Abstract
The oxide garnet Y3Al5O12 (YAG), when substituted with a few percent of the activator ion Ce3+ to replace Y3+, is a luminescent material that is nearly ideal for phosphor-converted solid-state white lighting. The local environments of the small number of substituted Ce3+ ions are known to critically influence the optical properties of the phosphor. Using a combination of powerful experimental methods, the nature of these local environments is determined and is correlated with the macroscopic luminescent properties of Ce-substituted YAG. The rigidity of the garnet structure is established and is shown to play a key role in the high quantum yield and in the resistance toward thermal quenching of luminescence. Local structural probes reveal compression of the Ce3+ local environments by the rigid YAG structure, which gives rise to the unusually large crystal-field splitting, and hence yellow emission. Effective design rules for finding new phosphor materials inferred from the results establish that efficient phosphors require rigid, highly three-dimensionally connected host structures with simple compositions that manifest a low number of phonon modes, and low activator ion concentrations to avoid quenching.
Original language | English |
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Pages (from-to) | 3979-3995 |
Number of pages | 17 |
Journal | Chemistry of Materials |
Volume | 25 |
Issue number | 20 |
DOIs | |
State | Published - Oct 22 2013 |
Keywords
- electron and nuclear magnetic resonance
- inorganic phosphors
- structure-property relations
- white solid-state lighting
- X-ray absorption
- X-ray and neutron scattering