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Advanced gas sensors based on substrate-integrated hollow waveguides and dual-color ring quantum cascade lasers

Erhan Tütüncü a, Vjekoslav Kokoric a, Rolf Szedlak b, Donald MacFarland b, Tobias Zederbauer c, Hermann Detz d, Aaron Maxwell Andrews b, Werner Schrenk c, Gottfried Strasser bc and Boris Mizaikoff *a
aInstitute of Analytical and Bioanalytical Chemistry, Ulm University, Germany. E-mail: boris.mizaikoff@uni-ulm.de
bInstitute of Solid State Electronics, TU Wien, Austria
cCenter for Micro- and Nanostructures, TU Wien, Austria
dAustrian Academy of Sciences, Austria

Received 17th May 2016 , Accepted 7th August 2016

First published on 8th August 2016


Abstract

This study shows the first combination of a ring-shaped vertically emitting quantum cascade laser (riQCL) providing two distinct emission wavelengths combined with a substrate-integrated hollow waveguide (iHWG). This ultra-compact riQCL-iHWG gas sensing device enables the simultaneous detection of two vapor phase species – here, furan and 2-methoxyethanol – providing distinctive absorption features at the emission wavelengths of the riQCL (i.e., 1144 and 1170 cm−1). Hence, multianalyte gas sensing via a unique mid-infrared (MIR) sensor concept is demonstrated.


Introduction

Infrared spectroscopy, and in particular the MIR spectral range (2–20 μm) provides a viable alternative to commonly used vapor phase analysis techniques (e.g., gas chromatography combined with various detection schemes, mass spectrometric techniques, etc.) for selectively, sensitively, and rapidly detecting or monitoring molecular constituents. Due to the substantial potential for miniaturization and given recent progress in IR waveguide, light source, and detector technology1–3 along with inherent molecular selectivity and minimal sample preparation, conventional infrared absorption spectroscopy has evolved into a versatile and modular sensing toolbox.4

The excitation of fundamental vibro-rotational transitions is usually initiated via either broadband light sources such as incandescent glow bars, or using narrowband emitters including initially lead salt laser diodes, and nowadays predominantly quantum cascade lasers (QCLs) and interband cascade lasers (ICLs). Clearly, MIR sensing applications benefit from a possibly broad wavelength coverage, if entire molecular spectra or the discrimination of a multitude of analytes with potentially overlapping spectral features is required. Alternatively, selected target analytes may be addressed via comparatively narrow spectral bands selecting a single yet analyte-specific vibro-rotational absorption line free from interferences with any other gas phase constituent present in the sampled scenario.

However, a variety of analytical applications demand for a compromise between these two scenarios (i.e., broadband vs. narrowband IR absorption spectroscopy) for addressing moderately complex samples containing a limited number of constituents, yet taking advantage of the spectral brightness and compactness of advanced laser light sources. This requirement may be met by either using tunable laser light sources, or lasers based on active gain media tailored to emit at two or more wavelengths. While the latter concept provides coverage of few selected wavelengths only, the advantages in terms of device complexity, laser control, compactness, robustness, and power consumption are immediately evident.

Quantum cascade lasers (QCL) were first reported in 1994,5 and offer nowadays access to almost any wavelength window in the MIR via engineering of the quantum heterostructure comprising the active gain medium. Efficient photon emission via intersubband transitions instead of electron–hole recombination prevalent in conventional heterostructure laser diodes has rendered QCLs the MIR light source of choice in a wide variety of state-of-the-art optical sensing and spectroscopy concepts. Thereby, one may directly capitalize on their compact dimensions, robustness, long life time, and superior emission characteristics.6–8

