Local microstructure and photoluminescence of Er-doped 12CaO-7Al2O3 powder

Er-doped 12Ca0.7Al2O3 (C12A7:Er) powders were prepared using the sol-gel method followed by annealing inorganic precursors. X-ray diffraction (XRD), Raman and absorption spectra revealed that Er ions existed and substituted Ca^2+ lattice site in C12A7. The photoluminescence of C12A7:Er at room tempe...

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Bibliographic Details
Published inJournal of rare earths Vol. 26; no. 3; pp. 433 - 438
Main Author 王丹 刘玉学 徐长山 刘益春 王国瑞 李兴华
Format Journal Article
LanguageEnglish
Published Jilin Teachers' Institute of Engineering and Technology, Changchun 130052, China%Center for Advanced Opto-Electronic Functional Materials Research, Northeast Normal University, Changchun 130024, China 01.06.2008
Center for Advanced Opto-Electronic Functional Materials Research, Northeast Normal University, Changchun 130024, China
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Summary:Er-doped 12Ca0.7Al2O3 (C12A7:Er) powders were prepared using the sol-gel method followed by annealing inorganic precursors. X-ray diffraction (XRD), Raman and absorption spectra revealed that Er ions existed and substituted Ca^2+ lattice site in C12A7. The photoluminescence of C12A7:Er at room temperature was observed in the visible and infrared region using 488 nm (2.54 eV) Ar^+ line as excitation source, respectively. The sharp and intense green emission bands with multi-peaks around 520 nm and 550 nm correspond to the transitions from the excited states ^2H11/2 and ^4S3/2 tO the ground state ^4I15/2, respectively. Furthermore, red emission band around 650 nm was also observed. It was attributed to the electronic transition from excited states ^4F9/2 to the ground state ^4I15/2 inside 4f-shell of Er^3+ ions. The intensive infrared emission at 1.54 μm was attributed to the transition from the fast excited states of ^4I13/2 to the ground state (^4I15/2). The temperature dependent photoluminescence of infrared emission showed that the integrated intensity reached a maximum value at near room temperature. The forbidden transitions of intra-4f shell electrons in free Er^3+ ions were allowed in C12A7 owing to lack of the inversion symmetry in the Er^3+ position in C12A7 crystal field. Our results suggested that C12A7:Er was a candidate for applications in Er-doped laser materials, and full color display.
Bibliography:C12A7:Er; sol-gel; photoluminescence; raman; absorption; rare earths
C12A7:Er
11-2788/TF
photoluminescence
absorption
O616
sol-gel
raman
rare earths
ISSN:1002-0721
2509-4963
DOI:10.1016/s1002-0721(08)60112-x