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91.
Siwach OP Sen P 《Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy》2008,69(2):659-663
Ag nanoparticles in water phase have been synthesized employing the electro-exploding wire technique. A surface plasmon peak is observed at 400nm, characteristic of the Ag nanoparticles. A fluorescence emission peak is recorded at 300nm for excitation wavelengths in two different ranges 215-230 and 255-280nm. The position of the fluorescence peak remains fixed, irrespective of the excitation wavelength employed. These are assigned to electronic transition from different higher excited states to d levels of the Ag nanoparticles. In concomitant with these, there are two resonant absorptions at 5.76 and 4.59eV as evident from the fluorescence excitation spectra. 相似文献
92.
Structural organization of gold nanoparticles onto the ITO surface and its optical properties as a function of ensemble size 总被引:1,自引:0,他引:1
Khatri OP Murase K Sugimura H 《Langmuir : the ACS journal of surfaces and colloids》2008,24(8):3787-3793
Self-assembly of citrate-stabilized gold nanoparticles (AuNPs) onto an optically transparent indium tin oxide (ITO) surface followed by neutralization of these particles using dodecanethiol as a surfactant have been demonstrated. X-ray photoelectron spectroscopic (XPS) studies revealed the partial removal of citrate ions from the immobilized AuNPs, which advances the dilution of electrostatic attraction between AuNPs and the APS (amino-terminated monolayer)-functionalized ITO surface. The resultant AuNPs restore their mobility to some extent and form small ensembles. Some of the immobilized AuNPs were completely removed from the surface due to neutralization, as confirmed by XPS studies. Interparticle distance and size of ensembles were manipulated by consecutive cycles of immobilization and neutralization of AuNPs. Controlled nanostructural fabrication progression, which leads to two-dimensional lateral growth of AuNPs, provides a method for systematically shifting the surface plasmon resonance band based on the increase in plasmon coupling among the closely placed AuNPs of an ensemble. The magnitude of shift increases with the size of ensemble. This manipulated chemical strategy offers a convenient and simple method to tune the optical properties of materials on a nanoscale. 相似文献
93.
Khatri OP Sano H Murase K Sugimura H 《Langmuir : the ACS journal of surfaces and colloids》2008,24(20):12077-12084
Photopatterning of a hexadecyl (HD) monolayer has been demonstrated using vacuum ultraviolet (VUV; lambda = 172 nm) light under controlled vacuum pressure with the objective of minimizing the pattern dimension. X-ray photoelectron spectroscopy (XPS) and lateral force microscopy (LFM) studies reveal that photodegradation of the HD monolayer not only is limited to the regions exposed to VUV but also spreads under the masked regions. The strong oxidants generated by VUV irradiation to atmospheric oxygen and water vapor diffuse toward the masked regions through the nanoscopic channels and photodissociate the monolayer under the masked area, near the photomask apertures, resulting in broadening of the photopattern. Such broadening decreases with decreased vacuum pressure inside the VUV chamber, associated with a decrease of oxidant concentration and reduction of their diffusion. Gold nanoparticles (AuNPs) were immobilized on the VUV patterned features to probe the dimension of the chemically active pattern. Field emission electron microscopy reveals the construction of 565 nm wide pattern features at a vacuum pressure of 10 Pa. This pattern widens to 1,030 nm at 10 (4) Pa using the same size apertures (500 nm) as printed on the photomask. This study provides insight for fabricating submicron patterns with high reproducibility and its exploitation for different applications, which includes the patterning of nanoparticles, biopolymers, and other nano-objects at submicron dimensions. 相似文献
94.
Parkash Chander 《International Journal of Game Theory》2007,35(4):539-556
This paper reinterprets the γ-core (Chander and Tulkens in Int Tax Pub Financ 2:279–293, 1995; in Int J Game Theory 26:379–401,
1997) and justifies it as well as its prediction that the efficient coalition structure is stable in terms of the coalition
formation theory. The problem of coalition formation is formulated as an infinitely repeated game in which the players must
choose whether to cooperate or not. It is shown that a certain equilibrium of this game corresponds to the γ-core assumption
that when a coalition forms the remaining players form singletons, and that the grand coalition is an equilibrium coalition
structure.
