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Slow-light photonic crystal waveguide (PCW) gas sensors based on infrared absorption spectroscopy play a pivotal role in enhancing the on-chip interaction between light and gas molecules, thereby significantly boosting sensor sensitivity. However, two-dimensional (2D) PCWs are limited by their narrow mode bandwidth and susceptibility to polarization, which restricts their ability for multigas measurement. Due to quasi-TE and quasi-TM mode guiding characteristics in one-dimensional (1D) PCW, a novel slow-light-enhanced polarization division multiplexing infrared absorption spectroscopy was proposed for on-chip wideband multigas detection. The optimized 1D PCW gas sensor experimentally shows an impressive slow-light mode bandwidth exceeding 100 nm (TM, 1500-1550 nm; TE, 1610-1660 nm) with a group index ranging from 4 to 25 for the two polarizations. The achieved bandwidth in the 1D PCW is 2-3 times that of the reported quasi-TE polarized 2D PCWs. By targeting the absorption lines of different gas species, multigas detection can be realized by modulating the lasers and demodulating the absorption signals at different frequencies. As an example, we performed dual-gas measurements with the 1D PCW sensor operating in TE mode at 1.65 µm for methane (CH4) detection and in TM mode at 1.53 µm for acetylene (C2H2) detection. The 1 mm long sensor achieved a remarkable limit of detection (LoD) of 0.055% for CH4 with an averaging time of 17.6 s, while for C2H2, the LoD was 0.18%. This polarization multiplexing sensor shows great potential for on-chip gas measurement because of the slow-light enhancement in the light-gas interaction effect as well as the large slow-light bandwidth for multigas detection.
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Compared to the most commonly used on-chip direct absorption spectroscopy (DAS) gas detection technique, the second harmonic (2f) based on-chip wavelength modulation spectroscopy (WMS) proposed by our group has the faculty to suppress noise and improve performance, but the accuracy of 2f WMS is easily affected by optical power variation. A mid-infrared auto-correction on-chip gas sensor based on 2f/1f WMS was proposed for decreasing the influence of the variation of optical power. The limit of detection of methane (CH4) obtained by a chalcogenide waveguide with a length of 10â mm is 0.031%. Compared with the 2f WMS, the maximum relative concentration error of the auto-correction on-chip gas sensor was decreased by â¼5.6 times. The measurement error is ≤2% in a temperature variation range of 30°C. This auto-correction sensor without a complicated manual calibration is helpful to the high accuracy measurement for on-chip integrated gas sensing.
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The 1550 nm band semiconductor optical amplifier (SOA) has great potential for applications such as optical communication. Its wide-gain bandwidth is helpful in expanding the bandwidth resources of optical communication, thereby increasing total capacity transmitted over the fiber. Its relatively low cost and ease of integration also make it a high-performance amplifier of choice for LiDAR applications. In recent years, with the rapid development of quantum-well (QW) material systems, SOAs have gradually overcome the shortcomings of polarization sensitivity and high noise. The research on quantum-dot (QD) materials has further improved the noise characteristics and transmission loss of SOAs. The design of special waveguide structures-such as plate-coupled optical waveguide amplifiers and tapered amplifiers-has also increased the saturation output power of SOAs. The maximum gain of the SOA has been reported to be more than 21 dB. The maximum saturation output power has been reported to be more than 34.7 dBm. The maximum 3 dB gain bandwidth has been reported to be more than 120 nm, the lowest noise figure has been reported to be less than 4 dB, and the lowest polarization-dependent gain has been reported to be 0.1 dB. This study focuses on the improvement and enhancement of the main performance parameters of high-power SOAs in the 1550 nm band and introduces the performance parameters, the research progress of high-power SOAs in the 1550 nm band, and the development and application status of SOAs. Finally, the development trends and prospects of high-power SOAs in the 1550 nm band are summarized.
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To realize early fire identification in cotton harvesting operations, a mid-infrared carbon monoxide (CO) sensor system was developed. To match the broadband light source with a 15° divergence angle, a multipass gas cell (MPGC) with an effective path length of 180 cm was designed to improve sensor sensitivity, leading to a limit of detection (LoD) of 0.83 parts-per-million by volume (ppmv). A damping module with springs at the bottom and front/back sides was fabricated, which can effectively reduce the vibration intensity by >80%. The sensor system can operate normally from -40 °C to 85 °C by stabilizing the temperature of the optical module through heating or cooling as well as using automotive electronic components. An adaptive early fire identification algorithm based on a dual-parameter threshold alarming method was proposed to avoid false and missing alarms. Field deployments on a harvester verified the good practicability of the sensor system.
