Field-assisted diffusion bonding and bond characterization of glass to aluminum

The bonding of glass wafers to aluminum foils in multi-layer assemblies was investigated by the field-assisted diffusion bonding process. Bonding was effected at temperatures in the range 350–450 °C and with an applied voltage in the range 400–700 V under a pressure of 0.05 MPa. The experimental parameters of voltage and temperature were the main factors in influencing the ionic current leading to the formation of the depleted layer. The peak current in three-layer samples (glass/aluminum/glass) during bonding is twice that for the case of the two-layer samples (aluminum/glass). SEM and EDS analyses showed the presence of transition layers near the glass/aluminum interface, and XRD data demonstrated the phase structure of the glass/aluminum interface. The tensile strength of the bonded material increased markedly with increasing temperature and applied voltage. Fracture occurred in the glass phase near the interface with the aluminum. Finite element analysis showed the residual deformation in three-layer samples to be significantly lower than in two-layer samples. The symmetry in three-layer samples resulted in the absence of strain, an important advantage in MEMS fabrication.     

Ag+在硅酸盐玻璃中电场诱导扩散与纳米晶析出

利用直流电场诱导热扩散技术,引导金属银离子扩散进入硅酸盐玻璃基片内部,并通过后续热处理析出金属银纳米晶体。研究发现,随着电场强度的增大和扩散温度的升高,扩散进入到玻璃基片中的金属银离子数量也随之增多。电场诱导热扩散后银以Ag+和Ag0的形式存在于玻璃基片中。经后续热处理在玻璃基片中形成2～5nm的金属银纳米晶粒,并在410nm附近产生明显的表面等离子共振吸收现象;银纳米晶体主要分布在基片表面以下30～100μm区域。     

Effect of etchant diffusion on tip profiles of glass fiber probes

The tips of the probes are the key components in scanning probe microscopes and their applications in nano-scale imaging and nanofabrications. We investigated first the change of near-field scanning optical microscopy probe tips from optical fiber against time by chemical static etching. Several coverlayer-hydrofluoric acid aqueous solution systems and their possible factors affecting the tips' profile were studied. Tips with shorter tapers, larger conical aperture angles, and reproducible shapes were successfully obtained in high yields. It was found that the taper profiles were affected to a great extent by the one-dimensional linear diffusion of etchants in the coverlayer caused by concentration gradients and convection.     

Plasmonic Au x Ag y bimetallic alloy nanoparticles enhanced photoluminescence upconversion of Er3+ ions in antimony glass hybrid nanocomposites

Er³⁺ ions and spherical (3–23?nm) Au _x Ag _y bimetallic alloy (where x?=?18–96 and y?=?4–82, atom %) nanoparticles incorporated novel antimony oxide based reducing dielectric (glass) matrix, K₂O–B₂O₃–Sb₂O₃ (KBS), has been synthesized by a new single step methodology involving selective thermochemical reduction. Their absorption spectra show a single tunable (536–679 nm) surface plasmon resonance band along with the typical absorption peaks of the Er³⁺ ion. X-ray and SAED indicate the formation of (111) and (200) planes of Au _x Ag _y alloy. The luminescence intensity of two prominent emission bands of Er³⁺ ions centered at 536 (green) and 645 (red) nm due to ⁴S_3/2 → ⁴I_15/2 and ⁴F_9/2 → ⁴I_15/2 transitions were observed to be strongly dependent on the Au _x Ag _y nanoparticle composition. Both the bands undergo a maximum of 1.5- and 4.5-fold intensity enhancement respectively in the presence of the Ag₅₆Au₄₄ alloy (atom %) due to plasmon induced local field enhancement.     

