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A comprehensive structural/architectural evaluation of the PtRu (1:1) alloy and Ru@Pt core-shell nanoparticles (NPs) provides spatially resolved structural information on sub-5 nm NPs. A combination of extended X-ray absorption fine structure (EXAFS), X-ray absorption near edge structure (XANES), pair distribution function (PDF) analyses, Debye function simulations of X-ray diffraction (XRD), and field emission transmission electron microscopy/energy dispersive spectroscopy (FE-TEM/EDS) analyses provides complementary information used to construct a detailed picture of the core/shell and alloy nanostructures. The 4.4 nm PtRu (1:1) alloys are crystalline homogeneous random alloys with little twinning in a typical face-centered cubic (fcc) cell. The Pt atoms are predominantly metallic, whereas the Ru atoms are partially oxidized and are presumably located on the NP surface. The 4.0 nm Ru@Pt NPs have highly distorted hcp Ru cores that are primarily in the metallic state but show little order beyond 8 A. In contrast, the 1-2 monolayer thick Pt shells are relatively crystalline but are slightly distorted (compressed) relative to bulk fcc Pt. The homo- and heterometallic coordination numbers and bond lengths are equal to those predicted by the model cluster structure, showing that the Ru and Pt metals remain phase-separated in the core and shell components and that the interface between the core and shell is quite normal.
ACS Nano 2009 Oct 27
PMID:Structural and architectural evaluation of bimetallic nanoparticles: a case study of Pt-Ru core-shell and alloy nanoparticles. 1973 34

We report on a real-time in situ TEM study of the coalescence of individual pairs of decahedral gold nanoparticles, which have been synthesized in solution. We observe the rate of growth of the neck that joins two particles during coalescence and compare this to classical continuum theory and to atomistic kinetic Monte Carlo simulations. We find good agreement between the observations and the simulations but not with the classical continuum model. This disagreement is attributed to the faceted nature of the particles.
ACS Nano 2009 Nov 24
PMID:Real-time TEM and kinetic Monte Carlo studies of the coalescence of decahedral gold nanoparticles. 1985 52

We describe molecular capturing properties of protein nanotubes with a controllable ligand binding affinity and size selectivity. These practical biocylinders were prepared using an alternating layer-by-layer (LbL) assembly of protein and oppositely charged poly(amino acid) into the nanoporous polycarbonate (PC) membrane (pore diameter, 400 nm), with subsequent dissolution of the template. The tube wall typically comprises six layers of poly-L-arginine (PLA) and human serum albumin (HSA) [(PLA/HSA)(3)]. Use of high molecular weight PLA (M(w) = ca. 70 000) yielded robust nanotubes, which are available as lyophilized powder. The (PLA/HSA)(3) nanotubes swelled considerably in water, although the outer diameter was almost unaltered. Uranyl ion, 3,3'-diethylthiacarbocyanine iodide, and zinc(II) protoporphyrin IX (ZnPP) were bound to the HSA component in the cylinder wall. Similar nanotubes comprising recombinant HSA mutant [rHSA(His)], which has a strong binding affinity for ZnPP, captured this ligand more tightly. Furthermore, addition of excess myristic acid released ZnPP from the tubes through a ligand replacement reaction. The hybrid nanotubes bearing a single avidin layer as an internal surface captured FITC-biotin efficiently. Biotin-labeled nanoparticles are also incorporated into the tubes when their particle size is sufficiently small to enter the pores. Subsequent TEM observation revealed a line of loaded nanoparticles (100 nm) in the one-dimensional space interior.
ACS Nano 2010 Jan 26
PMID:Molecular capture in protein nanotubes. 2002 Jul 54

Solution phase triangular silver nanoplates (TSNP) with versatile tunability throughout the visible-NIR wavelengths are presented as highly sensitive localized surface plasmon refractive index sensors. A range of 20 TSNP solutions with edge lengths ranging from 11 to 200 nm and aspect ratios from 2 to 13 have been studied comprehensively using AFM, TEM, and UV-vis-NIR spectroscopy. Studies of the localized surface plasmon resonance (LSPR) peak's sensitivity to refractive index changes are performed using a simple sucrose concentration method whereby the surrounding refractive index can solely be changed without variation in any other parameter. The dependence of the TSNP localized surface plasmon resonance (LSPR) peak wavelength lambda(max) and its bulk refractive index sensitivity on the nanoplate's structure is determined. LSPR sensitivities are observed to increase linearly with lambda(max) up to 800 nm, with the values lying within the upper limit theoretically predicted for optimal sensitivity, notwithstanding any diminution due to ensemble averaging. A nonlinear increase in sensitivity is apparent at wavelengths within the NIR region with values reaching 1096 nm.RIU(-1) at lambda(max) 1093 nm. Theoretical studies performed using a simple aspect ratio dependent approximation method and discrete dipole approximation methods confirm the dependence of the LSPR bulk refractive index sensitivity upon the TSNP aspect ratio measured experimentally. These studies highlight the importance of this key parameter in acquiring such high sensitivities and promote these TSNP sols for sensing applications at appropriate wavelengths for biological samples.
ACS Nano 2010 Jan 26
PMID:Versatile solution phase triangular silver nanoplates for highly sensitive plasmon resonance sensing. 2003 Mar 62

