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Optical discharge

The optical discharging condition is the same. The well width is 5.9 nm and the barrier width is kept at 2nm. The bias voltages are Vo=1.29,Via=-Vi=-0.30V, Vib=0 volts. The output power of the first harmonic is 24.2 mW for diode area of 100 pm. The embedding impedance for the first harmonic is 0.57+j0.86 2. Fig.2 shows simulation results. The residual gap is 0.162 eV, greater than in Example 1. Hence the dc bias voltage need be set at a higher value and the well width is assigned a smaller value. [Pg.146]

Recent research with the II-VI semiconductor material ZnO (band gap = 3.8 eV, similar to those of the heavy-metal azides) has revealed that the ability of the specimen to retain stable ions formed by electrostatic charging is a critical function of the degree of surface order A highly disordered surface allows the formation of stable adsorbed ions a highly ordered surface does not [43]. A semiquantitative theory to account for this has been proposed [44]. Further, with disordered surfaces, the location of the electronic state of the adsorbed ions relative to the band structure of the specimen can be probed by an optical discharge technique to yield information about the electronic properties of the surface [43]. These potentialities, coupled with the field-assisted initiation capabilities of an azide specimen, argue that the electrostatic charging technique should be applied quantitatively to explosive azides. [Pg.467]

Thermal Plasma Generation in Microwave and Optical Discharges... [Pg.211]

Figure 4-69. Continuous optical discharge (a) general view of the discharge (b) large image of the discharge with the beam traveling right to left (Generalov et al., 1971). Figure 4-69. Continuous optical discharge (a) general view of the discharge (b) large image of the discharge with the beam traveling right to left (Generalov et al., 1971).
Most ion-molecule techniques study reactivity at pressures below 1000 Pa however, several techniques now exist for studying reactions above this pressure range. These include time-resolved, atmospheric-pressure, mass spectrometry optical spectroscopy in a pulsed discharge ion-mobility spectrometry [108] and the turbulent flow reactor [109]. [Pg.813]

Larger molecules generally caimot be studied in quite the same way, as an electric discharge merely breaks them up into smaller molecules or atoms. In such a case excited states are usually produced by optical excitation using light of the same or higher energy. Many modem fluorimeters are made with two... [Pg.1120]

Thermospray interface. Provides liquid chromatographic effluent continuously through a heated capillary vaporizer tube to the mass spectrometer. Solvent molecules evaporate away from the partially vaporized liquid, and analyte ions are transmitted to the mass spectrometer s ion optics. The ionization technique must be specified, e.g., preexisting ions, salt buffer, filament, or electrical discharge. [Pg.433]

Until the advent of lasers the most intense monochromatic sources available were atomic emission sources from which an intense, discrete line in the visible or near-ultraviolet region was isolated by optical filtering if necessary. The most often used source of this kind was the mercury discharge lamp operating at the vapour pressure of mercury. Three of the most intense lines are at 253.7 nm (near-ultraviolet), 404.7 nm and 435.7 nm (both in the visible region). Although the line width is typically small the narrowest has a width of about 0.2 cm, which places a limit on the resolution which can be achieved. [Pg.122]

Explosion Suppression With explosion suppression, an incipient explosion is detected and—within a few milhseconds—a suppressant is discharged into the exploding medium to stop combustion. Pressure and optical detection systems are used suppressors are pressurized and release the suppressants when actuated by an electroexplosive device. [Pg.2318]

Elastic Recoil Detection Analysis Glow discharge mass spectrometry Glow discharge optical emission spectroscopy Ion (excited) Auger electron spectroscopy Ion beam spectrochemical analysis... [Pg.4]

Several ion sources are particularly suited for SSIMS. The first produces positive noble gas ions (usually argon) either by electron impact (El) or in a plasma created by a discharge (see Fig. 3.18 in Sect. 3.2.2.). The ions are then extracted from the source region, accelerated to the chosen energy, and focused in an electrostatic ion-optical column. More recently it has been shown that the use of primary polyatomic ions, e. g. SF5, created in FI sources, can enhance the molecular secondary ion yield by several magnitudes [3.4, 3.5]. [Pg.88]

Edited by H. Bubert and H. Jenett Copyright 2002 Wiley-VCH Verlag GmbH ISBNs 3-527-30458-4 (Hardback) 3-527-60016-7 (Electronic) 4.4 Clow Discharge Optical Emission Spectroscopy (CD-OESj... [Pg.221]

Clow Discharge Optical Emission Spectroscopy (CD-OESj 223... [Pg.223]

Chw Discharge Optical Emission Spectroscopy (CD-OES) 229 Tab. 4.2. Some typical applications of GD-OES depth-profile analysis. [Pg.229]

R. Payling, D. Jones, A. Bengtson (eds.J Glow Discharge Optical Emission Spectrometry, John Wiley and Sons, Chichester 1997. [Pg.321]


See other pages where Optical discharge is mentioned: [Pg.409]    [Pg.144]    [Pg.144]    [Pg.145]    [Pg.211]    [Pg.214]    [Pg.215]    [Pg.215]    [Pg.257]    [Pg.409]    [Pg.144]    [Pg.144]    [Pg.145]    [Pg.211]    [Pg.214]    [Pg.215]    [Pg.215]    [Pg.257]    [Pg.344]    [Pg.810]    [Pg.1330]    [Pg.2080]    [Pg.354]    [Pg.246]    [Pg.379]    [Pg.15]    [Pg.1]    [Pg.6]    [Pg.471]    [Pg.116]    [Pg.83]    [Pg.443]    [Pg.472]    [Pg.129]    [Pg.129]    [Pg.2331]    [Pg.431]    [Pg.622]    [Pg.625]    [Pg.221]    [Pg.221]    [Pg.224]    [Pg.225]    [Pg.235]   
See also in sourсe #XX -- [ Pg.211 , Pg.214 ]




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