Surface plasmon resonance of Ag nanoparticles in the vicinity of a high impedance surface

Surface Plasmon resonance of Ag nanoparticles in the vicinity of a high impedance surface is investigated. Mushroom-like nanostructures were vertically grown on silicon substrate to form a high impedance surface operating in the range of optical frequencies. Formation of Ag nanoparticles on the fabricated high impedance surface was realized using plasma bombardment process. Optical measurements show an enhancement in the surface plasmon resonances of Ag nanoparticles. Also it was shown that the plasmon resonance peak of the Ag nanoparticles shifts to blue when Ag nanoparticles approach to the high impedance surface.     

Surface plasmon polariton contributions to strokes emission from molecular monolayers on periodic Ag surfaces

Surface enhanced Raman scattering from molecular monolayers adsorbed on a holographic grating and covered by Ag has been studied. The coupling of surface plasmon polaritons to light through the grating produces emission similar to the continuum observed in other surface Raman experiments. The angular dependence of the surface Raman scattering shows that enhanced Raman cross-sections can arise from scattering of surface plasmon polaritons into light by the localized molecular vibrations.     

Purely quadratic dispersion of surface plasmon in Ag/Ni(111): the influence of electron confinement

Surface plasmon dispersion in nanoscale thin Ag films deposited onto the Ni(111) surface was investigated by angle‐resolved electron energy loss spectroscopy. We found that the dispersion curve contains only the quadratic term. The vanishing of the linear term was ascribed to the presence in the film of Ag 5sp‐related quantum well states. Screening effects enhanced by electron confinement in Ag quantum well states push the position of the centroid of the induced charge of the surface plasmon less inside the interface compared to other Ag systems, rendering null the linear coefficient of the dispersion curve. (© 2008 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim)     

Surface plasmon enhanced light emission of silicon-rich silicon nitride: Dependence on metal island size

Surface plasmon coupled light emission of silicon-rich silicon nitride (SRSN) was investigated as a function of metal island size. It was found that the emission intensity was enhanced by surface plasmon (SP) and the enhancement factors increase greatly with the increase of metal island size. Moreover, SP coupled emission spectral shape was found also correlating with Ag island size. By calculating the extinction characteristics of the Ag islands, it was believed that SP scattering and absorption efficiency of the metal islands decide the photoluminescence (PL) changes including emission intensity enhancement and band position shift.     

Why metallic surfaces with grooves a few nanometers deep and wide may strongly absorb visible light

It is theoretically shown that nanometric silver lamellar gratings present very strong visible light absorption inside the grooves, leading to electric field enhancement of several orders of magnitude. It is due to the excitation of quasistatic surface plasmon polaritons with particular small penetration depth in the metal. This may explain the abnormal optical absorption observed a long time ago on almost flat Ag films. Surface enhanced Raman scattering in rough metallic films could also be due to the excitation of such quasistatic plasmon polaritons in grain boundaries or notches of the films.     

Optical properties of Ag nanoparticle embedded silicate glass prepared by field-assisted diffusion

Ag nanoparticle embedded silicate glass was prepared by field-assisted diffusion, combined with post-annealing process. Surface plasmon resonance (SPR) bands were observed in the optical absorption measurement. The properties of optical absorption were strongly affected by the process parameters. With increasing electric field intensity and diffusion time, the SPR peak position and the full width at half maximum (FWHM) of the plasmon band were almost invariable. With increasing post-annealing time, the SPR peak was blue-shifted and the FWHM of SPR band decreased. The experimental results could be well simulated using modified Mie scattering theory considering the spill-out effects and the limitation of the mean free path.     

Ag纳米颗粒对有机小分子太阳能电池性能的改善

在有机小分子太阳能电池CuPc/C60和TiOPc/C60的阳极ITO表面分别制备了一层Ag纳米颗粒,并采用MoO3作为阳极缓冲层,器件的性能均得到有效改善.Ag纳米颗粒的引入所形成的表面等离子激元共振可显著提高有机光活性层的吸收效率和光生激子的分解效率;而MoO3有效抑制了光生激子在有机/金属界面处发生的猝灭,提高了...     

Surface plasmon optical sensor with enhanced sensitivity using top ZnO thin film

Surface plasmon resonance (SPR) is one of the most sensitive label-free detection methods and has been used in a wide range of chemical and biochemical sensing. Upon using a 200 nm top layer of dielectric film with a high value of the real part ε′ of the dielectric function, on top of an SPR sensor in the Kretschmann configuration, the sensitivity is improved. The refractive index effect of dielectric film on sensitivity is usually ignored. Dielectric films with different refractive indices were prepared by radio frequency magnetron (RF) sputtering and measured with spectroscopic ellipsometry (SE). The imaginary part ε′′ of the top nanolayer permittivity needs to be small enough in order to reduce the losses and get sharper dips. The stability of the sensor is also improved because the nanolayer is protecting the Ag film from interacting with the environment. The response curves of the Ag/ZnO chips were obtained by using SPR sensor. Theoretical analysis of the sensitivity of the SPR sensors with different ZnO film refractive indices is presented and studied. Both experimental and simulation results show that the Ag/ZnO films exhibit an enhanced SPR over the pure Ag film with a narrower full width at half maximum (FWHM). It shows that the top ZnO layer is effective in enhancing the surface plasmon resonance and thus its sensitivity.     

