Thermal rectification in novel two-dimensional hybrid graphene/BCN sheets: A molecular dynamics simulation.

The graphene-like monolayer of carbon, boron and nitrogen that maintains the native hexagonal atomic lattice (BCN), is a novel semiconductor with special thermal properties. Herein, with the aid of a non-equilibrium molecular dynamics approach (NEMD), we study phonon thermal rectification in a hybrid system of pure graphene and BCN (G-BCN) in various configurations under a series of positive and negative temperature gradients. We begin by investigating the relation of thermal rectification to sample's mean temperature, T, and the imposed temperature difference, ΔT, between the two heat baths at its ends. We then move to explore the effect of varying strain levels of our sample on thermal rectification, followed by Kapitza resistance calculations at the G-BCN interface, which shed light on the interface effects on thermal rectification. Our simulation results reveal a BCN-configuration-dependent behavior of thermal rectification. Finally, the underlying mechanism leading to a preferred direction for phonons is studied using phonon density of states (DOS) on both sides of the G-BCN interface.

Flexible thermoelectrics in crossed graphene/hBN composites.

Nanostructures exhibit unusual properties due to the dominance of quantum mechanical effects. In addition, the geometry of a nanostructure can have a strong influence on its physical properties. Using the tight-binding and force-constant approaches with the help of the non-equilibrium Green's function method, the transport and thermoelectric properties of cross-shaped (X-shaped) composite heterostructures are studied in two cases: Mixed graphene and h-BN (HETX-CBN) and all graphene (HETX-C) cross-shaped structures. Our numerical results show that an X-shaped structure helps to manipulate its electronic and phononic properties. The transport energy gap can be tuned in the range of ~ 0.8 eV by changing one arm width. Due to the drastic decrease in the electronic conductance of HETX-CBN and the dominance of the phononic thermal conductance, the ZT performance is degraded despite the high Seebeck coefficient value (in the order of meV). However, HETX-C has better ZT performance due to better electronic conductance and lower phononic/electronic thermal ratio, it can enhance the ZT ~ 2.5 times compared to that of zigzag graphene nanoribbon. The thermoelectric properties of the system can be tuned by controlling the size of the arms of the device and the type of its atoms.

Tuning phononic and electronic contributions of thermoelectric in defected S-shape graphene nanoribbons.

Thermoelectrics as a way to use waste heat, is essential in electronic industries, but its low performance at operational temperatures makes it inappropriate in practical applications. Tailoring graphene can change its properties. In this work, we are interested in studying the transport properties of S-shape graphene structures with the single vacancy (SV) and double vacancy (DV) models. The structures are composed of a chiral part, which is an armchair graphene nanoribbon, and two zigzag graphene ribbons. We investigate the changes in the figure of merit by means of the Seebeck coefficient, electronic conductance, and electronic and phononic conductances with the vacancies in different device sizes. The transport properties of the system are studied by using the non-equilibrium Green's function method, so that the related Hamiltonians (dynamical matrices) are obtained from the tight-binding (force constant) model. The maximum figure of merit (ZT) obtains for the DVs in all lengths. Physical properties of such a system can be tuned by controlling various parameters such as the location and the type of the defects, and the device size. Our findings show that lengthening the structure can reduce phononic contribution, and single vacancies than double vacancies can better distinguish between electronic thermal conductance behavior and electronic conductance one. Namely, vacancy engineering can significantly increase thermoelectric performance. In the large devices, the SVs can increase the ZT up to 2.5 times.

Vacancy tuned thermoelectric properties and high spin filtering performance in graphene/silicene heterostructures.

The main contribution of this paper is to study the spin caloritronic effects in defected graphene/silicene nanoribbon (GSNR) junctions. Each step-like GSNR is subjected to the ferromagnetic exchange and local external electric fields, and their responses are determined using the nonequilibrium Green's function (NEGF) approach. To further study the thermoelectric (TE) properties of the GSNRs, three defect arrangements of divacancies (DVs) are also considered for a larger system, and their responses are re-evaluated. The results demonstrate that the defected GSNRs with the DVs can provide an almost perfect thermal spin filtering effect (SFE), and spin switching. A negative differential thermoelectric resistance (NDTR) effect and high spin polarization efficiency (SPE) larger than 99.99% are obtained. The system with the DV defects can show a large spin-dependent Seebeck coefficient, equal to Ss ⁓ 1.2 mV/K, which is relatively large and acceptable. Appropriate thermal and electronic properties of the GSNRs can also be obtained by tuning up the DV orientation in the device region. Accordingly, the step-like GSNRs can be employed to produce high efficiency spin caloritronic devices with various features in practical applications.

Effect of graphene and carbon-nitride nanofillers on the thermal transport properties of polymer nanocomposites: A combined molecular dynamics and finite element study.

