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In this work, we implement a dual frequency (24 kHz and 1174 kHz) ultrasonic assisted liquid phase exfoliation (ULPE) technique in deionized water (DIW) and other eco-friendly solvents, to produce a variety of high-quality few-layer graphene (FLG) solutions under controlled ultrasonication conditions. The resulting FLG dispersions of variable sizes (∼0.2-1.5 μm 2 ) confirmed by characterisation techniques comprising UV-Vis spectroscopy, Raman spectroscopy and high-resolution transmission electron microscopy (HR-TEM). For the first time we demonstrate that high yield of FLG flakes with minimal defects, stable for 6 + months in a solution (stability ∼ 70 %), can be obtained in less than 1-hour of treatment in either water/ethanol (DIW:EtOH) or water/isopropyl alcohol (DIW:IPA) eco-friendly mixtures. We also scrutinized the underlying mechanisms of cavitation using high-speed imaging synchronized with acoustic pressure measurements. The addition of ethanol or IPA to deionized water is proposed to play a central role in exfoliation as it regulates the extend of the cavitation zone, the intensity of the ultrasonic field and, thus, the cavitation effectiveness. Our study revealed that lateral sizes of the obtained FLG depend on the choice of exfoliating media and the diameter of a sonotrode used. This variability offers flexibility in producing FLG of different sizes, applicable in a wide spectrum of size-specific applications., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 The Author(s). Published by Elsevier B.V. All rights reserved.)

This paper follows our earlier work where a strong high frequency pressure peak has been observed as a consequence of the formation of shock waves due to the collapse of cavitation bubbles in water, excited by an ultrasonic source at 24 kHz. We study here the effects of liquid physical properties on the shock wave characteristics by replacing water as the medium successively with ethanol, glycerol and finally a 1:1 ethanol-water solution. The pressure frequency spectra obtained in our experiments (from more than 1.5 million cavitation collapsing events) show that the expected prominent shockwave pressure peak was barely detected for ethanol and glycerol, particularly at low input powers, but was consistently observed for the 1:1 ethanol-water solution as well as in water, with a slight shift in peak frequency for the solution. We also report two distinct features of shock waves in raising the frequency peak at MHz (inherent) and contributing to the raising of sub-harmonics (periodic). Empirically constructed acoustic pressure maps revealed significantly higher overall pressure amplitudes for the ethanol-water solution than for other liquids. Furthermore, a qualitative analysis revealed that mist-like patterns are developed in ethanol-water solution leading to higher pressures., Competing Interests: Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2023 The Author(s). Published by Elsevier B.V. All rights reserved.)

Graphene dispersions in water are highly desirable for a range of applications such as biomedicines, separation membranes, coatings, inkjet printing and more. Recent novel research has been focussed on developing a green approach for scalable production of graphene. However, one important parameter, which is often neglected is the bulk temperature of the processing liquid. This paper follows our earlier work where optimal sono-exfoliation parameters of graphite in aqueous solutions were determined based on the measured acoustic pressure fields at various temperatures and input powers. Here, we take the next step forward and demonstrate using systematic characterisation techniques and acoustic pressure measurements that sonication-assisted liquid phase exfoliation (LPE) of graphite powder can indeed produce high quality few layer graphene flakes in pure water at a specific temperature, i.e. 40 °C, and at an optimised input generator power of 50%, within 2-h of processing. UV-vis analysis also revealed that the exfoliation, stability and uniformity of dispersions were improved with increasing temperature. We further confirmed the successful exfoliation of graphene sheets with minimal level of defects in the optimized sample with the help of Raman microscopy and transmission electron microscopy. This study demonstrated that understanding and controlling processing temperature is one of the key parameters for graphene exfoliation in water which offers a potential pathway for its large-scale production., Competing Interests: Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2022 The Authors. Published by Elsevier B.V. All rights reserved.)

Lead Iodide (PbI 2 ) is a large bandgap 2D layered material that has potential for semiconductor applications. However, atomic level study of PbI 2 monolayer has been limited due to challenges in obtaining thin crystals. Here, we use liquid exfoliation to produce monolayer PbI 2 nanodisks (30-40 nm in diameter and > 99% monolayer purity) and deposit them onto suspended graphene supports to enable atomic structure study of PbI 2 . Strong epitaxial alignment of PbI 2 monolayers with the underlying graphene lattice occurs, leading to a phase shift from the 1 T to 1 H structure to increase the level of commensuration in the two lattice spacings. The fundamental point vacancy and nanopore structures in PbI 2 monolayers are directly imaged, showing rapid vacancy migration and self-healing. These results provide a detailed insight into the atomic structure of monolayer PbI 2 , and the impact of the strong van der Waals interaction with graphene, which has importance for future applications in optoelectronics.

