An exceptional property of photo-acoustic spectroscopy is the zero-background in wavelength modulation configuration while the signal varies linearly as a function of absorbed laser power. Here, we make use of this property by combining a highly sensitive cantilever-enhanced photo-acoustic detector, a particularly stable high-power narrow-linewidth mid-infrared continuous-wave optical parametric oscillator, and a strong absorption cross-section of hydrogen fluoride to demonstrate the ability of cantilever-enhanced photo-acoustic spectroscopy to reach sub-parts-per-trillion level sensitivity in trace gas detection. The high stability of the experimental setup allows long averaging times. A noise equivalent concentration of 650 parts-per-quadrillion is reached in 32 minutes.

We report a photoacoustic spectroscopy setup with a high-power mid-infrared frequency comb as the light source. The setup is used in broadband spectroscopy of radiocarbon methane. Due to the high sensitivity of a cantilever-enhanced photoacoustic cell and the high power light source, we can reach a detection limit below 100 ppb in a broadband measurement with a sample volume of only a few milliliters. The first infrared spectrum of 14 CH 4 is reported and given a preliminary assignment. The results lay a foundation for the development of optical detection systems for radiocarbon methane.

We have improved the sensitivity of a state-of-the-art cantilever-enhanced photo-acoustic trace gas sensor by combining it with an optical power build-up cavity. The build-up cavity enhances the photoacoustic signal by a factor of ∼100, resulting in an exceptionally good normalised noise equivalent absorption (NNEA) value of 1.75 × 10 −12 W cm −1 Hz −1/2 . We demonstrate the sensor platform in the 1530 nm wavelength range with a simple distributed feedback diode laser, achieving 75 ppt sensitivity for C 2 H 2 with a 10 s integration time.

Background-free methods have potentially superior detection sensitivity because of their ability to take advantage of the full laser power; they are therefore attractive to spectroscopists. We implement background-free Fourier transform spectroscopy based on coherent suppression of the background using an interferometer, whereby the central peak of the interferogram is suppressed without losing molecular absorption signatures. This results in the appearance of peaks rather than dips in the measured spectrum. The technique can be used with a variety of broadband spectroscopies and features advantages such as a reduction in the required detector dynamic range, the capability to perform quantitative measurements, and strongly enhanced sensitivity down to the quantum limit. We validated our method experimentally by performing mid-infrared dual-comb spectroscopy with a mixture of multiple molecular species over a broad wavelength range of 3-5 μm.

Cantilever-enhanced photoacoustic spectroscopy coupled with gas chromatography is used to quantitatively analyze a mixture of alcohols in a quasi-online manner. A full identification and quantification of all analytes are achieved based on their spectral fingerprints using a widely tunable continuous-wave laser as a light source. This can be done even in the case of interfering column/septum bleed or simultaneously eluted peaks. The combination of photoacoustic spectroscopy and gas chromatography offers a viable solution for compact and portable instruments in applications that require straightforward analyses with no consumables.