Edge-emitting Fabry–Pérot (FP) resonators are the most common optical configuration applied in diode laser light sources with the facets of the active laser chip acting as cavity mirrors. Recently, the research group of Strasser has reported a new generation of surface emitting QCLs based on ring-shaped active structures (riQCL; Fig. 1) utilizing a second order distributed feedback (DFB) grating fabricated into the ring waveguide for efficient vertical light outcoupling.9–11 Besides facilitating pronounced optical power12 and excellent beam collimation,13–18 the integration of vertically emitting laser diodes facilitates their application within ultra-compact sensing concepts using a minimum of beam-guiding optical elements. From the perspective of optical efficiency, in addition a rotationally symmetric far field is achieved via dielectric meta-materials, thereby minimizing scattering losses.


image file: c6an01130f-f1.tif
Fig. 1 (a) Schematic composition of a ring-shaped quantum cascade laser (riQCL) heterostructure and waveguide. The InGaAs/InAlAs active region is sandwiched between two InGaAs layers for improving vertical mode confinement. Electrical current is injected via an extended gold contact. The second order distributed feedback (DFB) grating on top of the waveguide selects the lasing wavelength and enables surface emission. (b, c) Scanning electron microscopy images of a riQCL structure with etched second-order gratings.

Next to the light source, for the development of rapidly responding and portable gas analyzers miniaturized yet efficient gas cells are mandatory along with efficient coupling of the radiation emitted by the light source into the sample compartment. Conventional multipass gas cells are of limited utility in portable usage due to complex alignment, optical delicacy, and rather large required gas sample volumes. An innovative solution for highly miniaturized gas cells serving at the same time as efficient photon conduits has recently been presented by Mizaikoff and collaborators. These so-called substrate-integrated hollow waveguides (iHWGs) simultaneously serve as efficient optical waveguide and highly miniaturized gas cell.19–21 iHWGs enable addressing transient signals in minute gas sample volumes (i.e., few hundreds of microliters), and provide excellent signal-to-noise ratios (SNR) during absorption measurements. Hence, exquisite sensitivity along with ultra-fast sample transition times are achieved by the obtained so-called volumetric optical efficiency, which is superior to conventional long-path or multipass gas cells. Moreover, the design flexibility and mechanical robustness have proven iHWGs as a promising generic key component for a variety of infrared gas sensing scenarios including environmental analysis, process monitoring, and breath diagnostics.22,23

The aim of the present study was demonstrating the first riQCL-iHWG prototype providing a compact yet high-performance gas/vapor mid-infrared sensor system comprising a low volume (i.e., 600 μL) iHWG gas cell combined with a multi-color riQCL enabling multi-component gas sensing.

Experimental

Chemicals

The vapor phase samples were prepared by collecting the head space gas above the corresponding liquid phase analytes. Furan (99% stab. with 250 ppm butylhydroxytoluen Alfa Aeser, Germany) and 2-methoxyethanol (Sigma Aldrich, Germany) were transferred into serum vials. After sealing the vial with a serum cap, the vial containing 2-methoxyethanol was transferred into a 40 °C water bath at a depth slightly above the liquid level inside the vial for enhancing the vapour pressure. In contrast, the furan-containing vial was placed in an icebox at 0 °C during the experiments in order to correspondingly decrease the vapor phase.

Head space samples were then collected by inserting the needle of 50 mL plastic syringe (B. Braun Melsungen AG, Melsungen, Germany) through the cap into the vial. Gas mixtures 0 to 100% of each analyte were prepared via a static mixing procedure using two 50 mL plastic syringes ensuring thorough mixing. Each sample was analyzed three times.

Substrate integrated hollow waveguide

Radiation from the QCL was collimated into the iHWG gas cell, and propagated along the waveguiding channel. The iHWG was fabricated from brass with dimensions of 150 × 25 × 20 mm3 (L × W × H), and comprised a waveguiding channel with a cross-section of 2.0 mm2 simultaneously serving as miniaturized gas cell. As optimum waveguiding is achieved by high surface reflectivity, the top- and base-substrates were polished to a mirror-like finish using commercially available diamond polishing suspensions. Protection of brass from oxidation and for enhancing the adhesion between the substrate and the subsequently applied gold layer galvanic copper plating (copper film thickness approx. 1 μm) was applied. The gold layer was then galvanically deposited onto the Cu-coated brass substrate for improving the reflectivity. Detailed information on the surface quality and assembly of iHWGs has been published in detail elsewhere.19,24,25

