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Deposition Charges

It has become clear that the potentials needed to form atomic layers shift negatively as the semiconductor films grow, especially over the first 25 cycles. The most probable reason is formation of a junction potential between the Au substrate and the depositing compound semiconductor. [Pg.30]

Alternatively, it might be that the underpotentials needed to form atomic layers of the elements were decreasing, shifting closer to the formal potentials for deposition of the bulk elements. This scenario may be a factor, but it is frequently observed that the steady state potentials are more negative then the formal potentials for the elements, where bulk deposits of the elements would be expected to form. [Pg.30]

When the potentials are shifted a little each cycle, steady state potentials are generally achieved after about 25 cycles. The steady state potentials can be maintained, without shifting, through the rest of the deposit, with the amounts deposited remaining constant. [Pg.30]


Fig. 2. Schematics of (a) single-layer photoreceptor, where the + signs represent the corona-deposited charge, D the photoconductor, and 1 the conductive substrate and (b), the CdS Sej (Katsuragawa) photoreceptor, where D represents the insulating layer, the CdS Sej, and I the... Fig. 2. Schematics of (a) single-layer photoreceptor, where the + signs represent the corona-deposited charge, D the photoconductor, and 1 the conductive substrate and (b), the CdS Sej (Katsuragawa) photoreceptor, where D represents the insulating layer, the CdS Sej, and I the...
Fig. 7. Schematic of an organic layered photoreceptor, where the — signs represent the corona-deposited charge, which is typically negative D, the CTL ... Fig. 7. Schematic of an organic layered photoreceptor, where the — signs represent the corona-deposited charge, which is typically negative D, the CTL ...
Figure 3. Scanning electron microscopy images of gold electrodes coated by the nanostructured TMPP/C12 monolayer after the electrochemical platinum deposition. The deposition charge was 41 and 160Cm for the left and right images, respectively. (Reprinted from Ref [18], 2005, with permission from Wiley-VCH.)... Figure 3. Scanning electron microscopy images of gold electrodes coated by the nanostructured TMPP/C12 monolayer after the electrochemical platinum deposition. The deposition charge was 41 and 160Cm for the left and right images, respectively. (Reprinted from Ref [18], 2005, with permission from Wiley-VCH.)...
In the EPD process, a DC electric field is used to deposit charged particles from a colloidal suspension onto an oppositely charged substrate, as illustrated in Figure 6.8. The graphite rod used for the deposition substrate is later burned out prior to cell operation, leaving a hollow tube. The other fuel cell layers can be deposited by a similar process onto the anode support tube. [Pg.254]

Figure 8. LEED pattern and real-space model of partial coverage UPD Pb on Ag(100). Deposition charge density before emersion = 53 fiC/ca -, 0pb - 0.14, Ep - 27 eV. Figure 8. LEED pattern and real-space model of partial coverage UPD Pb on Ag(100). Deposition charge density before emersion = 53 fiC/ca -, 0pb - 0.14, Ep - 27 eV.
Fig. 3 Series of EFM images taken for PE (a), PVC (b), PMMA (c), and PA (d). The images show the initial states without deposited charges, the states immediately after deposition of charges by the silicon cantilever (t = 0) and after different time spans (t = /,). The positions of the deposited charges are indicated by a white circle. Negative charges appear pale, positive charges are dark. All measurements were carried out at a relative humidity of tp = 30%... Fig. 3 Series of EFM images taken for PE (a), PVC (b), PMMA (c), and PA (d). The images show the initial states without deposited charges, the states immediately after deposition of charges by the silicon cantilever (t = 0) and after different time spans (t = /,). The positions of the deposited charges are indicated by a white circle. Negative charges appear pale, positive charges are dark. All measurements were carried out at a relative humidity of tp = 30%...
PA is another polar polymer. It is able to take up and incorporate tidy amounts of water [12], Figure 3d shows a quick spreading of the deposited charges within a few... [Pg.52]

