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While nanocomposite electromechanical sensors are expected to display reasonable conductivity and high sensitivity, little consideration is given to eliminating hysteresis and strain rate/frequency dependence from their response. For example, while G-putty, a composite of graphene and polysiloxane, has very high electromechanical sensitivity, its extreme viscoelasticity renders it completely unsuitable for real sensors due to hysteretic and rate-/frequency-dependent effects. Here it is shown that G-putty can be converted to an ink and printed into patterned thin films on elastic substrates. A partial graphene-polymer phase segregation during printing increases the thin-film conductivity by ×106 compared to bulk, while the mechanical effects of the substrate largely suppress hysteresis and completely remove strain rate and frequency dependence. This allows the fabrication of practical, high-gauge-factor, wearable sensors for pulse measurements as well as patterned sensors for low-signal vibration sensing.

Here we describe using nanosheets of both graphene and boron nitride, produced by liquid phase exfoliation, as fillers in composite fibres. The fibres were prepared by coagulation spinning using polyvinylalcohol as a matrix. We obtained good quality fibres with diameter and nanosheet volume fraction which could be controlled via the ratio of nanosheet to polymer injection rates. The mechanical stiffness (modulus, Y) and strength, σ B , increased relatively slowly with volume fraction (dY/dV f ≤ 160 GPa and dσ B /dV f ≤ 0.8 GPa). However, both stiffness and strength continued increasing with nanosheet content to loading levels of ∼20vol%, after which the properties fell off. Such relatively high loading levels result in impressive mechanical properties with stiffness and strength of up to 30 GPa and 260 MPa observed. In addition, we found the graphene-filled fibres to be electrically conducting with conductivities of up to 3 S/m.

The ever-increasing demands for advanced lithium-ion batteries have greatly stimulated the quest for robust electrodes with a high areal capacity. Producing thick electrodes from a high-performance active material would maximize this parameter. However, above a critical thickness, solution-processed films typically encounter electrical/mechanical problems, limiting the achievable areal capacity and rate performance as a result. Herein, we show that two-dimensional titanium carbide or carbonitride nanosheets, known as MXenes, can be used as a conductive binder for silicon electrodes produced by a simple and scalable slurry-casting technique without the need of any other additives. The nanosheets form a continuous metallic network, enable fast charge transport and provide good mechanical reinforcement for the thick electrode (up to 450 µm). Consequently, very high areal capacity anodes (up to 23.3 mAh cm−2) have been demonstrated., Developing thick electrodes could enable high-energy-density Li-ion batteries, however, above a critical thickness, the mass transport issues become dominating. Here the authors show that MXene can serve as a conductive binder leading to thick silicon anodes (up to 450 µm) with high areal capacity.

To progress from the laboratory to commercial applications, it will be necessary to develop industrially scalable methods to produce large quantities of defect-free graphene. Here we show that high-shear mixing of graphite in suitable stabilizing liquids results in large-scale exfoliation to give dispersions of graphene nanosheets. X-ray photoelectron spectroscopy and Raman spectroscopy show the exfoliated flakes to be unoxidized and free of basal-plane defects. We have developed a simple model that shows exfoliation to occur once the local shear rate exceeds 10(4) s(-1). By fully characterizing the scaling behaviour of the graphene production rate, we show that exfoliation can be achieved in liquid volumes from hundreds of millilitres up to hundreds of litres and beyond. The graphene produced by this method performs well in applications from composites to conductive coatings. This method can be applied to exfoliate BN, MoS2 and a range of other layered crystals.

Few-layer black phosphorus (BP) is a new two-dimensional material which is of great interest for applications, mainly in electronics. However, its lack of environmental stability severely limits its synthesis and processing. Here we demonstrate that high-quality, few-layer BP nanosheets, with controllable size and observable photoluminescence, can be produced in large quantities by liquid phase exfoliation under ambient conditions in solvents such as N-cyclohexyl-2-pyrrolidone (CHP). Nanosheets are surprisingly stable in CHP, probably due to the solvation shell protecting the nanosheets from reacting with water or oxygen. Experiments, supported by simulations, show reactions to occur only at the nanosheet edge, with the rate and extent of the reaction dependent on the water/oxygen content. We demonstrate that liquid-exfoliated BP nanosheets are potentially useful in a range of applications from ultrafast saturable absorbers to gas sensors to fillers for composite reinforcement., While phosphorene is an exciting new 2D material, techniques to produce it in large quantities in a stable, processable form are lacking. Here, the authors achieve this using liquid phase exfoliation and demonstrate the resultant nanosheets to be useful in a number of applications.

