, assigned by K, as tabulated in the JPL spectral database.51 Multipeak fitting analysis was performed to determine a CH3CN partial pressure and the corresponding linewidth of the rotational transitions in which a Lorentzian lineshape was used for each rotational line and a global linewidth parameter was applied to all of the lines. The line positions and intensities were fixed parameters, while the acetonitrile partial pressure and linewidth were left as free parameters. An example is presented in the red and blue plots of Fig. 5(c), yielding a CH3CN partial pressure of 127 (±1) Pa and an FWHM linewidth of 77 (±2) MHz. The database fitting curve (red line) was in good agreement with the experimental data (blue line) for all peaks in the frequency range of 0.2 to 0.4 THz with a slight residual (black line). The reason for the periodic modulation of the residual is that the fitting model does not include the rotational transitions at the vibrationally excited states.51 This is better illustrated in an expanded view in Fig. 5(d) around 0.3310 and 0.3677 THz, which shows that the large residual is mostly around the vibrationally excited states. Figures 5(e) and 5(f) show zoomed-in spectra for J=17 at 0.3310 THz and J=19 at 0.3677 THz, in which the blue plots show the experimental data. The frequency spacing of the experimental data points, corresponding to the spectral sampling interval, was 48.8 MHz, equal to frep1. The curve fitting results based on multipeak fitting analysis are shown by the red line while literature values of JPL spectral database are shown by the green line in Figs. 5(e) and 5(f). Most of the absorption lines have frequency separation between each other equal to or less than the spectral sampling interval (see green lines and blue plots). Such undersampling acquisition of fine spectral features leads to disagreement between experimental plots and absorption line positions. However, it is important to note that even such an undersampling spectral acquisition is effective for near-Doppler-limited gas spectroscopy with the help of curve fitting analysis, which is discussed later.

    The validity of the adaptive sampling THz-DCS scheme was more precisely evaluated by measuring the pressure broadening characteristics of CH3CN rotation transition in the CH3CN/air-mixed gas. Similar to the procedure for 360 Pa as shown in Fig. 5, a series of absorption spectra of rotational transitions in J=17 at 0.331 THz was measured when reducing the total pressure of the CH3CN/air-mixed gas from 430, 330, 280, 256, 149, to 115 Pa with an uncertainty of ±2  Pa, as shown by blue plots in Figs. 6(a)6(f), respectively. To perform a quantitative analysis, we again performed multipeak fitting analysis based on a Lorentzian lineshape under the assumption that all K lines have the same linewidth. The total pressure was measured by a pressure gauge to help achieve a sample with the desired approximate concentration and was not used in the fitting procedure. As shown by the red lines in Fig. 6(a)6(f), the curve fitting spectra match the experimental spectra very well. Both the experimental data and the curve fitting results clearly indicate the pressure-dependent change in the shape of the absorption spectrum. Table 1 shows the result of quantitative analysis for the CH3CN partial pressure and the corresponding linewidth of rotational transition with respect to different total pressures of this mixed gas sample. The uncertainties provided in Table 1 are the confidence intervals calculated as part of the fitting procedure. The partial pressure and the linewidth were determined with good uncertainty under all total pressures, indicating the validity of the adaptive sampling THz-DCS and the following curve fitting analysis. In particular, the linewidth was determined to be 25 MHz at a total pressure of 115 Pa. This quantitative analysis indicates the capability of the proposed system to realize THz spectroscopy of MHz-order absorption features with the reduced system complexity.

    Mode-resolved absorption characterization of CH3CN around 0.331 THz at (a) 430 Pa, (b) 330 Pa, (c) 280 Pa, (d) 256 Pa, (e) 149 Pa, and (f) 115 Pa.

    Figure 6.Mode-resolved absorption characterization of CH3CN around 0.331 THz at (a) 430 Pa, (b) 330 Pa, (c) 280 Pa, (d) 256 Pa, (e) 149 Pa, and (f) 115 Pa.

    Total pressure of CH3CN/air mixed gas (Pa)Partial pressure of CH3CN gas (Pa)FWHM linewidth of CH3CN rotation transition (MHz)
    ResultUncertaintyResultUncertainty
    43014211022
    3601271772
    330871652
    280731532
    256681471
    149521371
    115421251

    Table 1. Quantitative analysis of CH3CN/air-mixed gas.

