Hybrid Nanostructures (hybrid + nanostructure)

Distribution by Scientific Domains
Distribution within Polymers and Materials Science


Selected Abstracts


Gas Sensors: Room-Temperature Gas Sensing Based on Electron Transfer between Discrete Tin Oxide Nanocrystals and Multiwalled Carbon Nanotubes (Adv. Mater.

ADVANCED MATERIALS, Issue 24 2009
24/2009)
Hybrid nanostructures consisting of multiwalled carbon nanotubes (CNTs) uniformly coated with SnO2 nanocrystals can be used as a novel gas sensing platform, exhibiting high sensitivity to low-concentration gases (NO2, H2, and CO) at room temperature, report Junhong Chen and co-workers on p. 2487. The hybrid nanomaterial provides a new opportunity to engineer sensing devices through electronic transfer between the nanocrystals and the CNT. [source]


From Molecular Machines to Microscale Motility of Objects: Application as "Smart Materials", Sensors, and Nanodevices

ADVANCED FUNCTIONAL MATERIALS, Issue 5 2007
I. Willner
Abstract Machinelike operations are common functions in biological systems, and substantial recent research efforts are directed to mimic such processes at the molecular or nanoscale dimensions. The present Feature Article presents three complementary approaches to design machinelike operations: by the signal-triggered mechanical shuttling of molecular components; by the signal-triggering of chemical processes on surfaces, resulting in mechanical motion of micro/nanoscale objects; and by the fuel-triggered motility of biomolecule,metal nanowire hybrid systems. The shuttling of molecular components on molecular wires assembled on surfaces in semirotaxane configurations using electrical or optical triggering signals is described. The control of the hydrophilic/hydrophobic surface properties through molecular shuttling or by molecular bending/stretching processes is presented. Stress generated on microelements, such as cantilevers, results in the mechanical deflection of the cantilever. The deposition of a redox-active polyaniline film on a cantilever allows the reversible electrochemically induced deflection and retraction of the cantilever by the electrochemical oxidation or reduction of the polymer film, respectively. A micro-robot consisting of the polypyrrole (PPy) polymer deposited on a multi-addressable configuration of electrodes is described. Au magnetic core/shell nanoparticles are incorporated into a polyaniline film, and the conductivity of the composite polymer is controlled by an external magnet. Finally, the synthesis of a hybrid nanostructure consisting of two actin filaments tethered to the two ends of a Au nanowire is described. The adenosine triphosphate (ATP)-fueled motility of the hybrid nanostructure on a myosin monolayer associated with a solid support is demonstrated. [source]


Hybrid ZnAl-LDH/CNTs nanocomposites: Noncovalent assembly and enhanced photodegradation performance

AICHE JOURNAL, Issue 3 2010
Hui Wang
Abstract In this article, we reported a facile and effective strategy for assembling hybrid ZnAl-layered double hydroxide/carbon nanotubes (ZnAl-LDH/CNTs) nanocomposites through noncovalent bonds, for the first time, in the presence of L -cysteine molecules. The materials have been characterized by powder X-ray diffraction (XRD), energy dispersive X-ray spectroscopy (EDS), transmission electron microscopy (TEM), thermogravimetry and differential scanning calorimetry (TG-DSC), X-ray photoelectron spectra (XPS) and specific surface area measurement. The results indicate that L -cysteine as bridging linker plays a key role for enhancing both adhesion and dispersion of LDH nanocrystallites onto the surface of CNTs matrix through the interfacial interaction, and effectively inhibits the in situ growth of LDH crystallites, thus resulting in remarkably reduced LDH crystallite sizes; the Eu(III) fluorescence quenching in intercalated-Eu(III)complex LDH/CNTs nanocomposite can occur because of the interaction between LDH crystallites and CNTs matrix. Furthermore, it is found that as-assembled hybrid LDH/CNTs nanocomposites exhibit excellent performance for photodegradation of methyl orange molecules under UV irradiation, which is closely related to the unique hybrid nanostructure and composition of composites. © 2009 American Institute of Chemical Engineers AIChE J, 2010 [source]


Formation of Gold and Silver Nanoparticle Arrays and Thin Shells on Mesostructured Silica Nanofibers,