Asunto(s)
Monóxido de Carbono , Frío , Temperatura , Límite de DetecciónRESUMEN
A trace gas sensing technique of light-induced off-axis cavity-enhanced thermoelastic spectroscopy (OA-CETES) in the near-infrared was demonstrated by combing a high-finesse off-axis integrated cavity and a high Q-factor resonant quartz tuning fork (QTF). Sensor parameters of the cavity and QTF were optimized numerically and experimentally. As a proof-of-principle, we employed the OA-CETES for water vapor (H2O) detection using a QTF (Q-factor â¼12000 in atmospheric pressure) and a 10cm-long Fabry-Perot cavity (finesse â¼ 482). By probing a H2O line at 7306.75â cm-1, the developed OA-CETES sensor achieved a minimum detection limit (MDL) of 8.7 parts per million (ppm) for a 300â ms integration time and a normalized noise equivalent absorption (NNEA) coefficient of 4.12 × 10-9cm-1 WHz-1/2. Continuous monitoring of indoor and outdoor atmospheric H2O concentration levels was performed for verifying the sensing applicability. The realization of the proposed OA-CETES technique with compact QTF and long effective path cavity allows a class of optical sensors with low cost, high sensitivity and potential for long-distance and multi-point sensing.
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This publisher's note contains corrections to Opt. Lett.46, 4797 (2021)OPLEDP0146-959210.1364/OL.440361.
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A novel, to the best of our knowledge, mid-infrared chalcogenide (ChG) on magnesium fluoride (MgF2) waveguide gas sensor was fabricated by using the lift-off method. MgF2 was used as a lower cladding layer to increase the external confinement factor for enhancing light-gas interaction. Wavelength modulation spectroscopy (WMS) was used in carbon dioxide (CO2) detection at the wavelength of 4319 nm (2315.2cm-1). The limit of detection for the 1-cm-long sensing waveguide based on WMS is â¼0.3%, which is >8 times lower than the same sensor using direct absorption spectroscopy (DAS). The combination of WMS with the waveguide gas sensor provides a new measurement scheme for the performance improvement of on-chip gas detection.
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A near-infrared methane (CH4) sensor system for carbon isotopic abundance analysis was developed based on laser absorption spectroscopy (LAS). For good thermal stability, two CH4 absorption lines with a similar low-state energy level were selected to realize relative weak temperature dependence. Wavelet denoising (WD) was employed for a pre-treatment of the direct absorption spectral (DAS) signal to perform a preliminary suppression of high-frequency noise. Due to the abnormal 13CH4 profile caused by superimposition of multiple lines, two statistical analysis algorithms including linear regression and neural network prediction were respectively employed on the retrieval of molecule fractions instead of the traditionally used standard absorption line fitting method. Performance assessment and a comparison between the two methods were carried out. Compared with the concentration deducing method based on the maximum absorbance in rough data, the linear regression and the neural network prediction obtained a sensitivity enhancement by â¼2 times and â¼10 times, respectively. A simultaneous measurement of pressure and concentration was performed using the neural network, which indicated a good potential of the technique for multi-parameter analysis using a single LAS-based sensor system.
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The development of an efficient, portable, real-time, and high-precision ammonia (NH3) remote sensor system is of great significance for environmental protection and citizens' health. We developed a NH3 remote sensor system based on tunable diode laser absorption spectroscopy (TDLAS) technique to measure the NH3 leakage. In order to eliminate the interference of water vapor on NH3 detection, the wavelength-locked wavelength modulation spectroscopy technique was adopted to stabilize the output wavelength of the laser at 6612.7 cm-1, which significantly increased the sampling frequency of the sensor system. To solve the problem in that the light intensity received by the detector keeps changing, the 2f/1f signal processing technique was adopted. The practical application results proved that the 2f/1f signal processing technique had a satisfactory suppression effect on the signal fluctuation caused by distance changing. Using Allan deviation analysis, we determined the stability and limit of detection (LoD). The system could reach a LoD of 16.6 ppm·m at an average time of 2.8 s, and a LoD of 0.5 ppm·m at an optimum averaging time of 778.4 s. Finally, the measurement result of simulated ammonia leakage verified that the ammonia remote sensor system could meet the need for ammonia leakage detection in the industrial production process.