Characterization of the riQCL

The experimental sensor setup is schematically illustrated in Fig. 2. MIR radiation emitted from the riQCL (A) was collimated via a 1.5′′ ZnSe lens (B), and then guided via a gold-coated iHWG with a waveguide channel/gas cell length of 15 cm. Radiation emanating at the distal end of the iHWG was directly illuminating a 4 mm2 HgCdTe (MCT) detector element (FTIR-16-2.00 MSL-12, InfraRed Associates Inc., Stuart, FL, USA) located in a dewar cooled with liquid nitrogen (D). In a next step, it is anticipated that the riQCL and a thermoelectrically cooled MCT will be directly integrated into the iHWG structure, thus eliminating even the beam collimating ZnSe lens by coupling the emitted radiation instantaneously into the waveguide/gas cell channel.
image file: c6an01130f-f2.tif
Fig. 2 Prototype sensing setup comprising a HgCdTe semiconductor detector (A), an iWHG with 15 cm waveguide/gas cell channel length (B), a ZnSe lens for beam collimation (C), and a riQCL (D). In a next step, it is anticipated that the riQCL and the detector will be directly integrated into the iHWG structure. (Dimensions are not to scale).

Current pulses at the required repetition frequency were applied to the riQCL via a pulse generator (HP 8114A, Hewlett Packard, Houston USA). The riQCL was modulated at 10 kHz at a pulse duration of either 250 ns or 100 ns. The MCT detector output was coupled to a lock-in amplifier (Model 5209, Princeton Applied Research, NJ, USA) locked to the modulation frequency of the emitter. Data was recorded via the lock-in amplifier, and simultaneously also directly from the MCT detector. The latter voltage measurements were performed using a digital oscilloscope (PicoScope 5444B, Picotech, Cambridgeshire, UK). The riQCL features a dual DFB grating16 promoting/facilitating dual-color vertical emission of MIR radiation. The two distinct emission wavelengths at 1144 cm−1 (5.5 kA cm−2), and at 1170 cm−1 (10 kA cm−2) are attributed to the 1st and 2nd order whispering gallery modes, respectively.

FT-IR spectroscopy studies

FT-IR measurements were performed for verification of the riQCL-iHWG sensor response to mixtures of furan and 2-methoxyethanol by focusing the external collimated IR beam provided by the spectrometer (Bruker Alpha, Bruker Optics, Ettlingen, Germany) onto the end facet of an iHWG (7.5 cm waveguide/gas cell channel length; 300 μL internal volume) using a gold-coated off-axis parabolic mirror (OAPM; focal length: 25.4 mm). IR radiation emanating at the distal end of the waveguide was focused onto the DTGS detector integrated into the FT-IR spectrometer.

In between each measurement, the iHWG was purged with nitrogen. Interferogram were recorded in a wavelength window of 400–4000 cm−1 averaging 30 spectra at a spectral resolution of 2 cm−1 using a Blackman–Harris 3-term apodization function.

Results and discussion

The characteristics of the riQCL in terms of optical emission power vs. applied voltage and current density are shown in Fig. 3. The threshold current density is 4 kA cm−2 with a resulting optical output power of 5 mW (@ 5.5 kA cm−2), and 80 mW (@10 kA cm−2), respectively.
image file: c6an01130f-f3.tif
Fig. 3 Voltage vs. current density curve of the riQCL representing the emitted optical output power operated at 293 K (room temperature) driving the riQCL either at 5.5 kA cm−2 (image file: c6an01130f-u1.tif: emission wavelength @ 1144 cm−1) or at 10 kA cm−2 (image file: c6an01130f-u2.tif: emission wavelength @ 1144 cm−1 and 1170 cm−1).

