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8.1 Introduction
Spectroscopy instrumentation is transforming, thanks to developments in advanced manufacturing techniques
in the integrated circuits (IC) and optical components (Crocombe 2013, 2018). With better lithographic
methods, such as nanoimprint lithography (Chou et al. 2014; Mohamed 2019) and extreme ultraviolet
lithography (Ogletree 2016; Radamson et al. 2018), it is now possible to pack millions of electronic components
within a single chip and even embed optical functionality. This has led to the realization of faster and powerful
on-chip computing, for instance, in our smartphones. High demand for these computing devices has driven
down costs and paved the way for field-level applications in virtually every industry. Whether it is in the form
of distributed sensing networks or Internet of Things (IoT) (Karanassios and Fitzgerald 2018)-based approaches
(Gubbi et al. 2013; Zanella et al. 2014), field-level instrumentation has dramatically changed over the last
decade.
Although spectrometers are routinely used in material analysis today, they have been more suited to
controlled laboratory environments (Nelson 2019). Several factors are responsible for this trend including the
cost of the instrument, need for an expert for interpretation, need for sample preparation, noise from ambient
light sources, and sensitivity to ambient conditions, among others. Among all the different spectral ranges for
spectrometers, from ultraviolet-visible (UV-Vis), near infrared (NIR), shortwave infrared (SWIR), mid-infrared
(MIR) and far infrared (FIR), the most successful field deployments have been possible for the UV–Vis
instruments. By far, instrumentation costs have limited the use of other optical spectrometers. Silicon (Si)-based
sensors and devices are low-cost, while those based on Germanium (Ge) and Indium–Gallium–Arsenide
(InGaAs) are expensive, and do not scale as well as Si. As a result, linear or image (2D) sensors based on these
detectors are not field-compatible due to much higher costs. Hence, innovative single-detector approaches have
been the focus of recent develop- ments (Gelabert et al. 2016), although the principles behind these techniques
(e.g. Hadamard transform) have been known for many years. Due to these constraints, UV–Vis spectrometers
have been more successfully demon- strated in portable configurations, although for a limited range of
applications, such as water quality analysis (Langergraber et al. 2004).
In this chapter, the basic instrumentation configurations for portable UV–Vis spectrometers will be
introduced. This will be followed by an in-depth review of various approaches for achieving spectral acquisition
from digital micromirror devices (DMD) to do-it-yourself (DIY) approaches for teaching or hobby to
smartphone spectrome- ters. Finally, some applications and challenges of portable UV–Vis spectrometers will
be discussed, followed by challenges and future prospects.
Although technically the UV–Vis spectrum spans from around 190–800 nm, most spectrometers will offer a
higher wavelength limit up to 1100 nm. This is because Si has an appreciable responsivity into the NIR region
(Pavesi et al. 2013). However, most common spectrometer configurations will not operate over this entire
wavelength range. There is generally a tradeoff between spectral bandwidth and wavelength resolution. So,
manufacturers will offer spectral ranges that are a subset of 190–1100 nm. Additionally, there are no light
sources that have such a broad emission spectrum. Generally, a combination of two or more light sources is
needed to achieve coverage from 190 to 1100 nm. Finally, most applications typically do not require their entire
bandwidth along with a high resolu- tion. Due to these factors, spectrometers operate in limited spectral
bandwidths within the entire UV–Vis–NIR spectrum.
Collimator
(lens) Wavelength selector Detector
(slit) (photocell)
0.20
Io It
Digital display
Light source Polychromator Sample or meter
(Prism or grating) solution
(in cuvette)
102
150 W Halogen
450 W Xe
Spectral irradiance at 0.5m (mw m−2 nm−1)
101
75W Xe UV
100 W Halogen 150 W Xe UV
100
30 W D2
150 W Xe
150 W Xe OFR
10−1 75 W Xe
75 W Xe OFR
200
300 400 500 600 700 800 900
Wavelength (nm)
Figure 8.2 Spectra of common UV–Vis light sources. Source: Spectroscopy Instruments Catalog, Zolix. © Zolix Instruments
Co.,Ltd.