ADVANCED FUNCTIONAL MATERIALS, Issue 16 2007
S. Zhang
Abstract Mesostructured silica nanofibers synthesized in high yields with cetyltrimethylammonium bromide as the structure-directing agent in HBr solutions are used as templates for the assembly of Au and Ag nanoparticles and the formation of thin Au shells along the fiber axis. Presynthesized spherical Au and Ag nanoparticles are adsorbed in varying amounts onto the silica nanofibers through bifunctional linking molecules. Nonspherical Au nanoparticles with sharp tips are synthesized on the nanofibers through a seed-mediated growth approach. The number density of nonspherical Au nanoparticles is controlled by varying the amount of seeded nanofibers relative to the amount of supplied Au precursor. This seed-mediated growth is further used to form continuous Au shells around the silica nanofibers. Both the Au- and Ag-nanoparticle/silica-nanofiber hybrid nanostructures and silica/Au core/shell fibers exhibit extinction spectra that are distinct from the spectra of Au and Ag nanoparticles in solution, indicating the presence of new surface plasmon resonance modes in the silica/Au core/shell fibers and surface plasmon coupling between closely spaced metal nanoparticles assembled on silica nanofibers. Spherical Au- and Ag-nanoparticle/silica-nanofiber hybrid nanostructures are further used as substrates for surface-enhanced Raman spectroscopy, and the enhancement factors of the Raman signals obtained on the Ag-nanoparticle/silica-nanofiber hybrid nanostructures are 2,×,105 for 4-mercaptobenzoic acid and 4-mercaptophenol and 7,×,107 for rhodamine,B isothiocyanate. These hybrid nanostructures are therefore potentially useful for ultrasensitive chemical and biological sensing by using molecular vibrational signatures. [source]


Nanoscale Organic Hybrid Electrolytes

ADVANCED MATERIALS, Issue 33 2010
Jennifer L. Nugent
Nanoscale organic hybrid electrolytes are composed of organic-inorganic hybrid nanostructures, each with a metal oxide or metallic nanoparticle core densely grafted with an ion-conducting polyethylene glycol corona - doped with lithium salt. These materials form novel solvent-free hybrid electrolytes that are particle-rich, soft glasses at room temperature ; yet manifest high ionic conductivity and good electrochemical stability above 5V. [source]


Microwave-assisted graft polymerization of ,-caprolactone onto magnetite

JOURNAL OF POLYMER SCIENCE (IN TWO SECTIONS), Issue 20 2009
Alexandrina Nan
Abstract The graft polymerization of ,-caprolactone (,-CL) onto magnetite was carried out under microwave irradiation in the presence of tin(II) 2-ethylhexanoate. The molar ratio of ,-CL to tin(II) 2-ethylhexanoate was 300, whereas the molar ratio of ,-CL to magnetite was 5. The chemical structures of the obtained poly(,-caprolactone) coated magnetic nanoparticles were characterized by FTIR and XPS spectroscopy. These magnetic-polymer hybrid nanostructures were further investigated by X-ray diffraction and magnetization measurements. The morphology of the magnetic core-shell nanostructures were determined by TEM. © 2009 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 47: 5397,5404, 2009 [source]


Nanogel-Templated Mineralization: Polymer-Calcium Phosphate Hybrid Nanomaterials

MACROMOLECULAR RAPID COMMUNICATIONS, Issue 6 2006
Ayae Sugawara
Abstract Summary: We report novel organic-inorganic hybrid nanomaterials that consist of polymer hydrogel nanoparticles (nanogels) and calcium phosphate. Hybrid nanoparticles that measure ca. 40 nm are synthesized from a dilute solution of hydroxyapatite using nanogels as templates for calcium phosphate mineralization. These nanoparticles show a narrow size distribution and high colloidal stability. Nanogel-adsorbed liposomes act as templates for hierarchical hybrid nanostructures. These nanohybrids can potentially be used as biocompatible drug carriers with controlled-release properties. TEM images of calcium phosphate nanoparticles formed in the presence of CHP nanogels (0.5 mg,·,mL,1) (left) and nanogel-liposomes (CHP 0.05 mg,·,mL,1, DPPC 0.08 mg,·,mL,1)(right). [source]


Template-directed synthesis of hybrid nanowires and nanorods

PHYSICA STATUS SOLIDI (B) BASIC SOLID STATE PHYSICS, Issue 10 2010
Jiayin Yuan
Abstract Recently, one-dimensional (1D) nanostructures, such as wires, rods, tubes, etc., have attracted considerable attention due to their unique shape- and size-dependant properties and many potential applications. Template-directed synthesis is a powerful and widely used method to prepare 1D objects. As robust unimolecular template, cylindrical polymer brushes have been exploited for the fabrication of various hybrid nanowires and nanorods, for instance, ,-Fe2O3, CdS, CdSe, TiO2, silica, Au, Te, etc. As a key advantage of this polymeric templating, the obtained 1D hybrid nanostructures are colloidally stable in solution, facilitating their further solution processing. Cryo-TEM image of organo-silica hybrid nanowires in aqueous solution (the inset shows a cartoon of the structure). [source]