Nanocrystal-semiconductor interface: Atomic-resolution cross-sectional transmission electron microscope study of lead sulfide nanocrystal quantum dots on crystalline silicon

We report on a cross-sectional high resolution transmission electron microscope study of lead sulfide nanocrystal quantum dots （NCQDs） dispersed on electron-transparent silicon nanopillars that enables nearly atomically-resolved simultaneous imaging of the entire composite： the quantum dot, the interfacial region, and the silicon substrate. Considerable richness in the nanocrystal shape and orientation with respect to the substrate lattice is observed. The average NCQD-substrate separation is found to be significantly smaller than the length of the ligands on the NCQDs. Complementary photoluminescence measurements show that light emission from PbS NCQDs on silicon is effectively quenched which we attribute to intrinsic mechanisms of energy and charge transfer from PbS NCQDs to Si.     

Tunable D peak in gated graphene

We report the gate-modulated Raman spectrum of defective graphene. We show that the intensity of the D peak can be reversibly tuned by applying a gate voltage. This effect is attributed to chemical functionalization of the graphene crystal lattice, generated by an electrochemical reaction involving the water layer trapped at the interface between silicon and graphene.     

Impact of nanocrystallinity segregation on the growth and morphology of nanocrystal superlattices

A colloidal solution of 5 nm Au tetradecanethiol-coated nanoparticles is syn-thesized. After fast evaporation of one drop, ordered monolayers both composed of single domain and polycrystalline nanocrystals are obtained. On increasing the amount of materials and the evaporation time, nanocrystal films with irregular outlines are produced together with close-packed 3D superlattices exhibiting a truncated-tetrahedral shape. Using low-frequency micro-Raman scattering spectroscopy and electron microscopy the building block nanocrystallinity is characterized. Spontaneous nanocrystallinity segregation is revealed： the truncated-tetrahedral supracrystals are shown to mainly contain single domain building blocks while the supracrystalline films are composed of a mixture of single domain and polycrystalline nanocrystals. This observation points out the correlation between the nanocrystallinity segregation involved in the growth of the nanocrystal superlattices and their morphology.     

Raman scattering study of the phonon dispersion in twisted bilayer graphene

Bilayer graphene with a twist angle θ between the layers generates a superlattice structure known as a Moiré pattern. This superlattice provides a θ-dependent q wavevector that activates phonons in the interior of the Brillouin zone. Here we show that this superlattice-induced Raman scattering can be used to probe the phonon dispersion in twisted bilayer graphene (tBLG). The effect reported here is different from the widely studied double-resonance in graphene-related materials in many aspects, and despite the absence of stacking order in tBLG, layer breathing vibrations (namely ZO’ phonons) are observed.      

Formation and optical properties of ZnO:ZnFe2O4 superlattice microwires

Pure ZnO hexagonal microwires and Fe(III)-doped ZnO microwires (MWs) with a novel rectangular cross section were synthesized in a confined chamber by a convenient one-step thermal evaporation method. An oriented attachment mechanism is consistent with a vapor-solid growth process. Photoluminescence (PL) and Raman spectroscopy of the Fe(III)-doped ZnO MWs and in situ spectral mappings indicate a quasi-periodic distribution of Fe(III) along a one-dimensional (1-D) superlattice ZnO:ZnFe₂O₄ wire, while PL mapping shows the presence of optical multicavities and related multimodes. The PL spectra at room temperature show weak near-edge doublets (376 nm and 383 nm) and a broad band (450–650 nm) composed of strong discrete lines, due to a 1-D photonic crystal structure. Such a 1-D coupled optical cavity material may find many applications in future photonic and spintronic devices.      

Enhanced π-π interactions between a C60 fullerene and a buckle bend on a double-walled carbon nanotube

In situ low-voltage aberration corrected transmission electron microscopy (TEM) observations of the dynamic entrapment of a C₆₀ molecule in the saddle of a bent double-walled carbon nanotube is presented. The fullerene interaction is non-covalent, suggesting that enhanced π-π interactions (van der Waals forces) are responsible. Classical molecular dynamics calculations confirm that the increased interaction area associated with a buckle is sufficient to trap a fullerene. Moreover, they show hopping behavior in agreement with our experimental observations. Our findings further our understanding of carbon nanostructure interactions, which are important in the rapidly developing field of low-voltage aberration corrected TEM and nano-carbon device fabrication.      

Superhydrophobic and antireflective nanograss-coated glass for high performance solar cells

We present a facile method for producing superhydrophobic nanograss-coated （SNGC） glass surfaces that possess both reduced reflectivity and self-cleaning properties at the air/glass interface. The refractive index of a CaF2 nanograss （NG） layer on a glass substrate, deposited by glancing angle vapor deposition, is 1.04 at 500 nm, which is the second-lowest value ever reported so far. The fluorinated NG layer gives rise to a high water contact angle （〉150°） and very efficient cleaning out of dust with water drops. Using the dual functionalities of the SNGC glass, we demonstrate superhydrophobic and antireflective organic photovoltaic cells with excellent power conversion efficiency.     