    4 Discussion

    We first discuss the potential of the adaptive sampling THz-DCS scheme for Doppler-limited gas spectroscopy. We confirmed clear differences in the absorption linewidth as the gas pressure was reduced, as shown in Fig. 6 and Table 1. Figure 7 shows a relation between partial pressure of CH3CN and absorption linewidth, namely the pressure broadening characteristic, of this mixed gas sample. The linear trend between them indicates that the pressure broadening characteristic of this mixed gas was correctly measured by the proposed system and the following quantitative analysis. We consider that the deviation from a strict linear relationship is caused by other experimental uncertainties such as a drift of TMF because the adaptive sampling corrects the nonlinearity of the time scale but does not ensure the accuracy of the time scale. From the slope of the linear trend, the observed pressure broadening coefficient lies between the values for self-broadening (912  kHz/Pa) and broadening by nitrogen (91.2  kHz/Pa).52,53 The Doppler-limited linewidth of CH3CN gas was 382 kHz (FWHM) at 0.2 THz and 1.34 MHz (FWHM) at 0.7 THz.54 Consistent with these values, the adaptive sampling THz-DCS has a potential to interrogate low-pressure gases with absorption features approaching the Doppler limit.

    Pressure broadening characteristic of CH3CN/air gas.

    Figure 7.Pressure broadening characteristic of CH3CN/air gas.

    We next discuss the possibility of the proposed method for THz spectroscopy with further enhanced precision. Although we demonstrated the near-Doppler-limited gas spectroscopy in the THz region, the frequency comb spacing frep1 of 48.8 MHz is still large for a full analysis of rotational transitions with MHz-order structure. A promising approach for this purpose is to use the gapless technique in the THz comb, in which the frequency spacing of two stabilized THz combs is precisely swept to interleave additional comb lines into the original comb lines.49,50 Based on the simple structure of the dual-comb fiber laser, it is also foreseeable to achieve a higher resolution equal to the comb linewidth (= 4.88 MHz) by shifting the comb lines through tuning the laser cavity. However, to expand this technique into the free-running THz combs generated by SCDCL, we have to consider the frequency instability of the THz comb line because it determines the spectrally interleaved interval. Although the frequency instability of the THz comb line depends on the fluctuations of both Δfrep and frep1, the former can be well compensated for by the adaptive sampling method, as shown in Fig. 4(a). The fluctuation of frep1 is a remaining factor associated with the fluctuation of the THz comb line position. As the frequency instability of frep1 was 108 from Fig. 3(d), it is expected that the THz comb line fluctuates within a frequency range of 3.3 kHz at 0.33 THz and 5.5 kHz at 0.55 THz. Because this kHz fluctuation is much smaller than the MHz comb linewidth determined by the inverse of the time window size (4.88 MHz in this article), the influence of the fluctuating frep1 is negligible for gapless THz-DCS. frep1 and frep2 will be tuned with little change in Δfrep by mechanically stretching a portion of the cavity fiber with an additional piezoelectric actuator or motor-driven translation stage. The combination of mode-resolved adaptive sampling THz-DCS with the gapless technique will be studied in a future work.

    In summary, we demonstrated the adaptive-sampling near-Doppler-limited THz comb spectroscopy with the SCDCL. Using the free-running SCDCL with the adaptive sampling method, the long-term instability of the TMF was effectively suppressed, facilitating the long-term acquisition and temporal accumulation of THz temporal waveforms with a time window extending to multiple laser pulse periods. This results in a broadband, mode-resolved THz comb spectrum with a frequency sampling spacing of 48.8 MHz, a spectral resolution of 4.88 MHz, and a power dynamic range of 50 dB. Low-pressure CH3CN/air gas with absorption spectral features approaching the MHz order was measured to be in good agreement with the theoretical predictions. The adaptive sampling scheme could be realized in the analog domain, like this demonstration, or the digital domain by resampling digitized signals. The resolving capability of MHz-level spectral characteristics using a simple SCDCL could greatly expand the applicability of precise THz spectroscopic techniques to much broader areas of applications.

    References

    [1] M. Tonouchi. Cutting-edge terahertz technology. Nat. Photonics, 1, 97-105(2007).

    [2] P. U. Jepsen, D. G. Cooke, M. Koch. Terahertz spectroscopy and imaging: modern techniques and applications. Laser Photonics Rev., 5, 124-166(2011).

    [3] K. Iwaszczuk, H. Heiselberg, P. U. Jepsen. Terahertz radar cross section measurements. Opt. Express, 18, 26399-26408(2010).

    [4] D. H. Auston et al. Cherenkov radiation from femtosecond optical pulses in electro-optic media. Phys. Rev. Lett., 53, 1555-1558(1984).

    [5] P. Y. Han, X. C. Zhang. Free-space coherent broadband terahertz time-domain spectroscopy. Meas. Sci. Technol., 12, 1747-1756(2001).