International audience; 2D metal chalcogenide (MC) nanosheets (NS) have displayed high capacities as lithium‐ion battery (LiB) anodes. Nevertheless, their complicated synthesis routes coupled with low electronic conductivity greatly limit them as promising LiB electrode material. Here, this work reports a facile single‐walled carbon nanotube (SWCNT) percolating strategy for efficiently maximizing the electrochemical performances of gallium chalcogenide (GaX, X = S or Se). Multiscaled flexible GaX NS/SWCNT heterostructures with abundant voids for Li+ diffusion are fabricated by embedding the liquid‐exfoliated GaX NS matrix within a SWCNT‐percolated network; the latter improves the electron transport and ion diffusion kinetics as well as maintains the mechanical flexibility. Consequently, high capacities (i.e., 838 mAh g−1 per gallium (II) sulfide (GaS) NS/SWCNT mass and 1107 mAh g−1 per GaS mass; the latter is close to the theoretical value) and good rate capabilities are achieved, which can be majorly attributed to the alloying processes of disordered Ga formed after the first irreversible GaX conversion reaction, as monitored by in situ X‐ray diffraction. The presented approach, colloidal solution processing of SWCNT and liquid‐exfoliated MC NS to produce flexible paper‐based electrode, could be generalized for wearable energy storage devices with promising performances.

We have developed methods to disperse and partially size separate NbSe(3) nanowires in aqueous surfactant solutions. These dispersions can easily be formed into thin films. Optical and electrical studies show these films to display sheet resistances and transmittances ranging from (460 Ω/□, 22%) to (12 kΩ/□, 79%) depending on thickness. For thicker films, we measured the transparent conducting figure of merit to be σ(DC, B)/σ(Op) = 0.32, similar to graphene networks. Thickness measurements gave individual values of σ(Op) = 17,800 S m(-1) and σ(DC, B) = 5700 S m(-1). Films thinner than ∼ 70 nm displayed reduced DC conductivity due to percolative effects.

Mixtures of 1D carbon nanotubes and 2D nanosheets are important in electrochemical applications where the nanosheets are the active material, while the nanotubes provide electrical conductivity and...

Liquid phase exfoliation has become an important method for the production of large quantities of two-dimensional (2D) nanosheets. This method is versatile, having been used to produce dozens of different 2D materials in a range of stabilizing liquids. The resultant liquid-suspended nanosheets have been characterized in great detail and have been processed into a number of structures for a wide range of applications. This has led to a growing number of researchers adopting this method. As a result, best practice in terms of experimental procedure has evolved rapidly over recent years. As experimental complexity has increased, it has become more and more difficult to discuss the rational behind a chosen experimental procedure in full detail using standard “Methods” sections due to the frequent use of procedures developed in related prior reports. This can make it difficult to reproduce complex procedures and acts as a barrier to new researchers entering the field. To address this shortcoming, here we descr...

Robust strain gauges are fabricated by growing PtSealt;subagt;2alt;/subagt; layers directly on top of flexible polyimide foils. These PtSealt;subagt;2alt;/subagt; layers are grown by low-temperature, thermally-assisted conversion of predeposited Pt layers. Under applied flexure the PtSealt;subagt;2alt;/subagt; layers show a decrease in electrical resistance signifying a negative gauge factor. The influence of the growth temperature and film thickness on the electromechanical properties of the PtSealt;subagt;2alt;/subagt; layers is investigated. The best-performing strain gauges fabricated have a superior gauge factor to that of commercial metal-based strain gauges. Notably, the strain gauges offer good cyclability and are very robust, surviving repeated peel tests and immersion in water. Furthermore, preliminary results indicate that the stain gauges also show potential for high-frequency operation. This host of advantageous properties, combined with the possibility of further optimization and channel patterning, indicate that PtSealt;subagt;2alt;/subagt; grown directly on polyimide holds great promise for future applications.