Differential photoacoustic-stimulated Raman spectroscopy (DPA-SRS) for high-sensitivity hydrogen detection

Abstract

To detect non-polar, infrared-inactive hydrogen, a Differential Photoacoustic-Stimulated Raman Spectroscopy (DPA-SRS) method is proposed. Utilizing the SRS process, a portion of the pump light is converted into intense Stokes light corresponding to the hydrogen Raman shift, eliminating complex dual-laser configurations. The nonlinear thermoacoustic effect is excited by this dual-color light field, endowing Photoacoustic Spectroscopy with the capability for hydrogen fingerprint identification. Raman cell pressure was optimized to achieve a synergistic enhancement of the Stokes conversion efficiency and the Four-Wave Mixing effect. Furthermore, an acoustic mode-optimized differential H-type resonant photoacoustic cell was designed, which effectively enhances anti-interference capability through the differential detection mechanism. Distinct from traditional lock-in amplification methods, a time-frequency transformation algorithm was employed to precisely extract the frequency-domain photoacoustic signal from the broadband time-domain acoustic signal. Experimental results demonstrate that the DPA-SRS system exhibits excellent linearity and achieves a Limit of Detection of 0.65 ppm under atmospheric conditions.