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<journal-meta>
<journal-id journal-id-type="publisher-id">Front. Sens.</journal-id>
<journal-title>Frontiers in Sensors</journal-title>
<abbrev-journal-title abbrev-type="pubmed">Front. Sens.</abbrev-journal-title>
<issn pub-type="epub">2673-5067</issn>
<publisher>
<publisher-name>Frontiers Media S.A.</publisher-name>
</publisher>
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<article-id pub-id-type="publisher-id">1513701</article-id>
<article-id pub-id-type="doi">10.3389/fsens.2025.1513701</article-id>
<article-categories>
<subj-group subj-group-type="heading">
<subject>Sensors</subject>
<subj-group>
<subject>Perspective</subject>
</subj-group>
</subj-group>
</article-categories>
<title-group>
<article-title>Making nanomaterial-enabled nitrate sensors useful for real water systems: user-centric design perspectives</article-title>
<alt-title alt-title-type="left-running-head">Defeo et al.</alt-title>
<alt-title alt-title-type="right-running-head">
<ext-link ext-link-type="uri" xlink:href="https://doi.org/10.3389/fsens.2025.1513701">10.3389/fsens.2025.1513701</ext-link>
</alt-title>
</title-group>
<contrib-group>
<contrib contrib-type="author" corresp="yes">
<name>
<surname>Defeo</surname>
<given-names>Shelby</given-names>
</name>
<xref ref-type="aff" rid="aff1">
<sup>1</sup>
</xref>
<xref ref-type="corresp" rid="c001">&#x2a;</xref>
<uri xlink:href="https://loop.frontiersin.org/people/2704942/overview"/>
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<role content-type="https://credit.niso.org/contributor-roles/Writing - review &#x26; editing/"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Erickson</surname>
<given-names>Samuel</given-names>
</name>
<xref ref-type="aff" rid="aff2">
<sup>2</sup>
</xref>
<uri xlink:href="https://loop.frontiersin.org/people/1398642/overview"/>
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<role content-type="https://credit.niso.org/contributor-roles/Writing - review &#x26; editing/"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Perez Mendoza</surname>
<given-names>Maria F.</given-names>
</name>
<xref ref-type="aff" rid="aff2">
<sup>2</sup>
</xref>
<role content-type="https://credit.niso.org/contributor-roles/writing-original-draft/"/>
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</contrib>
<contrib contrib-type="author">
<name>
<surname>Cooper</surname>
<given-names>Alexia</given-names>
</name>
<xref ref-type="aff" rid="aff1">
<sup>1</sup>
</xref>
<role content-type="https://credit.niso.org/contributor-roles/writing-original-draft/"/>
<role content-type="https://credit.niso.org/contributor-roles/Writing - review &#x26; editing/"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Barrios</surname>
<given-names>Bruce</given-names>
</name>
<xref ref-type="aff" rid="aff2">
<sup>2</sup>
</xref>
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</contrib>
<contrib contrib-type="author">
<name>
<surname>Malone</surname>
<given-names>Zachary</given-names>
</name>
<xref ref-type="aff" rid="aff1">
<sup>1</sup>
</xref>
<role content-type="https://credit.niso.org/contributor-roles/writing-original-draft/"/>
<role content-type="https://credit.niso.org/contributor-roles/Writing - review &#x26; editing/"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Baxter</surname>
<given-names>Ryan D.</given-names>
</name>
<xref ref-type="aff" rid="aff3">
<sup>3</sup>
</xref>
<role content-type="https://credit.niso.org/contributor-roles/writing-original-draft/"/>
<role content-type="https://credit.niso.org/contributor-roles/Writing - review &#x26; editing/"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Ghosh</surname>
<given-names>Sayantani</given-names>
</name>
<xref ref-type="aff" rid="aff2">
<sup>2</sup>
</xref>
<uri xlink:href="https://loop.frontiersin.org/people/1401291/overview"/>
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<contrib contrib-type="author">
<name>
<surname>Harmon</surname>
<given-names>Thomas C.</given-names>
</name>
<xref ref-type="aff" rid="aff1">
<sup>1</sup>
</xref>
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<aff id="aff1">
<sup>1</sup>
<institution>Environmental Systems Graduate Program</institution>, <institution>University of California</institution>, <addr-line>Merced</addr-line>, <addr-line>CA</addr-line>, <country>United States</country>
</aff>
<aff id="aff2">
<sup>2</sup>
<institution>Department of Physics</institution>, <institution>University of California</institution>, <addr-line>Merced</addr-line>, <addr-line>CA</addr-line>, <country>United States</country>
</aff>
<aff id="aff3">
<sup>3</sup>
<institution>Department of Chemistry and Biochemistry</institution>, <institution>University of California</institution>, <addr-line>Merced</addr-line>, <addr-line>CA</addr-line>, <country>United States</country>
</aff>
<author-notes>
<fn fn-type="edited-by">
<p>
<bold>Edited by:</bold> <ext-link ext-link-type="uri" xlink:href="https://loop.frontiersin.org/people/799623/overview">Sandeep Kumar</ext-link>, Punjab engineering college (Deemed to be University), India</p>
</fn>
<fn fn-type="edited-by">
<p>
<bold>Reviewed by:</bold> <ext-link ext-link-type="uri" xlink:href="https://loop.frontiersin.org/people/2261920/overview">Jaroslav Filip</ext-link>, Tomas Bata University in Zl&#xed;n, Czechia</p>
<p>
<ext-link ext-link-type="uri" xlink:href="https://loop.frontiersin.org/people/2854445/overview">Gaurav Bhanjana</ext-link>, Guru Jambheshwar University of Science and Technology, India</p>
<p>
<ext-link ext-link-type="uri" xlink:href="https://loop.frontiersin.org/people/2893270/overview">Vishal Singh</ext-link>, The Ohio State University, United States</p>
</fn>
<corresp id="c001">&#x2a;Correspondence: Shelby Defeo, <email>sdefeo@ucmerced.edu</email>
</corresp>
</author-notes>
<pub-date pub-type="epub">
<day>21</day>
<month>02</month>
<year>2025</year>
</pub-date>
<pub-date pub-type="collection">
<year>2025</year>
</pub-date>
<volume>6</volume>
<elocation-id>1513701</elocation-id>
<history>
<date date-type="received">
<day>18</day>
<month>10</month>
<year>2024</year>
</date>
<date date-type="accepted">
<day>05</day>
<month>02</month>
<year>2025</year>
</date>
</history>
<permissions>
<copyright-statement>Copyright &#xa9; 2025 Defeo, Erickson, Perez Mendoza, Cooper, Barrios, Malone, Baxter, Ghosh and Harmon.</copyright-statement>
<copyright-year>2025</copyright-year>
