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PubMed2001

Mapping the chemistry in nanostructured materials by energy-filtering transmission electron microscopy (EFTEM).

Energy-filtered transmission electron microscopy (EFTEM) can be used to acquire elemental distribution maps at high lateral resolution within short acquisition times, which makes it quite efficient for a detailed characterization of nanostructures, as illustrated with examples concerning a nanostructured substituted La-based cermet compound and a nanoscale multilayer. In the first example, we show how phases in a rapidly cooled substituted LaNi5 can be visualized by recording jump ratio images. Secondly, EFTEM was capable of imaging individual nanoscale layers in a magnetic multilayer consisting of 2 nm terbium and 3 nm iron.

Biophysical Phenomena↗
PubMed2003

Fourier transform infrared spectroscopy study of nanostructured nickel oxide.

Nanostructured nickel oxide having different average particle sizes ranging from 3 to 16 nm were synthesized and Fourier transform infrared (FTIR) spectra of the samples were recorded in the far infrared (IR) region. The spectra were found to be dominated by surface mode absorptions with no distinct absorption corresponding to the bulk transverse optical mode. IR absorption coefficient, alpha, for the nanostructured NiO samples were calculated as a function of frequency using a macroscopic approach devised by Fuchs. The effects of crystalline geometry, numerical values of optical constants, filling factor and increased damping on the spectral features of the samples were analyzed. Though the simulations approximately reproduced the occurrence of a shoulder in the experimental spectra, the most intense peak in the simulated spectra was found to be about 50 cm(-1) above the corresponding experimentally observed peak. It was shown that the experimentally observed absorption maximum of all the samples were in close agreement with that determined using a microscopic theory based on the rigid ion model. The weak absorption peaks in the frequency region 60-100 cm(-1) appearing in the spectra of all the samples were identified as surface induced transverse acoustical modes, omegaTA, which became IR active due to the breakdown of translational symmetry in the nanocrystallites.

Crystallization↗
PubMed2002

Nanostructure manipulation device for transmission electron microscopy: application to titania nanoparticle chain aggregates.

Experimental difficulties in studying nanostructures stem from their small size, which limits the use of traditional techniques for measuring their physical properties. We have developed a nanostructure manipulation device to apply tension to chain aggregates mounted in a transmission electron microscope. A 1-mm-long slit was cut in the center of a lead-tin alloy disc, measuring 3 mm in diameter and 200 microm in thickness. The disc was heated to about 140 degrees C before it was pressed between two quartz slides. The disc was then thinned by mechanical dimpling and ion milling until holes developed around the slit. The edges of the slit were 0.2 to 3 microm in thickness while the gap between them was up to a few microns. This disc was bonded to the two plates of a cartridge. The slit could be widened or narrowed at controlled speeds of 0.5 to 300 nm/s. The system was tested using titania (TiO2) nanoparticle chain aggregates (NCA) deposited across the slit. The ends of the NCA remained attached to the edges of the slit, which was widened at about 0.7 nm/s. In this way, the NCA was stretched up to 176% of its initial length before breaking.

Equipment Design↗
PubMed2004

Advanced electron microscopy characterization of nanostructured heterogeneous catalysts.

Heterogeneous catalysis is one of the oldest nanosciences. Although model catalysts can be designed, synthesized, and, to a certain degree, characterized, industrial heterogeneous catalysts are often chemically and physically complex systems that have been developed through many years of catalytic art, technology, and science. The preparation of commercial catalysts is generally not well controlled and is often based on accumulated experiences. Catalyst characterization is thus critical to developing new catalysts with better activity, selectivity, and/or stability. Advanced electron microscopy, among many characterization techniques, can provide useful information for the fundamental understanding of heterogeneous catalysis and for guiding the development of industrial catalysts. In this article, we discuss the recent developments in applying advanced electron microscopy techniques to characterizing model and industrial heterogeneous catalysts. The importance of understanding the catalyst nanostructure and the challenges and opportunities of advanced electron microscopy in developing nanostructured catalysts are also discussed.

