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Vanadium dioxide (VO(2)) is a well-known semiconductor material with a band gap of 0.7 eV, and is seldom used as a photocatalyst. We report here a new crystal structure for nanostructured VO(2), with body-centered-cubic (bcc) structure and a large optical band gap of approximately 2.7 eV, which surprisingly shows excellent photocatalytic activity in hydrogen production. The bcc VO(2) phase exhibited a high quantum efficiency of approximately 38.7% when synthesized as nanorods. Using films of the aligned VO(2) nanorods, the hydrogen production rate can be tuned by varying the incident angle of UV light on the films and reaches a high rate of 800 mmol/m(2)/h from a mixture of water and ethanol under UV light, at a power density of approximately 27 mW/cm(2), allowing possible commercial application of this material as photoassisted hydrogen generators.
ACS Nano 2008 Jul
PMID:Nanostructured VO2 photocatalysts for hydrogen production. 1920 20

Purification of high-quality few-walled carbon nanotubes (fWNTs) was developed by slow but selective oxidation in hydrogen peroxide (H(2)O(2)) at room temperature. The purity, nanotubes' structure, and thermal stability of purified fWNTs were characterized by transmission electron microscopy (TEM), Raman spectroscopy, and thermogravimetric analysis (TGA), respectively. The results showed that fWNTs could be selectively purified by prolonging the stirring time in 30 wt % H(2)O(2) solution. Highly purified fWNTs were obtained, having a high G/D ratio in Raman spectra and good thermal stability indicating the good quality of the purified fWNTs. The approach provides a simple low cost method for purification that also has higher nanotube yield than other purification methods.
ACS Nano 2008 Aug
PMID:Room temperature purification of few-walled carbon nanotubes with high yield. 1920 66

High-quality single-walled carbon nanotubes (SWNTs) with tunable diameters were synthesized by an improved H(2)/CH(4)-based floating catalyst method. Transmission electron microscopy observations and Raman results demonstrated the overall quality of the as-synthesized samples with finely tailored large diameters at 1.28, 1.62, 1.72, 1.91, and 2.13 nm, depending on the experimental conditions. In addition, Raman analysis revealed that the abundance of specific (n, m) SWNTs could be selectively enriched simultaneously along with the diameter modulation. It was found that the selective etching effects of high hydrogen flow stabilized the decomposition of ultralow CH(4) flow and considerably suppressed the deposition of amorphous carbon and small nanotubes, leading to very pure samples with high structural homogeneity suitable for further applications in practical electronic systems.
ACS Nano 2008 Aug
PMID:Diameter-selective growth of single-walled carbon nanotubes with high quality by floating catalyst method. 1920 77

We report the novel fabrication of a highly sensitive, selective, fast responding, and affordable amperometric glucose biosensor using exfoliated graphite nanoplatelets (xGnPs) decorated with Pt and Pd nanoparticles. Nafion was used to solubilize metal-decorated graphite nanoplatelets, and a simple cast method with high content organic solvent (85 wt %) was used to prepare the biosensors. The addition of precious metal nanoparticles such as platinum (Pt) and palladium (Pd) to xGnP increased the electroactive area of the electrode and substantially decreased the overpotential in the detection of hydrogen peroxide. The Pt-xGnP glucose biosensor had a sensitivity of 61.5+/-0.6 microA/(mM x cm(2)) and gave a linear response up to 20 mM. The response time and detection limit (S/N=3) were determined to be 2 s and 1 microM, respectively. Therefore, this novel glucose biosensor based on the Pt nanoparticle coated xGnP is among the best reported to date in both sensing performance and production cost. In addition, the effects of metal nanoparticle loading and the particle size on the biosensor performance were systematically investigated.
ACS Nano 2008 Sep 23
PMID:Nanometal-decorated exfoliated graphite nanoplatelet based glucose biosensors with high sensitivity and fast response. 1920 21

Isolated, carbon nanotube cups with diameters of 12-40 nm have been synthesized by chemical vapor deposition through incorporation of nitrogen atoms into graphitic carbon structure and subsequent mechanical separation. Incorporation of nitrogen affords carbon nanotube cups with a unique composition comprising multiwalled, graphitic lattice with nitrogen groups on the exterior rim and hollow interior cavities. These nanostructures demonstrate the ability to participate in hydrogen bonding because of nitrogen functionalities on their open edges. Furthermore, reaction with these nitrogen functionalities results in the coupling of gold nanoparticles (GNPs) to the open rim of carbon nanotube cups. Through atomic force microscopy manipulation and adhesion force measurements, we compare the mobility of these structures on a hydrophilic surface before and after GNP coupling. Understanding of these forces will aid in useful nanostructure assembly for energy and biomedical applications.
ACS Nano 2008 Sep 23
PMID:Synthesis, characterization, and manipulation of nitrogen-doped carbon nanotube cups. 1920 32