Buckminsterfullerenes (C 60 ) are near-spherical molecules, which freely rotate at room temperature in the solid state and when dissolved in solution. An intriguing question arises as to whether C 60 molecules can act as "molecular ball bearings," that is, preventing direct contact between two solid surfaces while simultaneously dissipating shear stress through fast rotation. To explore this, we performed measurements of friction across a solution of C 60 in the boundary lubrication regime. High-resolution shear and normal force measurements between mica sheets separated by C 60 solution were made using a surface force balance to provide single-asperity contact and sub-nanometer resolution in film thickness. We find that, even at a small volume fraction, C 60 forms a solidlike amorphous boundary film sustaining a high normal load, suggesting that this system undergoes a glass transition under confinement. The C 60 film gives rise to a low friction coefficient up to moderate applied loads, and we discuss the possible relevance of the ball-bearing effect at the molecular scale.

An N@C 60 -containing C 60 tetramer was synthesized by quadruple 1,3-dipolar cycloaddition (Prato) reaction. This molecule demonstrates the N@C 60 qubit's ability to form covalently linked arrays. Furthermore, it provides a promising scaffold with which to measure multiple qubit-qubit interactions; which must be well characterized for a functioning quantum information processing architecture., Competing Interests: We declare we have no competing interests.

A series of light-emitting perfluorinated polyanilines were synthesized by the oxidative polymerization of 3-perfluorooctyl aniline through a variety of aqueous/organic interfaces. According to the interfacial tension between the two solvents (the organic being chloroform, dichloromethane, perfluorinated ether, toluene, or o-dichlorobenzene), we obtain distinctive classes of materials based on the crystal packing, protonation, and oxidation state of the polymeric chains. We distinguish between soluble fractions with a distinctive, strong, and red-shifted photoluminescence pattern and an insoluble precipitate which can be subsequently solubilized in a mixture of acetone and toluene. The emission maximum for the insoluble fraction is located in the ultraviolet or blue region with a small Stokes shift; maxima for the soluble counterparts are in the green to yellow region. The soluble derivatives demonstrate a significantly smaller band gap compared to the monomer and large Stokes shifts up to 163 nm; the emission maximum for the most red-shifted emission was located at λ(em) = 548 nm. Their redox activity toward silver nanoparticles, their sensor reactivity with organic acid and bases, and the subsequent changes in the optical properties were demonstrated and the structure of the materials was evaluated with NMR, X-ray diffraction, and FTIR/Raman spectroscopy.

The Internet of Medical Things (IoMT) is increasingly utilized for patient health monitoring, treatment delivery, and healthcare enhancement. However, IoMT devices are vulnerable to attacks, posing risks to patient privacy and safety. Machine learning (ML) techniques are employed for attack detection to mitigate threats. IoMT devices generate substantial data, allowing ML algorithms to analyze and predict potential attacks. This study evaluates the performance of ML models for attack detection using datasets collected from medical devices. Both conventional and ensemble models are employed and trained on two datasets: one comprising all features and another with features selected based on importance. Ensemble models, which combine the strengths of multiple ML algorithms, are utilized to enhance detection accuracy and robustness. Results indicate that the ensemble model achieves superior detection rates and lower false positives than traditional ML algorithms. The stack ensemble model demonstrates the highest performance with a detection rate of 97.58%. Our proposed model outperforms existing models with a 5% improvement in detection rate and a 25% reduction in execution time. Proposed ensemble approaches hold promise for strengthening the security of IoMT devices and ensuring patient safety in fog-edge environments. [ABSTRACT FROM AUTHOR]

Quantum phenomena, including entanglement, superposition, tunneling, and spin-orbit interactions, among others, are foundational to the development of recent innovations in quantum computing, teleportation, encryption, sensing, and new modalities of electronics, such as spintronics, spinorbitronics, caloritronics, magnonics, twistronics, and valleytronics. These emerging technologies provide disruptive influences to global commercial markets. These remarkable advances in quantum technologies are nearly always enabled by the discovery of materials and their quantum behaviors. Such advances are governed by quantum principles that are strongly influenced by environmental, physical, topological, and morphological conditions such as very small length scales, short time durations, ultrahigh pressures, ultralow temperatures, etc., which lead to quantum behaviors that manifest as quantum tunneling, entanglement, superpositioning, superfluidity, low-dimensional, high-temperature and high-pressure superconductivity, quantum fluctuations, Bose-Einstein condensates, topological effects, and other phenomena that are not yet fully understood nor adequately explored. Here, we provide a review of quantum materials developed up to 2023. Remarkable advances in quantum materials occur daily, and therefore, by the time of publication, new and exciting breakthroughs will have occurred that are regrettably not covered herein. [ABSTRACT FROM AUTHOR]