<copyright-holder>Defeo, Erickson, Perez Mendoza, Cooper, Barrios, Malone, Baxter, Ghosh and Harmon</copyright-holder>
<license xlink:href="http://creativecommons.org/licenses/by/4.0/">
<p>This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.</p>
</license>
</permissions>
<abstract>
<p>Water quality monitoring is essential for identifying risks to environmental and human health. Nitrate monitoring is of particular importance, as its anthropogenic point and nonpoint sources are common globally and have deleterious effects on water quality and usability as well as aquatic ecosystem health. Standard methods for assessing nitrate concentrations in water generally involve laboratory techniques, as methods available for field testing face significant tradeoffs between cost, precision, and portability. Given its relatively ubiquitous nature and the widespread regulation of nitrate pollution, it is a prime target for sensor development. The growing field of nanomaterials (e.g., nanoparticles, nanotubes, and 2-dimensional materials) offers the potential to eliminate these tradeoffs through a new generation of field-ready nitrate sensors. However, transitioning nano-sensors from the lab to the field remains challenging. In this perspective we examine the challenges of lab-to-field transition of nano-sensors for nitrate, highlighting the importance of a user-centered design approach under the framework of FOCUS (form factor, operational robustness, cost, user interface, and sensitivity).</p>
</abstract>
<kwd-group>
<kwd>monitoring</kwd>
<kwd>nutrient</kwd>
<kwd>pollution</kwd>
<kwd>contamination</kwd>
<kwd>user</kwd>
<kwd>technology</kwd>
<kwd>device</kwd>
<kwd>field</kwd>
</kwd-group>
<contract-num rid="cn001">DGE-2125510</contract-num>
<contract-sponsor id="cn001">National Science Foundation<named-content content-type="fundref-id">10.13039/100000001</named-content>
</contract-sponsor>
<custom-meta-wrap>
<custom-meta>
<meta-name>section-at-acceptance</meta-name>
<meta-value>Sensor Devices</meta-value>
</custom-meta>
</custom-meta-wrap>
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</front>
<body>
<sec id="s1">
<title>1 Introduction</title>
<p>Nitrate (NO<sub>3</sub>
<sup>&#x2212;</sup>) pollution is a global concern because of its ubiquitous nature and negative effects on human health and ecosystem function. Elevated anthropogenic nitrate releases overwhelm crops, soil microbes, and aquatic ecosystems, leading to incomplete nitrogen assimilation (<xref ref-type="bibr" rid="B56">Zhang et al., 2015</xref>). Elevated concentrations can generally be traced to three sources: point discharges of treated and raw wastewater from municipal systems (<xref ref-type="bibr" rid="B9">Choudhary et al., 2022</xref>), releases from confined livestock operations (<xref ref-type="bibr" rid="B32">Lockhart et al., 2013</xref>), and land application of agricultural fertilizers resulting in diffuse or nonpoint source pollution (<xref ref-type="bibr" rid="B45">Singh and Craswell, 2021</xref>). While all these sources can be problematic, the nonpoint sources are the most challenging to delineate and control because of their connections with a variety of locations and activities (<xref ref-type="bibr" rid="B13">Drevno, 2016</xref>). The consumption of nitrate in drinking water is associated with deleterious health effects for pregnant people and infants, and there is growing evidence of negative health outcomes in other populations as well (<xref ref-type="bibr" rid="B50">Temkin et al., 2019</xref>; <xref ref-type="bibr" rid="B54">Ward et al., 2018</xref>). The United States Environmental Protection Agency established the maximum contaminant level (MCL) of 10 mg per liter (mg/L) nitrate-as-nitrogen or NO<sub>3</sub>
<sup>&#x2212;</sup>-N in public drinking water supplies in the United States at (<xref ref-type="bibr" rid="B51">US EPA, 2019</xref>), which is consistent with global limits set for the contaminant. Nitrate pollution does not affect all communities equally; agricultural areas, as well as rural and Hispanic communities, have been found to be at significantly higher risk for nitrate pollution exposure within the United States (<xref ref-type="bibr" rid="B43">Schaider et al., 2019</xref>). Given its diffuse distribution in surface water and groundwater, low cost and user-friendly nitrate sensing technologies would be highly desirable. For example, such sensors would enable rural water consumers to monitor their own tap water and empower citizen science groups to test their local rivers, lakes, and wetlands.</p>
<p>The current methodologies of measuring nitrate concentration involve huge trade-offs among prevailing methodologies with regard to precision, cost, and field usability. Although laboratory-based techniques can be highly accurate, they are unrealistic for many stakeholders due to the use of expensive equipment and personnel training. On the other side, simplistic field methods such as colorimetric test strips are imprecise, while the existing portable sensors face serious challenges on interference, calibration drift, and operational lifetime. The field of nanomaterials, currently under fast development, opens new perspectives in the overcoming of such limitations through tunable properties, high surface-to-volume ratio, and for selective detection potentially.</p>
<p>Successfully transitioning nanomaterial-based sensors from laboratory demonstrations to practical field applications requires careful consideration of multiple design factors. A systematic approach considering both technical performance and user needs is essential for developing sensors that will be adopted and used effectively in real-world settings. This work offers perspectives on leveraging the growing field of nanomaterials (e.g., nanoparticles, nanotubes, and 2-dimensional materials) to advance more quickly to a new generation of field-ready nitrate sensors. In this perspective we examine the challenges of lab-to-field transition of nano-sensors, highlighting the importance of a user-centered design approach under a framework we refer to as FOCUS (form factor, operational robustness, cost, user interface, and sensitivity).</p>
</sec>
<sec id="s2">
<title>2 Nitrate analysis background</title>