Low thermal conductivity of polymers, which is one of the considerable drawbacks of commonly used composite structures, has been the focus of many researchers aiming to achieve high-performance polymer-based nanocomposites through the inclusion of highly thermally conductive fillers inside the polymer matrices. Thus, in the present study, a multiscale scheme using nonequilibrium molecular dynamics and the finite element method is developed to explore the impact of different nanosized fillers (carbon-nitride and graphene) on the effective thermal conductivity of polyethylene-based nanocomposites. We show that the thermal conductivity of amorphous polyethylene at room temperature using the reactive bond order interatomic potential is nearly 0.36±0.05W/mK. Also, the atomistic results predict that, compared to the C_{3}N and graphene nanosheets, the C_{2}N nanofilm presents a much stronger interfacial thermal conductance with polyethylene. Furthermore, the results indicate that the effective thermal conductivity values of C_{2}N-polyethylene, C_{3}N-polyethylene, and graphene-polyethylene nanocomposite, at constant volume fractions of 1%, are about 0.47, 0.56, and 0.74W/mK, respectively. In other words, the results of our models reveal that the thermal conductivity of fillers is the dominant factor that defines the effective thermal conductivity of nanocomposites.

Predicting the new carbon nanocages, fullerynes: a DFT study.

In this study, based on density functional theory, we propose a new branch of pseudo-fullerenes which contain triple bonds with sp hybridization. We call these new nanostructures fullerynes, according to IUPAC. We present four samples with the chemical formula of C4nHn, and the structures derived from fulleranes. We compare the structural and electronic properties of these structures with those of two common fullerenes and fulleranes systems. The calculated electron affinities of the sampled fullerynes are negative, and much smaller than those of fullerenes, so they should be chemically more stable than fullerenes. Although fulleranes also exhibit higher chemical stability than fullerynes, but pentagon or hexagon of the fullerane structures cannot pass ions and molecules. Applications of fullerynes can be included in the storage of ions and gases at the nanoscale. On the other hand, they can also be used as cathode/anode electrodes in lithium-ion batteries.

Pure thermal spin current and perfect spin-filtering with negative differential thermoelectric resistance induced by proximity effect in graphene/silicene junctions.

The spin-dependent Seebeck effect (SDSE) and thermal spin-filtering effect (SFE) are now considered as the essential aspects of the spin caloritronics, which can efficiently explore the relationships between the spin and heat transport in the materials. However, there is still a challenge to get a thermally-induced spin current with no thermal electron current. This paper aims to numerically investigate the spin-dependent transport properties in hybrid graphene/silicene nanoribbons (GSNRs), using the nonequilibrium Green's function method. The effects of temperature gradient between the left and right leads, the ferromagnetic exchange field, and the local external electric fields are also included. The results showed that the spin-up and spin-down currents are produced and flow in opposite directions with almost equal magnitudes. This evidently shows that the carrier transport is dominated by the thermal spin current, whereas the thermal electron current is almost disappeared. A pure thermal spin current with the finite threshold temperatures can be obtained by modulating the temperature, and a negative differential thermoelectric resistance is obtained for the thermal electron current. A nearly zero charge thermopower is also obtained, which further demonstrates the emergence of the SDSE. The response of the hybrid system is then varied by changing the magnitudes of the ferromagnetic exchange field and local external electric fields. Thus, a nearly perfect SFE can be observed at room temperature, whereas the spin polarization efficiency is reached up to 99%. It is believed that the results obtained from this study can be useful to well understand the inspiring thermospin phenomena, and to enhance the spin caloritronics material with lower energy consumption.

Hydration effects and negative dielectric constant of nano-confined water between cation intercalated MXenes.

Using electrochemical methods a profound enhancement of the capacitance of electric double layer capacitor electrodes was reported when water molecules are strongly confined into the two-dimensional slits of titanium carbide MXene nanosheets [A. Sugahara et al., Nat. Commun., 2019, 10, 850]. We study the effects of hydration on the dielectric properties of nanoconfined water and supercapacitance properties of the cation intercalated MXene. A model for the electric double layer capacitor is constructed where water molecules are strongly confined in two-dimensional slits of MXene. We report an abnormal dielectric constant and polarization of nano-confined water between MXene layers. We found that by decreasing the ionic radius of the intercalated cations and in a critical hydration shell radius the capacitance of the system increases significantly (≃200 F g-1) which can be interpreted as a negative permittivity. This study builds a bridge between the fundamental understanding of the dielectric properties of nanoconfined water and the capability of using MXene films for supercapacitor technology, and in doing so provides a solid theoretical support for recent experiments.

Thermal rectification and interfacial thermal resistance in hybrid pillared-graphene and graphene: a molecular dynamics and continuum approach.

