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Journal ArticleDOI

Extremely Stretchable, Stable, and Durable Strain Sensors Based on Double-Network Organogels.

29 Aug 2018-ACS Applied Materials & Interfaces (American Chemical Society)-Vol. 10, Iss: 38, pp 32640-32648
TL;DR: This work provided a new elastic matrix platform for the fabrication of extremely stretchable, stable, and durable strain sensors, which could be further extended to the practical applications in electronic skin, human-machine interactions, and personalized health monitoring.
Abstract: Stretchable strain sensors offer great potential for diverse applications in modern electronics. However, it is still difficult to fabricate strain sensors with extreme stretchability, high stability, and superior durability because of the challenge in elastic matrix. In this work, the first example of extremely stretchable and highly stable double-networks ethylene glycol (EG) organogel is developed for the fabrication of wearable strain sensors with high performances. It is shown that the formation of hybrid physically and chemically cross-linked double-networks endows the EG organogel with an extraordinarily stretchability as high as 21 000%, which is the highest value for gels reported in the literature. Meanwhile, the low vapor pressure of EG gives the organogel high ambient stability. Benefiting from the intrinsic stretchability and stability of EG organogel, the strain sensors are fabricated easily by incorporating graphene as electrically conductive filler, which display extremely wide strain-sens...
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Journal ArticleDOI
TL;DR: This review summarizes the latest advances in this emerging field of "bio-integrated" technologies in a comprehensive manner that connects fundamental developments in chemistry, material science, and engineering with sensing technologies that have the potential for widespread deployment and societal benefit in human health care.
Abstract: Bio-integrated wearable systems can measure a broad range of biophysical, biochemical, and environmental signals to provide critical insights into overall health status and to quantify human performance. Recent advances in material science, chemical analysis techniques, device designs, and assembly methods form the foundations for a uniquely differentiated type of wearable technology, characterized by noninvasive, intimate integration with the soft, curved, time-dynamic surfaces of the body. This review summarizes the latest advances in this emerging field of “bio-integrated” technologies in a comprehensive manner that connects fundamental developments in chemistry, material science, and engineering with sensing technologies that have the potential for widespread deployment and societal benefit in human health care. An introduction to the chemistries and materials for the active components of these systems contextualizes essential design considerations for sensors and associated platforms that appear in f...

727 citations

Journal ArticleDOI
TL;DR: In this article, a conductive nanocomposite hydrogel comprised of oxidized multi-walled carbon nanotubes (oxCNTs) and polyacrylamide (PAAm) is developed.

268 citations

Journal ArticleDOI
TL;DR: This work provides new insight into the fabrication of stable, ultrastretchable, and ultrasensitive strain sensors using chemically modified organohydrogel for emerging wearable electronics.
Abstract: Ionic hydrogels, a class of intrinsically stretchable and conductive materials, are widely used in soft electronics. However, the easy freezing and drying of water-based hydrogels significantly limit their long-term stability. Here, a facile solvent-replacement strategy is developed to fabricate ethylene glycol (Eg)/glycerol (Gl)-water binary antifreezing and antidrying organohydrogels for ultrastretchable and sensitive strain sensing within a wide temperature range. Because of the ready formation of strong hydrogen bonds between Eg/Gl and water molecules, the organohydrogels gain exceptional freezing and drying tolerance with retained deformability, conductivity, and self-healing ability even stay at extreme temperature for a long time. Thus, the fabricated strain sensor displays a gauge factor of 6, which is much higher than previously reported values for hydrogel-based strain sensors. Furthermore, the strain sensor exhibits a relatively wide strain range (0.5-950%) even at -18 °C. Various human motions with different strain levels are monitored by the strain sensor with good stability and repeatability from -18 to 25 °C. The organohydrogels maintained the strain sensing capability when exposed to ambient air for nine months. This work provides new insight into the fabrication of stable, ultrastretchable, and ultrasensitive strain sensors using chemically modified organohydrogel for emerging wearable electronics.

260 citations

Journal ArticleDOI
TL;DR: Graphene-based sensors used for human health monitoring, their novel structures, sensing mechanisms, technological innovations, components for sensor systems and potential challenges will be discussed and outlined.
Abstract: Since the desire for real-time human health monitoring as well as seamless human-machine interaction is increasing rapidly, plenty of research efforts have been made to investigate wearable sensors and implantable devices in recent years. As a novel 2D material, graphene has aroused a boom in the field of sensor research around the world due to its advantages in mechanical, thermal, and electrical properties. Numerous graphene-based sensors used for human health monitoring have been reported, including wearable sensors, as well as implantable devices, which can realize the real-time measurement of body temperature, heart rate, pulse oxygenation, respiration rate, blood pressure, blood glucose, electrocardiogram signal, electromyogram signal, and electroencephalograph signal, etc. Herein, as a review of the latest graphene-based sensors for health monitoring, their novel structures, sensing mechanisms, technological innovations, components for sensor systems and potential challenges will be discussed and outlined.