<p>Observing aqueous nitrate concentrations <italic>in situ</italic> and in near-real time is valuable to water quality managers and stakeholders. It enables the mapping and understanding and analysis of nitrate distributions and dynamics in natural and engineered water systems. The field detection methods outlined here (colorimetric test strips, electrochemical sensors, and spectroscopic sensors) are not intended to be exhaustive. Instead, the methods and devices discussed are intended to highlight the common challenges associated with currently available field techniques, including lack of precision, robustness, and relatively high unit costs. It is worth noting that nitrate measurements can be expressed in various ways (ppb (parts per billion), ppm (parts per million), ppm-NO<sub>3</sub>
<sup>&#x2014;</sup>N (parts per million nitrate-as-nitrogen), mg/L (milligrams per liter), molarity, etc.). In this paper, we use ppm and ppb as nitrate for consistency and a broader audience (42&#xa0;ppm nitrate is the corresponding US EPA MCL).</p>
<p>Colorimetric nitrate test strips for predetermined ranges (0&#x2013;500&#xa0;ppm) can provide nitrate concentration assessments in less than 1&#xa0;min (<xref ref-type="bibr" rid="B5">Brockhage et al., 2022</xref>). The test colorimetric strips work through the reduction of nitrate to nitrite which can be visually quantified (or standardized for phone cameras). While such test strips are relatively inexpensive and easy to use, they are designed to quantify wide ranges and their readings may deviate from comparative laboratory results (<xref ref-type="bibr" rid="B5">Brockhage et al., 2022</xref>; <xref ref-type="bibr" rid="B33">Loperfido et al., 2010</xref>). However, test strips may be sufficient for uses such as rapid sample screening (e.g., prior to more precise lab analyses) and for community science projects, also known as citizen science projects, exploring nitrate presence/absence or identifying trends.</p>
<p>Electrochemical or spectroscopic nitrate sensing devices are also commercially available. Ion selective electrodes (ISE) operate potentiometrically and exist for a variety of environmental analytes of interest (<xref ref-type="bibr" rid="B11">Crespo, 2017</xref>). For a nitrate ISE, the working electrode material is coated with a membrane doped with an ionic carrier (e.g., quaternary ammonium ions, as noted in <xref ref-type="bibr" rid="B47">Singh et al. (2022)</xref>), which renders it selective for nitrate ions. The affinity of the nitrate ion for the surface of the working electrode alters the chemical potential (voltage) in a log-linear relationship with nitrate concentration. While nitrate ISEs can work well in laboratory and under carefully controlled field conditions, they are thus far unsuitable for autonomous field deployment. Hindrances to deployment include their lack of adequate sensitivity for some applications (often precision &#xb1;10% with detection limit of 0.5&#xa0;ppm in commercially available ISEs), need for frequent calibration, sensitivity to interfering ions, and need for frequent cleaning to prevent biofouling of the membrane surface (<xref ref-type="bibr" rid="B11">Crespo, 2017</xref>).</p>
<p>Spectroscopic devices for measuring nitrate concentrations operate in the ultraviolet (UV) range and can have limit of detections down to the sub ppb (<xref ref-type="bibr" rid="B35">Mahmud et al., 2020</xref>). Nitrate absorbs at specific wavelengths, generally within the range of 190&#x2013;250 nm (nm), though multiple wavelengths may be necessary due to interfering absorbance of other compounds also occurring in this range (<xref ref-type="bibr" rid="B46">Singh et al., 2019</xref>). Robust UV probes that limit interferences and are field-ready can be expensive ($10,000&#x2b;), bulky (on the order of a meter long), and complicated to operate, therefore presenting problems with implementation for a wide variety of aquatic research.</p>
<p>Laboratory techniques remain the standard for nitrate determination when high precision and accuracy are needed for scientific or regulatory purposes. Flow injection analysis is among the commonly used laboratory techniques for nitrate determination and generally utilizes a cadmium column to facilitate the reduction of nitrate to nitrite for analysis (<xref ref-type="bibr" rid="B24">Kazemzadeh and Ali, 2001</xref>). While this method provides results across a wide range of concentrations from the sub ppb to ppm level, there is debate regarding variation in results due to column preparation and influences of pH and dissolved oxygen (<xref ref-type="bibr" rid="B16">Gal et al., 2004</xref>).</p>
<p>Colorimetric methods for the detection of nitrate are predicated on the development of a visible color using reagents, in some cases through the development of color using Greiss reagents and the reduction of nitrate to nitrite (<xref ref-type="bibr" rid="B36">Michalski and Kurzyca, 2006</xref>). This method is relatively simple in application but requires the use of prefabricated reagent packets appropriate for a finite range of concentrations and therefore may require sample dilution for higher concentrations. In addition, these reagent packets are relatively expensive consumables and produce hazardous waste in the lab. Colorimetric methods are generally able to quantify nitrate concentrations between 0.05&#xa0;ppm and 22&#xa0;ppm, but high sensitivity <italic>versus</italic> broad sensitivity versions of the method require different procedures.</p>
<p>Ion chromatography is another common method for the determination of nitrate (<xref ref-type="bibr" rid="B36">Michalski and Kurzyca, 2006</xref>). Ions are separated by their interactions with a resin and progress through the system at differentiating rates. Chromatography provides highly accurate results (&#xb1;5%) with low detection limits in the ppb level, but the high cost of the instrument, time and cost associated with sample collection and transport, need for skilled technicians, and maintenance limit its use outside of a university, industry, or research laboratory. Raman spectroscopy is an optical-signal-based laboratory method capable of determining nitrate in water samples. The method utilizes light to quantify energy shifts originating from the vibrational modes of the chemical bonds of the molecule and is comparable to other laboratory techniques in accuracy. While similar in accuracy, the method is hindered by a higher detection limit of 0.5&#xa0;ppm (<xref ref-type="bibr" rid="B15">Gajaraj et al., 2013</xref>).</p>