Catalysis↗
PubMed2005

Electron microscopy study of exotic nanostructures of cadmium sulfide.

In this article, two simple methods, evaporation-condensation and catalytic thermal evaporation, were used to investigate the synthesis of CdS nanostructures for nanoscale optoelectronic applications. To understand their growth mechanisms, various electron microscopy and microanalysis techniques were utilized in characterizing their morphologies, internal structures, growth directions and elemental compositions. The electron microscopy study reveals that when using the evaporation-condensation method, branched CdS nanorods and self-assembled arrays of CdS nanorods were synthesized at 800 degrees C and 1000 degrees C, respectively. Instead of morphological differences, both types of CdS nanorods grew along the [0001] direction. However, when using the catalytic thermal evaporation method (Au as the catalyst), patterned CdS nanowires and nanobelts were formed at the temperature region of 500-600 degrees C and 600-750 degrees C, respectively. Their growth direction was along the direction [1010] instead of [0001]. Based on the microscopy and microanalysis results, we propose some growth mechanisms in relation to the growth processes of those exotic CdS nanostructures.

Journal Article↗
PubMed2007

Plasmonic nanostructures: artificial molecules.

This Account describes a new paradigm for the relationship between the geometry of metallic nanostructures and their optical properties. While the interaction of light with metallic nanoparticles is determined by their collective electronic or plasmon response, a compelling analogy exists between plasmon resonances of metallic nanoparticles and wave functions of simple atoms and molecules. Based on this insight, an entire family of plasmonic nanostructures, artificial molecules, has been developed whose optical properties can be understood within this picture: nanoparticles (nanoshells, nanoeggs, nanomatryushkas, nanorice), multi-nanoparticle assemblies (dimers, trimers, quadrumers), and a nanoparticle-over-metallic film, an electromagnetic analog of the spinless Anderson model.

Journal Article↗
PubMedDate not supplied

DNA hybridization in nanostructural molecular assemblies enables detection of gene mutations without a fluorescent probe.

We have developed a simple single nucleotide polymorphisms (SNPs) analysis utilizing DNA hybridization in nanostructural molecular assemblies. The novel technique enables the detection of a single-base mismatch in a DNA sequence without a fluorescent probe. This report describes for the first time that DNA hybridization occurs in the nanostructural molecular assemblies (termed reverse micelles) formed in an organic medium. The restricted nanospace in the reverse micelles amplifies the differences in the hybridization rate between mismatched and perfectly matched DNA probes. For a model system, we hybridized a 20-mer based on the p53 gene sequence to 20-mer complementary oligonucleotides with various types of mismatches. Without any DNA labeling or electrochemical apparatus, we successfully detected the various oligonucleotide mismatches by simply measuring the UV absorbance at 260 nm.

DNA Mutational Analysis↗
PubMedDate not supplied

Nanostructures of complexes formed by calf thymus DNA interacting with cationic surfactants.

Synchrotron small-angle X-ray scattering was used to study the nanostructures of the complexes formed by calf thymus DNA interacting with cationic lipids (or surfactants) of didodecyldimethylammonium bromide (DDAB), cetyltrimethylammonium bromide (CTAB), and their mixture with a zwitterionic lipid of 1-palmitoyl-2-hydroxy-sn-glycero-3-phosphocholine (PHGPC). The effects of lipid/DNA ratios, DNA chain flexibility, lipid topology, and neutral lipid mixing on the nanostructures of DNA-lipid complexes were investigated. The complexes between double-stranded DNA (dsDNA) and double-tailed DDAB formed a bilayered lamellar structure, whereas the complexes between dsDNA and single-tailed CTAB preferred a structure of 2D hexagonal close packing of cylinders. With single stranded DNA (ssDNA) interacting with CTAB, the complexes showed a Pm3n cubic structure due to the different chain flexibility between dsDNA and ssDNA. The lipid molecules bound by rigid dsDNA like to form cylindrical micelles, whereas lipids bound to flexible ssDNA could form spherical or short cylindrical micelles. The addition of the neutral single-chained PHGPC lipids to the CTAB lipids could induce a structural transition of dsDNA-lipid complexes from a 2D hexagonal to a multi-bilayered lamellar structure. The parallel DNA strands were intercalated in the water layers of lamellar stacks of the mixed lipid bilayers. The DNA-DNA spacing depended on the ratios of charged lipid to neutral lipid, and charged lipid to DNA, respectively.