Recently, there have been demonstrations of spectrometers without a traditional dispersing element. Config-
urations involving a miniature 2D sensor with suitable filters over each pixel have shown limited applicability
due to low spectral resolution (Oliver et al. 2013). However, they offer a simpler approach to achieve
wavelength separation and may find niche applications.
In many benchtop configurations, these gratings are mounted on precision rotation stages for wavelength
selec- tion. Although this approach offers very high spectral resolution, it is complex to implement and sensitive
to vibrations. Therefore, they are not generally suited for portable spectrometers. There are two most commonly
used grating mount configurations. One is a Czerny–Turner configuration, where a plane grating is used with
two concave mirrors. Light is incident from an entrance slit on to one of the concave mirrors that collimates the
beam on to the grating. The diffracted light from the grating is focused by the second concave mirror on to the
detector. The other is an aberration-compensated Paschen mount configuration, where the grating is etched on a
concave surface that acts as a dispersing and focusing element, as shown in Figure 8.15. The Paschen
configuration has fewer optical components and can be monolithically integrated on a chip. However, such
gratings are challenging to fabricate and less fiexible to employ.
8.2.4 Detectors
Almost all spectrometers that operate in the UV–Vis region have Si detectors (Acree 2006). Si has an excellent
responsivity over the entire UV–Vis–NIR range; and it is readily available and customizable into regular
photode- tectors, avalanche detector or photomultiplier tubes, depending on the sensitivity required. Most
portable UV–Vis spectrometers today use diode arrays in the complementary metal oxide semiconductor
(CMOS) or charge coupled device (CCD) configurations and can have several thousands of pixels for high-
resolution applications, as shown in Figure 8.4. These arrays are compact with fast readout times and can have
inbuilt high-resolution analog-to-digital (A/D) converters.
Figure 8.4 Photodiode arrays used in portable UV–Vis spectrometers. Source: Photo courtesy of Hamamatsu Photonics.
8.3 Measurement Configurations
(a) (b)
Figure 8.5 (a) Standalone spectrometer with display. Source: Permission from Sekonic. (b) Typical USB-type spectrometer.
Source: USB4000 Fiber Optic Spectrometer, Ocean Optics. © 2006 Ocean Optics, Inc.
distinction can be made that portability always does not imply field compatibility. Several popular
spectrometers like the one shown in Figure 8.5, do offer portability but their interface is USB-based, which
means they require an external laptop or desktop computer to visualize and process data. This does not support
standalone operation and is generally suited to lab-based studies. Standalone spectrometers with inbuilt displays
have local data storage and can have secure digital (SD) cards or USB storage capability for portability of data.
8.3.1 Reflection
In a refiection arrangement, the light source and detector are on the same side of the sample that is being exam-
ined. Upon illumination, the sample refiects certain wavelengths, which are collected by the detector.
Depending
184 8 Portable UV–Visible Spectroscopy – Instrumentation, Technology, and
Input end Figure 8.6 Typical setup for reflection spectroscopy using
optical fibers. Creative Commons license. Source: Edwards
et al. (2017). Licensed under CC BY 4.0.
Sample end
Scanning...
Collection end
on the sample surface, there can be diffuse and/or specular components. In some cases, an integrating sphere
may be required to capture both the diffuse and specular components simultaneously. Figure 8.6 shows a typical
refiec- tion arrangement using optical fibers. A fiber bundle with six illuminations and one centrally placed
collection fiber is used as the probe. The sample is illuminated by the six fibers on the periphery and the
refiected light is guided to the spectrometer using a splitter arrangement. This is a common refiection
configuration in portable spectrometers and the use of optical fibers minimizes any alignment issues. A similar
setup can be realized in a free-space arrangement without optical fibers.
This configuration is most commonly used for color-sensing applications, where the refiection spectrum of a
sample needs to be determined. Color measurements are used across several industries to characterize and stan-
dardize paints, pigments, and displays among others. Section 8.5 will discuss specific examples in color
sensing.
