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Pulse timing zero-crossing

The zero cross level adjustment minimises the timing jitter induced by amplitude jitter of the detector pulses. The zero cross level is therefore often called walk adjust". In early TCSPC systems the walk adjust had an enormous influenee on the shape of the instrument response function (IRF). In newer, more advaneed systems the influence is smaller. The reason is probably that detectors with shorter single electron response are used and the discriminators in the newer CFDs are faster. Therefore, the effective slope of the zero cross transition is steeper, with a correspondingly smaller influence of the zero eross level. Figure 7.63 shows the IRF for an XP2020UR linear-focused PMT and an H5773-20 photosensor module for different zero cross levels. [Pg.321]

The characterization of the laser pulse widths can be done with commercial autocorrelators or by a variety of other methods that can be found in the ultrafast laser literature. " For example, we have found it convenient to find time zero delay between the pump and probe laser beams in picosecond TR experiments by using fluorescence depletion of trans-stilbene. In this method, the time zero was ascertained by varying the optical delay between the pump and probe beams to a position where the depletion of the stilbene fluorescence was halfway to the maximum fluorescence depletion by the probe laser. The accuracy of the time zero measurement was estimated to be +0.5ps for 1.5ps laser pulses. A typical cross correlation time between the pump and probe pulses can also be measured by the fluorescence depletion method. [Pg.134]

FIGURE 2-4 Transport of a chemical in a river. At time zero, a pulse injection is made at a location defined as distance zero in the river. As shown in the upper panel, at successive times C, t2, and t3, the chemical has moved farther downstream by advection, and also has spread out lengthwise in the river by mixing processes, which include turbulent diffusion and the dispersion associated with nonuniform velocity across the river cross section. Travel time between two points in the river is defined as the time required for the center of mass of chemical to move from one point to the other. Chemical concentration at any time and distance may be calculated according to Eq. [2-10]. As shown in the lower panel, Cmax, the peak concentration in the river at any time t, is the maximum value of Eq. [2-10] anywhere in the river at that time. The longitudinal dispersion coefficient may be calculated from the standard deviation of the concentration versus distance plot, Eq. [2-7]. [Pg.74]

The lifetimes of the previous section depend on the concentration, capture cross-section and energy level of the impurities. Lifetime measurements, however, cannot easily be used for these determinations. DLTS is the technique most frequently used instead. It is based on the concept in Figure 5 (22). First consider the n-type Schottky barrier diode of Figure 5 (a) with no deep level impurities. A reverse bias -Vj creates a scr of width W. When the bias is reduced to zero, the scr is also reduced. The scr capacitance, being inversely proportional to W, is small and equal for cases A, C and D and large for case B. If the voltage is pulsed between zero and -V., the capacitance follows almost instantaneously and no time-dependent capacitance is observed. [Pg.29]

Pulse sequences can be used to manipulate information in other ways, as well. The chemical shift concertina uses it to manipulate the relative importance of two terms in the Hamiltonian, the chemical shift term and the spin-spin coupling term. Echo sequences can be viewed as causing the system to evolve back in time to enable us to view information that existed earlier but was obscured by instrumental problems. The same is true of the ZTR experiment to observe the FID at zero time. The cross polarization experiments enable us to exploit the thermodynamic properties of a spin system to enhance the spectrum S/N of a second spin system. [Pg.510]

The zero-crossing method reduces the errors due to jitter and walk by picking the time from the zero crossing of a bipolar pulse (Fig. 10.22). Ideally, all the pulses cross the zero at the same point, and the system is walk free. In practice, there is some walk because the position of zero crossing depends on pulse risetime. The dependence on pulse risetime is particularly important for Ge detectors because the pulses produced by Ge detectors exhibit considerable variations in their time characteristics. To reduce the uncertainties still present with the zero-crossing method, the constant-fraction method has been developed specifically for Ge detectors. [Pg.330]

Many different methods have been proposed and used for successful PSD. One method doubly differentiates the detector pulse, either using CR circuits or a delay line, and bases the PSD on the time interval between the beginning of the pulse and the zero crossing point. This time interval, which is... [Pg.337]

Figure 17. Contour plot of the 360MHz homonuclear spin correlation mpa of 10 (2 mg, CDCL, high-field expansion) with no delay inserted in the pulse sequence shown at the top of the figure. Assignments of cross peaks indicating coupled spins in the E-ring are shown with tljie dotted lines. The corresponding region of the one-dimensional H NMR spectra is provided on the abscissa. The 2-D correlation map is composed of 128 x 512 data point spectra, each composed of 16 transients. A 4-s delay was allowed between each pulse sequence (T ) and t was incremented by 554s. Data was acquired with quadrature phase detection in both dimensions, zero filled in the t dimension, and the final 256 x 256 data was symmetrized. Total time of the experiment was 2.31 h (17). Figure 17. Contour plot of the 360MHz homonuclear spin correlation mpa of 10 (2 mg, CDCL, high-field expansion) with no delay inserted in the pulse sequence shown at the top of the figure. Assignments of cross peaks indicating coupled spins in the E-ring are shown with tljie dotted lines. The corresponding region of the one-dimensional H NMR spectra is provided on the abscissa. The 2-D correlation map is composed of 128 x 512 data point spectra, each composed of 16 transients. A 4-s delay was allowed between each pulse sequence (T ) and t was incremented by 554s. Data was acquired with quadrature phase detection in both dimensions, zero filled in the t dimension, and the final 256 x 256 data was symmetrized. Total time of the experiment was 2.31 h (17).

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