An earlier version of this paper was presented at the conference on Game Theory and Its Applications held in Mumbai in 2003
and was subsequently circulated as CORE Discussion Paper 2003/46. 相似文献
95.
Gao H Ye C Gupta OD Xiao JC Hiskey MA Twamley B Shreeve JM 《Chemistry (Weinheim an der Bergstrasse, Germany)》2007,13(14):3853-3860
2,4,5-Trinitroimidazolate (TNI) salts with "high-nitrogen" cations tend to be highly hydrogen bonded and have heats of formation ranging up to 616 kJ mol(-1). Density, oxygen balance, and thermostability are enhanced by the presence of TNI. Based on theoretical calculations, all of the new salts are potential propellants. 相似文献
96.
97.
Journal of Statistical Physics - We establish the strong law of large numbers for Betti numbers of random ?ech complexes built on $${\mathbb {R}}^N$$ -valued binomial point processes and... 相似文献
98.
Visualization experiments in upward forced convective nucleate boiling flows were carried out. The bubble growth and collapse have been measured using high-speed photography technique with distilled water under atmospheric pressure. The experiments show that the bubbles depart from nucleating sites shortly after nucleation and slide along the heater surface. The bubbles grow while sliding, attain a maximum size, then lift from the surface sometime during condensation, and quickly vanish in the bulk liquid. Parametric studies show that bubble diameter and departure frequency increases with an increase in heat flux, a decrease in subcooling, and a decrease in mass flux. 相似文献
99.
We report on the effect of BaO on the crystallization kinetics of glasses in the diopside (CaMgSi2O6)-Ca-Tschermak (CaAl2SiO6) system. Partial substitution (i.e. 5%, 10% and 20%) of Ba2+ for Ca2+ was attempted in composition CaMg0.8Al0.4Si1.8O6, in three different glasses while partial substitution of B3+ for Al3+ was made in the fourth glass. Structural investigations on the glasses have been made by density measurements, molar volume and Infra-red spectroscopy (FTIR). Non-isothermal crystallization kinetic studies have been employed to study the mechanism of crystallization in all the four glasses. The Avrami parameter for the glass powders is ∼2, indicating the existence of intermediate mechanism of crystallization. Crystallization sequence in the glasses has been followed by X-ray diffraction (XRD) analysis, scanning electron microscopy (SEM) and FTIR. Augite crystallized out being the dominant phase in all the glass-ceramics, while different polymorphs of BaAl2Si2O8 were present as secondary or minor phases. 相似文献
100.
Self-organization of organic molecules through weak noncovalent forces such as CH/π interactions and creation of large hierarchical supramolecular structures in the solid state are at the very early stage of research. The present study reports direct evidence for CH/π interaction driven hierarchical self-assembly in π-conjugated molecules based on custom-designed oligophenylenevinylenes (OPVs) whose structures differ only in the number of carbon atoms in the tails. Single-crystal X-ray structures were resolved for these OPV synthons and the existence of long-range multiple-arm CH/π interactions was revealed in the crystal lattices. Alignment of these π-conjugated OPVs in the solid state was found to be crucial in producing either right-handed herringbone packing in the crystal or left-handed helices in the liquid-crystalline mesophase. Pitch- and roll-angle displacements of OPV chromophores were determined to trace the effect of the molecular inclination on the ordering of hierarchical structures. Furthermore, circular dichroism studies on the OPVs were carried out in the aligned helical structures to prove the existence of molecular self-assembly. Thus, the present strategy opens up new approaches in supramolecular chemistry based on weak CH/π hydrogen bonding, more specifically in π-conjugated materials. 相似文献