<p>Laboratory techniques of a wide variety are available for the detection of nitrate and serve a valuable purpose in scientific discovery, however they provide only partially the needs of nitrate determination due to their restrictive nature. While both laboratory and field methods have contributed to the current understanding of nitrates, gaps remain between available technology and the practical needs of users. Laboratory techniques are limited by their need for a skilled technician, high investment cost and cost of continuing maintenance, sample preparation, and delay in data analysis. Current field methods are restricted by tradeoffs between precision, cost, robustness, ease of use, and portability. The next-generation of nitrate sensors will need to bridge the associated gaps between lab and field detection, potentially through new technologies.</p>
</sec>
<sec id="s3">
<title>3 Recent nitrate sensors based on nanomaterials</title>
<p>The past decade has featured rapid growth in nanomaterial-based detectors for nitrate dissolved in water. While these lab devices are not yet commercialized or produced at scale, they present excellent detection limits as low as 0.045&#xa0;ppm and as high as 6,000&#xa0;ppm (<xref ref-type="bibr" rid="B19">Hassan et al., 2019</xref>; <xref ref-type="bibr" rid="B14">Essousi et al., 2019</xref>). Likewise, the hardware needed to make use of emergent nanomaterials is often compact and conducive to use in field sensors. Finally, many nanoscale sensors have few interfering ions, though nitrite (NO<sub>2</sub>
<sup>&#x2212;</sup>) is the most common (<xref ref-type="bibr" rid="B48">Stortini et al., 2015</xref>; <xref ref-type="bibr" rid="B30">Liang et al., 2016</xref>; <xref ref-type="bibr" rid="B49">Tang et al., 2016</xref>). <xref ref-type="sec" rid="s12">Supplementary Table S-1</xref> summarizes the parameters of nanomaterials based sensors highlighted in this perspective. This section will focus on promising electrochemical, spectroscopic, biological, and electrical nanosensors and their function (<xref ref-type="fig" rid="F1">Figure 1</xref>). The advantages and disadvantages of each will be discussed briefly, as will comparisons between devices to better understand their roles in future nitrate detection. Herein, electrochemical sensors will include voltametric and potentiometric devices, the latter using ion selective electrodes (ISEs). Similarly, electrical sensors will include chemiresistors, capacitors, and field effect transistors (FETs).</p>
<fig id="F1" position="float">
<label>FIGURE 1</label>
<caption>
<p>Schematic representation of typical nitrate sensing platforms. Both electrochemical and biological sensors rely on nitrate reduction to generate electrical responses, with the latter utilizing a biological molecule as the active medium. Optical techniques are non-invasive, leveraging changes in spectral absorption or emission properties of a substrate in response to nitrate adsorption. Electrical sensing devices use the same approach of molecular adsorption, but the detection method is a change of electrical conductivity of the sensor.</p>
</caption>
<graphic xlink:href="fsens-06-1513701-g001.tif"/>
</fig>
<sec id="s3-1">
<title>3.1 Electrochemical</title>
<p>Popular electrochemical nanosensors for nitrate detection include metal/metal oxide nanoparticles (NPs), graphene, carbon nanotubes (CNTs), electropolymerized films, and combinations of these. Most materials in this category act as electrode modifiers, as bulk copper (Cu) and other common conductors are poor nitrate detectors near neutral pH. These contacts also tend to degrade and experience interference with other molecules and ions, especially nitrite (NO<sub>2</sub>
<sup>&#x2212;</sup>) and chloride (Cl<sup>&#x2212;</sup>), without proper modifiers (<xref ref-type="bibr" rid="B28">Li et al., 2019</xref>). Copper nanoparticles (CuNPs) and nanowires in combination with various substates have nitrate detection ranges in the sub ppb (<xref ref-type="bibr" rid="B14">Essousi et al., 2019</xref>; <xref ref-type="bibr" rid="B48">Stortini et al., 2015</xref>). CuNPs deposited on graphene catalyzed nitrate reduction to ammonia with analysis by differential pulse voltammetry have been shown to have a detection limit of 0.49&#xa0;ppm (<xref ref-type="bibr" rid="B52">Wang et al., 2018</xref>). More recently, Cu nanowires were grown by galvanic deposition to detect nitrate by linear sweep voltammetry. This cost effective and stable growth technique enabled measurement of nitrate concentrations as low as 0.56&#xa0;ppm and performed well in natural water samples (<xref ref-type="bibr" rid="B40">Patella et al., 2021</xref>). An undesirable characteristic of these sensors is that they require a pH between two and three for proper electrocatalytic reduction of nitrate. Silver (Ag) nanostructures have low limits of detection (as low as 24&#xa0;ppb) near neutral pH and experience few interferents but are limited to concentrations under 62&#xa0;ppm (<xref ref-type="bibr" rid="B8">Chen Legrand et al., 2017</xref>; <xref ref-type="bibr" rid="B20">Hu et al., 2013</xref>). Potentiometric sensors utilize ISEs including multiwalled carbon nanotubes (MWCNTs), graphene, and polypyrrole (<xref ref-type="bibr" rid="B12">Cuartero et al., 2018</xref>; <xref ref-type="bibr" rid="B44">Schwarz et al., 2018</xref>; <xref ref-type="bibr" rid="B41">Pi&#x119;k et al., 2016</xref>; <xref ref-type="bibr" rid="B18">Gil et al., 2024</xref>). Work with organic nanotubes has also shown low detection limits of 0.02&#xa0;ppm (<xref ref-type="bibr" rid="B27">Kundu, 2023</xref>). Most ISEs are based on three nitrate ionophores: quaternary ammonium, nitrate ionophore V and VI, and tridodecylmethylammonium nitrate (TDMAN). Very low nitrate concentrations between 10<sup>&#x2212;7</sup>&#x2013;10<sup>&#x2212;2</sup>&#xa0;ppm have been detected by measuring the potential difference between the ISE and a reference electrode (<xref ref-type="bibr" rid="B47">Singh et al., 2022</xref>; <xref ref-type="bibr" rid="B31">Liu et al., 2020</xref>). Electrochemical sensors can be complicated in their construction, but recent work has highlighted alternative constructions with linear ranges between 10 and 100&#xa0;ppm with a detection limit of approximately 2&#xa0;ppm (<xref ref-type="bibr" rid="B10">Concepcion et al., 2024</xref>) while other work has highlighted possibilities for environmental sustainability with linear ranges of 1&#x2013;100&#xa0;ppm (<xref ref-type="bibr" rid="B42">Sarwar Inam et al., 2023</xref>).</p>
