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Synthesis And Fluorescence Control Of Nd 3+ Ion Sensitized NaLa(MoO 4 ) 2 Upconversion Phosphor

Posted on:2018-09-30Degree:MasterType:Thesis
Country:ChinaCandidate:J J LiFull Text:PDF
GTID:2350330518971727Subject:Subject teaching
Abstract/Summary:PDF Full Text Request
The rare-earth?RE?doped up-conversion?UC?materials have been widely used in various fields such as three-dimensional?3D?display,information storage and bio-imaging.UC luminescent materials have been paid more attention in biology thanks to their merits in non-autofluorescence,low photobleaching,less photodamage and high light penetration depth in tissues.Among these UC materials,Yb3+ ions are usually used as sensitizers and 980 nm infrared laser diodes are used as pumping sources.However,strong absorption of the water in organisms at 980 nm not only causes thermal damage to the body,but also reduces the penetration depth in biological tissue.It is found that using 808 nm lasers as excitation light sources can effectively avoid the above problems.In addition,Nd3+ ions show large absorption cross section near 808 nm and are ability to take place Yb3+.Therefore,the study of Nd3+ sensitized upconversion luminescent materials is of great significance in biomechanics.A series of NaLa?MoO4?2:Nd3+,Yb3+,Ho3+ upconversion phosphors were synthesized by sol-gel method.The crystal structures and optimum doped concentration of samples were determined by the X-ray diffraction and up-conversion spectra.A group of sharp line emissions peaked at 543,658 and 1187 nm were observed under 808 nm excitation,respectively,which corresponds to the transitions of 5F4/5S2 ? 5I8,5F5 ? 5I8 and 5Ie ? 5I8 of Ho3+ ions.The energy transfers among Nd3+,Yb3+ and Ho3+ were confirmed by comparing the fluorescence spectra and the lifetime of Ho3+ solely doped,Nd3+-Ho3+ and Nd3+-Yb3+ co-doped and Nd3+-Yb3+-Ho3+tri-doped samples.It is further proved that the Yb3+ ions act as the bridge in the energy transfer process.The Nd3+,Yb3+ and TDm3+ tri-doped NaLa?MoO4?2 up-conversion phosphors were aslo synthesized by sol-gel method.Under the excitation of 808 nm CW excitation,the emission peaks at 478,653 and 692 nm from the 1G4 ? 3H6,1G4 ? 3F4 and 3F3?3H6 transitions of Tm3+were found.The UC spectra of Tm3+ single-doped,Nd3+-Tm3+ co-doped Nd3+-Yb3+-Tm3+tri-doped samples and the lifetime of Nd3+ and Yb3+ in the NaLa?MoO4?2:Nd3+,Yb3+,Tm3+system,which prove the occurance of Nd3+?Tm3+ and Nd3+?Yb3+?Tm3+ energy transfer processes.Yb3+ ion play an efficient bridge in the process of energy transfer Nd3+?Yb3+ ?Tm3.Moreover,on the tuning of the emission color in the NaLa?MoO4?2:Nd3+,Yb3+,Ho3+system were also realized through changing the concentration,changing the pulse width and doping Ce3+ ions three methods.For these methods,the modulation of emitting color is achieved by changing the relative intensity ratio of red to green emission,but their mechanisms are different.Among them,the emission color of the samples change from orange to yellowish and from yellow to green were realizing by the different population processes of red and green emitting states of Ho3+ by adjusting Yb3+ concentration and changing excitation pulse width.In addition,introducing Ce3+ ion into Nd3+/Yb3+/Ho3+ doped sample also enhances the R/G ratio through increasing probability of nonradiation?NR?processes?5F4/5S2 ? 5F5 and 5I6?5I7?by two cross relaxations between Ho3+ and Ce3+,which change the fluorescence color from orange to red.
Keywords/Search Tags:Up-conversion, Energy transfer, Color modulation
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