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Silver layer

The preparation of the reflecting silver layers for MBI deserves special attention, since it affects the optical properties of the mirrors. Another important issue is the optical phase change [ ] at the mica/silver interface, which is responsible for a wavelength-dependent shift of all FECOs. The phase change is a fimction of silver layer thickness, T, especially for T < 40 mn [54]. The roughness of the silver layers can also have an effect on the resolution of the distance measurement [59, 60]. [Pg.1735]

Fig. 4.56. Schematic diagram of a SERS-active substrate and the measurement arrangement. Alumina nanoparticles are deposited on a glass surface and produce the required roughness. A thin silver layer is evaporated on to the nanoparticles and serves for the enhancement. Organic molecules adsorbed on the silver surface can be detected by irradiation with a laser and collecting the Raman scattered light. Fig. 4.56. Schematic diagram of a SERS-active substrate and the measurement arrangement. Alumina nanoparticles are deposited on a glass surface and produce the required roughness. A thin silver layer is evaporated on to the nanoparticles and serves for the enhancement. Organic molecules adsorbed on the silver surface can be detected by irradiation with a laser and collecting the Raman scattered light.
Figure 10-12. Lcfi hand side Slruclure of a PPV microcavily. A thin film of ihe conjugated polymer is deposited on top of a highly reflective distributed Bragg refieclor (DBR). The second mirror is then fabricated by evaporation of a silver layer. Right hand side Emission spectra of the microcavily at excitation cnetgics or 0.0S pJ (dashed line) and l. l pJ (solid line), respectively. Laser pulses ol duration 200-300 ps and a wavelength of 355 nm were used for optical excitation (according to Ref. [39]). Figure 10-12. Lcfi hand side Slruclure of a PPV microcavily. A thin film of ihe conjugated polymer is deposited on top of a highly reflective distributed Bragg refieclor (DBR). The second mirror is then fabricated by evaporation of a silver layer. Right hand side Emission spectra of the microcavily at excitation cnetgics or 0.0S pJ (dashed line) and l. l pJ (solid line), respectively. Laser pulses ol duration 200-300 ps and a wavelength of 355 nm were used for optical excitation (according to Ref. [39]).
Poly crystalline silver layer electrodeposited on a polycrystalline platinum electrode. [Pg.441]

For this micro reactor version, the catalyst was coated on the AlMg3 platelet as a thin silver layer by sputtering [43,44], A further set of platelets was covered with an a-alumina layer by sol-gel technique and impregnated by a three-step procedure with silver lactate. [Pg.265]

A specific example where heterogeneous supports provide nanoparticle size-control is the immobilization of homogeneous silver nanoparticles on polystyrene [366]. This work was extended later to the development of a one-pot method for the size-selective precipitation of silver nanoparticles on PVP-protected thiol-functionalized silica. During the immobilization of very small silver nanoclusters both the size of the silver nanoclusters and the thickness of the silver layer on the support could be controlled directly by the reaction parameters applied (Fi re 16) [367]. [Pg.36]

Therefore, the kinetics of generation of defects in surface-adjacent layers is similar to kinetics of emission of O-atoms. (The estimates indicate that the maximum concentration of vacancies in this case may attain the value of 10 for a sample with area 1 cm ). If one assumes that the emission of oxygen atoms is caused by processes of annihilation of vacancies in the sample, then the coincidence in time dependence of stationary concentration of defects can be indicative that these processes are limited by generation of defects, which, in its turn, is controlled by processes of formation of oxide phase in surface-adjacent silver layers. Oxidation, especially at initial stage, is characterized by intensive formation of defects [54]. [Pg.377]

The basic condition for experimental study of nucleation on an identical surface requires that this surface be a single crystal face without screw dislocations (page 306). Such a surface was obtained by Budevski et at. when silver was deposited in a narrow capillary. During subsequent deposition of silver layers the screw dislocations died out so that finally a surface of required properties was obtained. [Pg.383]

The pits are generally embossed into the substrate (polycarbonate or polymethylmethacrylate) layer by an injection-molding process, and are used to indicate whether a data bit is 0 or 1. An aluminum or silver layer provides a reflective surface, and is protected from corrosion and damage by a radiation-cured acrylate (lacquer) layer, onto which a label is usually printed.197... [Pg.604]

Fig. 7. The four silver layers of a 1 T FFC magnet. The picture shows also a detail of the inner wall of the smallest, most internal layer. The thickness of the cuts is 0.16 mm. At 400 A, the hottest spot power density dissipation reaches 1.1 W/mm. One of the most difficult engineering challenges is to cool these hot spots of the innermost layer efficiently enough to extract all the heat. If the cooling is inefficient, the layer can be seriously damaged or even destroyed. Fig. 7. The four silver layers of a 1 T FFC magnet. The picture shows also a detail of the inner wall of the smallest, most internal layer. The thickness of the cuts is 0.16 mm. At 400 A, the hottest spot power density dissipation reaches 1.1 W/mm. One of the most difficult engineering challenges is to cool these hot spots of the innermost layer efficiently enough to extract all the heat. If the cooling is inefficient, the layer can be seriously damaged or even destroyed.
Water adsorption on silver surfaces exposed into a ventilated shed in an urban-rural site of Cuba was studied [13] using quartz resonators covered with a silver layer. It was determined that in these indoor conditions water adsorption significantly diminishes when air temperature increases over 25°C at relative humidity ranges of 80-90% and 90-100%. All these results confirm the idea that an upper limit of temperature should be established for the estimation of time of wetness. [Pg.64]