There has been no attempt to date to specifically modify the nodes in carbon nanotube (CNT) networks. If the nodes can be modified in favorable ways, the electrical and/or thermal and/or mechanical properties of the CNT networks could be improved. In an attempt to influence the performance as a transparent conductive film, gold nanoparticles capped with the amino acid cysteine (Au-CysNP) have been selectively attached at the nodes of multiwalled carbon nanotubes (MWCNTs) networks. These nanoparticles have an average diameter of 5 nm as observed by TEM. FTIR and XPS were used to characterize each step of the MWCNT chemical functionalization process. The chemical process was designed to favor selective attachment at the nodes and not the segments in the CNT networks. The chemical processing was designed to direct formation of nodes where the gold nanoparticles are. The nanoparticles which were loosely held in the CNT network could be easily washed away by solvents, while those bound chemically remained. TEM results show that the Cys-AuNPs are preferentially located at the nodes of the CNT networks when compared to the segments. These nanoparticles at the nodes were also characterized by a novel technique called diffraction scanning transmission electron microscopy (D-STEM) confirming their identity. Four-probe measurements found that the sheet resistance of the modified CNT networks was half that of similarly transparent pristine multiwalled CNT networks.
ACS Nano 2010 Jan 26
PMID:Site-specific deposition of Au nanoparticles in CNT films by chemical bonding. 2005 76

Solid nanotubes comprising alpha-Fe2O3 nanoparticles were prepared from iron-storage protein ferritin. Their structure, magnetic properties, and photocatalytic activities were characterized. The initial ferritin nanotube precursors were fabricated using alternating layer-by-layer depositions of poly-L-arginine (PLA) and ferritin into a track-etched polycarbonate membrane (pore diameter, 400 nm) with subsequent dissolution of the template. The obtained uniform cylinders of (PLA/ferritin)3 (outer diameter, 410 +/- 14 nm) were calcinated at 500 degrees C under air, yielding reddish-brown iron oxide nanotubes. The one-dimensional hollow structure remained perfect, but its diameter, wall thickness, and maximum length were markedly diminished. Disappearance of the protein shell and the PLA layers were confirmed using IR and EDX spectroscopy. Subsequent SEM, TEM, and XPS measurements showed that the tubular walls comprise fine alpha-Fe2O3 nanoparticles with a 5 nm diameter. These alpha-Fe2O3 nanotubes demonstrated superparamagnetic properties with a blocking temperature of 37 K and efficient photocatalytic activity for degradation of 4-chlorophenol.
ACS Nano 2010 Mar 23
PMID:Solid nanotubes comprising alpha-Fe2O3 nanoparticles prepared from ferritin protein. 2016

Multipotent mesenchymal stem cells (MSCs) have attracted substantial attention in stem cell therapy and tissue engineering due to their ability to be cultured for successive passages and multilineage differentiation. Carbon nanotubes (CNTs) have been proposed to be used as potential biomedical structures for bone formation. Therefore, it is important to study the mechanisms of interaction between MSCs and CNTs. We demonstrated that carboxylated single-walled carbon nanotubes (SWCNTs) and carboxylated multiwalled carbon nanotubes (MWCNTs) inhibited the proliferation, osteogenic differentiation, adipogenic differentiation, and mineralization of MSCs. Oxidative stress assay indicated that reactive oxygen species (ROS) may not be responsible for the observed cytotoxicity of carboxylated CNTs. Quantitative real-time polymerase chain reaction (Q-PCR) experiments confirmed that the expression of osteoblast specific genes and adipocyte differentiation specific genes was greatly attenuated during the differentiation of MSCs in the presence of carboxylated CNTs. TEM images revealed that CNTs might interact with proteins located on the cell membrane or in the cytoplasm, which have a further impact on subsequent cellular signaling pathways. Q-PCR results and Western blot analysis together verified that the inhibition of proliferation and osteogenic differentiation of MSCs may be modulated through a Smad-dependent bone morphogenetic protein (BMP) signaling pathway.
ACS Nano 2010 Apr 27
PMID:Inhibition of proliferation and differentiation of mesenchymal stem cells by carboxylated carbon nanotubes. 2021 64

