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Graphene is a perfect 2D crystal of covalently bonded carbon atoms and constitutes the building block for all graphitic structures. Its superior properties make it an attractive material for a variety of technological applications. However, mass production does not meet the initial expectations. Chemical Vapor Deposition (CVD) is currently the only available method for large‐scale automated production, but the produced graphene sheets suffer from structural and morphological defects that degrade considerably the mechanical and other physical properties of synthesized graphene. Recently, the use of liquid metal catalysts (LMCat) has been proposed as an alternative platform for facile and high‐quality synthesis of single‐crystal graphene. Herein, simultaneous Raman spectroscopy combined with mechanical testing is adopted confirming that the reinforcing efficiency of the LMCat graphene is greatly improved. In fact, the effective Young's modulus of LMCat graphene has been found ≈630 GPa, which is significantly higher than the graphene grown on solid Cu substrate due to differences in the morphology of Cu substrate. Overall, this work paves the way for the development of defect‐free graphene of quality comparable to exfoliated flakes, and this will have a major technological impact for many applications. [ABSTRACT FROM AUTHOR]

Agglomerations effects of graphene‐based nanofillers are often reported in the literature to be the main reason on the deterioration of the mechanical properties, especially at high filler loadings. In our study, we focused on the correlated effects of plasma‐treated graphene nanofillers on the curing reaction and mechanical properties of an epoxy matrix. Specifically, we explored the effect of dispersion state, planar size, filler content, surface functionalization and stoichiometric ratio on the epoxy curing process. The surface of the treated graphene nanofillers were studied in detail by X‐ray photoelectron spectroscopy (XPS), Raman spectroscopy and X‐ray diffraction (XRD). The results indicated greater presence of oxygen containing groups with the crystallinity to be unaffected after the plasma process. Dynamic Mechanical Analysis (DMA) was used to assess the changes in both the Tg and the mechanical properties of graphene‐epoxy nanocomposites. Rheological and microscopic data showed that a well‐dispersed material was achieved at high filler loadings with the use of calendaring and plasma functionalization. Although, a well‐dispersed material was achieved on the bulk composite, no further mechanical reinforcement was observed at high filler loadings. The adsorption of epoxy groups onto the graphene nanofillers' surface, leading to a stoichiometric imbalance between the epoxy chains and hardener molecules, was proposed to explain the results. [ABSTRACT FROM AUTHOR]

Graphene and other two-dimensional materials (2DMs) have been shown to be promising candidates for the development of flexible and highly-sensitive strain sensors. However, the successful implementation of 2DMs in practical applications is slowed down by complex processing and still low sensitivity. Here, we report on a novel development of strain sensors based on Marangoni self-assemblies of graphene and of its hybrids with other 2DMs that can both withstand very large deformation and exhibit highly sensitive piezoresistive behaviour. By exploiting the Marangoni effect, reference films of self-assembled reduced graphene oxide (RGO) are first optimized, and the electromechanical behaviour has been assessed after deposition onto different elastomers demonstrating the potential of producing strain sensors suitable for different fields of application. Hybrid networks have been then prepared by adding hexagonal boron nitride (hBN) and fluorinated graphene (FGr) to the RGO dispersion. The hybrid integration of 2D materials is demonstrated to become a potential solution to increase substantially the sensitivity of the produced resistive strain sensors without compromising the mechanical integrity of the film. In fact, for large quasi-static deformations, a range of gauge factor values up to 2000 were demonstrated, while retaining a stable performance under cyclic deformations. [ABSTRACT FROM AUTHOR]

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. [ABSTRACT FROM AUTHOR]

The very serious problem of temperature and humidity regulation, especially for small and medium-sized museums, galleries, and private collections, can be mitigated by the introduction of novel materials that are easily applicable and of low cost. Within this study, archive boxes with innovative technology are proposed as "smart" boxes that can be used for storage and transportation, in combination with a nanocomposite material consisting of polyvinyl alcohol (PVA) and graphene oxide (GO). The synthesis and characterization of the PVA/GO structure with SEM, Raman, AFM, XRD, Optical Microscopy, and profilometry are fully discussed. It is shown that the composite material can be integrated into the archive box either as a stand-alone film or attached onto fitting carriers, for example, those made of corrugated board. By applying the PVA/GO membrane this way, even with strong daily temperature fluctuations of ΔT = ±24.1 °C, strong external humidity fluctuations can be reduced by −87% inside the box. Furthermore, these humidity regulators were examined as Volatile Organic Compounds (VOCs) adsorbers since gas pollutants like formic acid, formaldehyde, acetic acid, and acetaldehyde are known to exist in museums and induce damages in the displayed or stored items. High rates of VOC adsorption have been measured, with the highest ones corresponding to formic acid (521% weight increase) and formaldehyde (223% weight increase). [ABSTRACT FROM AUTHOR]

