Functionalized graphene reinforced thermoplastic nanocomposites as strain sensors in structural health monitoring
16 Aug 2011-Journal of Materials Chemistry (The Royal Society of Chemistry)-Vol. 21, Iss: 34, pp 12626-12628
TL;DR: In this article, a real-time strain response of functionalized graphene-polyvinylidene fluoride (f-G-PVDF) nanocomposite films was demonstrated under tensile loads.
Abstract: Functionalized graphene–polyvinylidene fluoride (f-G–PVDF) nanocomposite films were synthesized using a simple solvent casting technique. The investigation demonstrates the real time strain response of f-G–PVDF nanocomposites on the macro-scale under tensile loads and the use of this nanocomposite as strain sensor. This is ascribed to the variation of electrical properties of graphene–polymer upon mechanical deformation at the nanoscale.
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TL;DR: In this paper, the current status of the intrinsic mechanical properties of the graphene-family of materials along with the preparation and properties of bulk graphene-based nanocomposites is thoroughly examined.
1,531 citations
Cites background from "Functionalized graphene reinforced ..."
...Additionally, there are reports of the use of graphene as strain sensor in bulk composites, such as woven fabrics [197–199], elastomers [200–202], thermoplastics [203] and hybrids [204]....
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TL;DR: A simple method to infuse liquid-exfoliated graphene into natural rubber to create conducting composites is described, which are excellent strain sensors displaying 10(4)-fold increases in resistance and working at strains exceeding 800%.
Abstract: Monitoring of human bodily motion requires wearable sensors that can detect position, velocity and acceleration. They should be cheap, lightweight, mechanically compliant and display reasonable sensitivity at high strains and strain rates. No reported material has simultaneously demonstrated all the above requirements. Here we describe a simple method to infuse liquid-exfoliated graphene into natural rubber to create conducting composites. These materials are excellent strain sensors displaying 10(4)-fold increases in resistance and working at strains exceeding 800%. The sensitivity is reasonably high, with gauge factors of up to 35 observed. More importantly, these sensors can effectively track dynamic strain, working well at vibration frequencies of at least 160 Hz. At 60 Hz, we could monitor strains of at least 6% at strain rates exceeding 6000%/s. We have used these composites as bodily motion sensors, effectively monitoring joint and muscle motion as well and breathing and pulse.
667 citations
TL;DR: This work investigated graphene woven fabrics (GWFs) for strain sensing and investigated the main mechanism, resulting in a theoretical model that predicts very well the observed behavior.
Abstract: The use of nanomaterials for strain sensors has attracted attention due to their unique electromechanical properties. However, nanomaterials have yet to overcome many technological obstacles and thus are not yet the preferred material for strain sensors. In this work, we investigated graphene woven fabrics (GWFs) for strain sensing. Different than graphene films, GWFs undergo significant changes in their polycrystalline structures along with high-density crack formation and propagation mechanically deformed. The electrical resistance of GWFs increases exponentially with tensile strain with gauge factors of ~103 under 2~6% strains and ~106 under higher strains that are the highest thus far reported, due to its woven mesh configuration and fracture behavior, making it an ideal structure for sensing tensile deformation by changes in strain. The main mechanism is investigated, resulting in a theoretical model that predicts very well the observed behavior.
538 citations
TL;DR: In this article, the morphological control of conductive networks in conductive polymer composites (CPCs) has been extensively investigated as an important issue for the preparation of high performance CPCs.
525 citations
TL;DR: In this paper, carbon nanotubes (CNTs) and graphene bifillers were used to separate entangled CNTs from each other and the CNT bridged the broad gap between individual graphene sheets, which was beneficial for the dispersion of CNT and formation of effective conductive paths.
Abstract: Thermoplastic polyurethane (TPU) based conductive polymer composites (CPCs) with a reduced percolation threshold and tunable resistance–strain sensing behavior were obtained through the addition of synergistic carbon nanotubes (CNT) and graphene bifillers. The percolation threshold of graphene was about 0.006 vol% when the CNT content was fixed at 0.255 vol% that is below the percolation threshold of CNT/TPU nanocomposites. The synergistic effect between graphene and CNT was identified using the excluded volume theory. Graphene acted as a ‘spacer’ to separate the entangled CNTs from each other and the CNT bridged the broad gap between individual graphene sheets, which was beneficial for the dispersion of CNT and formation of effective conductive paths, leading to better electrical conductivity at a lower conductive filler content. Compared with the dual-peak response pattern of the CNT/TPU based strain sensors, the CPCs with hybrid conductive fillers displayed single-peak response patterns under small strain, indicating good tunability with the synergistic effect of CNT and graphene. Under larger strain, prestraining was adopted to regulate the conductive network, and better tunable single-peak response patterns were also obtained. The CPCs also showed good reversibility and reproductivity under cyclic extension. This study paves the way for the fabrication of CPC based strain sensors with good tunability.
444 citations
References
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TL;DR: Graphene is established as the strongest material ever measured, and atomically perfect nanoscale materials can be mechanically tested to deformations well beyond the linear regime.
