Interparticle Distance (interparticle + distance)

Distribution by Scientific Domains


Selected Abstracts


Interface Modifications of InAs Quantum-Dots Solids and their Effects on FET Performance

ADVANCED FUNCTIONAL MATERIALS, Issue 6 2010
Michal Soreni-Harari
Abstract InAs nanocrystals field-effect transistors with an ON/OFF ratio of 105 are reported. By tailoring the interface regions in the active layer step-by-step, the evolution of the ON/OFF ratio can be followed from approximately 5 all the way to around 105. The formation of a semiconducting solid from colloidal nanocrystals is achieved through targeted design of the nanocrystal,nanocrystal interaction. The manipulation characteristics of the nanocrystal interfaces include the matrix surrounding the inorganic core, the interparticle distance, and the order of nanocrystals in the 3D array. Through careful analysis of device characteristics following each treatment, the effect of each on the physical properties of the films are able to be verified. The enhanced performance is related to interparticle spacing, reduction in sub-gap states, and better electronic order (lower , parameter). Films with enhanced charge transport qualities retain their quantum-confined characteristics throughout the procedure, thus making them useful for optoelectronic applications. [source]


Highly Stable Au Nanoparticles with Tunable Spacing and Their Potential Application in Surface Plasmon Resonance Biosensors

ADVANCED FUNCTIONAL MATERIALS, Issue 1 2010
Shuyan Gao
Abstract Colloidal Au-amplified surface plasmon resonance (SPR), like traditional SPR, is typically used to detect binding events on a thin noble metal film. The two major concerns in developing colloidal Au-amplified SPR lie in 1) the instability, manifested as a change in morphology following immersion in organic solvents and aqueous solutions, and 2) the uncontrollable interparticle distance, determining probe spacing and inducing steric hindrance between neighboring probe molecules. This may introduce uncertainties into such detecting techniques, degrade the sensitivity, and become the barricade hampering colloidal Au-based transducers from applications in sensing. In this paper, colloidal Au-amplified SPR transducers are produced by using ultrathin Au/Al2O3 nanocomposite films via a radio frequency magnetron co-sputtering method. Deposited Au/Al2O3 nanocomposite films exhibit superior stability, and average interparticle distances between Au nanoparticles with similar average sizes can be tuned by changing surface coverage. These characteristics are ascribed to the spacer function and rim confinement of dielectric Al2O3 and highlight their advantages for application in optimal nanoparticle-amplified SPR, especially when the probe size is smaller than the target molecule size. This importance is demonstrated here for the binding of protein (streptavidin) targets to the probe (biotin) surface. In this case, the dielectric matrix Al2O3 is a main contributor, behaving as a spacer, tuning the concentration of Au nanoparticles, and manipulating the average interparticle distance, and thus guaranteeing an appropriate number of biotin molecules and expected near-field coupling to obtain optimal sensing performance. [source]


Cover Picture: Assembly of Wiseana Iridovirus: Viruses for Colloidal Photonic Crystals (Adv. Funct.

ADVANCED FUNCTIONAL MATERIALS, Issue 8 2006
Mater.
Abstract Assembly of colloids is a versatile tool for micro- and nanofabrication. Natural and artificially engineered viruses offer the opportunity to expand the functionality and versatility of such assemblies. The cover shows optically iridescent, thin polycrystalline arrays (background) as well as bulk pellets (inset right) that exhibit reversible hydration-dependent reflection spectra, as reported by Vaia and co-workers on p.,1086. The films and pellets were created in vitro with classical colloid-assembly techniques from Wiseana iridescent virus (inset, center) harvested from infected Wiseana spp larvae (inset, left). In,vitro assembly of Wiseana iridescent virus (WIV) yields iridescent pellets and films with structural color more vivid than in the native insect. WIV is icosahedral in shape, 140,nm in diameter, with 30,nm long fibrils attached to the outer surface, and exhibits a surface charge ca.,1/6th that of a comparable polymer colloid. The low surface charge and tethered chains on the virus surface allow the facile modification of the interparticle distance. Directed sedimentation yields predominantly an amorphous liquid-like packing of the virus. Such samples exhibit a broad reflection band that is angle independent and for which the broad maximum can be reversibly shifted from blue towards red with increased hydration. Slow sedimentation and flow-assisted assembly methods produce thin films with a polycrystalline morphology that exhibit narrower, more intense reflectivity peaks, which are hydration and angle dependent. This study points toward the potential of viral particles for photonic crystals where their unique structural features (icosahedral symmetry, extreme monodispersity, precise surface functionalization, and tethered surface chains of low surface-charge density) may lead to superior control of optical properties of their assembled arrays. [source]