Benzotriazole has also been used as an additive in anticorrosive coatings for silver layered on plastic film <89JAP8909733). An anticorrosive, electromagnetic wave-shielding coating containing tolyltriazole has been developed for aluminum <91EUP437979). [Pg.124]

Fig. 5 Montage image combining an STM image of the Ag oxide structure (from bottom left) superimposed over the proposed oxide structure (from top right). The numbers, n = 1-5, correspond to the symmetrically different positions within the middle silver layer sandwiched between two O layers. Agi and Ag2 have metallic character, as they are exclusively bonded to silver atoms in the substrate below, whereas Ags, Ag4, and Ags are directly bonded to oxygen inside the oxide rings and are ionic in nature. Both Ag4 and Ags sites sit above threefold sites of the underlying (111) lattice atoms, whereas Ags occupies a top site. Reprinted with permission from Bocquet et at.. Journal of the American Chemical Society, 2003, 125, 3119. 2003, American Chemical Society. Fig. 5 Montage image combining an STM image of the Ag oxide structure (from bottom left) superimposed over the proposed oxide structure (from top right). The numbers, n = 1-5, correspond to the symmetrically different positions within the middle silver layer sandwiched between two O layers. Agi and Ag2 have metallic character, as they are exclusively bonded to silver atoms in the substrate below, whereas Ags, Ag4, and Ags are directly bonded to oxygen inside the oxide rings and are ionic in nature. Both Ag4 and Ags sites sit above threefold sites of the underlying (111) lattice atoms, whereas Ags occupies a top site. Reprinted with permission from Bocquet et at.. Journal of the American Chemical Society, 2003, 125, 3119. 2003, American Chemical Society.
In the oxide region of gold electrodes, residual lead can be present, resulting from irreversible adsorption, and presence of hydroxide species has been postulated ]265]. Pb UPD on Au(lll) has also been studied in selected organic solvents, mainly propylene carbonate [284]. Results similar to those in aqueous solutions have been obtained. Deposition of Pb on Au electrodes coated by silver has also been studied [285]. Depending on the silver layer thickness, results typical for Pb deposited on Au or Ag have been obtained. [Pg.819]

Hasse et al. [366] have used in situ AFM for the detection of silver nucleation at the three-phase junction of the type metal-silver halide-electrolyte solution. At this phase boundary, electrochemical reduction of submicrometer size silver halide crystals immobilized on the surface of gold and platinum electrodes took place. Following nucleation, the reaction advanced until the entire surface of the silver hahde crystals was covered with 20 atomic layers of silver. Then, reduction was terminated. The obtained silver layer could be oxidized and the next layer of silver halide crystals became accessible for further reduction. [Pg.944]

The comparison of more complete kinetic equations (242) and (243) with experimentation is hampered by the instability of activity of silver catalysts (59). The effects arising from the penetration of oxygen into the subsurface silver layer (63) and the formation of a polymer film on the surface (70), an extremely high sensitivity of the catalyst to the traces of compounds of such elements as S and Cl that may be present in the reactants as impurities, can be the sources of this instability. [Pg.238]

Figure A is the dielectric. In B two thin silver layers have been applied. In C you can see the conduction wires and in D the capacitor... Figure A is the dielectric. In B two thin silver layers have been applied. In C you can see the conduction wires and in D the capacitor...
Figure 27 Schematic representation of the all-optical parallel processing in guided mode geometry and the calculated reflectance for a polymer film (1600 nm) on a silver layer (50 nm). The complex refractive index of a polymer layer is (a) 1.60, (b) 1.58, and (c) 1.60 + 0.02i. Figure 27 Schematic representation of the all-optical parallel processing in guided mode geometry and the calculated reflectance for a polymer film (1600 nm) on a silver layer (50 nm). The complex refractive index of a polymer layer is (a) 1.60, (b) 1.58, and (c) 1.60 + 0.02i.

See other pages where Silver layer is mentioned: [Pg.238]    [Pg.560]    [Pg.487]    [Pg.441]    [Pg.352]    [Pg.422]    [Pg.422]    [Pg.422]    [Pg.223]    [Pg.223]    [Pg.143]    [Pg.122]    [Pg.210]    [Pg.211]    [Pg.300]    [Pg.303]    [Pg.222]    [Pg.218]    [Pg.507]    [Pg.139]    [Pg.60]    [Pg.241]    [Pg.53]    [Pg.198]    [Pg.116]    [Pg.314]    [Pg.1483]    [Pg.444]    [Pg.140]    [Pg.142]    [Pg.127]    [Pg.427]   
See also in sourсe #XX -- [ Pg.193 , Pg.196 ]




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Oxygen Layers on Silver in Alkaline Electrolytes

Silver Nitrate-impregnated Silica Gel Layers

Silver bromide, determination layer

Silver ion thin-layer chromatography

Silver layers single-layer devices

Silver layers solutions

Silver layers spacers

Silver layers spin coating

Silver layers splitting

Silver layers stacking

Silver layers substituents

Silver layers substrates

Silver nitrate layers

Silver nitrate thin layer plate

Thin-layer silver electrodes

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