期刊
JOURNAL OF PHYSICAL CHEMISTRY C
卷 120, 期 8, 页码 4529-4537出版社
AMER CHEMICAL SOC
DOI: 10.1021/acs.jpcc.5b12501
关键词
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资金
- National Natural Science Foundation of China [21171176, U1232108, U1432249]
- Natural Science Foundation of Guangdong Province [S2013030012842]
- U.S. Department of Energy, Office of Basic Energy Sciences, Division of Chemical Sciences, Geosciences, and Biosciences [DE-AC02-06CH11357]
The lithium yttrium silicate series of LiY1-x-Ln(x)SiO(4) exhibits superb chemical and optical properties, and with Ln = Ce3+, Sm3+, its spectroscopic characteristics and luminescence dynamics are investigated in the present work. Energy transfer and nonradiative relaxation dramatically influence the Ln(3+) luminescence spectra and decay dynamics, especially in the Ce3+ Sm3+ codoped phosphors. It is shown that thermal-quenching of the blue Ce3+ luminescence is primarily due to thermal ionization in the 5d excited states rather than multiphonon relaxation, whereas cross-relaxation arising from electric dipole dipole interaction between adjacent Sm3+ ions is the leading mechanism that quenches the red Sm3+ luminescence. In the codoped systems, Ce3+-Sm3+ energy transfer in competing with the thermal quenching enhance the emission from Sm3+. The combined influences of concentration quenching, thermal ionization, and energy transfer including cross-relaxation on the luminescence intensity of single-center and codoped phosphors are analyzed based on the theories of ion-ion and ion-lattice interactions.
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