</sec>
<sec id="s3-2">
<title>3.2 Spectroscopic</title>
<p>Spectroscopic nitrate detection is the most popular method in the lab due to the highly precise nature of spectrometers and other optical instruments. By performing a nitrate to nitrite reduction via a Griess assay, nitrate concentrations as low as 10<sup>&#x2212;5</sup>&#xa0;ppm can be measured with high resolution fluorescence spectroscopy (<xref ref-type="bibr" rid="B55">Yang et al., 2015</xref>). Vanadium (III) chloride (VCl<sub>3</sub>) in hydrochloric acid (HCl) has also been used with limits of detection as low as 0.006 ppm, though sensing times range from 3&#x2013;60&#xa0;min (<xref ref-type="bibr" rid="B17">Garcia-Robledo et al., 2014</xref>; <xref ref-type="bibr" rid="B53">Wang et al., 2016</xref>). CNTs and CuNPs and been utilized in tandem with optical fibers for both surface plasmon resonance and ultraviolet-visible (UV-Vis) absorption detection techniques (<xref ref-type="bibr" rid="B57">Zhang et al., 2019</xref>; <xref ref-type="bibr" rid="B39">Parveen et al., 2017</xref>; <xref ref-type="bibr" rid="B38">Moo et al., 2016</xref>). Surface-enhanced Raman spectroscopy also offers large linear detection ranges spanning multiple orders of magnitude and low limits of detection of ppm or sub ppm (<xref ref-type="bibr" rid="B15">Gajaraj et al., 2013</xref>; <xref ref-type="bibr" rid="B29">Li et al., 2024</xref>). While these measurements take only milliseconds, have very low detection limits, and are highly reproducible, they require expensive optical systems and calibration training.</p>
</sec>
<sec id="s3-3">
<title>3.3 Biological</title>
<p>Biosensors based on nitrate reductase (NR) enzymes can detect nitrate with high specificity and sensitivity at neutral pH through adsorption onto electrodes. The primary drawbacks of NR sensors are their high cost and the low temperature required for storage (<xref ref-type="bibr" rid="B47">Singh et al., 2022</xref>). Some methods for improving the sensitivity and stability of NR sensors through biological enhancements include incorporating NR from plants and fungi (<xref ref-type="bibr" rid="B22">Kalimuthu et al., 2015</xref>; <xref ref-type="bibr" rid="B23">Kalimuthu et al., 2021</xref>), combining biosensing elements with nanomaterials such as carbon nanotubes and zinc oxide (ZnO) nanostructures (<xref ref-type="bibr" rid="B6">Can et al., 2012</xref>; <xref ref-type="bibr" rid="B2">Ahmad et al., 2017</xref>), and utilizing whole-cell organisms (<xref ref-type="bibr" rid="B34">Machado et al., 2022</xref>). While nanomaterials can improve the capabilities of biological nanosensors, enzymatic sensors are still susceptible to degradation under environmental conditions (<xref ref-type="bibr" rid="B47">Singh et al., 2022</xref>). To overcome the limitations of enzymatic sensors, there is a need for more research focused on developing novel designs and synthesis methods that can minimize degradation under environmental conditions.</p>
</sec>
<sec id="s3-4">
<title>3.4 Electrical</title>
<p>While potentiometric and optical sensors have very low detection limits, they require sample preparation including pH balance and control calibration. New chemiresistors, capacitors, and FETs avoid these problems, showing great aptitude as nitrate detectors largely due to their &#x2018;lab-on-a-chip&#x2019; design. In one recent study, graphene nanowire was created by melting high density polyethylene (HDPE) between two bulk Cu contacts. By measuring current-voltage response, nitrate concentrations between 50&#x2013;5,000&#xa0;ppm were successfully determined (<xref ref-type="bibr" rid="B3">Ahmadi et al., 2021</xref>). FETs in particular can provide extremely low detection limits (45&#xa0;ppb) with no interfering species (<xref ref-type="bibr" rid="B37">Minami et al., 2016</xref>). By replacing the gate metal on a standard FET with a nitrate sensing material, researchers created chemically sensitive FETs (CHEMFETs) in the early 1970s (<xref ref-type="bibr" rid="B21">Janata, 2022</xref>). The amount of nitrate present modulates the electric field in the gate, changing current flow across the device. As in all transistors, various forms of CHEMFETs allow minute field changes in the gate to produce large currents through the device. This sensitivity allowed for ppb detection in some ion selective FETs (ISFETs) and organic FETs (OFETs) over the past decade (<xref ref-type="bibr" rid="B37">Minami et al., 2016</xref>; <xref ref-type="bibr" rid="B25">Kim et al., 2020a</xref>). Other ISFETs have used nitrate selective membranes on chemical vapor deposited graphene and nitrone coated polyvinyl chloride for detection with impressive results (<xref ref-type="bibr" rid="B26">Kim et al., 2020b</xref>; <xref ref-type="bibr" rid="B7">Chaisriratanakul et al., 2020</xref>). These electrical sensors can easily be integrated into &#x2018;internet of things&#x2019; devices and are likely to see largescale field deployment with wireless data communication (<xref ref-type="bibr" rid="B1">Agir et al., 2021</xref>; <xref ref-type="bibr" rid="B4">Alahi et al., 2018</xref>).</p>
</sec>
</sec>
<sec id="s4">
<title>4 Considerations for the transition from lab to field</title>
<p>Contemporary laboratory sensors address some of the challenges with existing field methods, but there are additional considerations with their transition from the lab to field. Most novel sensors in the scientific literature remain at the proof-of-concept stage, with emphasis on unique materials or interesting transduction mechanisms. Integrating the transduction, signal acquisition/processing/conditioning, and power supply is a secondary step that takes time, money, and effort that is not typically rewarded in the academic world. Packaging the integrated sensor system to make it useable and resilient in the environment is a tertiary step which can sometimes involve innovation (e.g., creative geometry, filters, or other features for specific environmental sampling challenges). An additional hurdle to field implementation is that the end user of the device is important to consider ensuring the need and relevancy of a device. This translates to more time and effort for researchers to consult with users early in the development period. While each category of sensor has specific strengths and weaknesses, researchers need to consider form factor, operational robustness, cost, user interface, and sensitivity (FOCUS) during development if the gap between the lab and field is to be bridged.</p>