As the signal-to-noise ratio and background signal are dependent on the laser driving current, the SNR varied accordingly from 344 for a driving current density of 5.5 kA cm−2 to 1951 for 10 kA cm−2.

In order to verify suitable spectral overlap between both riQCL emission lines (i.e., @ 1144 and 1170 cm−1) and characteristic absorption bands of furan and 2-methoxyethanol, individual IR spectra of each gas phase constituent were recorded using an FT-IR spectrometer coupled to a suitable iHWG. The gas cell was filled with pure vapor of either furan or 2-methoxyethanol. Likewise, the FT-IR spectrum of the riQCL was recorded by coupling the emitted radiation in lieu of the broadband emitter of the spectrometer into the interferometer of the FT-IR spectrometer, thereby obtaining the emission characteristics of the riQCL. An emission wavelength of 1144 cm−1 was obtained by applying 5.5 kA cm−2 to the riQCL, whereas 10 kA cm−2 led to the emission of both wavelengths (i.e., 1144 cm−1 and 1170 cm−1). The IR spectrum of laser emission characteristics (black) are overlaid with the spectral signatures of furan (red) and 2-methoxyethanol (blue) in Fig. 4.


image file: c6an01130f-f4.tif
Fig. 4 Laser emission lines (black) overlaid with the IR spectrum of furan (red), and 2-methoxyethanol (blue). The emission spectrum of the riQCL was obtained by coupling the emitted laser radiation into a Fourier transform infrared (FT-IR) spectrometer.

Additional FT-IR spectroscopic studies of various furan and 2-methoxyethanol mixtures in a concentration range of 0–100% indicate distinctly changing spectral features, as shown in Fig. 5. After purging the iHWG with approx. 50 mL of gas mixture, the inlet/outlet gas ports of the iHWG were closed off via a T-valve, and 30 spectral scans were averaged.


image file: c6an01130f-f5.tif
Fig. 5 For comparison, IR spectra were recorded by coupling an iHWG with 7.5 cm channel length to a conventional FT-IR spectrometer analyzing vapor phase samples with increasing concentrations of furan, and correspondingly decreasing concentrations of 2-methoxyethanol (0 to 100% for each constituent).

The same experimental procedure was then applied for characterizing the performance and multicomponent detection capabilities of the riQCL-iHWG sensor system.

Fig. 6A shows the riQCL-iHWG sensor response as a function of increasing furan concentrations (2–20% in 2-methoxyethanol) at an applied laser voltage of 10 kA cm−2, at which both wavelengths (i.e., 1144 cm−1 and 1170 cm−1) are emitted. As the absorption of furan overlaps with the laser emission at 1170 cm−1, it is immediately evident that increasing concentrations of furan accordingly reduced the detected signal. The obtained response function is fitted with an exponential curve, thereby resulting in a calibration function with a coefficient of determination (R2) value >0.99.


image file: c6an01130f-f6.tif
Fig. 6 riQCL-iHWG sensor system response to furan (in 2-methoxyethanol) obtained via selective emission line damping at an applied voltage of 10 kA cm−2 (A), and of 5.5 kA cm−2 (B). An exponential fit was applied to the response function resulting in a calibration model with a coefficient of determination (R2) >0.99 for both curves.

Using the same procedure, the furan fractions were increased (20–80% in 2-methoxyethanol), and introduced into the iHWG. However, now the laser emission was tuned to 1144 cm−1 at 5.5 kA cm−2 of voltage applied to the riQCL, thus matching the absorption of 2-methoxyethanol (Fig. 6B).

Due to the decreasing concentrations of 2-methoxyethanol in the gas cell, a decreased in damping of the radiation emitted from the QCL readily verified that the narrow frequency band emitted at 1144 cm−1 overlapped with the absorption feature characteristic. The positive slope of the exponential fit (R2 > 0.99) reveals the expected behavior.

During these experiments, the riQCL-iHWG sensor system was operated at a repetition rate of 10 kHz with a pulse duration of 100 ns, whereby emission was achieved at room temperature for an applied voltage of 10 kA cm−2. Similar characteristics were ensured at an applied voltage of 5.5 kA cm−2 with a pulse duration of 250 ns at the same repetition rate.

