Enhanced Laser Cooling of Rare-Earth-Ion-Doped Glass Containing Nanometer-Sized Metallic Particles

The enhanced laser cooling performance ofrare-earth-ions-doped glasses containing small particles is predicted. Thisis achieved by the enhancement of local field around rare earth ions, owingto the surface plasmon resonance of small metallic particles. The role ofenergy transfer between ions and the particle is theoretical discussed.Depending on the particle size and the ion emission quantum efficiency, theenhancement of the absorption and the fluorescence is predicted. Moreover,taking Yb³⁺-doped ZBLAN as example, the cooling power and heat-lightconverting efficiency are calculated. It is finally concluded that theabsorption and the fluorescence are greatly enhanced in these compositematerials, the cooling power is increased compared to the bulk material.     

Electromagnetic interaction of fluorophores with designed two-dimensional silver nanoparticle arrays

We study the fluorescence enhancement of dye molecules adsorbed on regular two-dimensional arrays of designed silver nanoparticles. The silver particles show two orthogonal optical resonances at different wavelengths because of their elongated shape. The short-wavelength resonance was designed to fit to the absorption maximum of the fluorophore. When the excitation light drives the short-wavelength resonance, the measured fluorescence intensity is strongly enhanced compared to that for the orthogonal particle orientation. This shows directly a strong electromagnetic coupling between the nanoparticles and the fluorophore. Additionally enhanced photochemical bleaching is observed due to the interaction of fluorophores with the particles. Using a rate model describing the fluorescence enhancement and the bleaching enhancement, an average value for the particle-induced increase in the radiative fluorescence rate is obtained, together with a lower limit for the averaged particle-induced field intensity enhancement factor. Received: 3 July 2001 / Revised version: 3 September 2001 / Published online: 15 October 2001     

Giant magnetic susceptibility enhancement in field-structured nanocomposites

We demonstrate through experiment and simulation that when mono-domain Fe nanoparticles are formed into chains by the application of a magnetic field, the susceptibility of the resulting structure is greatly enhanced (11.4-fold) parallel to the particle chains and is much larger than transverse to the chains. Simulations show that this significant enhancement is expected when the susceptibility of the individual particles approaches 5 in MKS units, and is due to the spontaneous magnetization of individual particle chains, which occurs because of the strong dipolar interactions. This large enhancement is only possible with nanoparticles, because demagnetization fields limit the susceptibility of a spherical multi-domain particle to 3 (MKS). Experimental confirmation of the large susceptibility enhancement is presented, and both the enhancement and the susceptibility anisotropy are found to agree with simulation. The specific susceptibility of the nanocomposite is 54 (MKS), which exceeds the highest value we have obtained for field-structured composites of multi-domain particles by a factor of four.     

Second harmonic generation in composites of ellipsoidal particles with core–shell structure

We study the enhancement of the second-harmonic generation (SHG) coefficient in a random composite consisting of ellipsoidal particles with a core–shell structure in a linear dielectric host. The material making up the ellipsoidal core is assumed to be dielectric, but with a nonlinear susceptibility for SHG. The coating material is assumed to be metallic with a linear susceptibility. The effective SHG coefficient is derived and its expression is related to various local field factors. The numerical calculations of the effective SHG response per unit volume of nonlinear material can be greatly enhanced at certain frequencies. For coated ellipsoidal particles, the core–shell structure and the particle shape allow for tuning of the resonance through the choice of material parameters and/or the ratio of the core to shell volume fraction and the depolarization factor of the particles.     

Particle size reduction and enhanced diffusion of Fe and Pt atoms in FePt-C granular films by N addition

N-doped FePt-C nanocomposite films were fabricated using facing-target sputtering method under different N₂ partial pressures (P_N) at room temperature. Annealing at 650 °C turns the amorphous films into ordered structures. Nitrogen doping not only make the ordering of FePt particles easier than the ordering in FePt-C films, due to the enhanced diffusivity of Fe and Pt atoms, but also effectively limits the growth of the FePt particles during the thermal induced ordering, especially for the annealed films fabricated at P_N = 40%, where the average size of well-isolated FePt particles is only ∼8 nm. The particle size reduction and the enhanced diffusion of Fe and Pt atoms can be ascribed to the desorption of doped N atoms and dissociation of FeN bonds during annealing. The room-temperature coercivity of the samples decreases with the P_N due to the particle size reduction and thus the enhancement of the thermal agitation for small particles during the magnetizing procedure.     

