Synergistic Improvement in the Thermal Conductivity of Hybrid Boron Nitride Nanotube/Nanosheet Epoxy Composites.

Epoxy composites with excellent thermal properties are highly promising for thermal management applications in modern electronic devices. In this work, we report the enhancement of the thermal conductivity of two different nanocomposites, using epoxy resins LY564 (epoxy 1) and LY5052 (epoxy 2), by incorporating multiwalled boron nitride nanotubes (BNNT) and boron nitride nanosheets (BNNS) as fillers. The synergistic interaction between the 1D BNNT and 2D BNNS allows for improved thermal conductivity via several different mechanisms. The highest thermal conductivity was measured at a loading of 1/30 wt % of BNNT/BNNS, resulting in values of 2.6 and 3.4 Wm-1 K-1, respectively, for each epoxy matrix. This improvement is attributed to the formation of a three-dimensional heat flow path formed through intercalation of the nanotubes between the BNNS. The thermal conductivity of the epoxy 1 and 2 nanocomposites improved by 940 and 1500%, respectively, making them suitable as thermal interface materials in electronic applications requiring electrical resistivity.

Measuring the Capacitance of Carbon in Ionic Liquids: From Graphite to Graphene.

The physical electrochemistry of the carbon/ionic liquids interface underpins the processes occurring in a vast range of applications spanning electrochemical energy storage, iontronic devices, and lubrication. Elucidating the charge storage mechanisms at the carbon/electrolyte interface will lead to a better understanding of the operational principles of such systems. Herein, we probe the charge stored at the electrochemical double layer formed between model carbon systems, ranging from single-layer graphene to graphite and the ionic liquid 1-ethyl-3-methylimidazolium bis(trifluoromethylsulfonyl)imide (EMIM-TFSI). The effect of the number of graphene layers on the overall capacitance of the interface is investigated. We demonstrate that in pure EMIM-TFSI and at moderate potential biases, the electronic properties of graphene and graphite govern the overall capacitance of the interface, while the electrolyte contribution to the latter is less significant. In mixtures of EMIM-TFSI with solvents of varying relative permittivity, the complex interplay between electrolyte ions and solvent molecules is shown to influence the charge stored at the interface, which under certain conditions overcomes the effects of relative permittivity. This work provides additional experimental insights into the continuously advancing topic of electrochemical double-layer structure at the interface between room temperature ionic liquids and carbon materials.

Simultaneous Electrochemical Exfoliation and Functionalization of 2H-MoS2 for Supercapacitor Electrodes.

MoS2 is a promising semiconducting material that has been widely studied for applications in catalysis and energy storage. The covalent chemical functionalization of MoS2 can be used to tune the optoelectronic and chemical properties of MoS2 for different applications. However, 2H-MoS2 is typically chemically inert and difficult to functionalize directly and thus requires pretreatments such as a phase transition to 1T-MoS2 or argon plasma bombardment to introduce reactive defects. Apart from being inefficient and inconvenient, these methods can cause degradation of the desirable properties and introduce unwanted defects. Here, we demonstrate that 2H-MoS2 can be simultaneously electrochemically exfoliated and chemically functionalized in a facile and scalable procedure to fabricate functionalized thin (∼4 nm) MoS2 layers. The aryl diazonium salts used for functionalization have not only been successfully covalently grafted onto the 2H-MoS2, as verified by X-ray photoelectron spectroscopy (XPS) and Raman spectroscopy, but also aid the exfoliation process by increasing the interlayer spacing and preventing restacking. Electrochemical energy storage is one application area to which this material is particularly suited, and characterization of supercapacitor electrodes using this exfoliated and functionalized material revealed that the specific capacitance was increased by ∼25% when functionalized. The methodology demonstrated for the simultaneous production and functionalization of two-dimensional (2D) materials is significant, as it allows for control over the flake morphology with increased repeatability. This electrochemical functionalization technique could also be extended to other types of transition-metal dichalcogenides (TMDs), which are also typically chemically inert with different functional species to adjust to specific applications.

Dielectric-free electrowetting on graphene.

