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2p excitation

FIGURE 13.1 Graphs that have a one-dimensional data space, (a) Radial portion of the wave function for the hydrogen atom in the l.v ground state and 2p excited state. (A) Hypothetical salary chart. [Pg.116]

The proportions of ground-state and (2P ) excited iodine atoms produced in a photolysis using monochromatic radiation can be approximately calculated from Fig. 1. To conserve momentum, essentially all the energy from the primary process in excess of that used in bond dissociation (HI -> H+I) =... [Pg.144]

In this context, the threshold power is the minimum power necessary to obtain a well formed structure which is not deformed or washed away during the developing step. As the 2P-excitation rate does... [Pg.74]

As with radical polymerization, some studies have used well-established IP-initiators under 2P excitation conditions. For example, the commercially available photoacid generator p.l (Fig. 18), which has a peak cross section of only 16 GM at a photon wavelength of 5 3 0 nm [ 169 ], has b een used to fabricate... [Pg.80]

Fig. 5.2. Cross sections for the 2S-2P excitation of lithium obtained using the... Fig. 5.2. Cross sections for the 2S-2P excitation of lithium obtained using the...
Figure 5.14 The helium ionization yield for the ion being left in the He+(2s) and He+(2p) excited states as a function of the time delay between the initial XUV pump pulse and the IR probe pulse. The oscillations are due to breathing between different doubly excited states (resonances). Figure 5.14 The helium ionization yield for the ion being left in the He+(2s) and He+(2p) excited states as a function of the time delay between the initial XUV pump pulse and the IR probe pulse. The oscillations are due to breathing between different doubly excited states (resonances).
Fig. 7.1. Comparison of Tl with the approximation (7.153) for the 2p excitation of hydrogen and the 3p excitation of sodium. Curves are drawn for the energies (eV) indicated (Allen et al, 1988). Fig. 7.1. Comparison of Tl with the approximation (7.153) for the 2p excitation of hydrogen and the 3p excitation of sodium. Curves are drawn for the energies (eV) indicated (Allen et al, 1988).
Fig. 8.5. Differential cross section for the unresolved 2s and 2p excitations of hydrogen. Experimental data E < 50 eV, Williams (1976a) > 50 eV, Williams and Willis (1975) solid curve, coupled channels optical long-dashed curve, six-state coupled channels (Bray et al, 1991c) short-dashed curve, intermediate-energy R matrix (Scholz et al., 1991). From Bray et al. (1991c). Fig. 8.5. Differential cross section for the unresolved 2s and 2p excitations of hydrogen. Experimental data E < 50 eV, Williams (1976a) > 50 eV, Williams and Willis (1975) solid curve, coupled channels optical long-dashed curve, six-state coupled channels (Bray et al, 1991c) short-dashed curve, intermediate-energy R matrix (Scholz et al., 1991). From Bray et al. (1991c).
The resulting second-order polarization propagator approximation (SOPPA) was first described in its present form by Nielsen et al. (1980). Splitting h4 up into 2p-2h and 2h-2p excitation operators as was done for h2 in Eqs (95)-(97)... [Pg.229]

The cluster operators involve at least inactive (3h — 3p) excitations or excitations associated with active hne(s)— purely exi type and (f> Yi contains at most inactive (2h — 2p) excitations. Thus the contribution of the first and third terms of Eq. (25) will be zero. Using the same argument, it can be shown that the exp(T ) will not appear in the second term. [Pg.596]

In order to illustate this possibility, the SFg molecule, for which there exist experimental data has been tested [31]. For this purpose different basis sets for the different excitations have to be used. For Is excitations in the central sulfur atom, the standard chlorine atom basis was employed for describing all the sulfur electrons. For the 2s or 2p excitations in the same atom, the chlorine atom basis was employed for describing the sulfur L and M shells. The corresponding excitation values are given in Table 4. [Pg.268]

The calculation of excited-state energies has been attempted only occasionally with QMC methods. The simplest situation is to determine the excitation energy from the state of one symmetry to a state of different symmetry (e.g., the ls-to-2p excitation in hydrogen). Since both states are ground states within their symmetries, one can do fixed-node calculations for each state individually and get individual upper bounds to their energies. [Pg.22]

For the 2p state, a similar behavior to the 2p excitation of the target is present. Our results are higher for low energies than that reported by the experiment due to the same reason mentioned in the case of the target excitations. [Pg.270]

Fig. 2. Schematic diagram of the EXAFS process. The central atom (filled circle) absorbs an X-ray photon. Scattering of the outgoing wave is induced by the neighboring sites (open circles) (left) Schematic presentation of the experimental EXAFS-signal obtained from Ar 2p-excited argon clusters (right). Fig. 2. Schematic diagram of the EXAFS process. The central atom (filled circle) absorbs an X-ray photon. Scattering of the outgoing wave is induced by the neighboring sites (open circles) (left) Schematic presentation of the experimental EXAFS-signal obtained from Ar 2p-excited argon clusters (right).
Ground state configuration of boron atom Is 2s 2p Excited state of B atom Is 2s 2p 2p ... [Pg.18]

Make a rough estimate of the total number of determinants in the MR-CISD wave function for a system with 74 electrons, 154 orbitals and a CAS(2,2)CI reference wave function. Calculate the percentage of 2h-2p excitations in the MR-CISD wave function (neglect the Ih, Ip, Ih-lp, 2h and 2p excitations, they give rise to a very small number of determinants). [Pg.124]


See other pages where 2p excitation is mentioned: [Pg.301]    [Pg.307]    [Pg.308]    [Pg.157]    [Pg.72]    [Pg.78]    [Pg.80]    [Pg.81]    [Pg.73]    [Pg.217]    [Pg.218]    [Pg.297]    [Pg.301]    [Pg.200]    [Pg.23]    [Pg.200]    [Pg.414]    [Pg.189]    [Pg.88]    [Pg.537]    [Pg.136]    [Pg.220]    [Pg.198]    [Pg.203]    [Pg.204]    [Pg.228]    [Pg.230]    [Pg.296]    [Pg.212]    [Pg.160]    [Pg.389]    [Pg.94]    [Pg.123]   
See also in sourсe #XX -- [ Pg.132 , Pg.201 ]




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