The magnitude of the error bars shown for the experimental data points the calibration functions (Fig. 6) result predominantly from the manual gas mixing procedures, however suffice to demonstrate the analytical utility of the developed riQCL-iHWG sensor prototype in multicomponent vapor phase sensing scenarios.

Conclusions and outlook

In this study, we demonstrated the first combination of substrate-integrated hollow waveguides with vertically emitting ring-shaped two-color quantum cascade lasers for gas/vapor phase sensing applications. Specifically, the developed riQCL-iHWG sensor prototype comprises a riQCL with an embossed 2nd order DFB grating emitting at 1144 cm−1 and 1170 cm−1 at room temperature in pulsed mode, and a miniaturized iHWG gas cell simultaneously serving as MIR waveguide with a sample volume of only 600 μL.

By directly coupling the laser emission into the iHWG, two exemplary analytes – furan and 2-methoxyethanol – were simultaneously detected and quantified during proof-of-principle analytical studies. This innovative sensing concept not only promises exceptionally compact mid-infrared gas sensing platforms, but efficient quantitative vapor phase analysis in minute (i.e., few hundreds of microliters) sample volumes in sensing/monitoring scenarios requiring rapid measurements (i.e., few seconds) due to a transiently changing sample composition.

In a next step, a significant further reduction of the device footprint is anticipated by direct integration of the riQCL and a thermoelectrically cooled MCT detector or a pyroelectric detection device into the iHWG structure. Such hybrid integration not only ensures more efficient optical energy throughput, but also avoids usage of any additional beam guiding optics, while maintaining or even improving the device robustness (e.g., changes in optical alignment due to mechanical vibrations, etc.). Consequently, the application of such devices in sensing applications including environmental analysis, process monitoring, security and surveillance scenarios, and biomedical diagnostics appears a natural fit.

Acknowledgements

Partial support of this study by the project APOSEMA funded by the German BMBF within the M-Era.net program is greatly acknowledged. The Machine Shop at Ulm University is thanked for support during prototype development of the iHWG. This work was performed in part under the auspices of the U.S. Department of Energy by Lawrence Livermore National Laboratory (LLNL) under Contract DE-AC52-07NA27344. This project was funded in part under LLNL sub-contract No. B603018 and B607114. This work was also supported by the Austrian Science Fund (FWF) via project Next-Lite (F49-P09).