205 citations

References
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Journal ArticleDOI
06 Sep 2012-Nature
TL;DR: The synthesis of hydrogels from polymers forming ionically and covalently crosslinked networks is reported, finding that these gels’ toughness is attributed to the synergy of two mechanisms: crack bridging by the network of covalent crosslinks, and hysteresis by unzipping thenetwork of ionic crosslinks.
Abstract: Hydrogels with improved mechanical properties, made by combining polymer networks with ionic and covalent crosslinks, should expand the scope of applications, and may serve as model systems to explore mechanisms of deformation and energy dissipation. Hydrogels are used in flexible contact lenses, as scaffolds for tissue engineering and in drug delivery. Their poor mechanical properties have so far limited the scope of their applications, but new strong and stretchy materials reported here could take hydrogels into uncharted territories. The new system involves a double-network gel, with one network forming ionic crosslinks and the other forming covalent crosslinks. The fracture energy of these materials is very high: they can stretch to beyond 17 times their own length even when containing defects that usually initiate crack formation in hydrogels. The materials' toughness is attributed to crack bridging by the covalent network accompanied by energy dissipation through unzipping of the ionic crosslinks in the second network. Hydrogels are used as scaffolds for tissue engineering1, vehicles for drug delivery2, actuators for optics and fluidics3, and model extracellular matrices for biological studies4. The scope of hydrogel applications, however, is often severely limited by their mechanical behaviour5. 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 hydrogels6,7 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 cartilage9 and ∼10,000 J m−2 for natural rubbers10. Intense efforts are devoted to synthesizing hydrogels with improved mechanical properties11,12,13,14,15,16,17,18; 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.

3,856 citations

Journal ArticleDOI
28 Jan 2016-Nature
TL;DR: This work bridges the technological gap between signal transduction, conditioning, processing and wireless transmission in wearable biosensors by merging plastic-based sensors that interface with the skin with silicon integrated circuits consolidated on a flexible circuit board for complex signal processing.
Abstract: Wearable sensor technologies are essential to the realization of personalized medicine through continuously monitoring an individual's state of health. Sampling human sweat, which is rich in physiological information, could enable non-invasive monitoring. Previously reported sweat-based and other non-invasive biosensors either can only monitor a single analyte at a time or lack on-site signal processing circuitry and sensor calibration mechanisms for accurate analysis of the physiological state. Given the complexity of sweat secretion, simultaneous and multiplexed screening of target biomarkers is critical and requires full system integration to ensure the accuracy of measurements. Here we present a mechanically flexible and fully integrated (that is, no external analysis is needed) sensor array for multiplexed in situ perspiration analysis, which simultaneously and selectively measures sweat metabolites (such as glucose and lactate) and electrolytes (such as sodium and potassium ions), as well as the skin temperature (to calibrate the response of the sensors). Our work bridges the technological gap between signal transduction, conditioning (amplification and filtering), processing and wireless transmission in wearable biosensors by merging plastic-based sensors that interface with the skin with silicon integrated circuits consolidated on a flexible circuit board for complex signal processing. This application could not have been realized using either of these technologies alone owing to their respective inherent limitations. The wearable system is used to measure the detailed sweat profile of human subjects engaged in prolonged indoor and outdoor physical activities, and to make a real-time assessment of the physiological state of the subjects. This platform enables a wide range of personalized diagnostic and physiological monitoring applications.

3,235 citations

Journal ArticleDOI
TL;DR: Transparent, conducting spray-deposited films of single-walled carbon nanotubes are reported that can be rendered stretchable by applying strain along each axis, and then releasing this strain.
Abstract: Transparent films of carbon nanotubes can accommodate strains of up to 150% and demonstrate conductivities as high as 2,200 S cm−1 in the stretched state.

2,847 citations

Journal ArticleDOI
TL;DR: Flexible, capacitive pressure sensors with unprecedented sensitivity and very short response times that can be inexpensively fabricated over large areas by microstructuring of thin films of the biocompatible elastomer polydimethylsiloxane are demonstrated.
Abstract: The development of an electronic skin is critical to the realization of artificial intelligence that comes into direct contact with humans, and to biomedical applications such as prosthetic skin. To mimic the tactile sensing properties of natural skin, large arrays of pixel pressure sensors on a flexible and stretchable substrate are required. We demonstrate flexible, capacitive pressure sensors with unprecedented sensitivity and very short response times that can be inexpensively fabricated over large areas by microstructuring of thin films of the biocompatible elastomer polydimethylsiloxane. The pressure sensitivity of the microstructured films far surpassed that exhibited by unstructured elastomeric films of similar thickness, and is tunable by using different microstructures. The microstructured films were integrated into organic field-effect transistors as the dielectric layer, forming a new type of active sensor device with similarly excellent sensitivity and response times.

2,627 citations

Journal ArticleDOI
Morteza Amjadi1, Aekachan Pichitpajongkit1, Sangjun Lee1, Seunghwa Ryu1, Inkyu Park1 
29 Apr 2014-ACS Nano
TL;DR: The applicability of the high performance strain sensors based on the nanocomposite of silver nanowire network and PDMS elastomer in the form of the sandwich structure is demonstrated by fabricating a glove integrated with five strain sensors for the motion detection of fingers and control of an avatar in the virtual environment.
Abstract: The demand for flexible and wearable electronic devices is increasing due to their facile interaction with human body. Flexible, stretchable and wearable sensors can be easily mounted on clothing or directly attached onto the body. Especially, highly stretchable and sensitive strain sensors are needed for the human motion detection. Here, we report highly flexible, stretchable and sensitive strain sensors based on the nanocomposite of silver nanowire (AgNW) network and PDMS elastomer in the form of the sandwich structure (i.e., AgNW thin film embedded between two layers of PDMS). The AgNW network-elastomer nanocomposite based strain sensors show strong piezoresistivity with tunable gauge factors in the ranges of 2 to 14 and a high stretchability up to 70%. We demonstrate the applicability of our high performance strain sensors by fabricating a glove integrated with five strain sensors for the motion detection of fingers and control of an avatar in the virtual environment.

1,837 citations