8.3.2 Absorption
In an absorption measurement setup, the light source and detector are on either side of the sample, as shown in
Figure 8.7. Light first passes through a reference, which is typically a nonabsorbing material like distilled water.
The reference transmission spectrum is captured and saved. Next, the sample is introduced and another trans-
mission spectrum is recorded. By assuming that there are no other interactions like scattering or refiection, the
absorption spectrum can be deduced from the transmission spectrum by applying Beer–Lambert’s law.
Benchtop spectrometers generally have a double beam configuration for measuring absorption, wherein the
reference and sample measurements can be done simultaneously. However, in portable spectrometers, those are
not feasible, and measurements for the reference and sample need to be done sequentially. In such cases,
fiuctuations in the light source limit the sensitivity of detection. An example of a portable absorption
spectrometer is shown in Figure 8.7b.
8.3.3 Fluorescence
Another common configuration that is especially seen in biomedical applications involves detecting
fiuorescence (Lakowicz 2006). Depending on the use case and sample state, there are several geometries for
detecting fiuores- cence from thin films, solutions, droplets to powders among others. Typically, a narrowband
source is used for exciting the fiuorophore and the wavelength of the source chosen such that it coincides with
an absorption maxi- mum of the fiuorophore. In most cases, laser sources are used to obtain suitable signal
strength, but high-intensity LEDs have also been used in recent implementations. On the detector side, longpass
filters are generally used to reject the excitation wavelength and only transmit the fiuorescence signal
comprising longer wavelengths. This is a versatile configuration where the source and detector can be arranged
in absorption or refiection-like geometries.
8.3 Measurement Configurations
Reference measurement
Reference
Intens
Sample/reference
Transmissi
Wavelength
−log10(Sample/Reference)
Sample measurement
Sample
Absorban
Intens
Wavelength
Wavelength
Broadband
light source Cuvette Spectrometer
sample
(a)
(b)
Figure 8.7 (a) Absorption spectroscopy setup. Source: Permission from Ibsen Photonics. (b) Example of a portable
absorption spectrometer. Source: Permission from PASCO.
In applications where the fiuorophore has a weak fiuorescence or exists in low concentrations, additional focus-
ing optics are employed to increase the signal collected by the spectrometer. This geometry is routinely used in
confocal microscopy where a spectrometer is coupled to the microscopy objective and fiuorescence spectra are
captured at each point as a raster scan is carried out. However, in portable fiuorescence measurement configura-
tions, optical fibers are typically used to minimize alignment errors. In some cases, a custom sample holder has
been designed to house the filters and other optical components, as shown in Figure 8.8. Yu et al. demonstrated
a smartphone-based spectrometer, where the fiuorescence signal was incident on a grating placed at the camera
of the smartphone that played the role of a detector (Yu et al. 2014). The image captured by the camera could be
calibrated with known sources and a spectrum could be extracted based on that.
Although a spectrum can be obtained using the geometry shown in Figure 8.8, that is only the first step
toward a usable device. Several questions need to be addressed regarding the stability of the wavelength
calibration, the
186 8 Portable UV–Visible Spectroscopy – Instrumentation, Technology, and
(a) (b)
f1 = 40 mm
f2 = 50 mm
Test sample
(c)
Diffraction grating (1200 lines/mm) Smartphone camera (Lens and CMOS sensor)
Pinhole (d = 1 mm)
Cradle
Fluorescence
(d) (e)
200
150
Intensity
100
50
0
Broadband lightRed and green lasers 500 600 700
Wavelength (nm)
Figure 8.8 Smartphone-based portable fluorescence spectrometer arrangement. Source: Yu et al. (2014). © 2014 American
Chemical Society.
8.4 Types of Instrumentation Used in UV–Vis Spectroscopy
linearity of the response, effect of background noise, and summing of adjacent pixels. Without a complete
under- standing of the device performance and limitations, developing applications, particularly in the
biomedical field can lead to low sensitivity and specificity of tests. Section 8.6 discusses some of the parameters
to keep in mind when developing applications based on such spectrometer configurations.
