The photoluminescence properties of Eu2+-activated α’-Sr2SiO4 and α’-Ba2SiO4 with a high Eu2+ concentration were investigated. In the case of Sr2-xEuxSiO4, emission was shifted from 585 to 611 nm with increasing t...The photoluminescence properties of Eu2+-activated α’-Sr2SiO4 and α’-Ba2SiO4 with a high Eu2+ concentration were investigated. In the case of Sr2-xEuxSiO4, emission was shifted from 585 to 611 nm with increasing the total Eu2+ concentration (x) from 0.1 to 0.8. This trend was similar to that in Ba2-xEuxSiO4, where the emission was shifted from 513 to 545 nm. The large redshifts in both the excitation and emission spectra were discussed in terms of the Eu2+ occupancies on two kinds of M sites and their local structural changes (M: Sr and Ba).展开更多
Novel red-emitting Eu3＋, Sm3＋ singly doped and co-doped Ca14Mg2（SiO4）8 phosphors were prepared by conventional solidstate reaction. Powder X-ray diffraction patterns were employed to confirm phase pttrity. Ca14Mg2...Novel red-emitting Eu3＋, Sm3＋ singly doped and co-doped Ca14Mg2（SiO4）8 phosphors were prepared by conventional solidstate reaction. Powder X-ray diffraction patterns were employed to confirm phase pttrity. Ca14Mg2（SiO4）8：Eu3＋ phosphors exhibited intense red emission under 394 nm excitation and Ca14Mg2（SiO4）8：Sm3＋ phosphors, excited at 405 nm, also showed strong red emitting at 602 nm. The concentration quenching mechanism of Cal4Mg2（SiOa）s：Eu3＋ was dipole-dipole interaction, while that of CalnMg2（SiOn）8：Sm3＋ was energy migration among nearest neighbor ions. The results indicated that Ca14Mg2（SiOn）8：Eu3＋ and Ca14Mg2（SiOn）s：Sm3＋ were promising red-emitting phosphors for WLEDs. Meanwhile, the effect of co-doping Sm3＋ ions on photoluminescence properties of CalaMg2（SiO4）s：Eu3＋ was studied and energy transfer from Sm3＋ to Eu3＋ was discovered in Eu3＋, Sm3＋ co-doped phosphors.展开更多
文摘The photoluminescence properties of Eu2+-activated α’-Sr2SiO4 and α’-Ba2SiO4 with a high Eu2+ concentration were investigated. In the case of Sr2-xEuxSiO4, emission was shifted from 585 to 611 nm with increasing the total Eu2+ concentration (x) from 0.1 to 0.8. This trend was similar to that in Ba2-xEuxSiO4, where the emission was shifted from 513 to 545 nm. The large redshifts in both the excitation and emission spectra were discussed in terms of the Eu2+ occupancies on two kinds of M sites and their local structural changes (M: Sr and Ba).
基金supported by the Hong Kong,Macao and Taiwan Science and Technology Cooperation Special Project of Ministry of Science and Technology of China(2014DFT10310)the National Basic Research Program of China(973 Program,2014CB643801)the National Natural Science Foundation of China(51402288,51102229,21401184)
文摘Novel red-emitting Eu3＋, Sm3＋ singly doped and co-doped Ca14Mg2（SiO4）8 phosphors were prepared by conventional solidstate reaction. Powder X-ray diffraction patterns were employed to confirm phase pttrity. Ca14Mg2（SiO4）8：Eu3＋ phosphors exhibited intense red emission under 394 nm excitation and Ca14Mg2（SiO4）8：Sm3＋ phosphors, excited at 405 nm, also showed strong red emitting at 602 nm. The concentration quenching mechanism of Cal4Mg2（SiOa）s：Eu3＋ was dipole-dipole interaction, while that of CalnMg2（SiOn）8：Sm3＋ was energy migration among nearest neighbor ions. The results indicated that Ca14Mg2（SiOn）8：Eu3＋ and Ca14Mg2（SiOn）s：Sm3＋ were promising red-emitting phosphors for WLEDs. Meanwhile, the effect of co-doping Sm3＋ ions on photoluminescence properties of CalaMg2（SiO4）s：Eu3＋ was studied and energy transfer from Sm3＋ to Eu3＋ was discovered in Eu3＋, Sm3＋ co-doped phosphors.