Animals↗
PubMed2004

Highly efficient liquid-phase photooxidation of an azo dye methyl orange over novel nanostructured porous titanate-based fiber of self-supported radially aligned H2Ti8O17 x 1.5H2O nanorods.

Novel nanostructured porous fibers of self-supported, radially aligned H2Ti8O17 x 1.5H2O nanorods were prepared from layered H2Ti4O9 x 1.2H2O tetratitanate fibers by novel solvothermal reaction in glycerine at 150-250 degrees C. The H2Ti8O17 x 1.5H2O fibers with diameters of 0.5-1.5 microm and lengths of 10-20 microm consist of multi-scale nanopores and nanostructures. They also are of high crystallinity, large surface area of 127 m2 g(-1), and stable phase up to 350 degrees C. Photocatalytic activity of the H2Ti8O17 x 1.5H2O fibers was evaluated in aqueous photooxidation of an azo dye methyl orange in the presence of UV irradiation and 02, using P-25 as the standard sample. Both the photocatalytic activity and the dispersity-agglomeration property of H2Ti8O17 x 1.5H2O fibers are pH-controllable. Highly photooxidative activity, superior to that of P-25, occurs at pH 6.0-11.0 due to certain distinguishable material characteristics and to large amounts of adsorbed reactants of surface active OH* free radicals, surface hydroxyl OH, O2*-, O*OH, and methyl orange. The agglomeration of H2Ti8O17 x 1.5H2O fibers becomes more serious from pH 2.0 to pH 5.0 and from pH 6.0 to pH 11.0. Well-dispersed H2Ti8O17 x 1.5H2O fibers occur at pH 6.0. Both the total photodegradation of waste chemicals and the entire sedimentation of H2Ti8O17 x 1.5H2O fibers can be timed to end simultaneously at suitable pH value. The photocatalyst-free reaction solution is then easily removed, and the fresh wastewater is added again. Standard unit operation processes of chemical engineering are used to design a continuous, low-cost, large-scale, liquid-phase photocatalysis technique based on the H2Ti8O17 x 1.5H2O fibers.

Azo Compounds↗
PubMed2003

Nanostructured magnetic cuprate cluster: synthesis, structure, UV-Vis spectroscopy, and magnetic properties of a new copper(II) arsenate NaCuAsO4 containing discrete [Cu4O16]24- clusters.

Crystals of copper(II) arsenate NaCuAsO(4) were grown by conventional high-temperature, solid-state methods in molten-salt media. The compounds were characterized by single crystal X-ray diffraction, UV-vis spectroscopy, and magnetic susceptibility measurements. NaCuAsO(4) crystallizes in a monoclinic lattice with a = 6.002 (1) A, b = 10.853 (2) A, c = 10.373 (2) A, beta = 91.50 (3) degrees, and V = 675.4(2) A(3); P2(1)/c (No. 14); Z = 8. The newly isolated sodium copper(II) arsenate reveals a pseudo-one-dimensional channel structure where the sodium cations reside. The extended framework contains nanostructured [Cu(4)O(16)](24-) magnetic clusters that are interlinked by closed-shell, nonmagnetic AsO(4)(3-) oxy anions via sharing vertex oxygen atoms of the CuO(5) and AsO(4) polyhedral units. Each [Cu(4)O(16)](24-) cluster consists of four CuO(5) square pyramidal units in a chair configuration centered by a center of inversion. The two crystallographically independent Cu(2+) cations adopt the [4 + 1] CuO(5) Jahn-Teller distortion giving rise to an intense d-d transition in UV-vis absorption spectra. The magnetic susceptibility measurements reveal that the title compound is antiferromagnetic. At high temperatures, the data follows a pure Curie law, suggesting noninteracting spins, but with a rapid suppression of the effective spin below T = 70 K. At low temperature, the susceptibility collapses, indicating spin gap formation as the magnetic-cluster material settles into the lowest energy magnetic singlet state. The current work in the exploratory synthesis of oxy compounds containing nanostructured transition-metal-oxide magnetic clusters leads to new materials for experimental and theoretical developments of magnetic models.

