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Excitation Excited Exponentially Generated

H. Nakatsuji, J. Chem. Phys., 94, 6716 (1991). Exponentially Generated Configuration Interaction Theory. Descriptions of Excited, Ionized, and Electron Attached States. [Pg.183]

The value of k so determined could then be compared with the theoretical value of 4ttN aD. However, when viscosity is considerable and/or for short lifetimes, the transient effect in diffusion is not negligible and -30% of the transfer may be attributable to the transient phase. In such a case, the luminescence decay is not simply exponential (Sveshnikov, 1935). For a brief pulse excitation, a complicated decay ensures on the other hand, for so prolonged an excitation as to generate a steady state, the resultant decay curve in many cases is indistinguishable from an exponential (Yguerabide et ah, 1964). [Pg.87]

The background problem can be further overcome when using a surface-confined fluorescence excitation and detection scheme at a certain angle of incident light, total internal reflection (TIR) occurs at the interface of a dense (e.g. quartz) and less dense (e.g. water) medium. An evanescent wave is generated which penetrates into the less dense medium and decays exponentially. Optical detection of the binding event is restricted to the penetration depth of the evanescent field and thus to the surface-bound molecules. Fluorescence from unbound molecules in the bulk solution is not detected. In contrast to standard fluorescence scanners, which detect the fluorescence after hybridization, evanescent wave technology allows the measurement of real-time kinetics (www.zeptosens.com, www.affinity-sensors.com). [Pg.493]

Figure 8.9 Time-resolved fluorescent lifetime analysis of Cy3 attached to double-stranded DNA (Iqbal et al., 2008b). Fluorescent decay curve for Cy3 attached to a 16 bp DNA duplex, showing the experimental data and the instrument response function (IRF), and the fit to three exponential functions (line). The decay curve was generated using time-correlated single-photon counting, after excitation by 200 fs pulses from a titanium sapphire laser at 4.7 MHz. Figure 8.9 Time-resolved fluorescent lifetime analysis of Cy3 attached to double-stranded DNA (Iqbal et al., 2008b). Fluorescent decay curve for Cy3 attached to a 16 bp DNA duplex, showing the experimental data and the instrument response function (IRF), and the fit to three exponential functions (line). The decay curve was generated using time-correlated single-photon counting, after excitation by 200 fs pulses from a titanium sapphire laser at 4.7 MHz.
The authors included that the excited states created by the optical transition at peak absorption ( 620 nm) are not involved in carrier generation. Very interesting is the observation that photocurrents increased with decreasing temperature to the peak value at 175—225 °K. They proposed that carrier mobilities increase with decreasing temperature and that the increase is high enough to offset the exponential decrease in carrier separation and lifetime. [Pg.18]

Although the reverse current of an ideal Schottky barrier is J, in practice there are other current soitfces. Imperfect contacts have a leakage current which generally increases exponentially with bias. Even with an ideal contact, there is a thermal generation current caused by the excitation of electrons and holes from bulk gap states to the band edges. This mechanism determines the Fermi energy position under deep depletion conditions. The current density is the product of the density of states and the excitation rate and is approximately. [Pg.327]

The minimum prerequisite for generation of upconversion luminescence by any material is the presence of at least two metastable excited states. In order for upconversion to be efficient, these states must have lifetimes sufficiently long for ions to participate in either luminescence or other photophysical processes with reasonably high probabilities, as opposed to relaxing through nonradiative multiphonon pathways. The observed decay of an excited state in the simplest case scenario, as probed for example by monitoring its luminescence intensity I, behaves as an exponential ... [Pg.4]


See other pages where Excitation Excited Exponentially Generated is mentioned: [Pg.139]    [Pg.148]    [Pg.1105]    [Pg.291]    [Pg.274]    [Pg.460]    [Pg.171]    [Pg.277]    [Pg.290]    [Pg.418]    [Pg.286]    [Pg.372]    [Pg.397]    [Pg.139]    [Pg.225]    [Pg.222]    [Pg.231]    [Pg.395]    [Pg.472]    [Pg.212]    [Pg.29]    [Pg.651]    [Pg.115]    [Pg.117]    [Pg.176]    [Pg.132]    [Pg.142]    [Pg.26]    [Pg.316]    [Pg.96]    [Pg.150]    [Pg.363]    [Pg.147]    [Pg.202]    [Pg.554]    [Pg.195]    [Pg.1949]    [Pg.24]    [Pg.473]   


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