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Highly Flexible, Electrically Driven, Top-Emitting, Quantum Dot Light-Emitting Stickers
Strain and Orientation Modulated Bandgaps and Effective Masses of Phosphorene Nanoribbons
Mesoscale Imperfections in MoS2 Atomic Layers Grown by a Vapor Transport Technique
Formation of Stable Phosphorus–Carbon Bond for Enhanced Performance in Black Phosphorus Nanoparticle–Graphite Composite Battery Anodes
Multiphonon Relaxation Slows Singlet Fission in Crystalline Hexacene
Highly Intensified Surface Enhanced Raman Scattering through the Formation of p,p′-Dimercaptoazobenzene on Ag Nanoparticles/Graphene Oxide Nanocomposites
The reversible conversion between 4-aminothiophenol and p,p′-dimercaptoazobenzene is performed with a single Ag nanoparticles/graphene oxide nanocomposite (AgNPs/GO) via the assistance of local surface plasmons. The formation of p,p′-dimercaptoazobenzene on AgNPs/GO leads to the decrease in distance between adjacent AgNPs on a GO surface, enhancing the local electromagnetic field near AgNPs. This effect is beneficial to enhancing surface Raman enhanced scattering signals of Rhodamine 6G molecules.
Near-Infrared Photoluminescence Enhancement in Ge/CdS and Ge/ZnS Core/Shell Nanocrystals: Utilizing IV/II–VI Semiconductor Epitaxy
Black Phosphorus–Monolayer MoS2 van der Waals Heterojunction p–n Diode
Probing Electronic Excitations in Mono- to Pentalayer Graphene by Micro Magneto-Raman Spectroscopy
Ultraconformal Contact Transfer of Monolayer Graphene on Metal to Various Substrates
The direct transfer method of large area monolayer CVD graphene from Cu foil to various substrates such as PET, PDMS, and glass is developed using mechano-electro-thermal forces based on ultraconformal contact without any metal etching process or additional carrier layers in a solid-state process. Transferred graphene presents both excellent quality (with no residues, few defects, or no folding) and remarkable mechanical and electrical stability.
Atomic Structures and Gram Scale Synthesis of Three Tetrahedral Quantum Dots
Defect-Free, Size-Tunable Graphene for High-Performance Lithium Ion Battery
Highly Conductive Carbon Nanotube-Graphene Hybrid Yarn
An efficient procedure for the fabrication of highly conductive carbon nanotube/graphene hybrid yarns has been developed. To start, arrays of vertically aligned multi-walled carbon nanotubes (MWNT) are converted into indefinitely long MWNT sheets by drawing. Graphene flakes are then deposited onto the MWNT sheets by electrospinning to form a composite structure that is transformed into yarn filaments by twisting. The process is scalable for yarn fabrication on an industrial scale. Prepared materials are characterized by electron microscopy, electrical, mechanical, and electrochemical measurements. It is found that the electrical conductivity of the composite MWNT-graphene yarns is over 900 S/cm. This value is 400% and 1250% higher than electrical conductivity of pristine MWNT yarns or graphene paper, respectively. The increase in conductivity is asssociated with the increase of the density of states near the Fermi level by a factor of 100 and a decrease in the hopping distance by an order of magnitude induced by grapene flakes. It is found also that the MWNT-graphene yarn has a strong electrochemical response with specific capacitance in excess of 111 Fg−1. This value is 425% higher than the capacitance of pristine MWNT yarn. Such substantial improvements of key properties of the hybrid material can be associated with the synergy of MWNT and graphene layers in the yarn structure. Prepared hybrid yarns can benefit such applications as high-performance supercapacitors, batteries, high current capable cables, and artificial muscles.

Highly conductive hybrid multi-walled carbon nanotubes/graphene yarn are produced in a continuous, scalable process. Graphene dispersions are deposited onto the MWNT sheets by electrospinning to form a composite structure that is transformed by twist insertion into yarn filaments. The novel hybrid yarns will be useful in wearable electronic textiles applications such as batteries, high-performance supercapacitors, high current capable cables, and artificial muscles.
The Importance of the Heat Capacity of Lubricants With Nanoparticles in the Static Behavior of Journal Bearings
Frictional Behavior of Carbon Film Embedded with Controlling-Sized Graphene Nanocrystallites
Abstract
Graphene nanocrystallites embedded in amorphous carbon matrix can bring excellent tribological, electrical and magnetical properties to the carbon films. But too large size of graphene nanocrystallite would lead to degradation of the tribological performance. So it is necessary to clarify the dependence of frictional behavior of the carbon film on graphene nanocrystallite size. In order to control the size, different electron irradiation densities were introduced during film growth in the electron cyclotron resonance plasma sputtering process. Frictional tests on the films were carried out with a Pin-on-Disk tribometer. The evolution of graphene nanocrystallite size along with electron irradiation density was examined by transmission electron microscopy and Raman spectroscopy. The results showed that the graphene nanocrystallite size increased with increasing of the electron irradiation density. The film with a graphene nanocrystallite size of 1.09 nm exhibited a low friction coefficient of 0.03 and a long wear life. When nanocrystallite size increased, the friction coefficient increased and the wear life decreased. Observation on transfer film revealed that the nanocrystallite in transfer film grew larger when initial size was 1.09 nm, and changed smaller when initial size was 1.67 nm. The results suggested that embedded graphene nanocrystallite played an important role in the formation of transfer film, the initial size of graphene nanocrystallite strongly affected the frictional behavior of the film, and the graphene nanocrystallite needed to be controlled under a certain size in order to keep the good tribological performance.
