skip to main content
US FlagAn official website of the United States government
dot gov icon
Official websites use .gov
A .gov website belongs to an official government organization in the United States.
https lock icon
Secure .gov websites use HTTPS
A lock ( lock ) or https:// means you've safely connected to the .gov website. Share sensitive information only on official, secure websites.


Title: Zero‐Power, Optical Toxic Gas and Vapor Sensors Utilizing Printed Nematic Liquid Crystal Patterns on Selectively Reactive Substrates
Abstract Health risks affiliated with exposure to a wide variety of toxic gases and vapors are a certainty for first responders such as firefighters and HAZMAT team members but also for countless other professions from water purification and chemical manufacturing to the oil and gas industry, among others, and even the general public. Here the fabrication and testing of several prototypes for a novel toxic gas sensor platform based on ink‐jet printed nematic liquid crystal patterns are described. These sensors require zero power to operate and are characterized by high sensitivity down to highly relevant ppm and ppb levels, fast response times on the order of seconds, improved durability, and an overall design that is highly customizable by the potential end user. The response times of these sensors exponentially decrease with toxic gas concentration, thereby establishing the toxic gas diffusivity dependence of their mode of action. Such prototypes for two particular toxic gases, chlorine, and phosgene, performing interference testing in high humidity and smoke conditions as well as field testing with active firefighters are demonstrated.  more » « less
Award ID(s):
2122421
PAR ID:
10575955
Author(s) / Creator(s):
 ;  ;  ;  ;  ;  ;  ;  ;  ;  
Publisher / Repository:
Wiley Blackwell (John Wiley & Sons)
Date Published:
Journal Name:
Advanced Sensor Research
Volume:
4
Issue:
6
ISSN:
2751-1219
Format(s):
Medium: X
Sponsoring Org:
National Science Foundation
More Like this
  1. null (Ed.)
    Toxic gases, such as NOx, SOx, H2S and other S-containing gases, cause numerous harmful effects on human health even at very low gas concentrations. Reliable detection of various gases in low concentration is mandatory in the fields such as industrial plants, environmental monitoring, air quality assurance, automotive technologies and so on. In this paper, the recent advances in electrochemical sensors for toxic gas detections were reviewed and summarized with a focus on NO2, SO2 and H2S gas sensors. The recent progress of the detection of each of these toxic gases was categorized by the highly explored sensing materials over the past few decades. The important sensing performance parameters like sensitivity/response, response and recovery times at certain gas concentration and operating temperature for different sensor materials and structures have been summarized and tabulated to provide a thorough performance comparison. A novel metric, sensitivity per ppm/response time ratio has been calculated for each sensor in order to compare the overall sensing performance on the same reference. It is found that hybrid materials-based sensors exhibit the highest average ratio for NO2 gas sensing, whereas GaN and metal-oxide based sensors possess the highest ratio for SO2 and H2S gas sensing, respectively. Recently, significant research efforts have been made exploring new sensor materials, such as graphene and its derivatives, transition metal dichalcogenides (TMDs), GaN, metal-metal oxide nanostructures, solid electrolytes and organic materials to detect the above-mentioned toxic gases. In addition, the contemporary progress in SO2 gas sensors based on zeolite and paper and H2S gas sensors based on colorimetric and metal-organic framework (MOF) structures have also been reviewed. Finally, this work reviewed the recent first principle studies on the interaction between gas molecules and novel promising materials like arsenene, borophene, blue phosphorene, GeSe monolayer and germanene. The goal is to understand the surface interaction mechanism. 
    more » « less
  2. This study presents the fabrication and characterization of highly selective, room-temperature gas sensors based on ternary zinc oxide–molybdenum disulfide–titanium dioxide (ZnO-MoS2-TiO2) nanoheterostructures. Integrating two-dimensional (2D) MoS2 with oxide nano materials synergistically combines their unique properties, significantly enhancing gas sensing performance. Comprehensive structural and chemical analyses, including scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy (EDX), Raman spectroscopy, and Fourier transform infrared spectroscopy (FTIR), confirmed the successful synthesis and composition of the ternary nanoheterostructures. The sensors demonstrated excellent selectivity in detecting low concentrations of nitrogen dioxide (NO2) among target gases such as ammonia (NH3), methane (CH4), and carbon dioxide (CO2) at room temperature, achieving up to 58% sensitivity at 4 ppm and 6% at 0.1 ppm for NO2. The prototypes demonstrated outstanding selectivity and a short response time of approximately 0.51 min. The impact of light-assisted enhancement was examined under 1 mW/cm2 weak ultraviolet (UV), blue, yellow, and red light-emitting diode (LED) illuminations, with the blue LED proving to deliver the highest sensor responsiveness. These results position ternary ZnO-MoS2-TiO2 nanoheterostructures as highly sensitive and selective room-temperature NO2 gas sensors that are suitable for applications in environmental monitoring, public health, and industrial processes. 
