Abstract
Lanthanide doping through a crystal site engineering approach tunes the emission wavelength suitable for LED applications, but weak emission from low coordination sites remains a huge challenge. Herein the use of a sensitizer is reported to enhance the emission strength and unravel the crystallinity and phase, as this approach demands a large amount of dopants. Doping of Eu2+ ions at SrO10 and SrO9 sites of Sr2 SiO4 (S2 S), respectively, tunes the emission from green to yellow and controlled doping of a Ce3+ sensitizer quadruples the quantum efficiency of yellow emission. Remarkably, doping of Eu2+ at the SrO9 site produces polycrystals, whereas co-doping of Ce3+ and Eu2+ at the same site produces single crystals. DFT calculations further delineate the underlying changes wherein strong interaction of dopant with its neighbours determines the electron density, and thus the crystallinity and phase, rather than usual explanation of aliovalent conditions, which is further substantiated by TEM results. Irrespective of dopant valence, use of large amounts of dopants and their interaction with the host is responsible for the crystallinity and phase change (α'-S2 S to β-S2 S). The XPS valence band spectra experimentally evidences the changes in bonding nature of O 2p and O 2s orbitals of silicate and its electron density, due to doping at the two sites. In short, the outcomes resulting from this work could be extended for the development of other two-coordination site lanthanide-doped materials and crystallization of inorganic materials.
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