Channeling of fusion alpha-particle power using minority ion catalysis

Maintaining fuel ions hotter than electrons would greatly facilitate controlled nuclear fusion. The parameter range for achieving this temperature disparity is shown here to be enhanced by catalyzing the α-channeling effect (wave-induced simultaneous expulsion and cooling of α particles) through minority-ion heating. Specifically, a wave can extract energy from hot α particles and transfer it to colder minority ions, which act as a catalyst, eventually forwarding the energy to still colder fuel ions through collisions. In comparison with the traditional α-channeling mechanism, the requirements are thereby relaxed on the waves that accomplish the α channeling, which no longer have to interact simultaneously with α particles and fuel ions. Numerical simulations illustrate how the new scheme may increase, for example, the effective fusion reactivity of mirror-confined plasmas.     

Effects of volatile coatings on the laser-induced incandescence of soot

We have measured time-resolved laser-induced incandescence (LII) from combustion-generated mature soot extracted from a burner and (1) coated with oleic acid or (2) coated with oleic acid and then thermally denuded using a thermodenuder. The soot samples were size selected using a differential mobility analyzer and characterized with a scanning mobility particle sizer, centrifugal particle mass analyzer, and transmission electron microscope. The results demonstrate a strong influence of coatings on the magnitude and temporal evolution of the LII signal. For coated particles, higher laser fluences are required to reach signal levels comparable to those of uncoated particles. The peak LII curve is shifted to increasingly higher fluences with increasing coating thickness until this effect saturates at a coating thickness of ~75 % by mass. These effects are predominantly attributable to the additional energy needed to vaporize the coating while heating the particle. LII signals are higher and signal decay rates are significantly slower for thermally denuded particles relative to coated or uncoated particles, particularly at low and intermediate laser fluences. Our results suggest negligible coating enhancement in absorption cross-section for combustion-generated soot at the laser fluences used. Apparent enhancement in absorption with restructuring may be caused by less conductive cooling.     

Enhancement of non-leptonic decays of charmed particles

We suggest that non-leptonic decays of charmed particles are enhanced over semi-leptonic decays by a sizeable factor, in analogy with the situation encountered in strange particle decays. This conjecture is verified in a model octet enhancement based on asymptotically-free gauge theories of strong interactions. Arguments are given to support a specific SU(3) behavior of the enhanced part of the non-leptonic Hamiltonian for charmed particle decays. Consequent selection and intensity rules are discussed.     

Enhanced Fluorescence from Periodic Arrays of Silver Nanoparticles

Electron beam lithography was used to fabricate silver nanoparticle arrays and study the effects of geometrical properties of particles on metal-enhanced fluorescence. Nanoparticle size, shape, interparticle spacing, and nominal thickness were varied in a combinatorial pattern for investigation of the particle plasmon resonance effect on enhancement of fluorescence from three different fluorophores; Fluorescein, Cy3, and Cy5. A specific geometric property for optimal enhancement from each fluorophore was determined. For interparticle spacings greater or equal to 270 nm, the enhancement matched what is expected for a single-particle model. For those particles smaller than 210 nm, the enhancement was lower than for the larger spacing in the range studied. Triangular-shaped particles gave similar enhancement to those of square-shaped particles. This combinatorial pattern by e-beam lithography was found to be useful for studying how individual parameters enhance the fluorescence that are important for rational design of enhanced fluorescence sensors.     

Localization of the electromagnetic field in the vicinity of gold nanoparticles: Surface modification of different substrates

Theoretical predictions and experimental results for nanosized modification of metal (Au), semiconductor (Si), or dielectric (soda lime glass) substrates using near-electromagnetic field enhancement in the vicinity of gold nanoparticles are presented. The near field properties for the system consisting of an isolated gold nanoparticle or nanoparticle aggregate deposited on the substrates, which is irradiated by electromagnetic wave, are investigated using Finite Difference Time Domain Simulation technique. The influence of the substrate material on the near field distribution characteristics is predicted. The results reveal that the field on the substrate surface is enhanced in the three investigated cases, but its spatial distribution and magnitude depend on the substrate material. In the case of the metal and semiconductor substrate the enhanced near field is strongly localized in the vicinity of the contact point with the particle, in an area with diameter smaller than the particle's one. The intensity of the enhanced field on the glass is more than an order of magnitude lower than the case of using silicon substrate. The properties of the near field on the substrate surface also depend on the particle arrangement. For a two-dimensional gold nanoparticle array, when the particles are closely arrayed, the intensity of the enhanced field on the substrate surface is minimal. With the increase of the interparticle distance the near field intensity increases. The validity of the obtained theoretical results is confirmed experimentally.     