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System-level integration of a midinfrared carbon dioxide (CO2) sensor system based on tunable laser absorption spectroscopy (TLAS) was realized for the analysis of dissolved CO2 in seawater, employing an interband cascade laser (ICL) centered at 4319 nm and a multipass cell (MPC) with an optical path length of 29.8 m. At a low measurement pressure of 30 Torr, three absorption lines of 12CO2 were selected to realize different measurement ranges and a 13CO2 absorption line was targeted for simultaneous isotopic abundance analysis of δ13CO2. The sensor system was compactly integrated into a standalone system with automatic operation for underwater field deployment, and the working process was controlled by a specially designed electrical system. A gas-liquid separator system was developed for CO2 extraction from water, and a pressure-control mechanism with two operation modes (i.e., static and dynamic modes) was proposed to make the sensor system applicable under a deep-sea environment. A series of experiments were carried out in the laboratory for performance assessment of the developed sensor system employed for the analysis of dissolved CO2 in water. The sensor was deployed for a field test for natural gas hydrates exploration at an underwater depth of 0-2000 m in the South China Sea, with the sensor operating normally during the deployment.
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The reported chalcogenide (ChG) rectangular waveguide sensors with a small evanescent field need a large waveguide length to obtain an enhanced light-gas interaction effect. To make such sensors compact and improve the light-gas interaction effect, a microcavity-enhanced absorption spectroscopy technique for methane (CH4) detection was proposed using a mid-infrared chalcogenide/silica-on-fluoride horizontal slot-waveguide racetrack resonator. For the horizontal slot waveguide, an equivalent sensor model (ESM) and related formulations were proposed to simplify the analysis of the racetrack resonator sensor model (RRSM), and the ESM was verified through a comparison between the theoretical result of ESM and the simulation result of RRSM based on the finite element method (FEM). Due to the use of a chalcogenide/silica-on-fluoride horizontal slot-waveguide structure, the waveguide parameters were optimized to obtain a high power confinement factor of 44.63% at the wavelength of 3291â nm, which is at least 5 times higher than other ChG rectangular waveguides. The waveguide length is reduced at least 30 times due to the use of the optimized chalcogenide/silica-on-fluoride horizontal slot-waveguide and racetrack resonator. The limit of detection (LoD) is 3.87â ppm with an intrinsic waveguide loss of 3â dB/cm and an amplitude coupling ratio of 0.1 for the resonator. The response time is less than 5 µs due to the small light-gas interaction area. The influences of environmental pressure and waveguide intrinsic loss on the sensing characteristics were discussed. The compact racetrack resonator sensor structure and equivalent analytical model can also be adopted in the design of an on-chip waveguide sensor for the detection of other gas species.
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To overcome the limitations of size, optical alignment, and integration into photonic circuits in previous light-induced thermoelastic spectroscopy (LITES) using free-space optics, a compact all-fiber LITES was proposed for gas sensing. A hollow-core photonic crystal fiber was employed as a waveguide and a microcapillary gas cell simultaneously. A single-mode fiber (SMF) tip was employed to guide light on the quartz tuning fork (QTF) surface. The distance between the SMF tip and the QTF, and the light excitation position on the QTF's surface were optimized experimentally. The detection performance of the all-fiber LITES was evaluated by detecting methane, and a normalized noise equivalent absorption coefficient of ${9.66} \times {{10}^{ - 9}}\; {{\rm cm}^{ - 1}} \cdot {\rm W}\,{{\rm Hz}^{ - 1/2}}$9.66×10-9cm-1â WHz-1/2 was realized at a 1 atm pressure and an environmental temperature of $ {\sim} 297\;{\rm K}$â¼297K. The combination of fiber sensing and LITES allows a class of LITES sensors with compact size and potential for long-distance and multi-point sensing.
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By contrast with the widely reported traditional two mirror-based Herriott cell, a three mirror-based dense pattern gas cell was proposed, of which the modeling and design were proven to be effective through a comparison between the simulated spot pattern and effective path length and those of the experimental results. A mechanical structure was designed to adjust the position/angle of the three mirrors for aligning the optical path. The experimentally measured reflection number was 60, resulting in an optical path length of ~11 m, which agrees well with the theoretical value of 10.95 m. Combined with a near-infrared laser with a center wavenumber located at an acetylene (C2H2) absorption line of 6521.2 cm-1, a C2H2 sensor system was established to verify the feasibility of the three mirror-based gas cell. Assisted by a data acquisition (DAQ) card, a LabVIEW platform was developed to generate the drive signal of the laser and acquire the second harmonic (2f) signal from the output of the detector. Through Allan variance analysis, the limit of detection (LoD) of the sensor system is 4.36 ppm at an average time of 0.5 s; as the average time exceeds 10 s, the LoD is <1 ppm. The proposed model and design of the three mirror-based gas cell can be used to realize similar gas cells with different absorption path lengths for gas detection based on infrared absorption spectroscopy.
