chemosensors
Article
Non-Local Patch Regression Algorithm-Enhanced Differential
Photoacoustic Methodology for Highly Sensitive Trace
Gas Detection
Le Zhang
1,2
, Lixian Liu
1,2,3
, Huiting Huan
1,2,3
, Xukun Yin
1,2
, Xueshi Zhang
1,2
, Andreas Mandelis
3
and Xiaopeng Shao
1,2,
*
Citation: Zhang, L.; Liu, L.; Huan,
H.; Yin, X.; Zhang, X.; Mandelis, A.;
Shao, X. Non-Local Patch Regression
Algorithm-Enhanced Differential
Photoacoustic Methodology for
Highly Sensitive Trace Gas Detection.
Chemosensors 2021, 9, 268. https://
doi.org/10.3390/chemosensors9090268
Academic Editor: Chris Blackman
Received: 12 July 2021
Accepted: 16 September 2021
Published: 18 September 2021
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1
School of Physics and Optoelectronic Engineering, Xidian University, Xi’an 710071, China;
lezhangxd@163.com (L.Z.); lixianliu@xidian.edu.cn (L.L.); hthuan@xidian.edu.cn (H.H.);
xkyin@xidian.edu.cn (X.Y.); monomp@163.com (X.Z.)
2
Xi’an Key Laboratory of Computational Imaging, Xi’an 710071, China
3
Center for Advanced Diffusion-Wave and Photoacoustic Technologies (CADIPT), Department of Mechanical
and Industrial Engineering, University of Toronto, Toronto, ON M5S 3G8, Canada; mandelis@mie.utoronto.ca
* Correspondence: xpshao@xidian.edu.cn
Abstract: A non-local patch regression (NLPR) denoising-enhanced differential broadband photoa-
coustic (PA) sensor was developed for the high-sensitive detection of multiple trace gases. Using the
edge preservation index (EPI) and signal-to-noise ratio (SNR) as a dual-criterion, the fluctuation was
dramatically suppressed while the spectral absorption peaks were maintained by the introduction of
a NLPR algorithm. The feasibility of the broadband framework was verified by measuring the C
2
H
2
in the background of ambient air. A normalized noise equivalent absorption (NNEA) coefficient of
6.13 × 10
−11
cm
−1
·W·Hz
−1/2
was obtained with a 30-mW globar source and a SNR improvement
factor of 23. Furthermore, the simultaneous multiple-trace-gas detection capability was determined
by measuring C
2
H
2
,H
2
O, and CO
2
. Following the guidance of single-component processing, the
NLPR processed results showed higher EPI and SNR compared to the spectra denoised by the
wavelet method and the non-local means algorithm. The experimentally determined SNRs of the
C
2
H
2
,H
2
O, and CO
2
spectra were improved by a factor of 20. The NNEA coefficient reached a
value of 7.02 × 10
−11
cm
−1
·W·Hz
−1/2
for C
2
H
2
. The NLPR algorithm presented good performance
in noise suppression and absorption peak fidelity, which offered a higher dynamic range and was
demonstrated to be an effective approach for trace gas analysis.
Keywords: photoacoustic spectroscopy; gas sensors; multi-component; non-local denoising algorithm
1. Introduction
There is an ever-increasing need for non-destructive and rapid monitoring technolo-
gies for multiple trace gas species and their concentrations in the fields of environmental
protection, medical diagnosis, industrial production, and food safety [1,2]. Photoacoustic
spectroscopy (PAS) based technologies [3–6] feature the advantages of fast response, high
sensitivity, high selectivity, and a large dynamic detection range and have thus played
an important role in multi-component gas sensing. The basic principle of PAS is that
the gas molecules absorb the light energy at specific wavelengths and cause the local
temperature to increase. Combined with the periodic modulation of the light source,
the gas temperature thermally diffuses to generate pressure oscillations and acoustic sig-
nals [7]. Up until now, various PAS-based sensor modalities have been developed for
multi-gas analysis, such as the use of multi-lasers combined time-division multiplexing
methods [8–10], multi-resonators with various frequency demodulation schemes [11], and
broadband detection-based thermal emitters or blackbody radiators using several band-
pass filters [12]. However, use of multiple lasers yields narrowband wavelength selection
for specific gas absorption, limiting the capability to simultaneously detect multiple gases.
Chemosensors 2021, 9, 268. https://doi.org/10.3390/chemosensors9090268 https://www.mdpi.com/journal/chemosensors