Synchronization, anti-synchronization and current transports in non-identical chaotic ratchets

The synchronization (CS) and anti-synchronization (AS) of two non-identical inertial ratchets moving in different asymmetric potentials and transporting particles chaotically is demonstrated based on a technique derived from nonlinear control theory. It is shown that in the CS state, particle current is enhanced; while in the AS state, the particles transport current in different directions, suggesting that AS phenomenon could be exploited as a mechanism for particle separation.     

用于飞秒激光纳米加工的TiO_2粒子阵列诱导多种基底表面近场增强

利用纳米粒子辅助对飞秒激光能量进行空间局域化,使其在基底表面诱导产生纳米尺度的近场增强,这对超衍射极限微结构加工具有重要意义.目前对于粒子阵列诱导飞秒激光纳米孔加工的研究仅限于金属Au粒子及低折射率聚苯乙烯介电粒子等,本文提出并开展了应用高折射率TiO_2介电粒子阵列作为辅助诱导激光近场增强从而进行飞秒激光超衍射纳米孔加工的研究.对TiO_2介电粒子阵列在Si,Pt及SiO_2表面的近场强度分布进行了数值模拟,研究其基底表面近场增强的规律及物理过程.研究结果发现,使用硅基底时,阵列与单一TiO_2球形粒子相比其近场增强仅下降约30%;相对于入射激光强度而言,在直径约为100nm的空间范围内获得140倍的近场增强,这一现象可用于百纳米孔的激光加工.同时在其他典型基底的理论计算结果中也表明,几乎在所有金属及介电材料表面均可以实现良好的百纳米空间范围内的近场增强,并且具有近场随着基底折射率变大而增强的规律.这些现象的产生归因于TiO_2粒子中磁四极振荡产生的激光前向场增强及粒子与基底的耦合作用.进一步引入镜像电荷模型对基底光学参数对其表面近场增强的影响规律进行了分析和解释.本文的模拟结果对飞秒激光近场超衍射极限纳米加工的应用有着重要的意义.     

Effect of positional disorder in systems of ultrafine ferromagnetic particles

A simple model for systems of dipolarly interacting single-domain ultrafine ferromagnetic particles is studied by Monte Carlo simulations of zero field cooling and field cooling as well as relaxation experiments. By investigating systems characterized by an identical moderate concentration but different types of particle positions' disorder, it is shown that the positional disorder has a crucial influence on the magnetic behavior of the system. For extreme values of positional disorder, the interplay between spatial disorder and dipolar interaction can even lead to a cooperative freezing at low temperatures. Received 28 November 2001     

银纳米粒子阵列的自组装及其表面增强拉曼光谱应用

在以聚赖氨酸为表面耦联层分子的玻片基底制备了银纳米粒子阵列。ＳＥＭ表征结果表明,银粒子以亚单层的形式排列在基底表面。比较银溶胶和纳米粒子阵列的紫外可见光谱可见聚赖氨酸耦联层对银纳米粒子的粒径具有一定的选择性,甲基紫精在银纳米粒子阵列上的表面增强ＦＴ拉曼光谱表明在近红外区拉曼散射的表面增强主要来自于化学增强效应。     

Ferromagnetic properties of glucose coated Cu2O nanoparticles

Magnetic properties of glucose coated cuprous oxide nanoparticles of different sizes have been studied. Unlike bulk Cu₂O, which shows diamagnetic behavior, the nanoparticles show superparamagnetic behavior. A superparamagnetic blocking temperature of 21 K is observed for 5 nm particles. A magnetic hysteresis loop with a coercivity of 406 Oe is observed for these particles at 5 K. The magnetization and the coercivity increase with decreasing particle size. The superparamagnetic behavior, along with the increase in magnetization and coercivity with decreasing particle size, is due to the enhanced surface contributions to the magnetism.     