Notes and references

  1. B. Mizaikoff, Chem. Soc. Rev., 2013, 42, 8683 RSC.
  2. M. Sieger, J. Haas, M. Jetter, P. Michler, M. Godejohann and B. Mizaikoff, Anal. Chem., 2016, 88, 2558–2562 CrossRef CAS PubMed.
  3. J. Haas and B. Mizaikoff, Annu. Rev. Anal. Chem., 2016, 9(1), 45–68 CrossRef PubMed.
  4. B. Mizaikoff, Anal. Chem., 2003, 75, 258 A–267 A CrossRef CAS.
  5. J. Faist, F. Capasso, D. L. Sivco, C. Sirtori, A. L. Hutchinson and A. Y. Cho, Science, 1994, 264, 553–556 CAS.
  6. K. Wörle, F. Seichter, A. Wilk, C. Armacost, T. Day, M. Godejohann, U. Wachter, J. Vogt, P. Radermacher and B. Mizaikoff, Anal. Chem., 2013, 85, 2697–2702 CrossRef PubMed.
  7. C. Charlton, F. de Melas, A. Inberg, N. Croitoru and B. Mizaikoff, IEE Proc.: Optoelectron., 2003, 150, 306 CrossRef CAS.
  8. C. Charlton, A. Katzir and B. Mizaikoff, Anal. Chem., 2005, 77, 4398–4403 CrossRef CAS PubMed.
  9. E. Mujagić, L. K. Hoffmann, S. Schartner, M. Nobile, W. Schrenk, M. P. Semtsiv, M. Wienold, W. T. Masselink and G. Strasser, Appl. Phys. Lett., 2008, 93, 161101 CrossRef.
  10. E. Mujagić, S. Schartner, L. K. Hoffmann, W. Schrenk, M. P. Semtsiv, M. Wienold, W. T. Masselink and G. Strasser, Appl. Phys. Lett., 2008, 93, 011108 CrossRef.
  11. E. Mujagić, C. Deutsch, H. Detz, P. Klang, M. Nobile, A. M. Andrews, W. Schrenk, K. Unterrainer and G. Strasser, Appl. Phys. Lett., 2009, 95, 011120 CrossRef.
  12. Y. Bai, S. Tsao, N. Bandyopadhyay, S. Slivken, Q. Y. Lu, D. Caffey, M. Pushkarsky, T. Day and M. Razeghi, Appl. Phys. Lett., 2011, 99, 261104 CrossRef.
  13. C. Schwarzer, R. Szedlak, S. Il Ahn, T. Zederbauer, H. Detz, A. Maxwell Andrews, W. Schrenk and G. Strasser, Appl. Phys. Lett., 2013, 103, 081101 CrossRef.
  14. R. Szedlak, C. Schwarzer, T. Zederbauer, H. Detz, A. M. Andrews, W. Schrenk and G. Strasser, Opt. Express, 2014, 22, 15829 CAS.
  15. R. Szedlak, C. Schwarzer, T. Zederbauer, H. Detz, A. Maxwell Andrews, W. Schrenk and G. Strasser, Appl. Phys. Lett., 2014, 104, 151105 CrossRef.
  16. R. Szedlak, M. Holzbauer, D. MacFarland, T. Zederbauer, H. Detz, A. M. Andrews, C. Schwarzer, W. Schrenk and G. Strasser, Sci. Rep., 2015, 5, 16668 CrossRef CAS PubMed.
  17. A. Harrer, R. Szedlak, B. Schwarz, H. Moser, T. Zederbauer, D. MacFarland, H. Detz, A. M. Andrews, W. Schrenk, B. Lendl and G. Strasser, Sci. Rep., 2016, 6, 21795 CrossRef CAS PubMed.
  18. R. Szedlak, M. Holzbauer, P. Reininger, D. MacFarland, T. Zederbauer, H. Detz, A. M. Andrews, W. Schrenk and G. Strasser, Vib. Spectrosc., 2016, 84, 101–105 CrossRef CAS.
  19. A. Wilk, J. C. Carter, M. Chrisp, A. M. Manuel, P. Mirkarimi, J. B. Alameda and B. Mizaikoff, Anal. Chem., 2013, 85, 11205–11210 CrossRef CAS PubMed.
  20. J. F. da S. Petruci, P. R. Fortes, V. Kokoric, A. Wilk, I. M. Raimundo, A. A. Cardoso and B. Mizaikoff, Analyst, 2013, 139, 198–203 RSC.
  21. V. Kokoric, A. Wilk and B. Mizaikoff, Anal. Methods, 2015, 7, 3664–3667 RSC.
  22. J. F. da S. Petruci, A. A. Cardoso, A. Wilk, V. Kokoric and B. Mizaikoff, Anal. Chem., 2015, 87, 9580–9583 CrossRef CAS PubMed.
  23. J. F. da S. Petruci, A. Wilk, A. A. Cardoso and B. Mizaikoff, Anal. Chem., 2015, 87, 9605–9611 CrossRef CAS PubMed.
  24. E. Tütüncü, M. Nägele, P. Fuchs, M. Fischer and B. Mizaikoff, ACS Sens., 2016, 1(7), 847–851 CrossRef.
  25. I. José Gomes da Silva, E. Tütüncü, M. Nägele, P. Fuchs, M. Fischer, I. M. Raimundo and B. Mizaikoff, Analyst, 2016, 141, 4432–4437 RSC.

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