Surface‐enhanced Raman scattering studies of carbon nanotubes using Ag‐core Au‐shell nanoparticles

Surface‐enhanced Raman scattering from carbon nanotube bundles adsorbed with plasmon‐tunable Ag‐core Au‐shell nanoparticles (Ag@Au nps) was carried out for the first time. By utilizing nanoparticles whose plasmon resonance peak (541, 642 nm) closely matches the commonly used Raman excitation sources (532, 632.81 nm), we can observe a large enhancement in the Raman signatures of carbon nanotubes. We obtain greater enhancement in the Raman signal for the above case when compared to nanotubes adsorbed with conventional Ag, Au or other ‘off resonant’ Ag@Au nps. The power‐dependent SERS experiment on single‐walled nanotubes (SWNTs) with resonant Ag@Au nps reveals a linear behavior between the G‐band intensity and the photon flux density, which is in agreement with the vibrational pumping model of SERS. The observed enhancement by resonance matching is pronounced for carbon nanotubes and may lead to insights into understanding nanotube–nanoparticle interaction. Copyright © 2009 John Wiley & Sons, Ltd.     

Size dependence of the plasmon peak position in electron stimulated photon emission spectra of Ag clusters supported on amorphous carbon film

The plasmon energy of Ag clusters produced on an amorphous carbon substrate by gas-aggregation technique has been measured. It has been determined from the plasmon peak position in the light emission spectrum obtained during bombardment of Ag clusters by low-energy electrons. For Ag cluster films with maximum of the cluster size distribution at 30, 8 and 2.5 nm, the plasmon energy comprised 3.76, 4.13 and 4.28 eV (the wavelength was 330, 300 and 290 nm), respectively. The blue shift of the plasmon energy is probably related to the effect of confounding of collective and single-particle excitations.     

SURFACE PLASMON OF Ag CLUSTERS ON ALUMINA FILMS

The deposition of silver on an ordered alumina film prepared on Re(0001) surface has been studied by Auger electron spectroscopy (AES), low energy electron diffraction (LEED) and high resolution electron energy loss spectroscopy (HREELS). The results show that Ag grows initially as clusters at 90K and 300K. A red shift of the Ag surface plasmon as a function of decreasing coverage is observed, which is related to the cluster size effect. A surface plasmon characteristic of metallic Ag appears at coverages higher than 2.8 monolayer equivalent.     

In-situ study of Ag nanoparticle hydrosol optical spectra evolution during laser ablation/fragmentation

The results of in-situ monitoring of a laser fragmentation process of a largely polydisperse and morphologically heterogeneous citrate-reduced Ag hydrosol containing a fraction of Ag nanowires are presented. The laser fragmentation was performed using several wavelengths of the incident laser pulses (1064, 532 and 355 nm). Surface plasmon extinction spectra monitoring the nanoparticle fragmentation process were acquired pulse by pulse and related to transmission electron microscopy (TEM) images and statistical TEM image analysis of Ag nanoparticles collected in selected stages of the fragmentation. It was found that, due to different interactions of the laser pulses of various wavelengths with a specific fraction of the Ag nanoparticles in the hydrosol, the course of the fragmentation process depends on the wavelength, leading to different size distributions of the nanoparticles in the resulting hydrosol. The laser pulses of 532 nm wavelength are the most effective for the fragmentation process of the citrate-reduced Ag hydrosol, yielding the narrowest size distribution and the smallest mean radius of the Ag nanoparticles. PACS 81.07.-b; 73.21.-b; 81.16.-c     

Surface plasmon coupled fluorescence in deep-ultraviolet excitation by Kretschmann configuration

We report the experimental demonstration of fluorescence of CdSe quantum dots with surface plasmon excitation in deep-ultraviolet （deep-UV） region. Surface plasmon resonance in deep-UV is excited by aluminum thin film in the Kretschmann-Raether geometry. Considering the oxidation thickness of aluminum, the experimental results of incident angle dependence of reflectance show good agreement with Fresnel theory. Surface plasmon resonance with 19 nm-thick aluminum and 5 nm-thick almnina was excited at the incident angle of 48 degrees for 266 nm excitation. Fluorescence of CdSe quantum dots coated on this aluminum film was observed by the surface plasmon excitation.     

Surface structure influences on the absorptance of thick silver films

Thick Ag films were prepared on mica in UHV, and their absorptance was determined in situ for 260 < λ < 1300 nm. The surface structure was varied by variing thicknesses and by annealing, and was investigated by means of electron microscopy. For the Drude region values of the p-factor resulted between 0 and 1. Surface structure parameters were calculated by fitting the roughness induced surface plasmon peak to the theory of Kretschmann/Kröger with a Peklenik correlation function. It is shown that even at 300 K the roughness structure varies markedly with increasing age of the films. References to a surface roughness dependence of the interband absorption are found in the spectra.     