Electrochemical polymerization of benzene in the presence of Ag+, Pb2+ and Cu+ ions

Poly(p-phenylene) (PPP) films were synthesized by using benzene and fluorosulphonic acid (FSO₃H) as a strong acid containing Ag⁺, Pb²⁺ and Cu⁺ ions in methylene chloride (CH₂Cl₂) solution. Addition of Ag⁺ or Pb²⁺ ions into the polymerization medium improved the PPP films formation, but Cu⁺ ion did not have an effect on polymerization. PPP films were characterized by cyclic voltammetry, IR and TGA. Dry conductivities were measured by using four probe technique. Received: 18 September 2000 / Reviewed and accepted: 20 September 2000     

Field-assisted ion diffusion of transition metals for the synthesis of nanocomposite silicate glasses

Field-assisted ion diffusion of metals was realized for the controlled doping of silicate glasses. Metallic films deposited onto the substrates by the rf-sputtering technique were used as the metal ions source. In particular, cobalt was, for the first time, introduced into a soda-lime glass by field-assisted ion exchange, giving rise to diffusion profiles that were observed to depend on the preparation parameters, namely, temperature and electric field intensity across the samples. This technique, which allowed to dope the glass matrix with high metal concentration values, can be used as the first step in combined methodologies for the preparation of nanostructured glass composites. The shape of the measured Co diffusion profiles indicates that the migration process depends not only on the experimental parameters but also on the behavior of alkali ions within the glass. Chemical phenomena occurring at the metal/glass interface also play a significant role in the penetration of the Co ions. The possibility of doping the glass with two different metal species was also investigated, with the aim to create the condition for the formation of core-shell or alloy nanoclusters. In particular, preliminary results on Co + Au field-assisted co-diffusion are presented.     

Ag nanoparticles enhanced near-IR emission from Er3+ ions doped glasses

Vitreous materials containing rare-earth (RE) ions and metallic nanoparticles (NPs) attract considerable interest because the presence of the NPs may lead to an intensification of luminescence. In this work, the characteristics of 1.54 μm luminescence for the Er³⁺ ions doped bismuthate glasses containing Ag NPs were studied under 980 nm excitation. The surface plasmon resonance (SPR) band of Ag NPs appears from 500 to 1500 nm. Transmission electron microscopic (TEM) image reveals that the Ag NPs are dispersed homogeneously with the size from 2 to 7 nm. The strength parameters Ω_t(t = 2, 4, 6), spontaneous emission probability (A), radiative lifetime (τ) and stimulated emission section (σ_em) of Er³⁺ ions were calculated by the Judd–Ofelt theory. When the glass contains 0.2 wt% AgCl, the 1.54 μm fluorescence intensity of Er³⁺ reaches a maximum value, which is 7.2 times higher than that of glass without Ag NPs. The Ag NPs embedded glasses show significantly fluorescence enhancement of Er³⁺ ions by local field enhancement from SPR.     

Two-step K(+)-Na+ and Ag(+)-Na+ ion-exchanged glass waveguides for C-band applications

A two-step K(+)-Na+ and Ag(+)-Na+ ion-exchange technique is introduced to fabricate single-mode channel waveguides in BK7 glass for the telecom-wavelength region. The dependencies of insertion loss, polarization-dependent loss (PDL), end bending loss of curved waveguides on channel width, diffusion time, and annealing time are investigated. Results show that postannealing is a required process for improving waveguide properties and an optimal annealing time exists. Although relatively narrow mask openings are used in most one-step ion-exchange processes, a wider channel width, to as wide as 10 microm, is preferred for this two-step method. The minimum coupling loss to/from single-mode fiber and the propagation loss is found to be 0.4 dB and 0.3 dB/cm, respectively. For 5-cm-long waveguides the PDL is less than 0.1 dB. For the S-bend structure the cosine curve exhibit apparently a lower bending loss than the double-arc curve.     