Synthetic nanoscale motors represent a major step toward the development of practical nanomachines. Despite impressive progress, man-made nanomachines lack the efficiency and speed of their biological counterparts. Here we show that the incorporation of carbon nanotubes (CNT) into the platinum (Pt) component of asymmetric metal nanowire motors leads to dramatically accelerated movement in hydrogen-peroxide solutions, with average speeds (50-60 microm/s) approaching those of natural biomolecular motors. Further acceleration to 94 microm/s, with some motors moving above 200 microm/sis observed upon adding hydrazine to the peroxide fuel. Factors influencing the accelerated movement, including the CNT loading and fuel concentration, are examined. Such development of highly efficient and controllable nanomotors offers great promise for self-powered nanoscale transport and delivery systems.
ACS Nano 2008 May
PMID:Carbon-nanotube-induced acceleration of catalytic nanomotors. 1920 5

Self-assembling peptide-based nanotubes are among the most investigated bioactive compounds as a result of their numerous potential applications as novel biomaterials. To support rational bottom-up design of such artificial nanosystems, here we investigate structural and energetic properties of various sheet-derived nanotubes. We carried out high level quantum chemical calculations on large models, composed of up to 32 amino acids, and characterized structures from extended beta-sheets to the molecular framework of beta-barrel proteins. Surprisingly, enzyme-resistant nonnatural beta-peptides have an affinity to form nanotubes that is remarkably higher than that of natural alpha-peptides. We analyzed the stability of both systems depending on (i) parallel or antiparallel orientation, (ii) the number of peptide strands, and (iii) the formed hydrogen bond pattern. Applicability is outlined by investigating guest molecules in the tubes. It is hoped that the structural and energetic data presented here will be effectively used in the design of novel peptide nanosystems.
ACS Nano 2008 Mar
PMID:A theoretical comparison of self-assembling alpha- and beta-peptide nanostructures: toward design of beta-barrel frameworks. 1920 81

Using a novel hydrogen peroxide heating method, we synthesized milky white, water-soluble polyhydroxylated fullerenes (fullerenols) with 36-40 hydroxyl groups (estimated average) along with 8-9 secondary bound water molecules. The fullerenols exhibited high water solubility up to 58.9 mg/mL in a neutral (pH = 7) condition. Dynamic light scattering analysis showed a high dispersion property, to give a narrow particle size distribution within 0.7-2.0 nm.
ACS Nano 2008 Feb
PMID:Facile synthesis of highly water-soluble fullerenes more than half-covered by hydroxyl groups. 1920 34

We present the integration of amphiphilic block copolymer micelles as nanometer-sized vehicles for hydrophobic drugs within layer-by-layer (LbL) films using alternating hydrogen bond interactions as the driving force for assembly for the first time, thus enabling the incorporation of drugs and pH-sensitive release. The film was constructed based on the hydrogen bonding between poly(acrylic acid) (PAA) as an H-bond donor and biodegradable poly(ethylene oxide)-block-poly(epsilon-caprolactone) (PEO-b-PCL) micelles as the H-bond acceptor when assembled under acidic conditions. By taking advantage of the weak interactions of the hydrogen-bonded film on hydrophobic surfaces, it is possible to generate flexible free-standing films of these materials. A free-standing micelle LbL film of (PEO-b-PCL/PAA)60 with a thickness of 3.1 microm was isolated, allowing further characterization of the bulk film properties, including morphology and phase transitions, using transmission electron microscopy and differential scanning calorimetry. Because of the sensitive nature of the hydrogen bonding employed to build the multilayers, the film can be rapidly deconstructed to release micelles upon exposure to physiological conditions. However, we could also successfully control the rate of film deconstruction by cross-linking carboxylic acid groups in PAA through thermally induced anhydride linkages, which retard the drug release to the surrounding medium to enable sustained release over multiple days. To demonstrate efficacy in delivering active therapeutics, in vitro Kirby-Bauer assays against Staphylococcus aureus were used to illustrate that the drug-loaded micelle LbL film can release significant amounts of an active antibacterial drug, triclosan, to inhibit the growth of bacteria. Because the micellar encapsulation of hydrophobic therapeutics does not require specific chemical interactions, we believe this noncovalent approach provides a new route to integrating active small, uncharged, and hydrophobic therapeutics into LbL thin films for biological and biomedical coatings.
ACS Nano 2008 Feb
PMID:Hydrogen-bonding layer-by-layer-assembled biodegradable polymeric micelles as drug delivery vehicles from surfaces. 1920 41

A series of star-shaped oligofluorenes end-capped with carboxylic acid groups were synthesized. Different numbers of carboxyl groups that can form hydrogen bonds, and long alkane chains that have stabilizing effects, were intentionally introduced. The resulting molecular architectures of the so-prepared star-shaped oligofluorenes at the liquid-solid interface were investigated by scanning tunneling microscopy. It is found that the number of hydrogen-bonding groups and the symmetry of the target molecules have crucial influences on the structures of the ordered assemblies.
ACS Nano 2007 Oct
PMID:Star-shaped oligofluorenes end-capped with carboxylic groups: syntheses and self-assembly at the liquid-solid interface. 1920 46


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