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Titlebook: Electronic Defect States in Alkali Halides; Effects of Interacti Volkmar Dierolf Book 2003 Springer-Verlag Berlin Heidelberg 2003 Electron-

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https://doi.org/10.1007/978-3-030-81993-4ctron density has on the molecule, thereby simulating the effects occurring during the excitation/relaxation cycle of a F.(CN.). By comparison, a “feeling” for the interaction effects in the RES of the F electron can be obtained.
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Orthodoxy in Balkan Political Conflictsrence of vibrational luminescence (owing to the presence of effective nonradiative channels) and more difficult resonance Raman studies have to be employed, many of the other interaction effects are very pronounced for this defect type, and we shall put special emphasis on the following:
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Introduction and Historical Overview,ave been studied systematically since the early decades of the 20th century. It is a common belief that essentially everything is understood. While the latter statement is certainly not true even for individual defects, as becomes apparent as soon as one looks in somewhat more detail, it is quite su
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F Centers and Rare-Earth Ion Defects in Alkali Halides,basic properties of the defects considered in the remaining chapters of this book. As in the rest of the text we concentrate on F centers and divalent rare-earth ions. The properties of these defects have been reported in several other monographs, and we shall review here only those aspects that are
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,Theoretical Models for E—V Transfer,l results. The various different approaches will be reviewed and compared in the following. The main focus will be on a critical examination of the statements made by the respective authors about the agreement of their models with experimental data. In addition, the question of what kind of addition
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,FH(CN−) Centers,vation of E-V transfer in 1983 [., .]) both experimentally and theoretically (as reviewed in Sect. 4). The main interest of the studies was the very effective E-V transfer especially for Cs halides which leads to intense vibrational luminescence (VL) (see in Fig. 5.3). Even superfluoresence [.] and
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