DNA Base Detection Using a Single-Layer MoS2
Monolayers: Quick, Large-Area Assembly of a Single-Crystal Monolayer of Spherical Particles by Unidirectional Rubbing (Adv. Mater. 27/2014)
Unidirectional rubbing of a dry powder between two flat rubbery substrates enables quick large-area single-crystal monolayer assembly of microparticles. The rubbing process is applicable to curved surfaces, as shown here in this frontispiece. Various parameters for the rubbing conditions, such as pressure, rubbing speed, and adhesion energy of substrate, are discussed in detail by U. Jeong, J. Myoung, and co-workers on page 4633.
Enhanced Sodium-Ion Battery Performance by Structural Phase Transition from Two-Dimensional Hexagonal-SnS2 to Orthorhombic-SnS
Ambipolar Molybdenum Diselenide Field-Effect Transistors: Field-Effect and Hall Mobilities
Liquid Metal Actuator for Inducing Chaotic Advection
#TeddersRecommendsCHAOTIC ADVECTION
Chaotic advection plays an important role in microplatforms for a variety of applications. Currently used mechanisms for inducing chaotic advection in small scale, however, are limited by their complicated fabrication processes and relatively high power consumption. Here, a soft actuator is reported which utilizes a droplet of Galinstan liquid metal to induce harmonic Marangoni flow at the surface of liquid metal when activated by a sinusoidal signal. This liquid metal actuator has no rigid parts and employs continuous electrowetting effect to induce chaotic advection with exceptionally low power consumption. The theory behind the operation of this actuator is developed and validated via a series of experiments. The presented actuator can be readily integrated into other microfluidic components for a wide range of applications.
A soft actuator is developed which utilizes a droplet of Galinstan liquid metal to induce harmonic Marangoni flow at the surface of liquid metal when activated by a sinusoidal signal. This liquid metal actuator has no rigid parts and can be readily integrated into other microfluidic components for a wide range of applications.
Remarkably Improved Electrode Performance of Bulk MnS by Forming a Solid Solution with FeS – Understanding the Li Storage Mechanism
Transition metal compounds based on conversion reactions are promising electrode materials for lithium-ion batteries due to their higher lithium storage capacity compared with currently available commercial battery electrodes. Most of the studies on these materials in the literature focus on transition metal oxides and fluorides, and not much work on transition metal sulphides has been reported, partially due to their relatively poor electrochemical performance. Here, synthesis and characterization of a series of solid solution FexMn1-xS (x = 0.2, 0.5, 0.8) monosulphide compounds is reported. Interestingly, hexagonal FeS and cubic MnS can form a solid solution of FexMn1-xS (x < 0.57). It is demonstrated that the lithium storage voltage can be tuned by changing the Fe concentration in the FexMn1-xS matrix; meanwhile, the discharge-charge coulombic efficiency and cycle stability of FexMn1-xS are greatly enhanced in comparison with that of pure MnS. A half cell using Fe0.5Mn0.5S as electrode material achieves a high first cycle coulombic efficiency of 78.0% and a high reversible capacity of ca. 477 mAh g−1 after 35 cycles, while for pure MnS the first cycle coulombic efficiency is only 45.9% and the capacity rapidly fades to ≈200 mAh g−1 after 15 cycles. Although the solid solution state of Fe0.5Mn0.5S cannot be retained during conversion reaction as indicated by X-ray diffraction (XRD), X-ray absorption spectroscopy (XAS), and transmission electron microscopy (TEM), the initial discharge “polarization”, which has been considered as one of the major hurdles for conversion reaction, can be significantly reduced by this type of material design. In addition, the size and distribution of the nucleated nanophases might also be altered by the initial solid solution state of Fe0.5Mn0.5S, contributing to the improved electrochemical performance reported here.
A series of FexMn1-xS (x = 0.2, 0.5, 0.8) monosulphide compounds is synthesized using a simple solid state reaction method. The lithium storage voltage can be tuned by the content of Fe in FexMn1-xS, while the electrochemical performance of electrodes based on FexMn1-xS is greatly enhanced in comparison with that of MnS. The lithium storage mechanism of Fe0.5Mn0.5S is investigated in detail.
Epitaxially Aligned Cuprous Oxide Nanowires for All-Oxide, Single-Wire Solar Cells
Composite Titanium Dioxide Nanomaterials
Evolution of Graphene Molecules: Structural and Functional Complexity as Driving Forces behind Nanoscience
Large-Area Single-Layer MoSe2 and Its van der Waals Heterostructures
Charge Distribution View: Large Difference in Friction Performance Between Graphene and Hydrogenated Graphene Systems
Abstract
Density functional theory calculations including dispersion correction (DFT-D2) were used to investigate the relationship between charge distribution and nanofriction characteristics of graphene-based material systems. In our calculations, the single-side-hydrogenated graphene (SSHGraphene) system exhibits lower coefficient of friction, whereas the graphane system exhibits larger one compared with graphene system. These results are attributed to the adjustments of interfacial charge distribution that are induced by different hydrogen passivations. The charge distribution is smooth along the sliding direction for the SSHGraphene sheet, which yields a small potential barrier. Corrugation of the charge distribution in graphane system is much steeper than that in graphene system, which leads to a larger potential barrier. Comparative investigations reveal that the interfacial charge distributions determine the nanofriction performance, which may be helpful for friction modulation and design of new controlling lubricant material.



