Peptide Nanotubes: Simple Separation Using Size-Exclusion Columns and Use as Templates for Fabricating One-Dimensional Single Chains of Au Nanoparticles,

ADVANCED MATERIALS, Issue 14 2005
X. Gao
Straight single chains of Au nanoparticles have been synthesized using 10,nm diameter peptide nanotubes as templates (see Figure). The 6,nm Au nanoparticles grow in the gaps between the synthetic peptide coating the nanotubes which regulates the size, dispersity, interparticle distance, and crystallinity of the nanoparticles. The use of longer nanotubes results in longer chains. [source]


Controlled Assembly of Protein,Nanoparticle Composites through Protein Surface Recognition,

ADVANCED MATERIALS, Issue 5 2005
S. Srivastava
Controlled assembly of protein,nanoparticle composites through complementary protein surface recognition is demonstrated. Interaction of an unstable protein (chymotrypsin) with a gold nanoparticle results in close interparticle spacing, while a stable protein (cytochrome,C) that retains its structure upon binding produces a hybrid material with a larger interparticle distance (see Figure). [source]


Thomas,Fermi approximation for the quasi-two-dimensional electron gas

INTERNATIONAL JOURNAL OF QUANTUM CHEMISTRY, Issue 6 2001
M. Moreno
Abstract To take into account static correlation effects in the quasi-two-dimensional electron gas a screened Coulombic interaction between particles is studied. The Thomas,Fermi approximation is used and the potential screening appears as a function of the Wigner,Seitz density parameter rs and the effective width t of the system. With the self-consistent field theory applied to the modified deformable jellium, the ground-state energy per particle and the conditions for electron localization are obtained in terms of the interparticle distance and the screening parameter ,. A critical minimum characteristic width tc is obtained; below tc no long-range order is obtained. For larger widths a stable localized state is predicted at finite densities. © 2001 John Wiley & Sons, Inc. Int J Quant Chem 82: 269,276, 2001 [source]


New antistatic charge and electromagnetic shielding effectiveness from conductive epoxy resin/plasticized carbon black composites

POLYMER COMPOSITES, Issue 2 2008
Nadia Abdel Aal
Recently, there is an increasing interest in electromagnetic interference shielding due to the rapid increase in electromagnetic pollution and the wide use of commercial and military products. Conducting polymer composites were prepared in the presence of epoxy resin and plasticized carbon black (CB). The structural characteristics of the composites were examined by means of scanning electron microscopy, cross linking density, and interparticle distance among conductive particles. The mechanical properties such as Young's modulus, elongation at break, and hardness of the composites were investigated as a function of CB content. The results indicated that CB could improve the composite microstructure. The higher mechanical behavior than green epoxy can be attributed to the interaction between CB particles and epoxy resin. The conductivity, mobility carriers, and number of charges of the composites at room temperature were found to be dependent on CB content. The applicability of the composites to antistatic charge dissipation was examined. Dependence of the microwave properties of the epoxy/CB composites on the volume fraction of CB particles and frequency were studied. Moreover the permittivity as a function of frequency of the composites was studied. The electromagnetic wave shielding of epoxy/CB composites is dominant by both reflection and absorption. Composites can find applications in antistatic charge dissipation and in suppression of electromagnetic interference and stealth technology. POLYM. COMPOS., 2008. © 2007 Society of Plastics Engineers [source]


Effects of addition of functionalized SEBS on rheological, mechanical, and tribological properties of polyamide 6 nanocomposites

