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      Hydrogel- and organohydrogel-based stretchable, ultrasensitive, transparent, room-temperature and real-time NO 2 sensors and the mechanism

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          Abstract

          Highly stretchable, transparent, ultrasensitive, selective and room-temperature NO 2 sensors are created by using ion-conductive hydrogels/organohydrogels. The electrodes play a key role in sensing performances and NO 2 tend to react at the cathode.

          Abstract

          Highly stretchable, sensitive and room-temperature nitrogen dioxide (NO 2) sensors are fabricated by exploiting intrinsically stretchable, transparent and ion-conducting hydrogels and active metals as the novel transducing materials and electrodes, respectively. The NO 2 sensor exhibits high sensitivity (60.02% ppm −1), ultralow theoretical limit of detection (6.8 ppb), excellent selectivity, linearity and reversibility at room temperature. Notably, the sensitivity can be maintained even under 50% tensile strain. For the first time, it's found that the metal electrodes significantly impact the sensing performance. Specifically, the sensitivity is boosted from 31.18 to 60.02% ppm −1 by replacing the anodic silver with copper–tin alloy. Importantly, by applying specially designed sensing tests, and microscopic and composition analyses, we have obtained the inherent NO 2 sensing mechanism: the anodic metal tends to be oxidized and the NO 2 molecules tend to react in the cathode–gel interface. The introduction of glycerol converts the hydrogel into the organohydrogel with remarkably enhanced anti-drying and anti-freezing capacities and toughness, which effectively improved the long-time stability of the sensors. Importantly, we execute sound/light alarms and a wireless smartphone alarm by utilizing a designed circuit board and applet. This work gives an incisive investigation for the preparation, performance improvement, mechanism and application of hydrogel-based NO 2 sensors, promoting the evolution of hydrogel ionotronics.

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          Most cited references48

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          Highly stretchable and tough hydrogels.

          Hydrogels are used as scaffolds for tissue engineering, vehicles for drug delivery, actuators for optics and fluidics, and model extracellular matrices for biological studies. The scope of hydrogel applications, however, is often severely limited by their mechanical behaviour. Most hydrogels do not exhibit high stretchability; for example, an alginate hydrogel ruptures when stretched to about 1.2 times its original length. Some synthetic elastic hydrogels have achieved stretches in the range 10-20, but these values are markedly reduced in samples containing notches. Most hydrogels are brittle, with fracture energies of about 10 J m(-2) (ref. 8), as compared with ∼1,000 J m(-2) for cartilage and ∼10,000 J m(-2) for natural rubbers. Intense efforts are devoted to synthesizing hydrogels with improved mechanical properties; certain synthetic gels have reached fracture energies of 100-1,000 J m(-2) (refs 11, 14, 17). Here we report the synthesis of hydrogels from polymers forming ionically and covalently crosslinked networks. Although such gels contain ∼90% water, they can be stretched beyond 20 times their initial length, and have fracture energies of ∼9,000 J m(-2). Even for samples containing notches, a stretch of 17 is demonstrated. We attribute the gels' toughness to the synergy of two mechanisms: crack bridging by the network of covalent crosslinks, and hysteresis by unzipping the network of ionic crosslinks. Furthermore, the network of covalent crosslinks preserves the memory of the initial state, so that much of the large deformation is removed on unloading. The unzipped ionic crosslinks cause internal damage, which heals by re-zipping. These gels may serve as model systems to explore mechanisms of deformation and energy dissipation, and expand the scope of hydrogel applications.
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            Hydrogel ionotronics

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              Highly stretchable, transparent ionic touch panel.

              Because human-computer interactions are increasingly important, touch panels may require stretchability and biocompatibility in order to allow integration with the human body. However, most touch panels have been developed based on stiff and brittle electrodes. We demonstrate an ionic touch panel based on a polyacrylamide hydrogel containing lithium chloride salts. The panel is soft and stretchable, so it can sustain a large deformation. The panel can freely transmit light information because the hydrogel is transparent, with 98% transmittance for visible light. A surface-capacitive touch system was adopted to sense a touched position. The panel can be operated under more than 1000% areal strain without sacrificing its functionalities. Epidermal touch panel use on skin was demonstrated by writing words, playing a piano, and playing games.
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                Author and article information

                Contributors
                Journal
                MHAOAL
                Materials Horizons
                Mater. Horiz.
                Royal Society of Chemistry (RSC)
                2051-6347
                2051-6355
                July 04 2022
                2022
                : 9
                : 7
                : 1921-1934
                Affiliations
                [1 ]State Key Laboratory of Optoelectronic Materials and Technologies and the Guangdong Province Key Laboratory of Display Material and Technology, School of Electronics and Information Technology, Sun Yat-sen University, Guangzhou 510275, China
                [2 ]National Engineering Research Center of Novel Equipment for Polymer Processing, Key Laboratory of Polymer Processing Engineering (SCUT), Ministry of Education, South China University of Technology, Guangzhou, 510641, China
                [3 ]Ministry of Education Key Laboratory of Micro and Nano Systems for Aerospace, Northwestern Polytechnical University, Xi’an 710072, China
                Article
                10.1039/D2MH00284A
                35535754
                266d8a67-b58f-431b-b556-4e6bad971634
                © 2022

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

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