Spin glass behavior of Mn2+ ions in zeolite-Y at very low temperature

Magnetic properties of manganese ion spin systems in zeolite-Y have been measured. These ions act as almost free ions in the zeolite. Low frequency ac-susceptibility can be described with the Curie-Weiss law down to 50 mK. The susceptibility has a maximum around 30 mK showing a magnetic anomaly. Characteristic relaxation times deduced from frequency dependence of the maxima are studied. They diverge towardsT _c = 0 K according to the following formula, = ₀exp{(b/T)⁺¹} where ₀ = 3 x 10_–10 sec, b = 0.28K, and = 0.4, respectively. It is expected from ESR measurements that the dominant interaction between the manganese ions is dipole-dipole like. This divergence is interpreted as that of a dipolar spin glass.     

The structural influence of aluminium ions on emission characteristics of Sm3+ ions in lead aluminium silicate glass system

Optical absorption and photoluminescence characteristics of Sm³⁺ ions in lead silicate glasses mixed with different concentrations of Al₂O₃ (5–10 mol%) have been investigated. From these studies, the radiative properties viz., spontaneous emission probability A, the total emission probability, the radiative lifetime τ_R, the fluorescent branching ratio β of emission transition of ⁴G_5/2 → ⁶H_7/2 along with other transitions for Sm³⁺ have been evaluated and found to be the highest for the glass mixed with 8.0 mol% of Al₂O₃.The IR spectral studies have indicated that Al³⁺ ions do participate in the glass network with AlO₄ and AlO₆ structural units and further revealed that the concentration of octahedral aluminium ions induce bonding defects in the glass network. Such bonding defects are assumed to be responsible for low phonon losses in these glasses and lead to higher values of radiative parameters for the glass mixed with 8.0 mol% of Al₂O₃.     

Concentration profiles of Zn ions implanted with 60 keV for nanoparticle formation in silica glass

Surface recession due to sputtering under low-energy and high-fluence heavy-ion implantation makes shallower and broader depth profile of implanted ions than those calculated by conventional ion-range simulation-codes such as SRIM. Depth profiles of Zn atoms in silica glasses (SiO₂) implanted with Zn⁺ ions of 60 keV up to 1.0×10¹⁷ ions/cm² were evaluated using both experimental methods as Rutherford backscattering spectrometry (RBS), sputtering depth-profiling by X-ray photoelectron spectroscopy (XPS), and an advanced numerical simulation code TRIDYN, which includes the sputtering loss effects. The TRIDYN code predicts the shallowing of the projectile range from ∼46 to ∼27 nm with increasing the fluence up to 1×10¹⁷ ions/cm², and very high-concentration (∼20 at%) of Zn atoms close to the surface. However, RBS and XPS results exclude such high concentration close to the surface. These results suggest remarkable redistribution of Zn atoms from the nearer surface to the deeper region during the implantation. In fact, Zn-atom concentration near the surface and that near the projectile range are, respectively, lower and higher than those by the SRIM code predictions.     

Planar waveguides formed by Ag+-Na+ ion exchange in nonlinear optical glasses: diffusion and optical properties

All-optical communication systems are the subject of intense research related to the integration of nonlinear optical materials. In sodiocalcic borophosphate glasses that contain niobium oxide and exhibit high nonlinear optical indices, planar waveguides have been formed by a Ag(+)-Na(+) ion-exchange technique. WKB analysis has been used to characterize the diffusion profiles of silver ions exchanged in glass substrate samples chemically by an electron microprobe technique and optically by an M-line technique. These methods permit the Ag(+) penetration depth and diffusion profile shape and index profiles to be determined. The results are analyzed and discussed in relation to Ca(2+) concentration and exchange conditions in glasses. The Ag(+) diffusion in these glasses can be almost entirely controlled for index-profile engineering.     