Journal Article↗
PubMed2002

Modified phthalocyanines for efficient near-IR sensitization of nanostructured TiO(2) electrode.

A zinc phthalocyanine with tyrosine substituents (ZnPcTyr), modified for efficient far-red/near-IR performance in dye-sensitized nanostructured TiO(2) solar cells, and its reference, glycine-substituted zinc phthalocyanine (ZnPcGly), were synthesized and characterized. The compounds were studied spectroscopically, electrochemically, and photoelectrochemically. Incorporating tyrosine groups into phthalocyanine makes the dye ethanol-soluble and reduces surface aggregation as a result of steric effects. The performance of a solar cell based on ZnPcTyr is much better than that based on ZnPcGly. Addition of 3alpha,7alpha-dihydroxy-5beta-cholic acid (cheno) and 4-tert-butylpyridine (TBP) to the dye solution when preparing a dye-sensitized TiO(2) electrode diminishes significantly the surface aggregation and, therefore, improves the performance of solar cells based on these phthalocyanines. The highest monochromatic incident photo-to-current conversion efficiency (IPCE) of approximately 24% at 690 nm and an overall conversion efficiency (eta) of 0.54% were achieved for a cell based on a ZnPcTyr-sensitized TiO(2) electrode. Addition of TBP in the electrolyte decreases the IPCE and eta considerably, although it increases the open-circuit photovoltage. Time-resolved transient absorption measurements of interfacial electron-transfer kinetics in a ZnPcTyr-sensitized nanostructured TiO(2) thin film show that electron injection from the excited state of the dye into the conduction band of TiO(2) is completed in approximately 500 fs and that more than half of the injected electrons recombines with the oxidized dye molecules in approximately 300 ps. In addition to surface aggregation, the very fast electron recombination is most likely responsible for the low performance of the solar cell based on ZnPcTyr.

Journal Article↗
PubMed2002

Molecular "wiring" enzymes in organized nanostructures.

We report on the "molecular wiring" efficiency of glucose oxidase in organized self-assembled nanostructures comprised of enzyme layers alternating with layers of an osmium-derivatized poly(allylamine) cationic polyelectrolyte, acting as redox relays. Varying the relative position of the active enzyme layer in nanostructures alternating active enzyme and inactive apoenzyme we have demonstrated that the specific rate of bimolecular FADH(2) oxidation ("wiring efficiency") is limited by the diffusion-like electron hopping mechanism in the multilayers.

Electrochemistry↗
PubMed2002

Synthesis and explosive decomposition of organometallic dehydro[18]annulenes: an access to carbon nanostructures.

The synthesis of eight new cyclobutadiene or ferrocene-fused organometallic dehydroannulenes is reported. Cadiot-type coupling of a 1-bromoethynyl-2-silylethynylbenzene derivative to an organometallic diyne (1,2-diethynyl-3,4-bis(trimethylsilyl)cyclobutadiene(cyclopentadienyl )cobalt or 1,2-diethynylferrocene) is followed by deprotection and Cu(OAc)(2)-promoted ring closure. Five of the organometallic dehydroannulenes were structurally characterized. Three of the novel cycles explode at temperatures from 196 to 293 degrees C and form insoluble carbon materials. The soot produced from 13a shows a high abundance of onion-like carbon nanostructures. The nanostructures were characterized by high-resolution transmission electron microscopy.

Journal Article↗
PubMed2003

Complex alpha-MoO(3) nanostructures with external bonding capacity for self-assembly.

