Overview
- Authors:
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Charles W. Struck
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GTE Laboratories Inc., Waltham, USA
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William H. Fonger
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Princeton, USA
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Table of contents (14 chapters)
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Front Matter
Pages I-XIII
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- Charles W. Struck, William H. Fonger
Pages 1-18
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- Charles W. Struck, William H. Fonger
Pages 19-23
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- Charles W. Struck, William H. Fonger
Pages 24-31
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- Charles W. Struck, William H. Fonger
Pages 32-59
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- Charles W. Struck, William H. Fonger
Pages 60-74
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- Charles W. Struck, William H. Fonger
Pages 75-76
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- Charles W. Struck, William H. Fonger
Pages 77-85
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- Charles W. Struck, William H. Fonger
Pages 86-109
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- Charles W. Struck, William H. Fonger
Pages 110-128
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- Charles W. Struck, William H. Fonger
Pages 129-172
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- Charles W. Struck, William H. Fonger
Pages 173-193
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- Charles W. Struck, William H. Fonger
Pages 194-197
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- Charles W. Struck, William H. Fonger
Pages 198-200
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- Charles W. Struck, William H. Fonger
Pages 201-203
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Back Matter
Pages 204-255
About this book
There are both a remote and a proximate history in the development of this book. We would like to acknowledge first the perceptiveness of the technical administrators at RCA Laboratories, Inc. during the 1970s, and in particular Dr. P. N. Yocom. Buoyed up by the financial importance of yttrium oxysulfide: europium as the red phosphor of color television tubes, they allowed us almost a decade of close cooperation aimed at understanding the performance of this phosphor. It is significant that we shared an approach to research in an industrial laboratory which allowed us to avoid the lure of "first-principles" approaches (which would have been severely premature) and freed us to formulate and to study the important issues directly. We searched for a semiquantitative understanding of the properties observed in luminescence, i. e. , where energy absorption occurs, where emission occurs, and with what efficiency this conversion process takes place. We were aware that the nonradi ative transition rates found in practice vary enormously with temperature and, for a given activator, with small changes in its environment. We traced the source of this enormous variation to the magnitude of the vibrational overlap integrals, which have strong dependences on the rearrangements occurring during optical transitions and on the vibrational number of the initial electronic state. We were willing to excise from the problem the electronic aspects - the electronic wavefunctions' and their transition integrals -by treating them as parameters to be obtained from the experimental data.
Authors and Affiliations
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GTE Laboratories Inc., Waltham, USA
Charles W. Struck
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Princeton, USA
William H. Fonger