硅酸盐玻璃中银纳米颗粒的原子状态

在硅酸盐玻璃中原位合成了平均颗粒尺寸为2．8nm、4．0nm和7．0nm的银纳米颗粒．使用银K-边X-射线吸收精细结构谱（XAFS）研究了纳米银颗粒的尺寸和玻璃基质对银原子状态和纳米银颗粒热膨胀系数的影响．结果表明,随着纳米银颗粒尺寸的减小,银原子的静态无序度增大,非和谐振动加剧．根据非和谐爱因斯坦模型和热力学微扰理论,计算了银纳米颗粒的线性膨胀系数．结果表明,纳米银颗粒越小,热膨胀系数越大．     

Anomalous diffusion profiles of zinc in GaAs

A number of workers investigating diffusion in semiconductors using radio-tracer techniques have reported a type of profile which is not easily explained by current theories of diffusion. This anomalous profile is usually found in experiments in which the solute concentration is high and has often been associated with the substitutional-interstitial diffusion mechanism. The profile shape is considered in this paper, taking the diffusion of zinc in GaAs at 1000° C as an example. The use of the Boltzman-Matano technique for analysing complex diffusion profiles is considered and experiments are described which suggest that the technique is not appropriate for this type of profile. An adaptation of the substitutional-interstitial diffusion theory is presented in which allowance is made for the possibility of the gallium vacancy concentration falling below the thermal equilibrium value. Theoretical profiles are computed and compared to experiments. Reasonable agreement is found.     

Determination of refractive index profiles of Ag+ -Na+ ion-exchange multimode strip waveguides by variable wavefront shear double-refracting interferometry microinterferometry

The results of experimental determination of multimode strip waveguide refractive index profiles and Ag concentration profiles obtained by using the variable wavefront shear double-refracting interferometry microinterferometer Biolar PI and an electron microprobe are presented. The strip waveguides under investigation are formed in soda lime glass in an external electric-field-assisted Ag+ -Na+ ion-exchange process from the molten AgNO3 salt by use of dielectric masks with channel apertures. A dry electrochemical technique of dielectric mask formation is applied. The influence of waveguide-forming parameters on the shape of Ag concentration profiles and the range of silver diffusion are shown. Changes in the usually assumed boundary conditions of electric-field calculations in ion-exchange numerical modeling are suggested.     

Impact of Nd3+ ions on physical and optical properties of Lithium Magnesium Borate glass

Enhancing the up-conversion efficiency of borate glass via optimized doping of rare earth ions is an ever-ending quest in lasing glass. Neodymium (Nd³⁺) doped Lithium Magnesium Borate (LMB) glasses are prepared using the melt-quenching method. X-ray diffraction (XRD), Fourier transformed infrared (FTIR), UV–Vis–NIR absorption and Photoluminescence (PL) spectroscopic characterizations are made to examine the influence of Nd³⁺ concentration on physical properties and optical properties. Nd³⁺ contents dependent density, molar volume, refractive index, ion concentration, Polaron radius, inter nuclear distance, field strength, energy band gap and oscillator strength are calculated. XRD patterns confirm the amorphous nature of all glasses and the FTIR spectra reveal the presence of BO₃ and BO₄ functional groups. UV–Vis–IR spectra exhibit ten prominent bands centered at 871, 799, 741, 677, 625, 580, 522, 468, 426, 349 nm corresponding to the transitions from the ground state to ⁴F_3/2, (⁴F_5/2 + ²H_9/2), (⁴F_7/2 + ⁴S_3/2), ⁴F_9/2, ²H_11/2, (⁴G_5/2 + ²G_7/2), (²K_13/2 + ⁴G_7/2 + ⁴G_9/2), (²G_9/2 + ²D_3/2 + ²P_3/2), (²P_1/2 + ²D_5/2), (⁴D_3/2 + ⁴D_5/2) excited states, respectively. A hyper-sensitive transition related to (⁴G_5/2 + ²G_7/2) level is evidenced at 580 nm. The room temperature up-conversion emission spectra at 800 nm excitation displays three peaks centered at 660, 610 and 540 nm. Glass with 0.5 mol% of Nd³⁺ showing an emission enhancement by a factor to two is attributed to the energy transfer between Mg²⁺ and Nd³⁺ ions. Our results suggest that these glasses can be nominated for solid state lasers and other photonic devices.