<sec id="s4-1">
<title>4.1 Form factor</title>
<p>Different user groups will have different requirements relating to form factor (i.e., size, shape, and other physical considerations). Limnologists or oceanographers will likely find a device that falls into the probe or sonde category, as something 2-liter bottle sized, amenable to their needs, while a community member or farmer interested in well water testing will likely be interested in something less bulky. The nanomaterial-based sensors described previously in this paper all contain small components. However, the sensors integrated system can exist across a wide range of device sizes. The addition of extra components and detectors can hamper portability, and the devices best suited for small form factors would be those that have integrated readout electronics (and display) on the sensor, and do not rely on bulky external components to read results. The intended audience and uses of device, along with the necessary system components, will play a large part in shaping the appropriate form factor of the device.</p>
</sec>
<sec id="s4-2">
<title>4.2 Operational robustness</title>
<p>Device robustness is important to consider during the development as this will affect the appropriate uses and audience. The robustness of a sensor is important for technical applications like wastewater testing and extended field sampling events by scientists and water managers. Factors such as the length of time until failure, number of measurements until required calibration or maintenance, structural suitability for long term deployment, and accuracy, precision, and sensitivity with time all compose the idea of robustness. These factors will need to be investigated in different capacities depending on the intended application. Sensors based on nanomaterials, such as nanotubes and nanoparticles deposited on electrodes, show promise with respect to resistance to structural damage and chemical degradation, as such devices could still function if a certain portion of the nanomaterial is damaged or degraded. Other users of nitrate sensing devices may not require the same level of robustness, and sensors that excel in alternative categories may be more appropriate. Electrical FET sensors based on a single sheet of nanomaterials are among the least robust with respect to structural damage and chemical degradation, as damage of the nanomaterial can easily render the device unusable. In general, the anticipated device users need to be consulted regarding electrical FET design and packaging, as these devices are among the most sensitive.</p>
</sec>
<sec id="s4-3">
<title>4.3 Cost</title>
<p>Cost is an important consideration in the development of any device, although there is a market for nitrate sensing devices that span a broad price spectrum. Scientists and wastewater managers may need relatively expensive sensors, driven by requirements for low detection limits and high precision. In contrast, community-based science projects or water monitoring will likely require more affordable sensor options with detection limits and precision being less of an integral issue. Spatiotemporal coverage issues will also play a role in dictating the appropriate price point. If a scientific or regulatory question required occasional sampling or sampling in only one place, then devices that are expensive but reliable and rugged would be appropriate. Other applications may be willing to sacrifice accuracy and precision for smallness and inexpensiveness because of the need to deploy many sensors at one time. While it can be difficult to discern the exact cost of a device still in a proof-of-concept stage, the overall cost can be estimated with the given components. Sensors containing integrated electronic readout circuitry, which can be mass-produced, would end up being more cost effective than those requiring additional equipment for every single measurement. Additionally, sensors requiring materials that are easy to procure in scalable quantities or are commercially available would lend themselves to a lower final cost. A variety of devices across a price continuum are needed to meet the unique needs of users related to nitrate sensing.</p>
</sec>
<sec id="s4-4">
<title>4.4 User interface</title>
<p>Much of the literature surrounding the development of nitrate sensors neglects the user interface, but the usability and interfacing of a device is important for its transition to the field. Although some work does consider the user interface (<xref ref-type="bibr" rid="B1">Agir et al., 2021</xref>; <xref ref-type="bibr" rid="B4">Alahi et al., 2018</xref>), the majority of current devices fail to mention the user experience or the collection of data by a new user in the field. The difficulty and complexity of interface should reflect the intended audience a. The interface for scientists could include more data options and even statistics, while an interface for the general public should be simple, possibly even including easy to interpret colors and icons to be usable across literacy and languages. A major expense associated with sensors installed in the environment is associated with operation and maintenance (e.g., checking, resetting, and recalibrating) in the field because of the travel time and human hours expended. Thus, technicians, interns, and students often fulfill these duties, and the user interface needs to consider the appropriate complexity for people at these career and educational stages. In order to complete a transition from a laboratory tested device to a field utilized product, data and results must be available to the users of the sensors and therefore user interface must be considered.</p>
</sec>
<sec id="s4-5">
<title>4.5 Sensitivity</title>
