Spectrochimica Acta Part A 60 (2004) 3269–3275
VCSEL based detection of water vapor near 940 nm
Heidi Cattaneo
∗
, Toni Laurila, Rolf Hernberg
Optics Laboratory, Institute of Physics, Tampere University of Technology, P.O. Box 692, FIN-33101 Tampere, Finland
Received 1 October 2003; accepted 16 February 2004
Abstract
A vertical-cavity surface-emitting laser (VCSEL) was used to study the absorption spectrum of water vapor in the 940nm region. Mea-
surements were performed in ambient air at room temperature and in a hydrogen–oxygen flame over the temperature range of 1500–1800 K.
Several rotational absorption lines within the 2ν
1
+ ν
3
vibrational band were measured. The absorption spectra were well resolved, which
demonstrates the feasibility of VCSEL-based spectroscopic measurements of water vapor at room and high-temperature in this spectral region.
The results were in good agreement with the values obtained from the HITRAN-96 database.
© 2004 Elsevier B.V. All rights reserved.
Keywords: VCSEL; Gas detection; High-temperature; Water vapor
1. Introduction
Monitoring of water vapor is an important tool for diag-
nostics in many industrial processes. The concentration of
water vapor yields information on performance parameters
such as efficiency and heat release of the process. In addi-
tion, information on gas dynamic parameters, e.g., gas tem-
perature, pressure, and velocity, can be obtained from the
absorption spectrum of water vapor.
Water vapor has strong, temperature-sensitive absorption
features in the near infrared. The strongest absorption lines
occur in the 1.4 m region. For this region, line strengths and
pressure broadening parameters have been thoroughly inves-
tigated for a large temperature range [1–3]. Water absorbs
notable amounts of light also in the 940 nm region, where
several vibrational bands (of which the 2ν
1
+ ν
3
band is one
of the strongest) are present. However, significantly less at-
tention has been given to determining spectral absorption
parameters in this region, especially at high-temperatures.
Line strengths, positions, and broadening for several at-
mospheric molecules (including H
2
O) at room temperature
can be found in molecular databases such as HITRAN-96
[4]. The databases can also be used to model the temperature
dependence of the absorption features. Several authors have
∗
Corresponding author. Tel.: +358-3-3115-3417;
fax: +358-3-3115-2090.
E-mail address: heidi.cattaneo@tut.fi (H. Cattaneo).
recently pointed out systematic errors in the database for
water vapor. Giver et al. [5] suggested that the line strength
values of HITRAN-96 should be corrected by a factor of
1.144 for the 940 nm region. Schermaul et al. [6] also found
systematic differences between the measured line strengths
and the values of the HITRAN-96 database.
Tunable diode laser spectroscopy (TDLS) is a widely used
and acknowledged method for sensor applications in the
near-IR region. An important advantage of TDSL is the pos-
sibility of performing in situ measurements without the need
for sampling lines. TDLS has been applied to detect several
gas species such as CO, CO
2
, CH
4
, OH, O
2
, and H
2
O in
different environments [7–11]. With direct absorption tech-
niques optical absorbances of 10
-3
to 10
-4
can be detected
[7,8]. The detection limit can be improved by at least two
orders of magnitude with more sensitive methods involving
wavelength modulation and balanced detection, which have
been successfully used with TDLS [11–13].
The vast majority of TDSL measurements on water vapor
have made use of distributed feedback (DFB) semiconduc-
tor lasers [1–3,13–15]. DFB lasers have very narrow line
widths but are difficult to fabricate and, hence, are expensive
devices. Vertical-cavity surface-emitting diode lasers (VC-
SELs) have the potential of being low-cost devices, and can
be fabricated in high volumes. They can operate single-mode
with line widths that are narrow enough for most spec-
troscopic applications. Their advantages include very good
beam quality, large current tuning range, high modulation
1386-1425/$ – see front matter © 2004 Elsevier B.V. All rights reserved.
doi:10.1016/j.saa.2004.02.025