Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Crystallization crystal thinning

Figure 16-47. Emission spectra of a melt-crystallized thin (300 nm) film of Oocl-OPV5. Excitation energy (a) I pJ, (b) 10 pj, (c) 50 pJ, (el) 70 pJ excitation beam diameter x 1 mm. Figure 16-47. Emission spectra of a melt-crystallized thin (300 nm) film of Oocl-OPV5. Excitation energy (a) I pJ, (b) 10 pj, (c) 50 pJ, (el) 70 pJ excitation beam diameter x 1 mm.
Diamond is obtained as a polycrystalline material by CVD with properties similar to these of natural diamond. Efforts to produce single crystal thin films have so far been largely unsuccessful. [Pg.194]

Because of its piezoelectric properties, synthetic CC-quartz is used for frequency control in electrical oscillators and filters and in electromechanical transducers. When mechanically stressed in the correct direction, CC-quartz develops an electric polarization. The opposite is also tme an applied electric field gives rise to a mechanical distortion in the crystal. Thin sections of quartz are cut to dimensions that produce the desired resonance frequency when subjected to an alternating electric field the vibrating crystal then reacts with the driving circuit to produce an oscillation that can be narrowly controlled. Quartz is ideal for this application because it is hard, durable, readily synthesized, and can be tuned to high accuracy, for example, quartz crystal clocks can be made that are stable to one part in 109. [Pg.480]

D nanoribbons and nanowires of different metal-containing Pcs have also been prepared by organic vapor-phase deposition (OVPD), a technique used to fabricate organic millimeter-sized crystals, thin films, or nanostructures [211], Scanning electron microscopy (SEM), TEM, x-ray diffraction (XRD), and absorption measurement studies have revealed that the morphology of the nanostructures was strongly dependent on the chemical nature of the deposited macrocycle, the nature and the temperature of the substrate, and the source-to-substrate distance. [Pg.29]

To compare these methods, in Fig. 40 we show (a) EIX vs. J and (b) /Ph vs. E plots for a CVD single crystal thin-film electrode. We see that with increase in illumination intensity J, the open-circuit potential E(X approaches a limit of 0.7 V, which is close to the photocurrent onset potential (0.75 V). [The photocurrent density squared vs. potential dependence for this electrode, although far from linear (unlike that of Fig. 38), by the extrapolation to yph -> 0 gives the potential value of approx. 0.65 V.] It is concluded that, on the whole, methods (i) and (ii) are in a good agreement and can be used in the determination of the flat-band potential. Similar results were obtained with HTHP single crystals. [Pg.262]

Investigations of the interference figures may be performed with a polarizing microscope equipped with a four-axis universal stage. Normally, for polarizing microscope measurements, transparent crystal thin sections... [Pg.235]

The study of isopropyl benzene can be sumnarized as follows. The width of the UPS line corresponding to removal of the lowest binding energy ir-electron is temperature dependent. This temperature dependence contributes significantly to the UPS line-width at elevated temperatures. The fact that the width is temperature dependent indicates that the mechanism involves vibrations. Although experimentally, intramolecular and inter-molecular effects could not be separated, theoretical models predict that of the effect is mostly intermolecular. The small residual linewidth observed is due to sample inhomogeneities. Presumably, an ideal single crystal thin film would exhibit the same A(T) but have a smaller A. ... [Pg.135]

Nonlinear optical infrared-visible sum frequency generation (IR-vis SFG) is a versatile surface-specific vibrational spectroscopy that meets the requirements mentioned above. SFG provides vibrational spectra of molecules adsorbed on a surface, while the molecules in the gas phase do not produce a signal. Consequently, SFG can be operated in a pressure range from UFIV to ambient conditions and still detects only the adsorbed species. A direct comparison of adsorbate structures under UFIV and elevated pressure is therefore feasible. Furthermore, SFG can be applied to molecules adsorbed on single crystals, thin films, metal foils, and supported nanoparticles (46,116-121) and is thus a promising tool to extend surface science experiments to more realistic conditions. [Pg.144]

Decher, G., Maclennan, J., Sohling, U., Reibel, J. (1992). Creation and structural comparison of ultrathin film assemblies -transferred freely suspended films and Langmuir-Blodgett-films of liquid-crystals. Thin Solid Films 210 504-7. [Pg.872]

From the above observations, it can be assumed that the formation of protrusions is due to incomplete thermal decomposition of the Ti precursors in the relatively low temperature region. The non-cracked ligands incorporated into the film hinder the formation of a uniformly crystallized thin film. It is reasonable to assume that the protruded region contains some carbonate material even though the crystallographic analysis did not detect any carbonate phase due probably to the fact that the carbon containing phase has non-crystalline structure. [Pg.230]