    more » « less
  3. Abstract This paper describes the use of a highly crystalline conductive 2D copper3(hexaiminobenzene)2(Cu3(HIB)2) as an ultrasensitive (limit of detection of 1.8 part‐per‐billion), highly selective, reversible, and low power chemiresistive sensor for nitric oxide (NO) at room temperature. The Cu3(HIB)2‐based sensors retain their sensing performance in the presence of humidity, and exhibit strong signal enhancement towards NO over other highly toxic reactive gases, such as NO2, H2S, SO2, NH3, CO, as well as CO2. Mechanistic investigations of the Cu3(HIB)2‐NO interaction through spectroscopic analyses and density functional theory revealed that the Cu‐bis(iminobenzosemiquinoid) moieties serve as the binding sites for NO sensing, while the Ni‐bis(iminobenzosemiquinoid) MOF analog shows no noticeable response to NO. Overall, these findings provide a significant advance in the development of crystalline metal‐bis(iminobenzosemiquinoid)‐based conductive 2D MOFs as highly sensitive, selective, and reversible sensing materials for the low‐power detection of toxic gases. 
    more » « less
  4. Different materials are studied for environmental gas sensors as well as photodetection prototypes. A ZnO/MoS2 p-n junction was synthetized to act as a multifunctional sensor prototype. After the ZnO was prepared on a silicon substrate by using DC sputtering at room temperature, molybdenum disulfide layers were spin-coated on a nanostructured zinc oxide flake-shaped surface to form an active layer. The heterostructure’s composite surface was examined using scanning electron microscopy, energy-dispersed X-ray, and Raman spectroscopy. Responses to light frequencies, light intensities, and gas chemical tracing were characterized, revealing an enhanced multifunctional performance of the prototype. Characterizations of light-induced photocurrents indicted that the obtained response strength (photocurrent/illumination light power) was up to 0.01 A/W, and the response time was less than 5 ms. In contrast, the gas-sensing measurements showed that its response strength (variation in resistance/original resistance) was up to 3.7% and the response time was down to 150 s when the prototype was exposed to ammonia gas, with the concentration down to 168 ppm. The fabricated prototype appears to have high stability and reproducibility, quick response and recovery times, as well as a high signal-to-noise ratio. 
    more » « less
  5. With the rapid growth of emerging point-of-use (POU)/point-of-care (POC) detection technologies, miniaturized sensors for the real-time detection of gases and airborne pathogens have become essential to fight pollution, emerging contaminants, and pandemics. However, the low-cost development of miniaturized gas sensors without compromising selectivity, sensitivity, and response time remains challenging. Microfluidics is a promising technology that has been exploited for decades to overcome such limitations, making it an excellent candidate for POU/POC. However, microfluidic-based gas sensors remain a nascent field. In this review, the evolution of microfluidic gas sensors from basic electronic techniques to more advanced optical techniques such as surface-enhanced Raman spectroscopy to detect analytes is documented in detail. This paper focuses on the various detection methodologies used in microfluidic-based devices for detecting gases and airborne pathogens. Non-continuous microfluidic devices such as bubble/droplet-based microfluidics technology that have been employed to detect gases and airborne pathogens are also discussed. The selectivity, sensitivity, advantages/disadvantages vis-a-vis response time, and fabrication costs for all the microfluidic sensors are tabulated. The microfluidic sensors are grouped based on the target moiety, such as air pollutants such as carbon monoxide and nitrogen oxides, and airborne pathogens such as E. coli and SARS-CoV-2. The possible application scenarios for the various microfluidic devices are critically examined. 
    more » « less