Electrowetting is a simple way to induce the spreading and retraction of electrolyte droplets. This method is widely used in "device" applications, where a dielectric layer is applied between the electrolyte and the conducting substrate. Recent work, including contributions from our own laboratory, have shown that reversible electrowetting can be achieved directly on conductors. We have shown that graphite surfaces, in particular when combined with highly concentrated electrolyte solutions, show a strong wetting effect. The process is driven by the interactions between the electrolyte ions and the surface, hence models of double-layer capacitance are able to explain changes in the equilibrium contact angles. Herein, we extend the approach to the investigation of electrowetting on graphene samples of varying thickness, prepared by chemical vapor deposition. We show that the use of highly concentrated aqueous electrolytes induces a clear yet subtle electrowetting response due to the adsorption of ions and the suppression of the negative effect introduced by the surface impurities accumulating during the transfer process. The latter have been previously reported to fully hinder electrowetting at lower electrolyte concentrations. An amplified wetting response is recorded in the presence of strongly adsorbed/intercalated anions in both aqueous and non-aqueous electrolytes. The phenomenon is interpreted based on the anion-graphene interactions and their influence on the energetics of the interface. By monitoring the dynamics of wetting, an irreversible behaviour is identified in all cases as a consequence of the irreversibility of anion adsorption and/or intercalation. Finally, the effect of the underlying reactions on the timescales of wetting is also examined.

Tribology of Copper Metal Matrix Composites Reinforced with Fluorinated Graphene Oxide Nanosheets: Implications for Solid Lubricants in Mechanical Switches.

The potential for the use of copper coatings on steel switching mechanisms is abundant owing to the high conductivities and corrosion resistance that they impart on the engineered assemblies. However, applications of these coatings on such moving parts are limited due to their poor tribological properties; tendencies to generate high friction and susceptibility to degradative wear. In this study, we have fabricated a fluorinated graphene oxide-copper metal matrix composite (FGO-CMMC) on an AISI 52100 bearing steel substrate by a simple electrodeposition process in water. The FGO-CMMC coatings exhibited excellent lubrication performance under pin-on-disk (PoD) tribological sliding at 1N load, which reduced CoF by 63 and 69%, compared to the GO-CMMC and pure copper coatings that were also prepared. Furthermore, FGO-CMMC achieved low friction and low wear at higher sliding loads. The lubrication enhancement of the FGO-CMMCs is attributed to the tribochemical reaction of FGO with the AISI 52100 steel counterface initiated by the sliding load. The formation of an asymmetric tribofilm structure on the sliding track is critical; the performance of the FGO/Cu tribofilm formed in the track is boosted by the continued fluorination of the counterface surface during PoD sliding, passivating the tribosystem from adhesion-driven breakdown. The FGO-CMMC and GO-CMMC coatings also provide increased corrosion protection reaching 94.2 and 91.6% compared to the bare steel substrate, allowing for the preservation of the long-term low-friction performance of the coating. Other influences include the improved interlaminar shear strength of the FGO-containing composite. The excellent lubrication performance of the copper matrix composite coatings facilitated by FGO incorporation makes it a promising solid lubricant candidate for use in mechanical engineering applications.

Deformation of and Interfacial Stress Transfer in Ti3C2 MXene-Polymer Composites.

Transitional metal carbides and nitrides (MXenes) have promise for incorporation into multifunctional composites due to their high electrical conductivity and excellent mechanical and tribological properties. It is unclear, however, to what extent MXenes are also able to improve the mechanical properties of the composites and, if so, what would be the optimal flake size and morphology. Herein, Ti3C2Tx MXene is demonstrated to be indeed a good candidate for mechanical reinforcement in polymer matrices. In the present work, the strain-induced Raman band shifts of mono-/few-/multilayer MXenes flakes have been used to study the mechanical properties of MXene and the interlayer/interfacial stress transfer on a polymer substrate. The mechanical performance of MXene was found to be less dependent upon flake thickness compared to that of graphene. This enables Ti3C2Tx MXene to offer an efficient mechanical reinforcement to a polymer matrix with a flake length of >10 µm and a thickness of 10s of nanometers. Therefore, the degree of exfoliation of MXenes is not as demanding as other two-dimensional (2D) materials for the purpose of mechanical enhancement in polymers. In addition, the active surface chemistry of MXene facilitates possible functionalization to enable a stronger interface with polymers for applications, such as strain engineering and mechanical enhancement, and in materials including membranes, coatings, and textiles.