Paper-like hybrid films based on carbon nanotubes (CNTs) are considered as favorable materials for electromagnetic interference shielding, energy storage, water treatment, and other contemporary high-performance applications due to their unique combination of excellent physical properties, multifunctional capabilities, and ease of fabrication. The present work reports the development, mechanical, electrical, and thermal characterization of multiwalled CNTs-based paper-like networks supporting a wide variety of two-dimensional graphene related materials (2D GRMs), in the absence of a matrix, for rapid de-icing applications. A multitude of hybrid CNT/GRM papers were produced, using graphene oxide (GO), chemically reduced GO, thermally reduced GO, and graphene nanoplatelets at weight fractions ranging from 0 up to 100 wt %. The mechanical response of the papers under uniaxial tension revealed that their toughness was dependent on both the 2D GRM type and nanotube modification method, while the materials exhibited a favorable combination of multifunctional behavior and mechanical robustness. The latter was evidenced by high values of Young's modulus of up to 13 GPa, an ultimate strength of up to 120 MPa, and a fracture energy of up to 1.84 MJ/m3. High values of electrical conductivity of up to ca. 12,500 S/m were coupled with dramatically fast heating responses to temperatures above 300 °C due to the Joule heating effect, which reached unprecedented rates of 355 °C/s and brought forward an impressive potential of the materials for electrothermal applications. In particular, the observed unique combination of low power draw, up to 16 W, high heating power densities of ca. 40,000 W/m2, and small mass renders the films ideal candidates for de-icing applications with a negligible weight burden on critical surfaces. [ABSTRACT FROM AUTHOR]

Laser‐fabrication of graphene from cellulose‐based feedstock materials often requires extensive preprocessing. This work demonstrates laser fabrication of porous, 3D graphene from a new class of marine‐based sustainable materials–chitosan biopolymers. The biopolymer films contain only chitosan, acetic acid, glycerol, and water. Fourier transform infrared spectroscopy studies indicate that the cured chitosan films still retain a significant water content (≈30%), enabling production of flexible films. A simple 3‐step laser fabrication process is presented using low‐cost infrared (CO2, 2.1 W) and visible (405 nm, 0.5 W) hobbyist laser engravers, with measured sheet resistance values as low as 40 ohms sq.−1. Transient electrochemical detection of an inner sphere redox molecule is demonstrated using a graphene‐like carbon working electrode fabricated on a water‐soluble chitosan substrate. [ABSTRACT FROM AUTHOR]

Herein, the physicochemical properties and enhanced adsorption capacity of highly porous thin-layer graphitic carbon nitride (g-C3N4) nanosheets (CNNs) in relation to the separation of dyes are investigated. Cationic and anionic dyes with similar sizes are adopted to study the adsorption and separation properties of graphitic carbon nitride. Highly porous g-C3N4 nanosheets were synthesized via the direct thermal polycondensation of melamine followed by a thermal exfoliation. A comparative study of bulk g-C3N4 and porous thin-film g-C3N4 nanosheets was carried out. The results revealed the formation of highly porous g-C3N4 nanosheets with a well-oriented structure and adequate chemical stability. Porous thin-layer g-C3N4 nanosheets possess a high surface area of 212 m2/g as compared to 10 m2/g of the bulk material. Interestingly, adsorption experiments employing both cationic (methylene blue, rhodamine 6G, and rhodamine B) and anionic (methyl orange, eosin Y) dyes, as well as their mixtures, revealed that g-C3N4 nanosheets exhibited excellent selective adsorption capacity toward cationic dyes, which is followed by very short equilibrium times (e.g., 100% adsorption of MB within 10 min). The present findings can be well interpreted in terms of improved textural and structural properties of CNNs in conjunction to the dispersion and electrostatic interactions between the different dyes and the surface of CNNs. The experimental findings are further corroborated by means of periodic self-consistent charge density functional tight binding theoretical calculations. [ABSTRACT FROM AUTHOR]