Bivariate-continuous-tunable interface memristor based on Bi2S3 nested nano-networks

A memristor that can emulate biological synapses is a promising basic-processing unit in neural-network computation. Here we propose a new-conceptual memristor based on a memoristive interface composed of two types of non-memristive materials, successfully realizing continuously tunable resistance controlled by both voltage （current） and applied time of a single pulse with a swift response comparable with synapses. The brain-like memorizing capability of the memristor is demonstrated. The memoristive mechanism in the interface is thought to be dominated by a Schottky barrier tuned by the capture/release of the carriers in interface traps with dispersive energy.     

Cooperative effects at the interface of nanocrystalline metal–organic frameworks

Controlling the chemistry at the interface of nanocrystalline solids has been a challenge and an important goal to realize desired properties. Integrating two different types of materials has the potential to yield new functions resulting from cooperative effects between the two constituents. Metal–organic frameworks (MOFs) are unique in that they are constructed by linking inorganic units with organic linkers where the building units can be varied nearly at will. This flexibility has made MOFs ideal materials for the design of functional entities at interfaces and hence allowing control of properties. This review highlights the strategies employed to access synergistic functionality at the interface of nanocrystalline MOFs (nMOFs) and inorganic nanocrystals (NCs).

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Biomimetic corrugated silicon nanocone arrays for self-cleaning antireflection coatings

Corrugated silicon nanocone (SiNC) arrays have been fabricated on a silicon wafer by two polystyrene-sphere-monolayer-masked etching steps in order to create high-performance antireflective coatings. The reflectance was reduced from above 35% to less than 0.7% in the range 400–1050 nm, and it remained below 0.5% at incidence angles up to 70° at 632.8 nm for both s- and p-polarized light. The fluorinated corrugated SiNC array surface exhibits superhydrophobic properties with a water contact angle of 164°.      

Construction of two-dimensional hydrogen clusters on Au（111） directed by phthalocyanine molecules

Low-dimensional H2 aggregates have been successfully fabricated on Au（111） surfaces and investigated by means of low temperature scanning tunneling microscopy. We use manganese phthalocyanine （MnPc） molecules anchored on the Au（111） surface to efficiently collect and pin hydrogen molecules. A two-dimensional （2D） molecular hydrogen cluster is formed around the MnPc. The hydrogen cluster exhibits bias-dependent topography and spatial-dependent conductance spectra, which are rationalized by the exponentially decreasing threshold energy with distance from the central MnPc to activate the motion of the H2 molecules. This exponential drop reveals an interfacial phase behavior in the 2D cluster.     

Silicene nanoribbons as carbon monoxide nanosensors with molecular resolution

Applications based on silicene as grown on substrates are of high interest toward actual utilization of this unique material. Here we explore, from first principles, the nature of carbon monoxide adsorption on semiconducting silicene nanoribbons and the resulting quantum conduction modulation with and without silver contacts for sensing applications. We find that quantum conduction is detectably modified by weak chemisorption of a single CO molecule on a pristine silicene nanoribbon. This modification can be attributed to the charge transfer from CO to the silicene nanoribbon and the deformation induced by the CO chemisorption. Moderate binding energies provide an optimal mix of high detectability and recoverability. With Ag contacts attached to a -1 nm silicene nanoribbon, the interface states mask the conductance modulations caused by CO adsorption, emphasizing length effects for sensor applications. The effects of atmospheric gases--nitrogen, oxygen, carbon dioxide, and water--as well as CO adsorption density and edge-dangling bond defects, on sensor functionality are also investigated. Our results reveal pristine silicene nanoribbons as a promising new sensing material with single molecule resolution.     

Magnetoresistance oscillations of ultrathin Pb bridges

Pb nanobridges with a thickness of less than 10 nm and a width of several hundred nm have been fabricated from single-crystalline Pb films using low-temperature molecular beam epitaxy and focus ion beam microfabrication techniques. We observed novel magnetoresistance oscillations below the superconducting transition temperature (T _C ) of the bridges. The oscillations—which were not seen in the crystalline Pb films—may originate from the inhomogeneity of superconductivity induced by the applied magnetic fields on approaching the normal state, or the degradation of film quality by thermal evolution.      

Light-controlled synthesis of uniform platinum nanodendrites with markedly enhanced electrocatalytic activity

We report a fast in situ seeding approach based on zinc（II） porphyrin （ZnP） under white light irradiation, leading to uniform spherical platinum nanodendrites with tunable sizes. The platinum nanodendrites exhibit significantly improved electrocatalytic activities toward oxygen reduction reaction （ORR） and methanol oxidation reaction （MOR） compared with commercial platinum black.     