Investigation of Voltage Range and Self-Discharge in Aqueous Zinc-Ion Hybrid Supercapacitors.

Aqueous zinc-ion hybrid supercapacitors are a promising energy storage technology, owing to their high safety, low cost, and long-term stability. At present, however, there is a lack of understanding of the potential window and self-discharge of this aqueous energy storage technology. This study concerns a systematic investigation of the potential window of this device by cyclic voltammetry and galvanostatic charge-discharge. Hybrid supercapacitors based on commercial activated carbon (AC) demonstrate a wide and stable potential window (0.2 V to 1.8 V), high specific capacitances (308 F g-1 at 0.5 A g-1 and 110 F g-1 at 30 A g-1 ), good cycling stability (10000 cycles with 95.1 % capacitance retention), and a high energy density (104.8 Wh kg-1 at 383.5 W kg-1 ), based on the active materials. The mechanism involves simultaneous adsorption-desorption of ions on the AC cathode and zinc ion plating/stripping on the Zn anode. This work leads to better understanding of such devices and will aid future development of practical high-performance aqueous zinc-ion hybrid supercapacitors based on commercial carbon materials, thus accelerating the deployment of these hybrid supercapacitors and filling the gap between supercapacitors and batteries.

Graphene-Enabled Adaptive Infrared Textiles.

Interactive clothing requires sensing and display functionalities to be embedded on textiles. Despite the significant progress of electronic textiles, the integration of optoelectronic materials on fabrics remains as an outstanding challenge. In this Letter, using the electro-optical tunability of graphene, we report adaptive optical textiles with electrically controlled reflectivity and emissivity covering the infrared and near-infrared wavelengths. We achieve electro-optical modulation by reversible intercalation of ions into graphene layers laminated on fabrics. We demonstrate a new class of infrared textile devices including display, yarn, and stretchable devices using natural and synthetic textiles. To show the promise of our approach, we fabricated an active device directly onto a t-shirt, which enables long-wavelength infrared communication via modulation of the thermal radiation from the human body. The results presented here provide complementary technologies which could leverage the ubiquitous use of functional textiles.

Unravelling the Mechanism of Rechargeable Aqueous Zn-MnO2 Batteries: Implementation of Charging Process by Electrodeposition of MnO2.

Poor cycling stability and mechanistic controversies have hindered the wider application of rechargeable aqueous Zn-MnO2 batteries. Herein, direct evidence was provided of the importance of Mn2+ in this type of battery by using a bespoke cell. Without pre-addition of Mn2+ , the cell exhibited an abnormal discharge-charge profile, meaning it functioned as a primary battery. By adjusting the Mn2+ content in the electrolyte, the cell recovered its charging ability through electrodeposition of MnO2 . Additionally, a dynamic pH variation was observed during the discharge-charge process, with a precipitation of Zn4 (OH)6 (SO4 )⋅5H2 O buffering the pH of the electrolyte. Contrary to the conventional Zn2+ intercalation mechanism, MnO2 was first converted into MnOOH, which reverted to MnO2 through disproportionation, resulting in the dissolution of Mn2+ . The charging process occurred by the electrodeposition of MnO2 , thus improving the reversibility through the availability of Mn2+ ions in the solution.

Graphene-Based Materials as Strain Sensors in Glass Fiber/Epoxy Model Composites.