基于银/二氧化钛复合膜的表面等离子共振气体传感器

表面等离子体共振是一种免标记的传感技术,当介质周围的介电常数发生改变时,则SPR谐振光谱特性也会随之改变.因此表面等离子体共振传感技术已广泛应用于生物化学和环境监测等领域.由于二氧化钛(TiO2)覆盖层不仅可以保护金属层,还能调谐SPR谐振的光谱强度和谐振波长于近红外波段,应用于1550 nm的光纤传感,其氧化还原反应...     

Damping of the surface plasmon in clean and K-modified Ag thin films

The damping processes of electronic collective excitations of Ag/Ni(1 1 1) were studied by high-resolution electron energy spectroscopy. The FMHM of the Ag surface plasmon was reported as a function of Ag thickness, primary electron beam energy, Ag surface plasmon energy, and parallel momentum transfer. The broadening of the Ag surface plasmon was found to be related to 5sp–5sp transitions, for which a critical wave vector of 0.2 Å⁻¹ exists. Moreover, we provide a direct evidence of the occurrence of chemical interface damping in thin films, upon doping the Ag/Ni(1 1 1) system with K adatoms. The enhanced plasmon broadening in K/Ag/Ni(1 1 1) was ascribed to the existence of additional electron–hole decay channels at the K/Ag interface.     

偏振方向及结构间耦合作用对空心方形银纳米结构表面等离子体共振的影响

空心方形纳米结构能够激发更大面积的增强电场,故其可以作为衬底用于表面增强拉曼散射.应用离散偶极子近似算法研究了空心方形银纳米结构的消光光谱及其近场电场分布与入射光偏振方向之间的关系.研究表明,空心方形银纳米结构的表面等离子体共振峰不随入射光偏振方向的改变而移动,但是其表面增强电场分布却强烈地依赖于入射光的偏振方向.另外,还讨论了空心方形银纳米结构间的耦合作用对其表面等离子体共振模式的影响.结果发现,可以通过调节结构间的距离来改变结构间的耦合作用,同时改变了表面等离子体共振峰的位置.这些结果将为理解闭合纳米 关键词： 空心方形银纳米结构 表面等离子体 偏振 电场耦合     

Fabrication and optical study of Ag@SnO<Subscript>2</Subscript> core-shell structure nanoparticle thin films

Ag@SnO₂ core-shell nanoparticles dispersed in poly-(vinyl) alcohol films were fabricated on glass substrate by employing a dip-coating technique. Synthesis of Ag@SnO₂ nanoparticles with core-shell morphology is carried out by a soft-chemical technique in aqueous phase at 60°C. Formation of core-shell structure is monitored by the red-shift of the surface plasmon band of Ag nanoparticles (from 390 to 410 nm) in the UV-visible spectrum. These nanoparticles are deposited on the glass substrate. The structure and morphology of these films were investigated by X-ray diffraction technique and field-emission transmission electron microscopy, respectively. Optical properties of these pseudo-solids were studied by UV-visible spectroscopy. Surface plasmon spectrum of the core-shell nanoparticles film remained unaltered with increase in the number of layers. However, silver nanoparticles films have shown peak broadening and development of additional peaks with increase in the number of layers. Our investigations showed that the surface plasmon band of the silver nanoparticles could be preserved by controlled deposition of the tin dioxide shell.     

Ag/ZnO纳米结构的荧光增强效应

利用化学合成方法制备了Ag纳米线和ZnO量子点。对这两种纳米结构的表面形貌、晶体结构和光学性质分别进行了研究。结果表明：Ag纳米线和ZnO量子点均为单晶结构,平均直径分别为160 nm和5 nm左右。将Ag纳米线混入ZnO量子点可以使其紫外荧光显著增强,其中位于345 nm和383 nm 的荧光分别增强30倍和12倍。这与Ag纳米线和ZnO量子点混合体系的局域表面等离子体共振耦合吸收峰位相一致,说明该体系存在两种共振耦合模式。该研究结果为将来开发ZnO基纳米发光器件提供了一条新的途径。     

基于表面等离子体共振增强的硅基锗金属-半导体-金属光电探测器的设计研究

金属-半导体-金属光电探测器的光栅结构可激发表面等离子体, 有效增强探测器的吸收. 为深入研究器件结构对于表面等离子体的激发及共振增强的影响, 本文提出了一种具有超薄有源层的硅基锗金属-半导体-金属光电探测器的设计方法. 采用时域有限差分的方法详细分析了光栅周期、光栅厚度、 光栅间距及有源层厚度对于表面等离子体共振增强器件性能的影响, 通过仿真模拟获得了器件的最佳结构, 详细地分析了各个界面激发的表面等离子体及其共振模式对于光谱吸收增强的机理. 仿真结果表明, 有源层锗的厚度为400nm的超薄器件在通信波段具有较高的吸收, 尤其在1550nm波长处器件的归一化的光谱吸收率可以高达53.77%, 增强因子达7.22倍. 利用共振效应能够极大地提高高速器件的光电响应, 为解决光电探测器响应度与响应速度之间的相互制约关系提供了有效途径. 关键词： 表面等离子体 锗探测器 时域有限差分仿真