Effects of Kinetic Decoupling on Relic Density with Sommerfeld Enhancement

We investigate the effect of kinetic decoupling on the relic density of the non-relativistic particles whose annihilation rate is increased by Sommerfeld enhancement. We discuss the effect of kinetic decoupling both for the Sommerfeld enhanced s-wave annihilation and p-wave anihilation cross sections. We find after kientic decoupling Sommerfeld enhanced annihilations continue to change the particle abundance until the matter domination begins or
the Sommerfeld effect cuts off. We provide analytic estimates of this effect.     

Study of magnetically enhanced corona pre-charger

In this paper, experimental investigations of the discharge characteristics of magnetically enhanced corona discharges, for the purpose of capturing fine aerosol particles, are presented. The discharge mechanism during such a process is analyzed as well. The effects of magnetic enhancement under different magnet flux densities, and in positive- or negative-corona discharges, were experimentally compared. The magnetically enhanced effects in different inter-electrode regions were studied. Experimental results demonstrated that the magnetic field could efficiently increase the concentrations of both the negative ions and the free electrons during negative-corona discharge. The dominant mechanism of magnetic enhancement in a corona discharge involves the Larmor precessions of free electrons which enhance ionization of the gas molecules near the discharge electrode. A convenient configuration for enhancing corona discharge was formed by placing permanent magnets with a local strong magnetic field near the discharge electrode. A magnetically enhanced negative-corona (MNC) pre-charger was assembled in front of an electrostatic enhancement filter. The influence of the MNC pre-charger on the efficiencies of an electrostatic enhancement filter was measured and compared with that of a conventional corona pre-charger. The free-electron-charging mechanism of the MNC pre-charger was preliminarily analyzed. Our results show that the new pre-charging technique is promising for capturing fine aerosol particles in electrostatic enhancement filters or electrostatic precipitators.     

Using gold colloid nanoparticles to modulate the surface enhanced fluorescence of Rhodamine B

Enhanced fluorescence from Rhodamine B (RB) mixed with gold colloids has been observed under ultraviolet irradiation. Spectroscopic studies show that with the increasing gold colloids content, the fluorescence of RB at about 590 nm increases firstly and then decreases with slight red shift. These features observed in the experiment can be explained by the local electric field enhancement via surface plasmon resonance (SPR) of gold nanoparticles. Fluorescence enhancement is obtained when the emission frequency of RB lies within the bandwidth of local field enhancement from gold nanoparticles. Theoretical calculation results show that the local field band red shifts obviously with increase the thickness of dye shell which capped on gold particle, whereas the fluorescence band of RB is fixed around 590 nm. Therefore, the red shift and non-monotonic change of fluorescence intensity from RB is attributed to the dye shell dependent red shift of local field band of gold particles.     

Synthesis of nano-sized antimony-doped tin oxide (ATO) particles using a DC arc plasma jet

Nano-sized antimony-doped tin oxide (ATO) particles were synthesized using DC arc plasma jet. The precursors SnCl₄ and SbCl₅ were injected into the plasma flame in the vapor phase. ATO powder could conveniently be synthesized without any other post-treatment in this study. To control the doping amount of antimony in the ATO particles, the Sb/Sn molar ratio was used as an operating variable. To study the effect of carrier gas on the particle size, argon and oxygen gases were used. The results of XRD and TGA show that all Sb ions penetrated the SnO₂ lattice to substitute Sn ions. With the increased SbCl₅ concentration in source material, the Sb doping level was also increased. The size of the particles synthesized using the argon carrier gas was much smaller than that of the particles prepared using the oxygen carrier gas. For the argon gas, PSA results and SEM images reveal that the average particle size was 19 nm. However, for the oxygen gas, the average particle size was 31 nm.     

Temperature-induced particle self-assembly

Agglomeration of monodisperse thiol-stabilized gold particles with diameters of 6 nm, suspended in organic solvents, was induced by the cooling of the suspension. A sharp transition between the stable suspension and agglomeration resulted. The temperature of the transition depends on the concentration and the compatibility of the solvent. The morphology of the formed particle structures upon agglomeration implies that the used metal colloid can be described as a van der Waals-gas. The particles undergo phase transitions from a stable fluid phase to a metastable phase, in which nucleation and growth occur, or to an instable phase, in which spinodal decomposition occurs. The results will direct research on routes to nanostructured materials using nanoparticles as building blocks.