A detailed review on the development of quartz-enhanced photoacoustic sensors (QEPAS) for the sensitive and selective quantification of molecular trace gas species with resolved spectroscopic features is reported. The basis of the QEPAS technique, the technology available to support this field in terms of key components, such as light sources and quartz-tuning forks and the recent developments in detection methods and performance limitations will be discussed. Furthermore, different experimental QEPAS methods such as: on-beam and off-beam QEPAS, quartz-enhanced evanescent wave photoacoustic detection, modulation-cancellation approach and mid-IR single mode fiber-coupled sensor systems will be reviewed and analysed. A QEPAS sensor operating in the THz range, employing a custom-made quartz-tuning fork and a THz quantum cascade laser will be also described. Finally, we evaluated data reported during the past decade and draw relevant and useful conclusions from this analysis.

The paper provides an overview on the use of photoacoustic sensors based on semiconductor laser sources for the detection of trace gases. We review the results obtained using standard, differential and quartz enhanced photoacoustic techniques.

We compare the electronic temperatures and the population inversion both below and above the lasing threshold in three quantum-cascade lasers ͑QCLs͒ operating at 2.8 THz, 3.2 THz, and 3.8 THz using microprobe band-to-band photoluminescence. In the lasing range, while the ground-state temperature remains close to the lattice one ͑90 K-100 K͒, the upper radiative state heats up to ϳ200 K. From the measured thermal resistance and the power dependence of the ground-state electronic temperature, we get a value of the electron-lattice energy relaxation rate comparable with that typical of midinfrared QCLs.

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A sensitive spectroscopic sensor based on a hollow-core fiber-coupled quantum cascade laser (QCL) emitting at 10.54 μm and quartz enhanced photoacoustic spectroscopy (QEPAS) technique is reported. The design and realization of mid-IR fiber and coupler optics has ensured single-mode QCL beam delivery to the QEPAS sensor. The collimation optics was designed to produce a laser beam of significantly reduced beam size and waist so as to prevent illumination of the quartz tuning fork and microresonator tubes. SF(6) was selected as the target gas. A minimum detection sensitivity of 50 parts per trillion in 1 s was achieved with a QCL power of 18 mW, corresponding to a normalized noise-equivalent absorption of 2.7×10(-10) W·cm(-1)/Hz(1/2).

This review aims to discuss the latest advancements in quartz-enhanced photoacoustic spectroscopy (QEPAS) based trace-gas sensing. Starting from the QEPAS basic physical principles, the most used QEPAS configurations will be described. This is followed by a detailed theoretical analysis and experimental study regarding the influence of quartz tuning forks (QTFs) geometry on their optoacoustic transducer performance. Furthermore, an overview of the latest developments in QEPAS trace-gas sensor technology employing custom QTFs will be reported. Results obtained by exploiting novel micro-resonator configurations, capable of increasing the QEPAS signal-to-noise ratio by more than two orders of magnitude and the utilization of QTF overtone flexural modes for QEPAS based sensing will be presented. A comparison of the QEPAS performance of different spectrophone configurations is reported based upon signal-to-noise ratio. Finally, a novel QEPAS approach allowing simultaneous dual-gas detection will be described.

Geometrical parameters of micro-resonator for a quartz enhanced photoacoustic spectroscopy sensor are optimized to perform sensitive and background-free spectroscopic measurements using mid-IR quantum cascade laser (QCL) excitation sources. Such an optimized configuration is applied to nitric oxide (NO) detection at 1900.08 cm(-1) (5.26 µm) with a widely tunable, mode-hop-free external cavity QCL. For a selected NO absorption line that is free from H(2)O and CO(2) interference, a NO detection sensitivity of 4.9 parts per billion by volume is achieved with a 1-s averaging time and 66 mW optical excitation power. This NO detection limit is determined at an optimal gas pressure of 210 Torr and 2.5% of water vapor concentration. Water is added to the analyzed mixture in order to improve the NO vibrational-translational relaxation process.

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