Through manipulating crystal growth directions, we devised a versatile synthetic method to fabricate complex alpha-MoO(3) nanostructures with external bonding capacity for self-organization. Using four-armed forklike alpha-MoO(3) as nanobuilding blocks, we assembled more complex crystal morphologies, such as centrally holed nanorods, tridents, and paintbrushes. With prolonged ultrasonic treatments, pristine forklike alpha-MoO(3) crystals can be turned into less armed nanostructures, giving away the secondary arms (width < 100 nm) at the same time. On the other hand, the resultant alpha-MoO(3) itself can act as a template to produce shaped TiO(2) and other nanocrystals. Square- and horseshoe-shaped nanocrystals of anatase TiO(2) are left undissolved after removing alpha-MoO(3) templates in basic medium.

Journal Article↗
PubMed2004

Photon antibunching from oriented semiconducting polymer nanostructures.

Fluorescence intensity correlation measurements reveal that z-oriented nanostructures from single chains of a cyano-substituted polyphenylene vinylene (CN-PPV) polymer act as single-quantum emitters. Photon antibunching is observed for the first time on individual polymer nanostructures with a modulation depth exceeding 90%, providing definitive proof that radiative recombination of molecular excitons occurs at a single localized site within the folded polymer chain.

Journal Article↗
PubMed2003

Synthesis, self-assembly, and switching of one-dimensional nanostructures from new crowded aromatics.

This study outlines a versatile and expeditious synthesis of the first derivatives of a new class of benzene that is substituted with both three amide and three alkyne substituents. Sparsely covered monolayer films, made through spin-casting, reveal one-dimensional nanostructures that can be visualized with atomic force microscopy. In bulk, synchrotron X-ray diffraction and polarized light microscopy show that these nanostructured columns assemble further into a two-dimensional liquid crystalline phase. The birefringence of this phase can be switched by application of an electric field. The half-time for the liquid crystalline phase to switch is very fast and proportional to the applied voltage.

Journal Article↗
PubMed2004

Understanding the high activity of a nanostructured catalyst obtained by a deposit of Pd on Ni: first principle calculations.

The catalytic activity of a 4 monolayer deposit of Pd on a Ni(110) surface toward the hydrogenation of ethylene is investigated by using gradient-corrected periodic density functional calculations. The Pd/Ni(110) surface is strongly nanostructured, due to the anisotropic stress induced by the Ni(110) substrate on the Pd layer. A kinetic analysis, based on the investigation of the optimal reaction pathway for the hydrogenation of ethylene to ethane, is presented, allowing a comparison between Pd/Ni(110) and pure Pd(110) surfaces. The calculated activation energies allow one to reproduce the experimental result, which shows that the Pd/Ni(110) surface is about 30 times more active than the pure Pd(110) surface. This marked increase of the catalytic activity is a consequence of the specific nanostructure of the Pd/Ni(110) surface. By examining the structure of the adsorbed species and of the transition states and by analyzing the electronic properties, we show that this rate increase can be associated to the fact that the ethylene adsorption energy in the first hydrogenation step and the ethyl-hydrogen coadsorption energy in the second step are both much lower on Pd/Ni(110) than on pure Pd(110).

Journal Article↗
PubMed2004

Modular DNA-programmed assembly of linear and branched conjugated nanostructures.

A new strategy for self-assembly and covalent coupling of encoded molecular modules into nanostructures with predetermined connectivity has been developed. The method uses DNA-functionalized oligo(phenylene ethynylene)-derived organic modules for controlling the assembly and covalent coupling of multiple modules. Rigid linear modules (LM) and tripoidal modules (TM) were functionalized with short oligonucleotides at each terminus. They can hybridize and thereby link up modules containing complementary sequences. Each terminus of the oligo(phenylene ethynylene) modules also consists of a salicylaldehyde moiety, which can form metal-salen complexes with other modules. The salicylaldehyde groups of two modules are brought in proximity when their adjoining DNA sequences are complementary, and they selectively form a manganese-salen complex in the presence of ethylenediamine and manganese acetate. The resulting structures consist of a matrix of linear and branched oligo(phenylene ethynylene)s which are linked by conjugated and rigid manganese-salen complexes. These nanostructures are potential conductors for applications in molecular electronics.

Acrylic Resins↗