    [6] H. Harde, R. A. Cheville, D. Grischkowsky. Terahertz studies of collision-broadened rotational lines. J. Phys. Chem. A, 101, 3646-3660(1997).

    [7] T. Q. Luong et al. Onset of hydrogen bonded collective network of water in 1,4-dioxane. J. Phys. Chem. A, 115, 14462-14469(2011).

    [8] R. J. Falconer, A. G. Markelz. Terahertz spectroscopic analysis of peptides and proteins. J. Infrared. Millimeters Terahertz Waves, 33, 973-988(2012).

    [9] I. Coddington, N. Newbury, W. Swann. Dual-comb spectroscopy. Optica, 3, 414-426(2016).

    [10] N. Picqué, T. W. Hänsch. Frequency comb spectroscopy. Nat. Photonics, 13, 146-157(2019).

    [11] T. Yasui et al. Terahertz frequency comb by multifrequency-heterodyning photoconductive detection for high-accuracy, high-resolution terahertz spectroscopy. Appl. Phys. Lett., 88, 241104(2006).

    [12] T. Yasui et al. Fiber-based, hybrid terahertz spectrometer using dual fiber combs. Opt. Lett., 35, 1689-1691(2010).

    [13] Y. Hsieh et al. Terahertz comb spectroscopy traceable to microwave frequency standard. IEEE Trans. Terahertz Sci. Technol., 3, 322-330(2013).

    [14] G. Villares et al. Dual-comb spectroscopy based on quantum-cascade-laser frequency combs. Nat. Commun., 5, 5192(2014).

    [15] Y. Yang et al. Terahertz multiheterodyne spectroscopy using laser frequency combs. Optica, 3, 499-502(2016).

    [16] Y. Ren et al. High-resolution heterodyne spectroscopy using a tunable quantum cascade laser around 3.5 THz. Appl. Phys. Lett., 98, 231109(2011).

    [17] J. T. Good et al. A decade-spanning high-resolution asynchronous optical sampling terahertz time-domain and frequency comb spectrometer. Rev. Sci. Instrum., 86, 103107(2015).

    [18] T. Yasui et al. Enhancement of spectral resolution and accuracy in asynchronous-optical-sampling terahertz time-domain spectroscopy for lowpressure gas-phase analysis. Opt. Express, 20, 15071-15078(2012).

    [19] X. Zhao et al. Switchable, dual-wavelength passively mode-locked ultrafast fiber laser based on a single-wall carbon nanotube modelocker and intracavity loss tuning. Opt. Express, 19, 1168-1173(2011).

    [20] X. Zhao et al. Polarization-multiplexed, dual-comb all-fiber mode-locked laser. Photonics Res., 6, 853-857(2018).

    [21] Y. Liu et al. Unidirectional, dual-comb lasing under multiple pulse formation mechanisms in a passively mode-locked fiber ring laser. Opt. Express, 24, 21392-21398(2016).

    [22] T. Ideguchi et al. Kerr-lens mode-locked bidirectional dual-comb ring laser for broadband dual-comb spectroscopy. Optica, 3, 748-753(2016).

    [23] Q.-F. Yang et al. Counter-propagating solitons in microresonators. Nat. Photonics, 11, 560(2017).

    [24] N. B. Hébert et al. Self-corrected chip-based dual-comb spectrometer. Opt. Express, 25, 8168-8179(2017).

    [25] S. M. Link et al. Dual-comb spectroscopy of water vapor with a free-running semiconductor disk laser. Science, 356, 1164-1168(2017).

    [26] R. M. Li et al. All-polarization-maintaining dual-wavelength mode-locked fiber laser based on Sagnac loop filter. Opt. Express, 26, 28302-28311(2018).

    [27] E. Lucas et al. Spatial multiplexing of soliton microcombs. Nat. Photonics, 12, 699-705(2018).

    [28] Y. Nakajima, Y. Hata, K. Minoshima. High-coherence ultra-broadband bidirectional dual-comb fiber laser. Opt. Express, 27, 5931-5944(2019).

    [29] X. Zhao et al. Picometer-resolution dual-comb spectroscopy with a free-running fiber laser. Opt. Express, 24, 21833-21845(2016).

    [30] S. Mehravar et al. Real-time dual-comb spectroscopy with a free-running bidirectionally mode-locked fiber laser. Appl. Phys. Lett., 108, 231104(2016).

    [31] R. Liao et al. Dual-comb spectroscopy with a single free-running thulium-doped fiber laser. Opt. Express, 26, 11046-11054(2018).