This study investigated the adsorption properties of graphene oxide in a magnetic-assisted adsorber for the depollution of water containing heavy metals. Two samples of graphene oxide with different surface chemistry were synthetized and assessed using the magnetic-assisted adsorption systems. One graphene oxide sample exhibited a dual magnetic behavior presenting both diamagnetic and ferromagnetic phases, while the other graphene oxide was diamagnetic. The adsorption properties of these graphene oxide samples for removing Pb2+ and Cu2+ were tested and compared with and without a magnetic field exposure. The results showed that the Pb2+ removal increased using both graphene oxide samples in the magnetic-assisted configuration, while Cu2+ adsorption was less sensitive to the application of the magnetic field. A monolayer model was used to simulate all the heavy metal adsorption isotherms quantified experimentally. It was concluded that the adsorption mechanism designed to remove Pb2+ and Cu2+ using tested graphene oxide samples was mainly multi-ionic where two metallic cations could interact with one active site (i.e., oxygenated functional groups) from the adsorbent surface. The oxygenated surface functionalities of graphene oxide samples played a relevant role in determining the impact of magnetic field exposure on the heavy metal removal efficacy. Magnetic-assisted adsorption using graphene oxide is an interesting alternative to reduce the concentration of Pb2+ in polluted effluents, and it can also be applied to improve the performance of adsorbents with a limited concentration of oxygenated functional groups, which usually show poor removal of challenging water pollutants such as toxic heavy metals. [ABSTRACT FROM AUTHOR]

The orientation of different N-substituted [N@C60]fulleropyrrolidine derivatives hosted in a nematic liquid crystal matrix has been studied by electron spin resonance spectroscopy. In this study, variations on the zero field splitting parameter of the guest species are employed as a means of determining their degree of orientation. Fulleropyrrolidines with more rigid N-substituents are preferentially oriented in the liquid crystal matrix, whereas those with less rigid substituents are almost randomly distributed. Additionally, the orientation of a C60 fullerene cage bearing a nitroxide radical has also been investigated in comparison.

CH4@C60 was the first example within which an organic molecule has been embedded in C60. CH4 can rotate freely in the molecular cage, and the carbon skeleton structure of the C60 has no obvious deformation. The electronic structure of CH4@C60 and interaction between C60 and CH4 were studied under quantum mechanical calculation method. The different reaction sites on C–C bonds in C60 and the weak Van der Waals interaction between CH4 and C60 were shown clearly. These results and the orbital interaction between CH4 and C60 were helpful for understanding and further application of this unique biggest organic molecule CH4 contained in C60 structure so far. [ABSTRACT FROM AUTHOR]

Certain migratory birds can sense the Earth's magnetic field. The nature of this process is not yet properly understood. Here we offer a simple explanation according to which birds literally see the local magnetic field through the impact of a physical rather than a chemical signature of the radical pair: a transient, long-lived electric dipole moment. Based on this premise, our picture can explain recent surprising experimental data indicating long lifetimes for the radical pair. Moreover, there is a clear evolutionary path toward this field-sensing mechanism: it is an enhancement of a weak effect that may be present in many species., (Copyright © 2012 Biophysical Society. Published by Elsevier Inc. All rights reserved.)

Carbon nanotubes (CNTs) are often regarded as semi-rigid, all-carbon polymers. However, unlike conventional polymers that can form 3D networks such as hydrogels or elastomers through crosslinking in solution, CNTs have long been considered non-crosslinkable under mild conditions. This perception changed with our recent discovery of UV-defluorination-driven direct crosslinking of CNTs in solution. In this study, we further investigate the thermal stability of UV-defluorination-driven crosslinked CNTs, revealing that they are metastable and decompose more readily than either pristine or fluorinated CNTs under Raman laser irradiation. Using Raman spectroscopy under controlled laser power, we examined both single-walled and multi-walled fluorinated CNTs. The results demonstrate that UV-defluorinated CNTs exhibit reduced thermal stability compared to their pristine or untreated fluorinated counterparts. This instability is attributed to the strain on the intertube crosslinking bonds resulting from the curved carbon lattice of the linked CNTs. The metallic CNTs in the crosslinked CNT networks decompose and revert to their pristine state more readily than the semiconducting ones. The inherent instability of crosslinked CNTs leads to combustion at temperatures approximately 100 °C lower than those required for non-crosslinked fluorinated CNTs. This property positions crosslinked CNTs as promising candidates for applications where mechanically robust, lightweight materials are needed, along with feasible post-use removal options. [ABSTRACT FROM AUTHOR]