Slit
Slit
Focusing
Focusing lens
lens
Single Point
DLP InGaAs detector
Detector:
InGaAs micromirror array ADC
linear array (wavelength selector)
Collection
lens
Figure 8.9 (a) Traditional array-based spectrometer. (b) Micromirror-based spectrometer. Source: © Texas Instruments.
This allows for fast acquisition of spectra with minimal postprocessing requirements, based on a Hadamard
trans- form. Recently, Texas Instruments (TI) commercialized micromirror-based spectrometers using their
digital light projector (DLP) technology (Gelabert et al. 2016), as shown in Figure 8.9b. Figure 8.10 shows a
micromirror-based spectrometer using the DLP2010NIR module, which can operate from 700 to 2000 nm.
Collection lenses
Grating
DLP2010NIR
885 nm wavepass filter
Collimating lenses
Slit
Figure 8.10 Micromirror-based spectrometer developed by Texas Instruments. Source: Texas Instruments Incorporated.
Light source
Filter array
CCD array
C CD
Analog to digital converter
Raw spectrum, y
(a) (b)
Figure 8.11 (a) Filter array-based portable spectrometers. Source: Wang et al. (2007). © 2007 The Optical Society (b) Filter
array with the random transmission. Source: Oliver et al. (2013). © 2013 The Optical Society.
Even though this approach is promising for realizing ultracompact spectrometers, most demonstrations have
been shown in laboratories. There is one commercial instance of a spectrometer based on this approach called
SCiO (SCiO n.d.). This product uses 12 filters in an array and operates from 700 to 1100 nm. Limited studies have
shown reasonable prediction accuracy for measuring fat and moisture using this approach.
(a) (b)
(c) (d)
Figure 8.12 Quantum dot spectrometer. (a) Schematic and (b) detailed configuration. Source: Bao and Bawendi (2015).
© 2015 Springer Nature.
eliminates the need for components, like displays, A/D converters, and other peripheral communication circuitry
(Long et al. 2014; McGonigle et al. 2018). An external battery-powered light source can be used with a grating
directly in line with the smartphone camera, as shown in Figure 8.13. A test sample is introduced in this path
and the spatially dispersed light is captured on the smartphone camera (de Oliveira et al. 2017). By accessing
the raw optical data, the effect of Bayer color filters can be suppressed. Finally, using light sources with known
wavelengths, a calibration can be set up.
This approach offers a cost-effective way to realize spectrometers without designing displays and other
electronic components. However, not many commercial spectrometers based on this approach have reached the
market, except for some do-it-yourself (DIY) kits that will be introduced in the next subsection. The technical
details of smartphone-based spectrometers are described in the chapter in this Volume by Scheeline, and the
field clinical applications in the chapter by Algar in Volume 2.
8.4 Types of Instrumentation Used in UV–Vis Spectroscopy
(2.5
(3
(3
(9 cm)
Battery
Battery
(9 cm)
(f)
Figure 8.13 Spectrometer design utilizing the camera of a smartphone as the detector. Source: Permission from Oliviera
et al. (2017). © 2017 Elsevier.
(a) (b)
Figure 8.14 DIY Spectrometer Kits. (a) Attachment for a smartphone. (b) Complete assembly. Source: Permission from
Jeffrey Yoo Warren and Public Lab.
192 8 Portable UV–Visible Spectroscopy – Instrumentation, Technology, and
High-sensitivity
CMOS linear image Incident light
sensor with slit
Input slit
Hollow
KACCC0757EB
(a) (b)
Figure 8.15 (a) Architecture of MEMS-based spectrometer. Source: Structure/Technology | Mini-spectrometers, Hamamatsu.
© Hamamatsu Photonics K.K. (b) Line of micro-spectrometers from Hamamatsu Photonics. Source: Photo courtesy
of Hamamatsu Photonics.
limited applicability in scenarios that require high sensitivity and robust operation. In one instance, a webcam
was modified with fiber optic cables to perform the action of an n-channel spectrometer (Sumriddetchkajorn
and Intaravanne 2012).