POLYMER ENGINEERING & SCIENCE, Issue 1 2010
Yosuke Nishitani
The effects of the addition of styrene-ethylene/butylene-styrene copolymer (SEBS) with various functionalized groups on the rheological, mechanical, and tribological properties on polyamide 6 nanocomposite filled with layered silicate (PA6/Clay) were investigated. Four types of SEBS: unmodified SEBS (SEBS), maleic anhydride grafted SEBS (SEBS- g -MA), amine group grafted SEBS (SEBS- g -NH2), and carboxyl group grafted SEBS (SEBS- g -COOH) were added with PA6/Clay nanocomposite to prepare various polymer blends. These polymer blends were extruded by a twin screw extruder and injection molded. Dynamic viscoelastic properties of these blends in the molten state and their tensile, impact, and tribological properties were evaluated. The viscoelastic properties were found to increase with the addition of SEBS and were highly influenced by the types of functionalized groups contained. Influence of the addition of SEBS on the mechanical properties of these systems differed for each mechanical property. Although the tensile properties decreased with SEBS, Izod impact properties improved with the addition of various functionalized SEBS. These mechanical properties and viscoelastic properties correlated closely with the size of dispersed SEBS particles and interparticle distance. The tribological properties also improved with the addition of SEBS, and the influence of the amount added was higher than the type of SEBS used. POLYM. ENG. SCI., 2010. © 2009 Society of Plastics Engineers [source]


Functional renormalization group approach to the BCS-BEC crossover

ANNALEN DER PHYSIK, Issue 9 2010
S. Diehl
Abstract The phase transition to superfluidity and the BCS-BEC crossover for an ultracold gas of fermionic atoms is discussed within a functional renormalization group approach. Non-perturbative flow equations, based on an exact renormalization group equation, describe the scale dependence of the flowing or average action. They interpolate continuously from the microphysics at atomic or molecular distance scales to the macroscopic physics at much larger length scales, as given by the interparticle distance, the correlation length, or the size of the experimental probe. We discuss the phase diagram as a function of the scattering length and the temperature and compute the gap, the correlation length and the scattering length for molecules. Close to the critical temperature, we find the expected universal behavior. Our approach allows for a description of the few-body physics (scattering and molecular binding) and the many-body physics within the same formalism. [source]


Highly Stable Au Nanoparticles with Tunable Spacing and Their Potential Application in Surface Plasmon Resonance Biosensors

ADVANCED FUNCTIONAL MATERIALS, Issue 1 2010
Shuyan Gao
Abstract Colloidal Au-amplified surface plasmon resonance (SPR), like traditional SPR, is typically used to detect binding events on a thin noble metal film. The two major concerns in developing colloidal Au-amplified SPR lie in 1) the instability, manifested as a change in morphology following immersion in organic solvents and aqueous solutions, and 2) the uncontrollable interparticle distance, determining probe spacing and inducing steric hindrance between neighboring probe molecules. This may introduce uncertainties into such detecting techniques, degrade the sensitivity, and become the barricade hampering colloidal Au-based transducers from applications in sensing. In this paper, colloidal Au-amplified SPR transducers are produced by using ultrathin Au/Al2O3 nanocomposite films via a radio frequency magnetron co-sputtering method. Deposited Au/Al2O3 nanocomposite films exhibit superior stability, and average interparticle distances between Au nanoparticles with similar average sizes can be tuned by changing surface coverage. These characteristics are ascribed to the spacer function and rim confinement of dielectric Al2O3 and highlight their advantages for application in optimal nanoparticle-amplified SPR, especially when the probe size is smaller than the target molecule size. This importance is demonstrated here for the binding of protein (streptavidin) targets to the probe (biotin) surface. In this case, the dielectric matrix Al2O3 is a main contributor, behaving as a spacer, tuning the concentration of Au nanoparticles, and manipulating the average interparticle distance, and thus guaranteeing an appropriate number of biotin molecules and expected near-field coupling to obtain optimal sensing performance. [source]


Polystyrene Arrays: Non-Close-Packed Crystals from Self-Assembled Polystyrene Spheres by Isotropic Plasma Etching: Adding Flexibility to Colloid Lithography (Adv. Funct.