We investigate thermal rectification and thermal resistance in a hybrid pillared-graphene and graphene (PGG) system by both molecular dynamics (MD) simulation and a continuum model. First, the thermal conductivity of both pillared-graphene and graphene is calculated by employing MD simulation and Fourier's law. Our results show that the thermal conductivity of the pillared-graphene is much smaller than that of graphene by one order of magnitude. Next, by applying positive and negative temperature gradients along the longitudinal direction of the PGG, the thermal rectification is examined. The MD results indicate that for the lengths in the range of 3686 nm, the thermal rectification remains almost constant (~3%-5%). We have also studied the phonon density of states (DOS) on both sides of the interface of PGG. The DOS curves show that there is phonon scattering at low frequencies that depends on the imposed temperature gradient direction in the system. Therefore, we can introduce the PGG as a thermal rectifier at room temperature. Furthermore, next, we also explore the temperature distribution over the PGG by using the continuum model. The results obtained from the continuum model predict the MD results, such as the temperature distribution in the upper half-layer and lower full-layer graphene, the temperature gap, and also the thermal resistance at the interface. This study could help in the design of chip coolers, and phononic devices such as thermal nanodiodes.

Topological and transport properties of graphene-based nanojunctions subjected to a magnetic field.

We study the topological properties of finite-size S-shaped graphene junctions with distinctive edge features subjected to the perpendicular magnetic field, using the tight-binding model. The quantum confinement and edge effects induced by the specific junction give rise to significant modifications in the Hofstadter spectra of the bent flakes, when compared to those of their perfect forms. Moreover, the results show that in absence of a magnetic field, the sharpest zigzag-edged corners support the edge states rather than the others, but the magnetic field leads to the localization of the edge states along the whole perimeter of the flakes. Furthermore, based on the Green's function method, we investigate the electron transport through our proposed junctions. We show that, under magnetic flux, one can effectively control the energy gap and the conductance around the Fermi energy. Moreover, the transitions between metallic, semimetallic, and semiconducting phases are possible by the magnetic flux in the S-shaped junctions.

Thermal transport across grain boundaries in polycrystalline silicene: A multiscale modeling.

During the fabrication process of large scale silicene, through common chemical vapor deposition (CVD) technique, polycrystalline films are quite likely to be produced, and the existence of Kapitza thermal resistance along grain boundaries could result in substantial changes of their thermal properties. In the present study, the thermal transport along polycrystalline silicene was evaluated by performing a multiscale method. Non-equilibrium molecular dynamics simulations (NEMD) was carried out to assess the interfacial thermal resistance of various constructed grain boundaries in silicene. The effects of tensile strain and the mean temperature on the interfacial thermal resistance were also examined. In the following stage, the effective thermal conductivity of polycrystalline silicene was investigated considering the effects of grain size and tensile strain. Our results indicate that the average values of Kapitza conductance at grain boundaries at room temperature were estimated to be nearly 2.56 × 109 W/m2 K and 2.46 × 109 W/m2 K through utilizing Tersoff and Stillinger-Weber interatomic potentials respectively. Also, in spite of the mean temperature, whose increment does not change Kapitza resistance, the interfacial thermal resistance could be controlled by applying strain. Furthermore, it was found that by tuning the grain size of polycrystalline silicene, its thermal conductivity could be modulated up to one order of magnitude.

Vesicle-like structure of lipid-based nanoparticles as drug delivery system revealed by molecular dynamics simulations.

Lipid-based drug delivery systems are considered as promising vehicles for hydrophobic drug compounds. Lipid distribution within the droplet can affect drug loading capacity in these carriers. However, it is extremely challenging to determine the nanostructure within these carriers through the implementation of the direct experimental methods due to the ultrafine size. Therefore, coarse grained molecular dynamics (MD) simulation was utilized to model different kinds of lipid-based nanoparticles of the diameter about 12 nm including solid lipid nanoparticles (SLN), nanoemulsion (NE), and nanostructured lipid carriers (NLC), and the organization of the lipids within the carriers was explored. The aforementioned nanoparticles consisted of stearic acid, oleic acid as lipids, and sodium dodecyl sulfate (SDS) as a surfactant in water medium. Furthermore, the impact of solid to liquid mass ratio on the lipid distribution within the lipid matrix was investigated regarding the NLC simulations. In the equilibrium state, we observed the vesicle-like structure for all the investigated systems in which the hydrophilic moieties of the lipids and surfactant organized a semi-bilayer fold into the droplet and the hydrophobic tails accumulated among them. It is worth mentioning although SDS as a harsh surfactant, which is a special case, was expected to be present in the surface of the droplet, it penetrated into the lipids. Additionally, our results showed remarkable entrapped water beads inside the droplet in the form of one or more cavities along the internal layer of the head groups which was surrounded by lipid head groups. It was also reported that in the building structure of the nanoemulsion and SLN, in the central parts of the droplets, lipids were denser than the case of NLCs. Moreover, no crystallization occurred within the lipid-based carriers. Finally, the results indicated that, in the case of NLC simulations, the lipid distribution within the lipid matrix was insensitive to the mass fraction of solid to liquid lipids.

