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One-photon emission

Figures 9A and 9B are photofragment images of D+ following irradiation of D2 with 532-nm light. All of the features can be assigned to dissociation of different vibrational levels of D2 by nominally either one-, two, or three-photon absorption. Because two-photon absorption to the 2p Figures 9A and 9B are photofragment images of D+ following irradiation of D2 with 532-nm light. All of the features can be assigned to dissociation of different vibrational levels of D2 by nominally either one-, two, or three-photon absorption. Because two-photon absorption to the 2p<xu repulsive state of the ion is parity forbidden, what appears as two-photon dissociation energetically is proposed to be three-photon absorption followed by one-photon emission as the molecule dissociates [46, 62, 63]. In the dressed state picture of the potentials (Figure 11), there is a series of crossings near 4 Bohr radii where the repulsive state of D2 shifted by the energy of a photon crosses the bound state. It is at this crossing that photon emission must occur so that the system can curve cross onto the two-...
The Fence description is completed with the asymptotic states of the EM field k lB), where the emission source is located at the origin of the k-vector that also identifies a direction k/ k in reciprocal space. Thus, conventionally, IT jl-kMa) signals an EM field in a direction pointing to the I-frame sustaining IT ) whereas ITqi+k 1 ) stands for one photon emission from the I-frame. These base states supplement a real-space (Fence) description. [Pg.74]

Where the medium is initially in an excited eigenstate, the resonant active process in this two-level problem is one-photon emission, or fluorescence. In this case, the resonant state would lie below the initial state. The field gains energy through the interaction while the medium loses energy. [Pg.71]

One-Photon Processes OPA, OPE, BCD One-photon absorption (OPA), electronic circular dichroism (ECD) and one-photon emission (OPE) spectra can be generally written in the form... [Pg.369]

The above fomuilae for the absorption spectrum can be applied, with minor modifications, to other one-photon spectroscopies, for example, emission spectroscopy, photoionization spectroscopy and photodetachment spectroscopy (photoionization of a negative ion). For stimulated emission spectroscopy, the factor of fflj is simply replaced by cOg, the stimulated light frequency however, for spontaneous emission... [Pg.248]

All nonlinear (electric field) spectroscopies are to be found in all temis of equation (B 1.3.1) except for the first. The latter exclusively accounts for the standard linear spectroscopies—one-photon absorption and emission (Class I) and linear dispersion (Class II). For example, the temi at third order contains by far the majority of the modem Raman spectroscopies (table B 1.3.1 and tableBl.3.2). [Pg.1181]

If certain quanta suitable for the excitation of a line are absorbed without photon emission, a radiationless transition is likely. This transition is known as the Auger effect,39 and it may be thought to involve an absorption by the atom of the photon produced when the hole in the K shell is filled by an electron from one of the external shells such as the L shell. The absorption of this photon results in the ejection of a second electron from one of the shells to leave a doubly charged residue of what had been a normal atom. The atom in this condition is described by naming the two states in which the electron holes are to be found e.g., the atom is in the LL or LM or LN state. An atom in such a state is, of course, vastly different from the usual divalent cation. [Pg.37]

UE provides an important potential advantage beyond small size. The excited states in Si-based electronics decay by phonons, and thus a huge heat dissipation problem faces nanoscale inorganic electronics at DR = 3 nm. In contrast, UE devices may be able to decay from their excited states by photon emission [15]. If the photon decay channel can be maximized, UE devices will have a great heat advantage over inorganic ones. [Pg.41]

Spectroscopic techniques look at the way photons of light are absorbed quantum mechanically. X-ray photons excite inner-shell electrons, ultra-violet and visible-light photons excite outer-shell (valence) electrons. Infrared photons are less energetic, and induce bond vibrations. Microwaves are less energetic still, and induce molecular rotation. Spectroscopic selection rules are analysed from within the context of optical transitions, including charge-transfer interactions The absorbed photon may be subsequently emitted through one of several different pathways, such as fluorescence or phosphorescence. Other photon emission processes, such as incandescence, are also discussed. [Pg.423]


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