    [32] J. Chen et al. Dual-comb spectroscopy of methane based on a free-running erbium-doped fiber laser. Opt. Express, 27, 11406-11412(2019).

    [33] J. Nürnberg et al. An unstabilized femtosecond semiconductor laser for dual-comb spectroscopy of acetylene. Opt. Express, 27, 3190-3199(2019).

    [34] G. Hu et al. Dual terahertz comb spectroscopy with a single free-running fiber laser. Sci. Rep., 8, 11155(2018).

    [35] R. D. Baker et al. Self-triggered asynchronous optical sampling terahertz spectroscopy using a bidirectional mode-locked fiber laser. Sci. Rep., 8, 14802(2018).

    [36] G. B. Rieker et al. Frequency-comb-based remote sensing of greenhouse gases over kilometer air paths. Optica, 1, 290-298(2014).

    [37] D. Burghoff, N. Han, J. H. Shin. Generalized method for the computational phase correction of arbitrary dual comb signals. Opt. Lett., 44, 2966-2969(2019).

    [38] L. A. Sterczewski et al. Computational Doppler-limited dual-comb spectroscopy with a free-running all-fiber laser. APL Photonics, 4, 116102(2019).

    [39] T. Yasui et al. Adaptive sampling dual terahertz comb spectroscopy using dual free-running femtosecond lasers. Sci. Rep., 5, 10786(2015).

    [40] J. Roy et al. Continuous real-time correction and averaging for frequency comb interferometry. Opt. Express, 20, 21932(2012).

    [41] G. Ycas et al. High-coherence mid-infrared dual-comb spectroscopy spanning 2.6 to 5.2  μm. Nat. Photonics, 12, 202-208(2018). https://doi.org/10.1038/s41566-018-0114-7

    [42] G. Ycas et al. Mid-infrared dual-comb spectroscopy of volatile organic compounds across long open-air paths. Optica, 6, 165-168(2019).

    [43] L. A. Sterczewski, J. Westberg, G. Wysocki. Computational coherent averaging for free-running dual-comb spectroscopy. Opt. Express, 27, 23875-23893(2019).

    [44] N. B. Hébert et al. Self-correction limits in dual-comb interferometry. IEEE J. Quantum Electron., 55, 8700311(2019).

    [45] C. Janke et al. Asynchronous optical sampling for high-speed characterization of integrated resonant terahertz sensors. Opt. Lett., 30, 1405-1407(2005).

    [46] T. Yasui, E. Saneyoshi, T. Araki. Asynchronous optical sampling terahertz time-domain spectroscopy for ultrahigh spectral resolution and rapid data acquisition. Appl. Phys. Lett., 87, 061101(2005).

    [47] H. G. Von Ribbeck et al. Spectroscopic THz near-field microscope. Opt. Express, 16, 3430-3438(2008).

    [48] M. Kessler et al. Microwave spectra and molecular structures of methyl cyanide and methyl isocyanide. Phys. Rev., 79, 54-56(1950).

    [49] T. Yasui et al. Super-resolution discrete Fourier transform spectroscopy beyond time-window size limitation using precisely periodic pulsed radiation. Optica, 2, 460-467(2015).

    [50] Y. D. Hsieh et al. Spectrally interleaved, comb-mode-resolved spectroscopy using swept dual terahertz combs. Sci. Rep., 4, 3816(2014).

    [51] H. M. Pickett et al. Submillimeter, millimeter, and microwave spectral line catalog. J. Quant. Spectrosc. Radiat. Transfer, 60, 883-890(1998).

    [52] A. S. Dudaryonok, N. N. Lavrentieva, J. V. Buldyreva. CH3CN self-broadening coefficients and their temperature dependences for the Earth and Titan atmospheres. Icarus, 250, 76-82(2015). https://doi.org/10.1016/j.icarus.2014.11.020

    [53] A. S. Dudaryonok, N. N. Lavrentieva, J. V. Buldyreva. N2-broadening coefficients of CH3CN. Icarus, 256, 30-36(2015). https://doi.org/10.1016/j.icarus.2015.04.025

    [54] S. Svanberg, M. W. Sigrist, J. D. Winefordner, I. M. Kolthoff. Differential absorption lidar (DIAL). Air Monitoring by Spectroscopic Techniques(1994).

    Jie Chen, Kazuki Nitta, Xin Zhao, Takahiko Mizuno, Takeo Minamikawa, Francis Hindle, Zheng Zheng, Takeshi Yasui. Adaptive-sampling near-Doppler-limited terahertz dual-comb spectroscopy with a free-running single-cavity fiber laser[J]. Advanced Photonics, 2020, 2(3): 036004
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