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Probe charge

TPi c point r is the position of a positive probe charge. is the n IIclear charge on atom A located at position The function p(r ) IS the electronic density. In the above equation, the first term represen ts the con tribii tion of tli e n nclei to the electrostatic poten tial and the second term is the electronic con tribiition. Siibstitii ting the electron density expression ... [Pg.245]

Rahimi M, Hegg M (2009) Probing charge transport in single-molecule break junctions using inelastic tunneling. Phys Rev B 79 081404(R)... [Pg.213]

When the characteristic time for charge diffusion is lower than the experiment timescale, not all the redox sites in the film can be oxidized/reduced. From experiments performed under these conditions, an apparent diffusion coefficient for charge propagation, 13app> can be obtained. In early work choroamperometry and chronocoulometry were used to measure D pp for both electrostatically [131,225] and covalently bound ]132,133] redox couples. Laviron showed that similar information can be obtained from cyclic voltammetry experiments by recording the peak potential and current as a function of the potential scan rate [134, 135]. Electrochemical impedance spectroscopy (EIS) has also been employed to probe charge transport in polymer and polyelectrolyte-modified electrodes [71, 73,131,136-138]. The methods... [Pg.81]

A fine example of the use of pulse radiolysis technique in combination with steady-state product distribution is the recent study by Schuler and co-workers to probe charge distribution in aromatics. Their initial studies on biphenyf which were extended recently to phenof have been concerned with the determination of relative yields at o-, m- and -positions to examine the substituent effects on charge distribution. For example, Fig. 2 shows the contour plot of HPLC chromatographic data obtained in the OH radical reaction following the irradiation of phenol in the presence of the oxidant ferricyanide. Figure 3 shows the transient absorption spectra recorded in the reactions of OH and Ng radicals with phenol. The absorption... [Pg.388]

In sec. 1.4.3c we have already introduced the mean (average) electrostatic potential. The mean electrostatic potential yr x ) is related to the work necessary to bring an Infinitely small probe charge from Infinity to Xj without disturbing the environment. This potential can be defined In terms of the one- and two-body interactions, mentioned above, according to... [Pg.294]

Yan and Hupp used nanosecond transient absorption to probe charge recombination after selective excitation of a hexaphosphonated Ru(bpy)3 + derivative bound to DeGussa Ti02 as a function of pH [212]. They found that a fast first-order charge recombination process was insensitive to pH over 13 decades of H+ concentration. Assuming the sensitizer oxidation potential is independent of pH and... [Pg.2772]

A theoretical ab initio approach to assess the basicity of ionic liquid anions has been presented, based on the proton as a probe charge to determine the charge on the anion. According to the equilibrium... [Pg.65]

In this section, after a brief introduction of the OFET operation principles, we outline the main signatures of the intrinsic polaronic transport observed in the experiments with single-crystal OFETs. We compare them to the results of TOF and space-charge limited current (SCLC) experiments that probe charge transport in the bulk. [Pg.38]

COO- Carboxylic acid anion Multi-atom probe, charge — 1... [Pg.412]

This result is also related to the earlier derived image potential in Ek. (2.306). The image charge becomes screened if the external probe charge has a distance / to the surface. Lang and Williams improved Lang s result by solving the Kohn... [Pg.169]

Fig. 2 Illustration of two possible routes of probe-charge transfer in a correctly connected circuit. Fig. 2 Illustration of two possible routes of probe-charge transfer in a correctly connected circuit.
M.C., and Kavan, L. (2011) Probing charge transfer between shells of double-walled carbon nanotubes sorted by outer-wall electronic type. Chem. [Pg.26]


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See also in sourсe #XX -- [ Pg.11 , Pg.60 , Pg.101 ]




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