Abstract:Quenching experiments were performed on manganese‐activated calcium fluoro‐chlorophosphate phosphors. Changes in the optical properties of the manganese ions due to quenching were studied in order to explain the manganese fluorescent envelope shift in quenched phosphors reported by other workers. We find that quenching causes a change in the nearest halogen neighbors of manganese ions located on the so‐called “Ca(II)” positions. In slowly cooled phosphors these ions have mostly chlorine ions as nearest neighbo… Show more
“…This causes a slight expansion of the lattice with the C1 ions displaced slightly above and below the would-be F position. If at least 36% of the halogens in the mixed chlorofluorophosphate are fluorines, then the halophosphate remains at all temperatures in the hexagonal apatite structure (18).…”
A review of the role played by color centers in the deterioration of lumen output of lamp phosphors with special attention to the halophosphates is presented. Color center dynamics in halophosphates result in a rapid degradation in phosphor brightness within minutes after the beginning of lamp life. An examination of the extent and rapidity of this effect is reviewed. Unirradiated spectral characteristics of halophosphates are dependent on growth stoichiometry. Radiatively induced spectral absorptions are dependent on the relative intensity of Hg u.v. components and crystal deformation and show thermal and optical bleaching effects. A dynamical model of color centers in halophosphates is extracted from the literature that explains the essential experimental dependencies. Related color center effects in phosphors including defect generation considerations for long‐term brightness deterioration are also presented.
“…This causes a slight expansion of the lattice with the C1 ions displaced slightly above and below the would-be F position. If at least 36% of the halogens in the mixed chlorofluorophosphate are fluorines, then the halophosphate remains at all temperatures in the hexagonal apatite structure (18).…”
A review of the role played by color centers in the deterioration of lumen output of lamp phosphors with special attention to the halophosphates is presented. Color center dynamics in halophosphates result in a rapid degradation in phosphor brightness within minutes after the beginning of lamp life. An examination of the extent and rapidity of this effect is reviewed. Unirradiated spectral characteristics of halophosphates are dependent on growth stoichiometry. Radiatively induced spectral absorptions are dependent on the relative intensity of Hg u.v. components and crystal deformation and show thermal and optical bleaching effects. A dynamical model of color centers in halophosphates is extracted from the literature that explains the essential experimental dependencies. Related color center effects in phosphors including defect generation considerations for long‐term brightness deterioration are also presented.
Es werden Abschreckversuche durchgeführt, um die dadurch bedingte Änderung der optischen Eigenschaften in mit Mn aktivierten Ca‐fluoridchloridphosphat‐Phosphoren zu untersuchen und die früher beobachtete Fluoreszenzverschiebung zu erklären.
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