<p>The necessary sensitivity of a device is directly related to the purpose of the sensing effort. Falling within the category of sensitivity are also important considerations of accuracy, precision, and reproducibility. Sensitivity is important for ecological applications in less impacted areas, especially in cases like alpine lake ecology monitoring, or in the low nitrate concentrations of the open ocean. Accuracy and reproducibility are critical in regulatory situations, which are typically associated with human-impacted areas and therefore less likely to need low detection limits. Instead, they need reliable measurements which can meet regulatory standards and legally binding agreements. Less precise sensors can also still be relevant to community science projects or personal home monitoring, such as a sensor that simply indicates the presence or absence of nitrate to the user. Electrical devices that are 2-dimensional material-based FET sensors may be among the sensors that can provide the best sensitivity in the low ppb range, however the consumer and intended use are important to consider when developing highly sensitive devices. Future work will need to consider the tradeoffs between sensitivity, accuracy, and robustness and would benefit from a comprehensive evaluation of the device and user.</p>
</sec>
<sec id="s4-6">
<title>4.6 The FOCUS parameter space</title>
<p>To link prospective nitrate sensors to users, we identified four broad user groups: wastewater managers, farmers, scientists, and community members. For each user, we assigned numerical scores to each FOCUS parameter on the scale of 1&#x2013;5, where one is least important to the user and five the most, and plotted these in <xref ref-type="fig" rid="F2">Figure 2A</xref>. Wastewater managers prioritize operational robustness (O &#x3d; 5) the most because monitoring systems must function reliably in harsh environments with varying conditions. Sensitivity (S &#x3d; 4) follows next as accurate measurements are needed to ensure regulatory compliance and early detection of relevant issues. Cost (C &#x3d; 3) takes middle priority as while budgets matter, reliable equipment justifies higher expenses. User interface (U &#x3d; 2) is less critical since staff are trained in complex systems, and form factor (F &#x3d; 1) ranks lowest as treatment plants have adequate installation space. Scientists place S highest because research demands precise, reliable data for experimental validity. U is also crucial for detailed control over measurements and comprehensive data access. O ranks third as scientists work in a mix of controlled and uncontrolled environments, while F is less important as lab setups are adaptable to research needs and end goals. C ranks lowest because most scientists value data quality data over quantity, justifying higher equipment expenses. This contrasts with farmers, whose priorities center on practical and economic factors, with C ranking highest. O follows next as their equipment must withstand outdoor conditions and physical impacts. F and U share lower priority. While portability and ease of use matter, they are secondary to cost and robustness. S ranks lowest since basic accuracy typically meets agricultural monitoring needs. Community members prioritize C as the main barrier to adoption in voluntary monitoring situations. U ranks second as systems must be accessible without technical training, while F takes middle priority to as portability and power needs are often important for community engaged sampling. O ranks lower as short-term durability often suffices for citizen groups, and S is least important since community monitoring typically emphasizes large numbers of less precise data.</p>
<fig id="F2" position="float">
<label>FIGURE 2</label>
<caption>
<p>The concept of FOCUS. <bold>(A)</bold> The five FOCUS metrics with allocated numerical values for four likely groups of users highlight their varied needs. <bold>(B)</bold> Principal Component Analysis of the relevant citations as a bubble plot showing three distinct clusters (1&#x2013;3). The data are mapped onto two principal components (PC1 and PC2), with bubble sizes proportional to cluster membership. The specific works that aligned with each end user group are indicated in the vicinity of their clusters by the citation numbers.</p>
</caption>
<graphic xlink:href="fsens-06-1513701-g002.tif"/>
</fig>
<p>We applied the FOCUS analysis to all relevant sensors cited in this perspective (<xref ref-type="sec" rid="s12">Supplementary Figure S-2</xref>). The analysis of the entire dataset of 37 entries indicates that U and S show a clear and consistent negative correlation (<xref ref-type="sec" rid="s12">Supplementary Figure S-3</xref>). This reflects a fundamental design challenge: Highly sensitive sensors require more complex controls, calibration options, and detailed readouts, which lead to less user-friendly interfaces. The relationship demonstrates the inherent challenge of balancing sophisticated measurement capabilities with user friendliness. We performed a cluster analysis on the FOCUS ratings and, as shown in <xref ref-type="fig" rid="F2">Figure 2B</xref>, it reveals three clusters. We plot the results as functions of two principal components (PC1 and PC2), which is a dimensionality reduction technique to reduce the number of variables while preserving as much variance as possible in the data. PC1 is measuring a trade-off between sensitivity/operational robustness <italic>versus</italic> user interface/form factor, while PC2 compares cost/form factor <italic>versus</italic> operational robustness. Cluster 1, with positive PC1 and PC2 values, is a collection of sensors with high sensitivity, good operational robustness, strong form factors, but more complicated user interface and higher cost. Cluster two includes sensors that have moderate scores across the FOCUS board, while cluster three comprises sensors with strong operational robustness at lower cost.</p>
<p>Next, we performed a similarity analysis to find which of the 37 entries align best with preferences of each of the end users, based on the profiles for them in <xref ref-type="fig" rid="F2">Figure 2A</xref>. Our results implementing a recommendation system based on cosine similarity reveals the best matches for each user type and are indicated in <xref ref-type="fig" rid="F2">Figure 2B</xref> relative to the three main clusters. <xref ref-type="bibr" rid="B15">Gajaraj et al. (2013)</xref> describes a SERS-based nitrate detection system using commercially available gold nano substrates. This scores highest for both wastewater management and scientific research, offering precision equivalent to ion chromatography, suitable detection range (1&#x2013;100&#xa0;mg/L), and reliability when faced with interfering compounds. Its quick analysis time, minimal preparation needs, and non-destructive approach support high-throughput monitoring and research requirements. Despite initial equipment costs, the lower per-test expenses and reduced preprocessing make it cost-effective for both routine wastewater testing and scientific studies.</p>