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In order to improve the performance of the large divergence angle mid-infrared source in gas sensing, this paper aims at developing a methane (CH4) sensor with non-dispersive infrared (NDIR) technology using a compact pentahedron gas-cell. A paraboloid concentrator, two biconvex lenses and five planar mirrors were used to set up the pentahedron structure. The gas cell is endowed with a 170 mm optical path length with a volume of 19.8 mL. The mathematical model of the cross-section and the three-dimension spiral structure of the pentahedron gas-cell were established. The gas-cell was integrated with a mid-infrared light source and a detector as the optical part of the sensor. Concerning the electrical part, a STM32F429 was employed as a microcontroller to generate the driving signal for the IR source, and the signal from the detector was sampled by an analog-to-digital converter. A static volumetric method was employed for the experimental setup, and 20 different concentration CH4 samples were prepared to study the sensor's evaluation, which revealed a 1σ detection limit of 2.96 parts-per-million (ppm) with a 43 s averaging time.
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For deep-sea natural gas hydrate exploration, highly sensitive detection of the dissolved gas in seawater near the seabed is significant because it requires the sensor system to be small in size, low in power consumption, and high in sensitivity. A mid-infrared sensor system was developed to detect dissolved carbon dioxide (CO2) in sea-water, while employing a 4319 nm continuous-wave interband cascade laser (ICL) and a multi-pass gas cell (MPGC) with a 29.8 m optical path length. A compact rectilinear optical structure was proposed by using the free-space-emitting ICL and tunable laser absorption spectroscopy (TLAS). This leads to a minimized sensor size and a simple optical alignment for deep-sea operation. A strong CO2 absorption line, located at 2315.19 cm-1 and a weak 2315.28 cm-1 line and at a low pressure of 40 Torr, was targeted for low- and high-concentration CO2 detection within a concentration range of 0-1000 parts per billion by volume (ppbv) and 0-40 parts per million by volume (ppmv), respectively. The limit of detection (LoD) was assessed to be 0.72 ppbv at an averaging time of 2 s, and the response time was measured to be ~30 s at a flow rate of ~180 standard cubic centimeters per minute (sccm). Deployment of the CO2 sensor combined with a gas-liquid separator was carried out for the CO2 detection in the gas extracted from water, which validated the reported sensor system's potential application for deep-sea natural gas hydrate exploration.
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In order to achieve a high acoustic coupling strength and detection sensitivity and to simplify the assembly and alignment process in quartz-enhanced photoacoustic spectroscopy (QEPAS) technique, a novel quartz tuning fork (QTF) embedded off-beam QEPAS (E-OB-QEPAS) spectrophone was proposed. The structural parameters of the acoustic micro-resonator of the E-OB-QEPAS spectrophone were optimized for enhancing the signal-to-noise ratio gain based on experimental investigation. Compared with the on-beam configuration using a bare QTF, a detection sensitivity enhancement by a factor of â¼25 was achieved by embedding the QTF in one resonant tube. By using two resonant tubes simultaneously embedded with a QTF, dual-channel detection and a two-fold photoacoustic signal enhancement were realized and a detection sensitivity enhancement by a factor of â¼20 and â¼40 were achieved for the single-tube-enhanced and dual-tube-enhanced E-OB-QEPAS spectrophone, respectively.
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By combining frequency division multiplexing assisted wavelength modulation spectroscopy (FDM-WMS) and off-axis integrated-cavity output spectroscopy (OA-ICOS), a near-infrared (near-IR) dual-gas sensor system was demonstrated for simultaneous chemical gas-phase detection of acetylene (C2H2) and methane (CH4). Two distributed feedback (DFB) lasers modulated at the frequency of 3 kHz and 4 kHz with an emitting wavelength of 1532 and 1653 nm were used to target two absorption lines, C2H2 at 6523.88 cm-1 and CH4 at 6046.95 cm-1, respectively. A 6 cm-long cavity was fabricated, which reveals an effective path length of 9.28 m (@1532 nm, C2H2) and 8.56 m (@1653 nm, CH4), respectively. Performances of the dual-gas sensor system were experimentally evaluated using C2H2 and CH4 samples generated by an Environics gas mixing system. An Allan deviation of 700 parts-per-billion in volume (ppbv) for C2H2 with an averaging time of 200 s and 850 ppbv for CH4 with an averaging time of 150 s was achieved for these two gas species. Dynamic measurements of a C2H2/CH4 : N2 mixture were performed for monitoring both C2H2 and CH4 simultaneously. This dual-gas sensor has the merits of reduced size and cost compared to two separate OA-ICOS sensors and reveals the minimum detectable column density (DCD) compared to other reported C2H2 and CH4 sensor systems.