Multicomponent nanocrystal assemblies have received great attention due to their fundamental role in the study of self-assembly and novel physical properties arising from particle interactions. Here, we report the formation of the first binary nanocrystal superlattices (BNSLs) consisting of different-sized Fe3O4 nanocrystals. We establish a framework to systematically study the structure of BNSLs using a dual-axis tomography TEM holder. The tilt series obtained not only allows us to map the three-dimensional (3D) structure of icosahdedral AB(13) (ico-AB(13)) and AlB(2)-type BNSLs but also uncovers the structural differences among the projections of ico-AB(13), cuboctahedral AB(13) (cub-AB(13)), and AlB(2). This structural characterization method is general and is important for further exploration of structural diversity in BNSLs and in the development of rigorous structure-property relationships in BNSLs. The formation of ico-AB(13) and AlB(2) BNSLs from electrostatically neutral Fe3O4 nanoparticles is consistent with the space-filling principles and further supports entropy as the dominant factor during the growth of these BNSLs.
ACS Nano 2010 Apr 27
PMID:Systematic electron crystallographic studies of self-assembled binary nanocrystal superlattices. 2030 47

The conformal deposition of metal nanoparticles (Au, Pd, and Pt) onto natural cellulose fibers using two chemical strategies is reported. The driven mechanism responsible for the high surface coverage of the substrates was identified as the electrostatic interactions between the positively charged cellulose and the either negatively charged nanoparticles or negative metal complex ions. The natural cellulose fibers were rendered cationic by grafting ammonium ions, using an epoxy substitution reaction, to the abundant hydroxyl groups present in cellulose molecules. The first method involved the electrostatic assembly of citrate-stabilized metal nanoparticles directly onto the cationic surfaces of cellulose. The second method involved the adsorption of negative metal complex ions onto the cationic cellulose followed by a reduction reaction. The attained metal nanoparticles bound with cellulose fibers were characterized by electron microscopy (TEM and SEM) and energy-dispersive X-ray spectroscopy (EDX). Both pathways generated metal nanoparticles with high packing densities on the cellulose substrates even when very dilute solutions of metal colloids or metal salts were used. Achieving high surface coverage with low-concentration precursor solutions may open an avenue for the production of flexible catalytic mantles or highly functionalized textile substrates.
ACS Appl Mater Interfaces 2009 Apr
PMID:Metal nanoparticles on natural cellulose fibers: electrostatic assembly and in situ synthesis. 2035 4

Nanocrystalline mesoporous gamma-Al2O3 film of high thickness has been developed and characterized. The films were prepared on ordinary glass substrates by a single dip-coating method using boehmite (AlOOH) sols derived from aluminum tri-sec-butoxide in presence of cetyltrimethylammonium bromide (CTAB) as structure-directing agent. The dried films were heat-treated at 500 degrees C in air to remove the organics and strengthen the network. The GIXRD of the heat-treated (500 degrees C) film shows a broad peak in the low-angle region supporting the formation of worm-hole-like disordered mesostructures. The high-angle GIXRD, FTIR, and TEM of the films confirm the formation of gamma-Al2O3. N2 adsorption-desorption analyses showed that the heat-treated (500 degrees C) film has a BET surface area of 171 m(2) g(-1) with a pore volume of 0.188 cm(3) g(-1) and mean pore diameter 4.3 nm. Pt nanoparticles (NPs) (approximately 2.7 mol % with respect to the equivalent AlO(1.5)) were generated inside the mesopores of the heat-treated films simply by soaking H2PtCl6 solutions into it, and followed by thermal decomposition at 500 degrees C. The surface area and pore volume of the Pt-incorporated film have been reduced to 101 m(2) g(-1) and 0.119 cm(3) g(-1) respectively, confirming the inclusion of Pt NPs inside the pores. FESEM and TEM studies revealed uniform distribution of Pt NPs (2-8.5 nm; average diameter 4.9 nm) in the films. Catalytic properties of the Pt-incorporated films were investigated in two model (one inorganic and other organic) systems: reduction of hexacyanoferrate(III) ions by thiosulfate to ferrocyanide, and p-nitrophenol to p-aminophenol. In both the cases, the catalyst showed excellent activities, and the reduction reactions followed smoothly, showing isosbestic points in the UV-visible spectra. The catalyst films can be separated easily after the reactions and reused several times.
ACS Appl Mater Interfaces 2009 Apr
PMID:Synthesis of thick mesoporous gamma-alumina films, loading of Pt nanoparticles, and use of the composite film as a reusable catalyst. 2035 9


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