Figure H.4. The crystals are manipulated by scooping them up with a small loop of nylon that is glued to the end of a pin. Surface tension firom the liquid will hold the crystal in the loop, but the crystal can also be held by using a loop that is smaller in size than the crystal of interest. This technique will work particularly well with fragile crystals, thin plates for example, that would normally fall apart in a capillary mount. Once the crystal is frozen, it is placed on an axis in line of both an X-ray source and a stream of nitrogen set to about 100,000to keep the crystal frozen. The crystal is rotated in increments during the data collection procedure to collect a full data set (typically one or two degrees per frame, depending on the resolution limits, mosaicity of the crystal, unit cell lengths, etc.). Figure H.4. The crystals are manipulated by scooping them up with a small loop of nylon that is glued to the end of a pin. Surface tension firom the liquid will hold the crystal in the loop, but the crystal can also be held by using a loop that is smaller in size than the crystal of interest. This technique will work particularly well with fragile crystals, thin plates for example, that would normally fall apart in a capillary mount. Once the crystal is frozen, it is placed on an axis in line of both an X-ray source and a stream of nitrogen set to about 100,000to keep the crystal frozen. The crystal is rotated in increments during the data collection procedure to collect a full data set (typically one or two degrees per frame, depending on the resolution limits, mosaicity of the crystal, unit cell lengths, etc.).
I, Spread potassium chlorate crystals thinly on a hard surface. Roll the round stick over crystals to crush into a very fine powder until It looks like face powder or wheat flour. [Pg.283]

M. H. Francombb and H. Sato (Eds.), Single Crystal Thin Films, Pergamon Press, Oxford, 1964. [Pg.271]

Paulmier, D Le Huu, T Zaidi, H. Growth and orientation of diamond crystal thin films obtained by the combustion flame method. Surface Sci. 1997, 377-379, 866-870. [Pg.97]

Alzawa et al. (51-54) incorporated chlorophyll molecules into a liquid crystal thin membrane, which was deposited on a platinum electrode. The liquid crystal molecules were found to be effective in the inhibition of intermolecular interaction of chlorophylls and the formation of the chlorophyll-hydrate, which could enhance the charge separation in photoexcitation. [Pg.458]


See other pages where Crystallization crystal thinning is mentioned: [Pg.443]    [Pg.480]    [Pg.25]    [Pg.3]    [Pg.469]    [Pg.240]    [Pg.273]    [Pg.443]    [Pg.136]    [Pg.484]    [Pg.207]    [Pg.25]    [Pg.26]    [Pg.88]    [Pg.276]    [Pg.298]    [Pg.191]    [Pg.340]    [Pg.401]    [Pg.329]    [Pg.1651]    [Pg.60]    [Pg.824]    [Pg.124]    [Pg.664]    [Pg.664]    [Pg.665]    [Pg.665]    [Pg.144]    [Pg.5]    [Pg.168]    [Pg.175]    [Pg.8]    [Pg.579]   
See also in sourсe #XX -- [ Pg.185 ]




SEARCH



Alloy single-crystal surface, thin anodic

Alloy single-crystal surface, thin anodic oxide overlayers

CVD of TBCCO Thin Films on Single Crystal Substrates

Crystal structure, thin films

Crystal structure, thin films 3-carbon atoms

Crystal structure, thin films bridged structures

Crystal structure, thin films changes with oxidation

Crystal structure, thin films linear

Crystal structure, thin films model compounds

Crystal structure, thin films techniques

Crystal thin plates

Crystallization in thin films

Crystallization of Thin Polymer Films on Amorphous Foreign Surface

Crystallization thin-film stage

Metal single-crystal surface, thin anodic

Microwave properties of dielectric single crystals, ceramics and thin films

Oxide Surfaces Single Crystals, Powders, Thin Films

Poly crystals from thin films

Polyethylene thin crystals, structure

Quartz crystal microbalance thin surface films

Quartz crystal thin liquid film

Scattering, from thin crystals

Secondary crystallization crystal thinning

Single crystal thin films

Single-crystal surfaces, thin anodic oxide

Single-crystal surfaces, thin anodic oxide overlayers

The Thin Crystal Case

Thin Films in Complete Wetting and the Specific Case of Nematic Liquid Crystals

Thin crystal

Thin crystallization

Thin crystals in circularly polarized laser fields

Thin crystals, scattering

Thin film characterization quartz crystal microbalance

Thin film growth quartz crystal microbalance

Thin films crystallization

Thin liquid crystal films

© 2024 chempedia.info