Rechargeable bettery
LED
Power switch
Spectrometer chip
Arduino pro mini
LED
Figure 8.16 Components involved in a standalone smartphone spectrometer developed by Labby Inc. Source: Das et al.
(2016). Licensed under CC BY 4.0.
circuitry along with a customized smartphone app that could calibrate and process the data on the phone itself.
This configuration is advantageous for remote operation where the smartphone needs to be at a distance from
the spectrometer. Bluetooth antenna can communicate with the smartphone at a distance of up to 9–12 m for
classic chips and beyond 100 m for low-energy chips. Additionally, it can work with any smartphone that has
the app installed, without having to deal with specific camera configurations. However, they are more expensive
mainly due to the chip.
8.5 Applications
In this section, various applications of portable UV–Vis spectrometers will be discussed.
(a) (b)
(c) (d)
Figure 8.17 Some portable color-sensing spectrometers. (a) Hach DR900. Source: Courtesy of Hach. (b) HunterLab Miniscan
EZ 4500L. Source: Hunter Associates Laboratory, Inc. (c) Nix QC. Source: NIX SENSOR, LTD. (d) X-Rite eXact. Source: X-Rite,
Incorporated.
beverage (Giusti and Wrolstad 2001), anthocyanins (Giusti and Wrolstad 2001), and textile (Berns 1992; Zhang and
Li 2008) industries among many others. Spectrometers are used to obtain a calibrated refiection spectrum which
is the first step in color measurement. Depending on the illuminant and International Commission on
Illumination (CIE) color space, a refiection spectrum can be transformed to RGB, Lab, cyan, magenta, yellow, and
key (CMYK), and other systems. Notable examples of portable color sensors are X-Rite, HunterLab, Nix, and
Hach, as shown in Figure 8.17. Some color sensors, based on discrete filter sensors, are the size of a lipstick and
can cost as low as
$59.
In addition to color systems like RGB and Lab, industrial applications have their own standards for quality
control of oils, lubricants, beer, wine, etc. For instance, ASTM D1500D and D6045 are color-based methods for
quantifying oil quality. ASBC 10 (standard reference method, SRM) is a standard for measuring beer color,
whereas OIV-MA-AS2-07B is a standard for wine color (tone and intensity) using spectrophotometric methods
(Streitberger and Dössel 2008).
Absorbance
Absorbance at 450
0.4
Optical cradle
0.2
0
400 450 500 550
Wavelength (nm)
(a) (b)
Figure 8.18 (a) Smartphone spectrometer arrangement for ELISA. (b) Absorption spectra correlated to peanut allergen.
Source: Long et al. (2014). © 2014 Optical Society of America.
described in Section 8.4.4. A schematic of their setup is shown in Figure 8.18a along with the absorption spectra
in Figure 8.18b.
Nucleic acids like deoxyribonucleic acid (DNA) and ribonucleic acid (RNA) have a characteristic absorption
peak at around 260 nm, which can be used to detect and quantify their concentration (Desjardins and Conklin
2010). Additionally, proteins have an absorption centered at around 280 nm. Portable UV spectrometers are
well-suited for these applications. For instance, the NanoDropTM is a portable spectrophotometer that only
intakes 1–2 μl of a sample and can analyze absorption or fiuorescence spectra to detect concentrations of
nucleic acids and proteins. Figure 8.19a shows the NanoDrop One/OneC spectrophotometer manufactured by
Thermo Fisher. Another small-volume spectrometer is the UV5Nano from Mettler Toledo, as shown in Figure
8.19b.
(a) (b)
Figure 8.19 (a) NanoDrop One/OneC spectrophotometer. Source: Permission from Thermo Fisher. (b) UV5Nano small
volume spectrometer. Source: METTLER TOLEDO.
196 8 Portable UV–Visible Spectroscopy – Instrumentation, Technology, and
Figure 8.20 Smartphone-based fluorescence spectrometer for the screening of skin disease. Source: Poojary et al. (2019).
(c) 1
0.8
4.8 mm
4.4 mm
0.6
Intensity
5.1 mm
0.4
6 nm
0.2
0
400 500 600 700 800 900
wavelength (nm)
Figure 8.21 G-Fresnel spectrometer for detecting hemoglobin concentration. Source: Edwards et al. (2017). Licensed under
CC BY 4.0.