The ability of graphene-based materials to act as strain sensors in glass fiber/epoxy model composites by using Raman spectroscopy has been investigated. The strain reporting performance of two types of graphene nanoplatelets (GNPs) was compared with that of graphene produced by chemical vapor deposition (CVD). The strain sensitivity of the thicker GNPs was impeded by their limited aspect ratio and weak interaction between flakes and fibers. The discontinuity of the GNP coating and inconsistency in properties among individual platelets led to scatter in the reported strains. In comparison, continuous and homogeneous CVD grown graphene was more accurate as a strain sensor and suitable for point-by-point strain reporting. The Raman mapping results of CVD graphene and its behavior under cyclic deformation show reversible and reliable strain sensing at low strain levels (up to 0.6% matrix strain), above which interfacial sliding of the CVD graphene layer was observed through an in situ Raman spectroscopic study.

3D Printing of Freestanding MXene Architectures for Current-Collector-Free Supercapacitors.

Additive manufacturing (AM) technologies appear as a paradigm for scalable manufacture of electrochemical energy storage (EES) devices, where complex 3D architectures are typically required but are hard to achieve using conventional techniques. The combination of these technologies and innovative material formulations that maximize surface area accessibility and ion transport within electrodes while minimizing space are of growing interest. Herein, aqueous inks composed of atomically thin (1-3 nm) 2D Ti3 C2 Tx with large lateral size of about 8 µm possessing ideal viscoelastic properties are formulated for extrusion-based 3D printing of freestanding, high specific surface area architectures to determine the viability of manufacturing energy storage devices. The 3D-printed device achieves a high areal capacitance of 2.1 F cm-2 at 1.7 mA cm-2 and a gravimetric capacitance of 242.5 F g-1 at 0.2 A g-1 with a retention of above 90% capacitance for 10 000 cycles. It also exhibits a high energy density of 0.0244 mWh cm-2 and a power density of 0.64 mW cm-2 at 4.3 mA cm-2 . It is anticipated that the sustainable printing and design approach developed in this work can be applied to fabricate high-performance bespoke multiscale and multidimensional architectures of functional and structural materials for integrated devices in various applications.

Correction: Synthetic 2-D lead tin sulfide nanosheets with tuneable optoelectronic properties from a potentially scalable reaction pathway.

[This corrects the article DOI: 10.1039/C8SC04018D.].

Synthetic 2-D lead tin sulfide nanosheets with tuneable optoelectronic properties from a potentially scalable reaction pathway.

Solventless thermolysis of molecular precursors followed by liquid phase exfoliation allows access to two-dimensional IV-VI semiconductor nanomaterials hitherto unreachable by a scalable processing pathway. Firstly, the use of metal dithiocarbamate precursors to produce bulk alloys in the series Pb1-x Sn x S (0 ≤ x ≤ 1) by thermolysis is demonstrated. The bulk powders are characterised by powder X-ray diffraction (pXRD), Raman spectroscopy, scanning electron microscopy (SEM) and energy dispersive X-ray (EDX) spectroscopy. It was found that there is a transition from cubic structures for the Pb-rich alloys including the end compound, PbS (0 ≤ x ≤ 0.4) to layered orthorhombic structures for Sn-rich alloys and the end compound SnS (0.5 ≤ x ≤ 1.0). A smooth elemental progression from lead-rich to tin-rich monochalcogenides across the series of materials is observed. Liquid phase exfoliation was applied to produce two dimensional (2D) nanosheets for a mixed Pb1-x Sn x S alloy (where x = 0.8) in 1-methyl-2-pyrrolidone (NMP) using the synthetic bulk powder as starting material. The nanosheet products were characterized by SEM, atomic force microscopy (AFM) and high angle annular dark field scanning transmission electron microscopy (HAADF STEM). First principle calculations of Pb1-x Sn x S alloys show that the Sn content x modifies the size of the band gap by several 100 meV and that x changes the gap type from indirect in SnS to direct in Pb0.2Sn0.8S. These results are supported by UV-Vis spectroscopy of exfoliated Pb0.2Sn0.8S. The method employed demonstrates a new, scalable, processing pathway which can potentially be used to synthesize a range of synthetic layered structures that can be exfoliated to as-yet unaccessed 2D materials with tunable electronic properties.

Capacitance of Basal Plane and Edge-Oriented Highly Ordered Pyrolytic Graphite: Specific Ion Effects.