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A mid-infrared cavity-enhanced sensor system was demonstrated for the detection of formaldehyde (H2CO) using a continuous-wave (cw) interband cascade laser (ICL) centered at 3599 nm. A compact Fabry-Perot (F-P) cavity with a physical size of 38 × 52 × 76 mm3 was developed consisting of two concave mirrors with a radius of curvature of 80 mm and a reflectivity of 99.8% at 3.6 µm. Different from the widely reported electro-optical (EO) external modulation based Pound-Drever-Hall (PDH) locking technique, a radio-frequency electrical internal modulation based PDH technique was used for locking the laser mode to the cavity mode. A dual-feedback control on the laser current and on the piezo transducer (PZT) displacement was utilized for further stabilizing mode locking. A 20 m effective optical path length was achieved with a cavity length of 2 cm and a finesse of 1572. The effectiveness and sensitivity of the sensor system were demonstrated by targeting an absorption line at 2778.5 cm-1 for H2CO measurements. A linear relation between the cavity transmitted signal amplitude and the H2CO concentration was obtained within the range of 0-5 ppm. A 1σ detection limit of 25 parts-per-billion (ppb) was achieved with an averaging time of 1 s based on Allan-Werle variance analysis. The reported dual-feedback RF modulation based PDH technique led to a method for gas detection using a similar experimental setup and measurement scheme.
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Design and fabrication of a dual spot-ring Herriott cell (DSR-HC) were proposed. The sealed Herriott cell with a dimensional size of 5.5 cm × 9.2 cm × 32.1 cm, possessed two input/output coupling holes leading to two absorption path lengths of ~20 m and ~6 m, respectively. An acetylene (C2H2) sensor system with a double-range was developed using the DSR-HC and wavelength modulation spectroscopy (WMS) technique. A near-infrared distributed feedback (DFB) laser was employed for targeting a C2H2 absorption line at 6521.2 cm-1. C2H2 concentration measurements were carried out by modulating the laser at a 5 kHz frequency and demodulating the detector signal with LabVIEW software. An Allan-Werle deviation analysis indicated that the limit of detection (LoD) for the two absorption path lengths of 20 m and 6 m are 7.9 parts-per-million in volume (ppmv) and 4.0 ppmv, respectively. The DSR-HC concept can be used to fabricate similar cells for single-gas detection requiring two different detection ranges as well as for dual-gas detection requiring different absorption path lengths.
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For highly sensitive and accurate acetylene (C2H2) detection, a near-infrared (NIR) off-axis integrated-cavity output spectroscopy (OA-ICOS) sensor system based on an ultra-compact cage-based absorption cell was proposed. The absorption cell with dimensions of 10 cm × 8 cm × 6 cm realized a dense-pattern and an easily-aligned stable optical system. The OA-ICOS sensor system employed a 6cm-long optical cavity that was formed by two mirrors with a reflectivity of 99.35% and provided an effective absorption path length of â¼9.28 m. The performance of the C2H2 sensor system based on two measurement schemes, i.e. laser direct absorption spectroscopy (LDAS) and wavelength modulation spectroscopy (WMS) is reported. A NIR distributed feedback (DFB) laser was employed for targeting a C2H2 absorption line at 6523.88 cm-1. An Allan deviation analysis yielded a detection sensitivity of 760 parts-per-billion in volume (ppbv) for an averaging time of 304 s using the LDAS-based OA-ICOS. A detection sensitivity of 85 ppbv for an averaging time of 250 s was obtained using the WMS-based OA-ICOS, which was further improved by a factor of ~9 compared to the result obtained with the LDAS method. The proposed sensor system has the advantages of reduced size and cost with acceptable detection sensitivity, which is suitable for applications in trace gas sensing in harsh environments and weight-limited balloon-embedded observations.