Highly tunable charge and spin transport in silicene junctions: phase transitions and half-metallic states.

We report peculiar charge and spin transport properties in S-shaped silicene junctions with the Kane-Mele tight-binding model. In this work, we investigate the effects of electric and exchange fields on the charge and spin transport properties. Our results show that by applying a perpendicular electric field, metal-semiconductor and also semimetal-semiconductor phase transitions occur in our systems. Furthermore, full spin current can be obtained in the structures, so the half-metallic states are observable. Our results enable us to control charge and spin currents and provide new opportunities and applications in silicene-based electronics, optoelectronics, and spintronics.

Synthesis and characterization of dextran coated magnetite nanoparticles for diagnostics and therapy.

INTRODUCTION: Expansion of efficacious theranostic systems is of pivotal significance for medicine and human healthcare. Magnetic nanoparticles (MNPs) are known as drug delivery system and magnetic resonance imaging (MRI) contrast agent. MNPs as drug carriers have attracted significant attention because of the delivery of drugs loaded onto MNPs to solid tumors, maintaining them in the target site by an external electromagnetic field, and subsequently releasing drugs in a controlled manner. On the other hand, it is believed that MNPs possess high potential as MRI contrast agents. The aim of this work was to payload curcumin into dextran coated MNPs and investigate their potential as theranostic systems for controlled drug delivery and MRI imaging. METHODS: MNPs were synthesized as a core and coated with dextran as polymeric shell to provide steric stabilization. Curcumin as anticancer drug was selected to be loaded into NPs. To characterize the synthesized NPs, various techniques (e.g., DLS, FESEM, FT-IR, XRD, and VSM) were utilized. In vitro drug release of curcumin was evaluated at 37˚C at the pH value of 5.4 and 7.4.The feasibility of employment of dextran coated MNPs as MRI contrast agents were also studied. RESULTS: Formulations prepared from dextran coated MNPs showed high loading (13%) and encapsulation efficiency (95%). In vitro release study performed in the phosphate-buffered saline (PBS, pH= 7.4, 5.4) revealed that the dextran coated MNPs possess sustained release behavior at least for 4 days with the high extent of drug release in acidic media. Vibrating sample magnetometer (VSM) analysis proved the superparamagnetic properties of the dextran coated MNPs with relatively high-magnetization value indicating that they were sufficiently sensitive to external magnetic fields as magnetic drug carriers. Furthermore, dextran coated MNPs exhibited high potential as T2 contrast agents for MRI. CONCLUSION: Based on our findings, we propose the dextran coated MNPs as promising nanosystem for the delivery of various drugs such as curcumin and MRI contrast agent.

The impact of polymer coatings on magnetite nanoparticles performance as MRI contrast agents: a comparative study.

BACKGROUND: Superparamagnetic iron oxide nanoparticles (SPIONs) are the most commonly used negative MRI contrast agent which affect the transverse (T2) relaxation time. The aim of the present study was to investigate the impact of various polymeric coatings on the performance of magnetite nanoparticles as MRI contrast agents. METHODS: Ferrofluids based on magnetite (Fe3O4) nanoparticles (SPIONs) were synthesized via chemical co-precipitation method and coated with different biocompatible polymer coatings including mPEG-PCL, chitosan and dextran. RESULTS: The bonding status of different polymers on the surface of the magnetite nanoparticles was confirmed by the Fourier transform infrared spectroscopy (FT-IR) and thermogravimetric analysis (TGA). The vibrating sample magnetometer (VSM) analysis confirmed the superparamagnetic behavior of all synthesized nanoparticles. The field-emission scanning electron microscopy (FE-SEM) indicated the formation of quasi-spherical nanostructures with the final average particle size of 12-55 nm depending on the type of polymer coating, and X-ray diffraction (XRD) determined inverse spinel structure of magnetite nanoparticles. The ferrofluids demonstrated sufficient colloidal stability in deionized water with the zeta potentials of -24.2, -16.9, +31.6 and -21 mV for the naked SPIONs, and for dextran, chitosan and mPEG-PCL coated SPIONs, respectively. Finally, the magnetic relaxivities of water based ferrofluids were measured on a 1.5 T clinical MRI instrument. The r2/r1 value was calculated to be 17.21, 19.42 and 20.71 for the dextran, chitosan and mPEG-PCL coated SPIONs, respectively. CONCLUSIONS: The findings demonstrated that the value of r2/r1 ratio of mPEG-PCL modified SPIONs is higher than that of some commercial contrast agents. Therefore, it can be considered as a promising candidate for T2 MRI contrast agent.