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      Novel gas sensing platform based on a stretchable laser-induced graphene pattern with self-heating capabilities

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          Abstract

          Laser-induced graphene based gas sensor conformable to skin with low detection limit at low temperature.

          Abstract

          Measurements of the gas sensing performance of nanomaterials typically involve the use of interdigitated electrodes (IDEs). A separate heater is often integrated to provide elevated temperature for improved sensing performance. However, the use of IDEs and separate heaters increases fabrication complexity. Here, a novel gas sensing platform based on a highly porous laser-induced graphene (LIG) pattern is reported. The LIG gas sensing platform consists of a sensing region and a serpentine interconnect region. A thin film of metal ( e.g., Ag) coated in the serpentine interconnect region significantly reduces its resistance, thereby providing a localized Joule healing in the sensing region ( i.e., self-heating) during typical measurements of chemoresistive gas sensors. Dispersing nanomaterials with different selectivity in the sensing region results in an array to potentially deconvolute various gaseous components in the mixture. The self-heating of the LIG gas sensing platform is first studied as a function of the applied voltage during resistance measurement and LIG geometric parameters ( e.g., linewidth from 120 to 240 μm) to achieve an operating temperature from 20 to 80 °C. Systematic investigations of various nanomaterials demonstrate the feasibility of the LIG gas sensing performance. Taken together with the stretchable design layout in the serpentine interconnect region to provide mechanical robustness over a tensile strain of 20%, the gas sensor with a significant response (6.6‰ ppm −1), fast response/recovery processes, excellent selectivity, and an ultralow limit of detection (1.5 parts per billion) at a modest temperature from self-heating opens new opportunities in epidermal electronic devices.

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          Most cited references76

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          Laser-induced porous graphene films from commercial polymers

          Synthesis and patterning of carbon nanomaterials cost effectively is a challenge in electronic and energy storage devices. Here report a one-step, scalable approach for producing and patterning porous graphene films with 3-dimensional networks from commercial polymer films using a CO2 infrared laser. The sp3-carbon atoms are photothermally converted to sp2-carbon atoms by pulsed laser irradiation. The resulting laser-induced graphene (LIG) exhibits high electrical conductivity. The LIG can be readily patterned to interdigitated electrodes for in-plane microsupercapacitors with specific capacitances of >4 mF·cm−2 and power densities of ~9 mW·cm−2. Theoretical calculations partially suggest that enhanced capacitance may result from LIG’s unusual ultra-polycrystalline lattice of pentagon-heptagon structures. Combined with the advantage of one-step processing of LIG in air from commercial polymer sheets, which would allow the employment of a roll-to-roll manufacturing process, this technique provides a rapid route to polymer-written electronic and energy storage devices.
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            Practical chemical sensors from chemically derived graphene.

            We report the development of useful chemical sensors from chemically converted graphene dispersions using spin coating to create single-layer films on interdigitated electrode arrays. Dispersions of graphene in anhydrous hydrazine are formed from graphite oxide. Preliminary results are presented on the detection of NO(2), NH(3), and 2,4-dinitrotoluene using this simple and scalable fabrication method for practical devices. Current versus voltage curves are linear and ohmic in all cases, studied independent of metal electrode or presence of analytes. The sensor response is consistent with a charge transfer mechanism between the analyte and graphene with a limited role of the electrical contacts. A micro hot plate sensor substrate is also used to monitor the temperature dependence of the response to nitrogen dioxide. The results are discussed in light of recent literature on carbon nanotube and graphene sensors.
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              Flexible Graphene-Based Wearable Gas and Chemical Sensors.

              Wearable electronics is expected to be one of the most active research areas in the next decade; therefore, nanomaterials possessing high carrier mobility, optical transparency, mechanical robustness and flexibility, lightweight, and environmental stability will be in immense demand. Graphene is one of the nanomaterials that fulfill all these requirements, along with other inherently unique properties and convenience to fabricate into different morphological nanostructures, from atomically thin single layers to nanoribbons. Graphene-based materials have also been investigated in sensor technologies, from chemical sensing to detection of cancer biomarkers. The progress of graphene-based flexible gas and chemical sensors in terms of material preparation, sensor fabrication, and their performance are reviewed here. The article provides a brief introduction to graphene-based materials and their potential applications in flexible and stretchable wearable electronic devices. The role of graphene in fabricating flexible gas sensors for the detection of various hazardous gases, including nitrogen dioxide (NO2), ammonia (NH3), hydrogen (H2), hydrogen sulfide (H2S), carbon dioxide (CO2), sulfur dioxide (SO2), and humidity in wearable technology, is discussed. In addition, applications of graphene-based materials are also summarized in detecting toxic heavy metal ions (Cd, Hg, Pb, Cr, Fe, Ni, Co, Cu, Ag), and volatile organic compounds (VOCs) including nitrobenzene, toluene, acetone, formaldehyde, amines, phenols, bisphenol A (BPA), explosives, chemical warfare agents, and environmental pollutants. The sensitivity, selectivity and strategies for excluding interferents are also discussed for graphene-based gas and chemical sensors. The challenges for developing future generation of flexible and stretchable sensors for wearable technology that would be usable for the Internet of Things (IoT) are also highlighted.
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                Author and article information

                Journal
                JMCAET
                Journal of Materials Chemistry A
                J. Mater. Chem. A
                Royal Society of Chemistry (RSC)
                2050-7488
                2050-7496
                2020
                2020
                Affiliations
                [1 ]Hebei Key Laboratory of Robot Perception and Human-robot Interaction
                [2 ]School of Mechanical Engineering
                [3 ]Hebei University of Technology
                [4 ]Tianjin 300401
                [5 ]China
                [6 ]Department of Materials Science and Engineering
                [7 ]The Pennsylvania State University
                [8 ]University Park
                [9 ]USA
                [10 ]Department of Engineering Science and Mechanics
                [11 ]Department of Mechanical and Industrial Engineering
                [12 ]Northeastern University
                [13 ]Boston
                [14 ]Plant Fiber Research Center
                [15 ]Department of Chemical Engineering
                Article
                10.1039/C9TA07855J
                92aa3fce-bd6c-450b-904d-d931d89b3799
                © 2020

                http://rsc.li/journals-terms-of-use

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