Abstract: We measured the elastic properties and intrinsic breaking strength of free-standing monolayer graphene membranes by nanoindentation in an atomic force microscope. The force-displacement behavior is interpreted within a framework of nonlinear elastic stress-strain response, and yields second- and third-order elastic stiffnesses of 340 newtons per meter (N m(-1)) and -690 Nm(-1), respectively. The breaking strength is 42 N m(-1) and represents the intrinsic strength of a defect-free sheet. These quantities correspond to a Young's modulus of E = 1.0 terapascals, third-order elastic stiffness of D = -2.0 terapascals, and intrinsic strength of sigma(int) = 130 gigapascals for bulk graphite. These experiments establish graphene as the strongest material ever measured, and show that atomically perfect nanoscale materials can be mechanically tested to deformations well beyond the linear regime.
18,008 citations
TL;DR: The bottom-up chemical approach of tuning the graphene sheet properties provides a path to a broad new class of graphene-based materials and their use in a variety of applications.
Abstract: The remarkable mechanical properties of carbon nanotubes arise from the exceptional strength and stiffness of the atomically thin carbon sheets (graphene) from which they are formed. In contrast, bulk graphite, a polycrystalline material, has low fracture strength and tends to suffer failure either by delamination of graphene sheets or at grain boundaries between the crystals. Now Stankovich et al. have produced an inexpensive polymer-matrix composite by separating graphene sheets from graphite and chemically tuning them. The material contains dispersed graphene sheets and offers access to a broad range of useful thermal, electrical and mechanical properties. Individual sheets of graphene can be readily incorporated into a polymer matrix, giving rise to composite materials having potentially useful electronic properties. Graphene sheets—one-atom-thick two-dimensional layers of sp2-bonded carbon—are predicted to have a range of unusual properties. Their thermal conductivity and mechanical stiffness may rival the remarkable in-plane values for graphite (∼3,000 W m-1 K-1 and 1,060 GPa, respectively); their fracture strength should be comparable to that of carbon nanotubes for similar types of defects1,2,3; and recent studies have shown that individual graphene sheets have extraordinary electronic transport properties4,5,6,7,8. One possible route to harnessing these properties for applications would be to incorporate graphene sheets in a composite material. The manufacturing of such composites requires not only that graphene sheets be produced on a sufficient scale but that they also be incorporated, and homogeneously distributed, into various matrices. Graphite, inexpensive and available in large quantity, unfortunately does not readily exfoliate to yield individual graphene sheets. Here we present a general approach for the preparation of graphene-polymer composites via complete exfoliation of graphite9 and molecular-level dispersion of individual, chemically modified graphene sheets within polymer hosts. A polystyrene–graphene composite formed by this route exhibits a percolation threshold10 of ∼0.1 volume per cent for room-temperature electrical conductivity, the lowest reported value for any carbon-based composite except for those involving carbon nanotubes11; at only 1 volume per cent, this composite has a conductivity of ∼0.1 S m-1, sufficient for many electrical applications12. Our bottom-up chemical approach of tuning the graphene sheet properties provides a path to a broad new class of graphene-based materials and their use in a variety of applications.
11,866 citations
TL;DR: The use of colloidal suspensions to produce new materials composed of graphene and chemically modified graphene is reviewed, which is both versatile and scalable, and is adaptable to a wide variety of applications.
Abstract: Interest in graphene centres on its excellent mechanical, electrical, thermal and optical properties, its very high specific surface area, and our ability to influence these properties through chemical functionalization. There are a number of methods for generating graphene and chemically modified graphene from graphite and derivatives of graphite, each with different advantages and disadvantages. Here we review the use of colloidal suspensions to produce new materials composed of graphene and chemically modified graphene. This approach is both versatile and scalable, and is adaptable to a wide variety of applications.
6,178 citations
TL;DR: Modulus, ultimate strength and thermal stability follow a similar trend, with values for functionalized graphene sheet- poly(methyl methacrylate) rivaling those for single-walled carbon nanotube-poly(methyl methamphetamine) composites.
Abstract: Polymer-based composites were heralded in the 1960s as a new paradigm for materials. By dispersing strong, highly stiff fibres in a polymer matrix, high-performance lightweight composites could be developed and tailored to individual applications. Today we stand at a similar threshold in the realm of polymer nanocomposites with the promise of strong, durable, multifunctional materials with low nanofiller content. However, the cost of nanoparticles, their availability and the challenges that remain to achieve good dispersion pose significant obstacles to these goals. Here, we report the creation of polymer nanocomposites with functionalized graphene sheets, which overcome these obstacles and provide superb polymer-particle interactions. An unprecedented shift in glass transition temperature of over 40 degrees C is obtained for poly(acrylonitrile) at 1 wt% functionalized graphene sheet, and with only 0.05 wt% functionalized graphene sheet in poly(methyl methacrylate) there is an improvement of nearly 30 degrees C. Modulus, ultimate strength and thermal stability follow a similar trend, with values for functionalized graphene sheet- poly(methyl methacrylate) rivaling those for single-walled carbon nanotube-poly(methyl methacrylate) composites.
3,245 citations