Nitrogen-doped graphene supported Pd@PdO core-shell clusters for C-C coupling reactions

The introduction of nitrogen significantly decreases the metal particle size and improves the performance of metal-based graphene-supported catalysts. In this work, the density functional theory is used to understand the interaction between nitrogen-doped graphene and Pd@PdO clusters. Experiments show that small size Pd@PdO clusters （1-2 nm） can be grown uniformly on nitrogen-doped graphene sheets by a facile oxidation-reduction method. The nanoscale interaction relationship between nitrogen-doped graphene and Pd@PdO clusters is investigated through X-ray photoelectron spectroscopy （XPS） and X-ray absorption spectra （XAS）. The composite catalysts are applied in Suzuki-Miyaura reactions giving high yields and good structural stability. These results have potential impact in design and optimization of future high performance catalyst materials for cross coupling reactions.     

Redox-sensitive colorimetric polyaniline nanoprobes synthesized by a solvent-shift process

We have synthesized water-stable polyaniline nanoparticles coated with triarmed polyethylene glycol chains using a solvent-shift method and confirmed their colloidal size and aqueous solubility. Furthermore, we have demonstrated that the polyaniline nanoparticles can be doped with biological dopants to produce distinct color changes allowing the detection of live cancer cells.      

Curved carbon nanotubes: From unique geometries to novel properties and peculiar applications

Incorporating pentagons and heptagons into the hexagonal networks of pristine carbon nanotubes （CNTs） can form various CNT-based nanostructures, as pentagons and heptagons will bend or twist the CNTs by introducing positive and negative curvature, respectively. Some typical so-made CNT-based nanostructures are reviewed in this article, including zero-dimensional toroidal CNTs, and one-dimensional kinked and coiled CNTs. Due to the presence of non-hexagonal rings and curved geometries, such nanostructures possess rather different structural, physical and chemical properties from their pristine CNT counterparts, which are reviewed comprehensively in this article. Additionally, their synthesis, modelling studies, and potential applications are discussed.     

Inhibitory activity of gold and silica nanospheres to vascular endothelial growth factor （VEGF）-mediated angiogenesis is determined by their sizes

Nanoparticles can be involved in biological activities such as apoptosis, angiogenesis, and oxidative stress by themselves. In particular, inorganic nanoparticles such as gold and silica nanoparticles are known to inhibit vascular endothelial growth factor （VEGF）-mediated pathological angiogenesis. In this study, we show that anti-angiogenic effect of inorganic nanospheres is determined by their sizes. We demonstrate that 20 nm size gold and silica nanospheres suppress VEGF-induced activation of VEGF receptor-2, in vitro angiogenesis, and in vivo pathological angiogenesis more efficiently than their 100 nm size counterparts. Our results suggest that modulation of the size of gold and silica nanospheres determines their inhibitory activity to VEGF-mediated angiogenesis.     

One-pot synthesis of thermally stable gold@mesoporous silica core-shell nanospheres with catalytic activity

A facile one-pot method has been developed to synthesize uniform gold@mesoporous silica nanospheres (Au@MSNs), which have a well-defined core-shell structure with ordered mesoporous silica as a shell. The resulting Au@MSNs have a high surface area (～521 m2/g) and uniform pore size (～2.5 nm) for the mesoporous silica shell. The diameter of the gold core can be regulated by adjusting the amount of HAuCl₄. The catalytic performance of the Au@MSNs was investigated using the reduction of 4-nitrophenol as a model reaction. The mesopores of the silica shells provide direct access for the reactant molecules to diffuse and subsequently interact with the gold cores. In addition, the Au@MSNs display the great advantage of sintering-resistance to 950 °C because the mesoporous silica shells inhibit aggregation or deformation of the gold cores. The high thermal stability enables the Au@MSNs to be employed in high-temperature catalytic reactions.      

ZnO hierarchical aggregates: Solvothermal synthesis and application in dye-sensitized solar cells

ZnO hierarchical aggregates have been successfully synthesized by solvothermal methods through reaction of zinc acetate and potassium hydroxide in methanol solution. The shapes of the aggregates were controlled by varying the ratio of Zn²⁺ and OH^? ions in the reaction system, while the size can be tuned from 2 μm to 100 nm. Oriented attachment was found to be the main mechanism of the three-dimensional assembly of small ZnO nanocrystallites into large aggregates. The performance of these aggregates in dye-sensitized solar cells (DSCs) indicated that hierarchical structured photoelectrodes can increase energy conversion efficiency of DSCs effectively when the sizes of aggregates match the wavelengths of visible light.