<p>However, while technically sophisticated, the SERS-based approach is less suitable for farmers and community members primarily due to its complexity and operational requirements. It demands complex sample preparation and advanced Raman spectroscopy instrumentation. While highly sensitive, its technical requirements added to high equipment costs make it impractical for non-technical users. Instead, we find the sensor described in <xref ref-type="bibr" rid="B2">Ahmad, et al. (2017)</xref> to be ideal for farmers, featuring durable zinc oxide nanorods for field conditions, rapid response time, and minimal sample preparation. The reported detection range suits agricultural needs, covering trace to excess nitrate levels. With proven reliability in real samples, interference resistance, and month-long stability, it enables quick on-site testing for timely fertilizer and irrigation decisions. And finally, <xref ref-type="bibr" rid="B34">Machado et al. (2022)</xref> describes the best sensor for community users, with affordable materials and simple construction, while also maintaining good sensitivity. Its cartridge-based design, minimal sample preparation, and Arduino-based system make it user-friendly for citizen scientists. With reliable reproducibility and real-time measurements, it enables effective community water monitoring without requiring technical expertise.</p>
</sec>
</sec>
<sec id="s5">
<title>5 Looking ahead</title>
<p>Nanomaterials are part of an exciting new era in sensor technology research and development, and there is a great opportunity for new field devices for sensing nitrate. A variety of sensors exist at the proof-of-concept stage, and different types of sensors excel and struggle under various categories within the FOCUS (form factor, operational robustness, cost, user interface, and sensitivity) framework. With the many possible applications of nitrate sensors, there is no single ideal sensor, instead the ideal is found in successfully meeting the needs of the intended application and user. Electrochemical sensors that are easy to use, low power, and inexpensive could be adequate for monitoring agricultural watersheds, where the limited range of detection overlaps typical field observations (e.g., <xref ref-type="bibr" rid="B40">Patella et al. (2021)</xref>). However, to our knowledge, the electrochemical nitrate sensing literature has yet to deeply explore critical FOCUS aspects like operational longevity. Similarly, the impressive detection ranges offered by spectroscopic approaches (e.g., <xref ref-type="bibr" rid="B29">Li et al. (2024)</xref>) begs for effort dedicated to lowering the cost of high precision optical components. Integrated lab-on-a-chip sensors can likely overcome these (and other) challenges by enabling self-calibration to extend the lifecycle and autonomy of electrochemical sensors or component miniaturization to reduce material costs. Such approaches are ripe for further developments in nano-enabled materials. As mentioned above, moving beyond the proof-of-concept stage requires attention to all FOCUS aspects, including system integration, power supply optimization, followed by environmental packaging and user interface design. These are steps that are often not rewarded or supported in the academic realm. It would prove beneficial to the field of sensing if funding bodies began investing in the connection of academia and industry to embrace the secondary and tertiary steps of full development, hardening, and environmental packaging. This cross-boundary collaboration, coupled with a new starting lens in research considering the target user first, could prove to be the push the field needs to revolutionize nitrate (and other) sensing technology.</p>
</sec>
</body>
<back>
<sec sec-type="data-availability" id="s6">
<title>Data availability statement</title>
<p>The original contributions presented in the study are included in the article/<xref ref-type="sec" rid="s12">Supplementary Material</xref>, further inquiries can be directed to the corresponding author.</p>
</sec>
<sec sec-type="author-contributions" id="s7">
<title>Author contributions</title>
<p>SD: Writing&#x2013;original draft, Writing&#x2013;review and editing. SE: Writing&#x2013;original draft, Writing&#x2013;review and editing. MP: Writing&#x2013;original draft, Writing&#x2013;review and editing. AC: Writing&#x2013;original draft, Writing&#x2013;review and editing. BB: Writing&#x2013;original draft, Writing&#x2013;review and editing. ZM: Writing&#x2013;original draft, Writing&#x2013;review and editing. RB: Writing&#x2013;original draft, Writing&#x2013;review and editing. SG: Writing&#x2013;original draft, Writing&#x2013;review and editing. TH: Writing&#x2013;original draft, Writing&#x2013;review and editing.</p>
</sec>
<sec sec-type="funding-information" id="s8">
<title>Funding</title>
<p>The author(s) declare that financial support was received for the research, authorship, and/or publication of this article. This work was funded by grant no. DGE-2125510 from the National Science Foundation.</p>
</sec>
<sec sec-type="COI-statement" id="s9">
<title>Conflict of interest</title>
<p>The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.</p>
</sec>
<sec sec-type="ai-statement" id="s10">
<title>Generative AI statement</title>
<p>The authors declare that no Generative AI was used in the creation of this manuscript.</p>
</sec>
<sec sec-type="disclaimer" id="s11">
<title>Publisher&#x2019;s note</title>
<p>All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.</p>
</sec>
<sec id="s12">
<title>Supplementary material</title>
<p>The Supplementary Material for this article can be found online at: <ext-link ext-link-type="uri" xlink:href="https://www.frontiersin.org/articles/10.3389/fsens.2025.1513701/full#supplementary-material">https://www.frontiersin.org/articles/10.3389/fsens.2025.1513701/full&#x23;supplementary-material</ext-link>
</p>
<supplementary-material xlink:href="DataSheet1.docx" id="SM1" mimetype="application/docx" xmlns:xlink="http://www.w3.org/1999/xlink"/>
</sec>
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