Journal
DALTON TRANSACTIONS
Volume 43, Issue 37, Pages 13845-13851Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/c4dt01524j
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Funding
- National Natural Science Foundation of China [61274053, 90922037, 51372121]
- Natural Science Foundation of Tianjin [14JCYBJC17800]
- Program for New Century Excellent Talents in University of China [NCET-11-0258]
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In this combined X-ray diffraction and photoluminescence study, the coordination environment of Mn2+ and the photoluminescence of single Mn2+ doped KMgBO3 phosphors were studied. Mn2+ occupies Mg2+ sites, which were coordinated by six O2-. The strong absorption of KMgBO3:Mn2+ was ascribed to the strong relaxation of spin and parity forbidden d-d transitions of Mn2+. The emission bands were centered at 636 nm, regardless of the excitation wavelength and Mn2+ doping concentration. Mn2+ activated KMgBO3 could be efficiently excited with the excitation of Mn2+ d-d transitions in the wavelength range of 300-475 nm. The red-shift of Mn2+ emission was because of the strong crystal field environment of Mn2+ afforded by KMgBO3. The potential applications of the phosphors have been pointed out based on their absorption spectra, excitation and emission spectra, thermal quenching properties, and decay properties.
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