Figure 8.22 Hach DR3900 spectrophotometer for water quality analysis. Source: Courtesy of Hach.
198 8 Portable UV–Visible Spectroscopy – Instrumentation, Technology, and
0.6
H
0.2
Figure 8.23 Smartphone spectrometer for detecting methylene blue in the water. (a) Smartphone spectrometer prototype
with an optical fiber coupled to the camera flash. (b) Images of light output from the fibers. (c) Spectra corresponding to the
fibers compared with a standard spectrometer. Source: Özdemir et al. (2017). © 2017 Royal Society of Chemistry
In a recent study, Özdemir et al. (2017) demonstrated a smartphone spectrometer for detecting dyes like
methy- lene blue by adsorbing dye molecules on polyacrylonitrile (PAN)/zeolite nanofibers, as shown in Figure
8.23. In another example, Wang et al. used a DVD grating-based smartphone spectrometer to detect neurotoxins
in water (Wang et al. 2016).
(c)
(e)
Figure 8.24 Smartphone spectrometer for detecting ripeness of apples using chlorophyll fluorescence. Source: Permission
from Das et al. (2016).
Figure 8.25 Linksquare smartphone spectrometer being used in fruit freshness analysis. Source: Permission from
Linksquare and You et al. (2017).
In this application space, there are a few commercial portable Vis spectrometers out in the market, such as
Linksquare, which have shown some success in classifying food and detecting freshness, as shown in Figure
8.25a. You et al. (2017) used the Linksquare spectrometer to classify identical-looking food powders, like sugar,
salt, rice, etc., using refiection spectroscopy, as shown in Figure 8.25b. They used machine learning algorithms
for classification and achieved near 100% accuracy for eight different types of food powders.
In another report, Cai et al. (2017) demonstrated pencil-like spectrometer using a prism-grating configuration
with an image sensor, as shown in Figure 8.26a. The spectrometer operated in the 400–675 nm region with a
200 8 Portable UV–Visible Spectroscopy – Instrumentation, Technology, and
Intensity
Intensity
150 620 2
1st order diffraction
437 579
620
th
100 1
0 order diffraction
50 596
0
400 450 500 550 600 650 400 450 500 550 600 650
Wavelength (nm) Wavelength (nm)
(a)
(a)
1 (b)
1
0.8
0.6 Reflectance
0.8
Reflectance
0.4
0.6
0.2
0
500 550 600 650 0.4
500 550 600 650
Wavelength (nm)
Wavelength (nm)
(c)
1 0.35 (d) 0.58
1
Reflectance
Reflectance
0.56
0.8 0.54
0.3 0.8
530 540 550 530 540 550
Reflectance
0.6
0.6
0.4 0.4
0.2 0.2
0
542 nm 0
500 550 600 650 500 550 600 650
Wavelength (nm) Wavelength (nm)
(b)
Figure 8.26 Top. Panel A, Pencil-like smartphone spectrometer. Panel B, Mercury lamp spectrum captured by the pencil
spectrometer. Panel C, Mercury lamp spectrum obtained using a commercial spectrometer. Bottom. Panel A, Reflectance
spectrum of unripe banana. Panel B, Reflectance spectrum of ripe banana. Panel C, Reflection spectrum of pork muscle. Panel
D, Reflection spectrum of pork fat. Source: Cai et al. (2017). © 2017 Optical Society of America.
resolution of 17 nm. The spectrometer was used for several applications including detecting ripeness of bananas
and freshness of pork, as shown in Figure 8.26b.