Carbon materials are ubiquitous in energy storage; however, many of the fundamental electrochemical properties of carbons are still not fully understood. In this work, we studied the capacitance of highly ordered pyrolytic graphite (HOPG), with the aim of investigating specific ion effects seen in the capacitance of the basal plane and edge-oriented planes of the material. A series of alkali metal cations, from Li+, Na+, K+, Rb+, and Cs+ with chloride as the counterion, were used at a fixed electrolyte concentration. The basal plane capacitance at a fixed potential relative to the potential of zero charge was found to increase from 4.72 to 9.39 µF cm-2 proceeding down Group 1. In contrast, the edge-orientated samples display capacitance ca. 100 times higher than those of the basal plane, attributed to pseudocapacitance processes associated with the presence of oxygen groups and largely independent of cation identity. This work improves understanding of capacitive properties of carbonaceous materials, leading to their continued development for use in energy storage.

Long-range oriented graphene-like nanosheets with corrugated structure.

A facile molten-salt (MS) route for the scalable synthesis of free-standing, long-range oriented and corrugated graphene-like sheets from a copper phthalocyanine (CuPc) precursor is reported. Their unique arrangement and transformation behavior in molten potassium chloride (KCl) play a key role in promoting the successful synthesis of the anisotropic nanostructure.

Black phosphorus with near-superhydrophobic properties and long-term stability in aqueous media.

Black phosphorus is a two-dimensional material that has potential applications in energy storage, high frequency electronics and sensing, yet it suffers from instability in oxygenated and/or aqueous systems. Here we present the use of a polymeric stabilizer which prevents the degradation of nearly 68% of the material in aqueous media over the course of ca. 1 month.

Desalination and Nanofiltration through Functionalized Laminar MoS2 Membranes.

Laminar membranes of two-dimensional materials are excellent candidates for applications in water filtration due to the formation of nanocapillaries between individual crystals that can exhibit a molecular and ionic sieving effect, while allowing high water flux. This approach has been exemplified previously with graphene oxide, however these membranes suffer from swelling when exposed to liquid water, leading to low salt rejection and reducing their applicability for desalination applications. Here, we demonstrate that by producing thin (∼5 µm) laminar membranes of exfoliated molybdenum disulfide (MoS2) in a straightforward and scalable process, followed by a simple chemical functionalization step, we can efficiently reject ∼99% of the ions commonly found in seawater, while maintaining water fluxes significantly higher (∼5 times) than those reported for graphene oxide membranes. These functionalized MoS2 membranes exhibit excellent long-term stability with no swelling and consequent decrease in ion rejection, when immersed in water for periods exceeding 6 months. Similar stability is observed when exposed to organic solvents, indicating that they are ideal for a variety of technologically important filtration applications.

Enhanced Photoluminescence of Solution-Exfoliated Transition Metal Dichalcogenides by Laser Etching.

Using a conventional Raman experimental apparatus, we demonstrate that the photoluminescent (PL) yield from ultrasonication-exfoliated transition metal dichalcogenides (TMDs) (MoS2 and WS2) can be increased by up to 8-fold by means of a laser etching procedure. This laser etching process allows us to controllably pattern and reduce the number of layers of the solution-exfoliated material, overcoming the key drawback to solvent-based exfoliation of two-dimensional (2D) semiconducting materials for applications in optoelectronics. The successful laser thinning of the exfoliated 2D crystals was investigated systematically by changes in both Raman and PL spectra. A simple proof-of-principle of the scalability of this laser etching technique for solution-exfoliated TMD crystals was also demonstrated. As well as being applicable for individual materials, it is also possible to use this simple laser etching technique to investigate the structure of solution-generated van der Waals heterostructures, consisting of layers of both MoS2 and WS2.

Asymmetric MoS2 /Graphene/Metal Sandwiches: Preparation, Characterization, and Application.

The polarizable organic/water interface is used to construct MoS2 /graphene nanocomposites, and various asymmetrically dual-decorated graphene sandwiches are synthesized. High-resolution transmission electron microscopy and 3D electron tomography confirm their structure. These dual-decorated graphene-based hybrids show excellent hydrogen evolution activity and promising capacitance performance.