Fig. 2.11. Cyclic voltammograms of a poly(aniline)-coated glassy carbon electrode (deposition charge ISO mC, geometric area 0.38 cm2), recorded at 5 mV s 1 in oxygen-free 0.1 mol dm 3 citrate/phosphate buffer at pH 5 in the absence (—), and in the presence (—), of 1 mmol dm-3 NADH. Before each scan the electrode was held at -0.3 V for 3 min to ensure complete reduction of the film. Fig. 2.11. Cyclic voltammograms of a poly(aniline)-coated glassy carbon electrode (deposition charge ISO mC, geometric area 0.38 cm2), recorded at 5 mV s 1 in oxygen-free 0.1 mol dm 3 citrate/phosphate buffer at pH 5 in the absence (—), and in the presence (—), of 1 mmol dm-3 NADH. Before each scan the electrode was held at -0.3 V for 3 min to ensure complete reduction of the film.
Fig. 2.12. Plot of the current as a function of time for the oxidation of 4 mmol dm- 1 NADH at 0.2 V at a poly(aniline)-coated rotating disc electrode (area 0.38 cm2, deposition charge ISO mC) in 0.1 mol dm 1 citrate/phosphate buffer, pH 5. The rotation speed of the electrode was increased in the sequence I, 4, 9, 16, 25, 36 and 49Hz and reduced in sequence back to 1 Hz. The broken line connects segments of the curve corresponding to the different rotation speeds. Note The current decays more rapidly at the higher rotation speeds and responds rapidly to changes in rotation speed. Fig. 2.12. Plot of the current as a function of time for the oxidation of 4 mmol dm- 1 NADH at 0.2 V at a poly(aniline)-coated rotating disc electrode (area 0.38 cm2, deposition charge ISO mC) in 0.1 mol dm 1 citrate/phosphate buffer, pH 5. The rotation speed of the electrode was increased in the sequence I, 4, 9, 16, 25, 36 and 49Hz and reduced in sequence back to 1 Hz. The broken line connects segments of the curve corresponding to the different rotation speeds. Note The current decays more rapidly at the higher rotation speeds and responds rapidly to changes in rotation speed.
Fig. 2.17. Plots of the current at +0.1 V for a poly(aniline)/poly(vinylsulfonate)-coated glassy carbon electrode (deposition charge 150 mC, geometric area 0.38 cm2) rotated at 9 Hz in 0.1 mol dm- 1 citrate/phosphate buffer at pH 7 as a function of the NADH concentration showing the stability of the electrode response. Four replicate calibration curves recorded in succession over 4h using the same electrode are shown ( ) run 1 ( ) run 2 (A) run 3 and (O) run 4. The solid line is drawn as a guide for the eye. Fig. 2.17. Plots of the current at +0.1 V for a poly(aniline)/poly(vinylsulfonate)-coated glassy carbon electrode (deposition charge 150 mC, geometric area 0.38 cm2) rotated at 9 Hz in 0.1 mol dm- 1 citrate/phosphate buffer at pH 7 as a function of the NADH concentration showing the stability of the electrode response. Four replicate calibration curves recorded in succession over 4h using the same electrode are shown ( ) run 1 ( ) run 2 (A) run 3 and (O) run 4. The solid line is drawn as a guide for the eye.

See other pages where Deposition Charges is mentioned: [Pg.324]    [Pg.213]    [Pg.30]    [Pg.30]    [Pg.146]    [Pg.146]    [Pg.146]    [Pg.147]    [Pg.147]    [Pg.148]    [Pg.148]    [Pg.206]    [Pg.105]    [Pg.22]    [Pg.302]    [Pg.241]    [Pg.242]    [Pg.42]    [Pg.42]    [Pg.42]    [Pg.329]    [Pg.38]    [Pg.503]    [Pg.48]    [Pg.49]    [Pg.51]    [Pg.51]    [Pg.51]    [Pg.53]   


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