ADVANCED FUNCTIONAL MATERIALS, Issue 20 2009
Mater.
Hexagonally ordered arrays of non-close-packed spherical polystyrene (PS) particles are prepared by A. Plettl et al. on page 3279, and exhibit precisely controlled diameters and interparticle distances. An isotropic low-temperature plasma-etching process is applied to extended monolayers of PS colloids deposited onto hydrophilic silicon. These non-close-packed PS arrays are used as masks for the fabrication of arrays of cylindrical nanopores by reactive ion etching. [source]


Non-Close-Packed Crystals from Self-Assembled Polystyrene Spheres by Isotropic Plasma Etching: Adding Flexibility to Colloid Lithography

ADVANCED FUNCTIONAL MATERIALS, Issue 20 2009
Alfred Plettl
Abstract Hexagonally ordered arrays of non-close-packed nanoscaled spherical polystyrene (PS) particles are prepared exhibiting precisely controlled diameters and interparticle distances. For this purpose, a newly developed isotropic plasma etching process is applied to extended monolayers of PS colloids (starting diameters <300,nm) deposited onto hydrophilic silicon. Accurate size, shape, and smoothness control of such particles is accomplished by etching at low temperatures (,150,°C) with small rates not usually available in standard reactive ion etching equipment. The applicability of such PS arrays as masks for subsequent pattern transfer is demonstrated by fabricating arrays of cylindrical nanopores into Si. [source]


Non,Born,Oppenheimer calculations of the ground state of H3

INTERNATIONAL JOURNAL OF QUANTUM CHEMISTRY, Issue 14 2007
Mauricio Cafiero
Abstract We present quantum,mechanical calculations for the ground state of the H3 system performed without the Born-Oppenehimer approximation. In the calculations we use explicitly correlated Gaussian basis functions that explicitly depend on all of the interparticle distances. These basis functions allow us to achieve high accuracy while explicitly describing nucleus,nucleus, nucleus,electron, and electron,electron correlation effects. Gaussian basis sets ranging in size from 85 to 950 functions have been optimized using a gradient-based procedure. The issue of defining and extracting the H3 molecular structure based on the non-BO wave function is also discussed. © 2007 Wiley Periodicals, Inc. Int J Quantum Chem, 2007 [source]


Reaction-induced nucleation and growth v. grain coarsening in contact metamorphic, impure carbonates

JOURNAL OF METAMORPHIC GEOLOGY, Issue 8 2010
A. BERGER
Abstract The understanding of the evolution of microstructures in a metamorphic rock requires insights into the nucleation and growth history of individual grains, as well as the coarsening processes of the entire aggregate. These two processes are compared in impure carbonates from the contact metamorphic aureole of the Adamello pluton (N-Italy). As a function of increasing distance from the pluton contact, the investigated samples have peak metamorphic temperatures ranging from the stability field of diopside/tremolite down to diagenetic conditions. All samples consist of calcite as the dominant matrix phase, but additionally contain variable amounts of other minerals, the so-called second phases. These second phases are mostly silicate minerals and can be described in a KCMASHC system (K2O, CaO, MgO, Al2O3, SiO2, H2O, CO2), but with variable K/Mg ratios. The modelled and observed metamorphic evolution of these samples are combined with the quantification of the microstructures, i.e. mean grain sizes and crystal size distributions. Growth of the matrix phase and second phases strongly depends on each other owing to coupled grain coarsening. The matrix phase is controlled by the interparticle distances between the second phases, while the second phases need the matrix grain boundary network for mass transfer processes during both grain coarsening and mineral reactions. Interestingly, similar final mean grain sizes of primary second phase and second phases newly formed by nucleation are observed, although the latter formed later but at higher temperatures. Moreover, different kinetic processes, attributed to different driving forces for growth of the newly nucleated grains in comparison with coarsening processes of the pre-existing phases, must have been involved. Chemically induced driving forces of grain growth during reactions are orders of magnitudes larger compared to surface energy, allowing new reaction products subjected to fast growth rates to attain similar grain sizes as phases which underwent long-term grain coarsening. In contrast, observed variations in grain size of the same mineral in samples with a similar T,t history indicate that transport properties depend not only on the growth and coarsening kinetics of the second phases but also on the microstructure of the dominant matrix phase during coupled grain coarsening. Resulting microstructural phenomena such as overgrowth and therefore preservation of former stable minerals by the matrix phase may provide new constraints on the temporal variation of microstructures and provide a unique source for the interpretation of the evolution of metamorphic microstructures. [source]