Emissivity of cluster

Table 10. Exotic Radioactive Decay and Emissions of Clusters...

Recent and detailed reanalysis can be found in Arnaud and Evrard (1999) and Markevitch (1998). The X-ray bremsstrahlung emission of clusters can generally be fitted by the emission of a gas distributed accordingly to the so called... 

Spontaneous emission of particles heavier than a particles is called cluster radioactivity. Theoretical calculations, published since 1980, showed that spontaneous fragmentation of nuclei with atomic numbers Z > 40 by emission of cluster nuclei, such as Li, Be, 20-2S]qg jg energetically possible... 

Many of the adsorbents used have rough surfaces they may consist of clusters of very small particles, for example. It appears that the concept of self-similarity or fractal geometry (see Section VII-4C) may be applicable [210,211]. In the case of quenching of emission by a coadsorbed species, Q, some fraction of Q may be hidden from the emitter if Q is a small molecule that can fit into surface regions not accessible to the emitter [211]. 

Static SIMS entails the bombardment of a sample surface with an energetic beam of particles, resulting in the emission of surface atoms and clusters. These ejected species subsequendy become either positively or negatively charged and are referred to as secondary ions. The secondary ions are the actual analytical signal in SIMS. A mass spectrometer is used to separate the secondary ions with respect to their charge-to-mass ratios. The atomic ions give an elemental identification (see... 

Palladium clusters deposited on amorphous carbon have been studied by XPS and UPS [28] and both techniques show broadening of the d-band peak as cluster size increases. The d-threshold shifts towards Ep as cluster size increases. In UPS studies the d-emission of the single atom has its peak at 3.0 eV below Ep, whereas the d-threshold is 2eV below Ep. Palladium clusters evaporated onto Si02 have been studied by UPS [38]. At large coverages of the Pd metal evaporated (> 10 atoms/cm ), a high emission intensity at Ep excited with photons of 21.2 eV (He(I)) or 40.8 eV (He(II)) as excitation source, is observed. This feature is characteristic in the spectra from bulk Pd samples. At the lowest metal coverage (3 x 10 atoms/cm ),... 

Tables 11-6, 11-7, and 11-8 show calculated solvatochromic shifts for the nucle-obases. Solvation effects on uracil have been studied theoretically in the past using both explicit and implicit models [92, 94, 130, 149, 211-214] (see Table 11-6). Initial studies used clusters of uracil with a few water molecules. Marian et al. [130] calculated excited states of uracil and uracil-water clusters with two, four and six water molecules. Shukla and Lesczynski [122] studied uracil with three water molecules using CIS to calculate excitation energies. Improta et al. [213] used a cluster of four water molecules embedded into a PCM and TDDFT calculations to study the solvatochromic shifts on the absorption and emission of uracil and thymine. Zazza et al. [211] used the perturbed matrix method (PMM) in combination with TDDFT and CCSD to calculate the solvatochromic shifts. The shift for the Si state ranges between (+0.21) - (+0.54) eV and the shift for the S2 is calculated to be between (-0.07) - (-0.19) eV. Thymine shows very similar solvatochromic shifts as seen in Table 11-6 [92],...

In general, silver clusters in solution are prepared by reduction of silver ions. Proper scaffolds, e.g., DNA, proteins, dendrimers and polymers, are essential to prevent the aggregation of clusters to larger nanoparticles. Although it is clear that the emission originates from few-atom silver clusters, many aspects of this exciting class of nanoscopic metals are not yet fully understood. 

Fig. 6 Luminescent profile of Au23 cluster before (pink trace) and after (orange trace) phase transfer. Emission of the cluster enhances considerably after phase transfer. Photographs of the aqueous-toluene mixture containing the cluster before and after phase transfer under white light (A and B, respectively) and UV light (C and D, respectively). In C, only the interface is illuminated as the UV radiation is attenuated as the sample was irradiated from the top [15]...

Two-photon emission is a process in which electronic transition between quantum levels occurs through the simultaneous emission of two photons. [27] presents more details about two-photon emission. Since metal clusters emit in the near-infrared region, they can be made useful for two-photon imaging with infrared excitation. Two-photon emission of Au25 clusters is observed at 830 nm by exciting at... 

Lee and Meisel incorporated Py, at levels of 10 M or more, into 1200 EW acid form samples that were swollen with water and with ferf-butyl alcohol. It was concluded based on the /3//1 value for water swollen samples that the Py molecules were located in the water clusters and were most likely near fluorocarbon—water interfaces. It was also concluded, based on both absorption and emission spectra, that the probes had strong interactions with the SO3 groups that were exchanged with Ag+ and Pb + cations in the case of water containing samples. Likewise, the pyrene molecules were rationalized as being surrounded by terf-butanol molecules in that case. However, excimer formation (due to the presence of adjacent pyrene molecules) in the ferf-butyl alcohol system suggested the loss of cluster morphology-... 

In Section 2 we briefly present the theoretical framework and schemes of the hybrid method used to compute the electronic states of clusters and the algorithm used for structure optimizations. Section 3 is devoted to the presentation and discussion of our results and a comparison with the DIM computations of Tutein and Mayne The emission lines originating from Na(3p)Ar excited states are also calculated and discussed. 

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