¼λ
pol. 2×4λ Camera lens Detector chip
Figure 8.27 Smartphone spectropolarimeter for sensing atmospheric aerosols. Source: Snik et al. (2014). © 2014 John
Wiley & Sons
gases, like SO2, among other applications. For instance, Snik et al. (2014) demonstrated a smartphone
spectropo- larimeter for aerosol mapping, which measured the degree of linear polarization as a function of
wavelength, as shown in Figure 8.27. They designed a low-cost add-on comprising polarizers and a
transmission grating, which was attached to the camera of the smartphone. Using this miniature arrangement,
multiple (over 3000) measure- ments could be conveniently made by “citizen spectroscopists.” Reasonable
agreement between ground-based spectrometers was observed, which establishes the potential of portable
spectrometers for aerosol sensing.
Galle et al. (2003) developed a portable UV spectrometer for sensing SO 2 emissions for applications in vol-
canic surveillance. The spectrometer had a Czerny–Turner configuration and operated in the 245–380 nm
spectral range for achieving differential optical absorption. A telescope was used to capture the scattered UV
light from aerosols, which was then coupled to the spectrometer using an optical fiber cable, as shown in Figure
8.28a. The telescope-spectrometer arrangement could be mounted on a car, a helicopter, or a tripod, such that
measurements
Telescope
Optical fibre
Figure 8.28 Portable UV spectrometer for SO2 detecting during volcanic eruptions. (a) Spectrometer design. (b) Field
implementation. Source: Permission from Galle et al.
202 8 Portable UV–Visible Spectroscopy – Instrumentation, Technology, and
Figure 8.29 Ocean Optics STS spectrometer mounted on a drone. Source: Ocean Optics Inc. and VOXearch Inc.
could be made close to the site of the volcanic eruption, as shown in Figure 8.28b. Compared to the existing SO2
detectors, this approach was attractive as the spectrometer could capture the entire UV spectrum, thereby
provid- ing greater fiexibility to identify errors and apply better statistical methods. Furthermore, a good
agreement was observed with a standard correlation spectrometer, which established the accuracy of their
prototype.
acquisition, spectral data conditioning, postprocessing, and, finally, interpretation. Without careful assessments
at each stage, errors can propagate and result in less-effective measurements. A distinction should be made
whether the spectrometer is a “toy” or a “tool.” A toy version would be great for educational and hobby use,
whereas a tool version would be imposed with stringent performance requirements. The issues involved in the
construction of appropriate libraries and calibrations are described in the chapter by Schreyer.
Although there are several approaches and reports of new spectrometer designs, only a few of them have
made it to the market. Within them, a smaller subset has been commercially successful. By looking at
established spec- trometers in the market, it is possible to impose certain constraints, such as ease of
manufacturing, scalability, robustness, among others, that will determine the successful deployment of newer
portable spectrometer tech- nologies. This section highlights a few aspects that will aid in the development of
robust spectrometers.
8.6.4 Calibration
Wavelength calibration is a critical process in spectroscopy and plays an important role in determining the accu-
racy of measurements. All factors that can affect calibration need to be considered, such that their effect can be
quantified and minimized (Burggraaff et al. 2019). For instance, in camera-based spectrometers, internal Bayer
filters in the image sensor can disrupt the calibration. The use of RAW format images has shown to minimize
the effect of these filters. The positioning of the grating must be robust and not change, as that can affect the
calibration. In the case of filter array-based spectrometers, the spectral overlap of the filters needs to be
considered.
204 8 Portable UV–Visible Spectroscopy – Instrumentation, Technology, and
8.7 Outlook
The notion of a “lab” is taking a new meaning thanks to new sensors, the increased computing power of smart-
phones and the emergence of cloud functionality. On the one hand, today’s smartphones boast of 6 GB random
access memory (RAMs), 2 GHz processors, and a range of wireless communication approaches with the
availabil- ity of programmable open source components. On the other hand, miniaturized spectrometers have
been realized due to advanced fabrication approaches. The merger of these technologies offers promising
opportunities for a range of applications that were not feasible earlier. Today, portable spectrometers can be
seamlessly integrated into smartphones via apps and be made more effective through cloud computing and
machine learning. It will be possible to generate large spectroscopic datasets for a range of food, beverage, and
agricultural products that will pave the way for intelligent sensors that “learn” over time and enable new
applications like counterfeit detection, predict harvest times, and improve the distribution of produce among
other uses: so-called “smart agriculture.”
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