As the power‐conversion efficiency (PCE) of organic–inorganic lead halide perovskite solar cells (PSCs) is approaching the theoretical maximum, the most crucial issue concerns long‐term ambient stability. Here, the application of PCN‐224 quantum dots (QDs) is reported, a typical Zr‐based porphyrinic metal–organic framework (MOF), to enhance the ambient stability of PSCs. PCN‐224 QDs with abundant Lewis‐base groups (e.g., CO, C−N, CN) contribute to high‐quality perovskite films with enlarged grain size and reduced defect density by interaction with under‐coordinated Pb2+. Meanwhile, PCN‐224 QDs enable the well‐matched energy level at the perovskite/hole transport layer (HTL) interface, thereby facilitating hole extraction and transport. More importantly, PCN‐224 QDs‐treated HTL can capture Li+ from bis(trifluoromethanesulfonyl)imide additive, leading to the reduced aggregation and less direct contact with moisture for hygroscopic Li‐TFSI. Moreover, PCN‐224 QDs mitigated Li+ ion migration into the perovskite layer, thus avoiding the formation of deleterious defects. The resultant devices yield a champion PCE of 22.51%, along with substantially improved durability, including humidity, thermal and light soaking stabilities. The findings provide a new approach toward efficient and stable PSCs by applying MOF QDs. [ABSTRACT FROM AUTHOR]

Ultrathin carbon nanomembranes (CNMs) are two-dimensional materials (2DM) of a few nm thickness with sub-nm intrinsic pores that mimic the biofiltration membranes found in nature. They enable highly selective, permeable, and energy-efficient water separation and can be produced at large scales on porous substrates with tuned properties. The present work reports the mechanical performance of such CNMs produced by p-nitrobiphenyl phosphonic acid (NBPS) or polyvinylbiphenyl (PVBP) and their composite membranes of microporous supporting substrates, which constitute indispensable information for ensuring their mechanical stability during operation. Measuring the nanomechanical properties of the ultrathin material was achieved by atomic force microscopy (AFM) on membranes both supported on flat substrates and suspended on patterned substrates ("composite membrane"). The AFM analysis showed that the CNMs presented Young's modulus in the range of 2.5–8 GPa. The composite membranes' responses were investigated by tensile testing in a micro-tensile stage as a function of substrate thickness and substrate pore density and diameter, which were found to affect the mechanical properties. Thermogravimetric analysis was used to investigate the thermal stability of composite membranes at high temperatures. The results revealed the structural integrity of CNMs, while critical parameters governing their mechanical response were identified and discussed. [ABSTRACT FROM AUTHOR]

The combination of two-dimensional materials (2D) into heterostructures enables their integration in tunable ultrathin devices. For applications in electronics and optoelectronics, direct growth of wafer-scale and vertically stacked graphene/hexagonal boron nitride (h-BN) heterostructures is vital. The fundamental problem, however, is the catalytically inert nature of h-BN substrates, which typically provide a low rate of carbon precursor breakdown and consequently a poor rate of graphene synthesis. Furthermore, out-of-plane deformations such as wrinkles are commonly seen in 2D materials grown by chemical vapor deposition (CVD). Herein, a wrinkle-facilitated route is developed for the fast growth of graphene/h-BN vertical heterostructures on Cu foils. The key advantage of this synthetic pathway is the exploitation of the increased reactivity from inevitable line defects arising from the CVD process, which can act as active sites for graphene nucleation. The resulted heterostructures are found to exhibit superlubric properties with increased bending stiffness, as well as directional electronic properties, as revealed from atomic force microscopy measurements. This work offers a brand-new route for the fast growth of Gr/h-BN heterostructures with practical scalability, thus propelling applications in electronics and nanomechanical systems. [ABSTRACT FROM AUTHOR]

The development of innovative materials for preventive conservation of cultural objects against known threats, such as fungi and volatile organic compounds (VOCs) that often exist in museums and galleries, is still challenging. In this work, graphene‐based aerogels with an ionic liquid (IL) additive were prepared, and their anti‐fungal and VOCs absorption properties were investigated. Several IL contents were evaluated and the graphene aerogel containing 10 wt.% IL was found to have the best anti‐fungal activity, preventing the aerogel contamination with Aspergillus niger. When exposed to a VOC saturated micro‐environment, this aerogel was highly suitable for the absorption of acetaldehyde, formic acid, acetic acid, and formaldehyde. This combined anti‐fungal and VOC absorption properties are prerequisites for bringing preventive conservation to a higher level. [ABSTRACT FROM AUTHOR]