简介:(Ba0.66Sr0.33)Mg0.8Al11.47O19:Tm0.013+(BSMA:Tm3+)phosphorwassynthesizedbysolid-statereactions.ThesamplewascharacterizedbyX-raydiffraction(XRD),scanningelectronicmicroscope(SEM),vacuumultraviolet(VUV)spectra,ultraviolet(UV)spectraandFT-IRspectrum.XRDpatternrevealsthatBSMA:Tm3+hasthesamestructureasBaAl12O19phase.SEMimageillustratesthatthephosphorhasthehexagonalshapeanddeepslicestructure.VUVandUVemissionspectraat20,50and100Kshowthatthelowtemperatureluminescenceintensitiesbecomeweakgraduallywiththeincreasingofthetemperatureunder147and254nmexcitation.Thestrongbroadbandpeaksataround357and397nmandthepeakat516nmunder147nmexcitationallcorrespondtothecharacteristictransitionsofTm3+ions.However,underUV(254nm)excitation,themainpeakbecomes530nmwhichhasveryhighlineintensity,andthepeaksatabout362and403nmareveryweak.Theexcitationspectrumat20Kshowsthattherearethreeabsorptionpeaksataround153,186and193nmwhen516nmemissionismonitored.Theabsorptionpeaksof[AlO4],[AlO6]andAl-OcanbeobservedinFT-IRspectrum.
简介:Differentfluxeswereusedtosynthesizelongpersistencephosphors,calciumsulfidesactivatedbyEu2+andTm3+,byconvenientsolid-statemethod.ThephosphorusingNH4Fasafluxhasgoodcrystallinityandlargeparticlesize,itsstabilityagainstwaterandotheratmosphericcomponentsisenhanced,anditsafterglowislongerandfluorescentintensityismoreintensethanthoseofthephosphorusingNH4Clasflux.TheirPLintensitiesvariedwithtimeinmoistairweremeasured,noremarkablechangewasfoundforthosepreparedwithNH4FfluxincontrastwithNH4Clasflux.SousingNH4Fasfluxisagoodmethodtoenhancethestabilityofalkalineearthsulfides.
简介:Thesolutionreactionmechanisms,composition,donoratoms,propertiesofcoordinatelinkandstabilityofthecomplexesonthesystemsofadrenalinewithNa3+,Gd3+andTm3+havebeenstudiedbypH-potentiometrictitrationandelectronicspectroscopy.Adrenalineperturbsthef-felectronictransitionofNd3+andTm3+sothattheabsorptionspectraoftheircomplexesareshiftedtowardlongerwavelengths.Theabsorptionspectraofthecomplexesformedbythethreef-blockelementionswithadrenalineareshiftedtowardshorterwavelengthswiththeincreaseofPHinΔγ=350~650nm
简介:Glasseswiththecompositionof65GeO212Ga2O3-10BaO-8Li2O-5La2O3(molarratio)dopedwith1.526wt.%,3.006wt.%,5.836wt.%,11.028wt.%,and15.678wt.%Tm2O3,respectively,werefabricatedbyconventionalmeltingmethod.AccordingtotheabsorptionspectraandtheJudd-Ofelttheory,theJ-Ostrengthparameters(Ω2,Ω4,Ω6)werecalculated,withwhichtheradiativetransitionprobabilities,branchingratiosandradiativelifetimeswereobtained.Theinfraredemissionspectra(with808nmLDexcitation)at~1.47and~1.8μmofvariousconcentrationsofTm3+-dopedglasseswerestudied.Theemissionintensityat~1.8μmreachedtothemaximumwhentheTm2O3-dopingconcentrationwasneartobe~3.006wt.%(1.0mol.%),andthendecreasedasdopingconcentrationincreasedfurther.Themechanismofthefluorescenceintensitychangewasexplainedwiththecross-relaxationeffectandtheconcentrationquenchingeffectofTm3+.Meanwhile,accordingtoMcCumbertheory,theabsorptionandemissioncross-sectionscorrespondingtothe3F4→3H6transitionsofTm3+at1.8μmwasobtained.ForTm3+-dopedgermanateglasses,themaximumemissioncross-sectionreachedavaluehigherthanthatre-portedforfluorozircoaluminateglasses.Itisexpectedtobeafavorablecandidatehostfor~2.0μmmid-inflatedlaserbecausetheglassshowsfavorableopticalspectra.
简介:LanthanidedopedNaYF4microcrystalsweresynthesizedviaafacilehydrothermalmethod.MulticolorupconversionluminescencewasobservedinNaYF4microcrystalsdopedwithYb3+/Er3+,Yb3+/Tm3+,andYb3+/Er3+/Tm3+undertheexcitationof980nminfraredlight.Importantly,theexcitationpowerdensitydependenceofupconversionemissionintensityindicatedclearlytheenergytransferfromTm3+toEr3+ionsundertheexcitationoflowpowerdensity(5×102–9×102W/cm2).Meanwhile,theinverseenergytransferfromEr3+toTm3+ionsundertheexcitationofrelativelyhigherpowerdensity(4.1×104–4.9×104W/cm2)wasalsorevealed.ThiswasadirectevidenceforreversibleenergytransferbetweenEr3+andTm3+ions.Undertheexcitationofhighpowerdensity(4.1×104–4.9×104W/cm2),darksensitizerswerealsomotivatedsothatthebottleneckeffectofhighconcentrationYb3+iondopingwasbroken.ThiswasthemainreasonforrealizinghighupconversionefficiencyofthesampleswithheavydopingofYb3+ion.
简介:Er3+-Tm3+-Yb3+tri-dopedBaMoO4phosphorsweresynthesizedbyco-precipitationtechniqueandcharacterizedbyX-raydiffractionanalysis,absorptionstudyandfieldemissionscanningelectronmicroscopyanalysis.Upconversionaswellasdownconversionluminescencestudieswereperformedbyusingnearinfrared(980nm)andultraviolet(380nm)excitations.Energyleveldiagram,pumppowerdependenceandcolourcoordinatestudywereutilizedtodescribethemulticolorupconversionemissionproperties.Undersingle980nmdiodelaserexcitationthedualmodesensingbehaviourisrealizedviaStarksublevelsandthermallycoupledenergylevelsoftheTm3+andEr3+ionsinthepreparedtri-dopedphosphors.AcomparativefluorescenceintensityratioanalysisforintegratedemissionintensitiesarisingfromtheStarksublevels{1G4(a)and1G4(b)}andthermallycoupledenergylevels{2H11/2and4S3/2}oftheTm3+andEr3+ions,respectivelywascarriedoutinthepreparedtri-dopedBaMoO4phosphors.ThemaximumsensitivityforthermallycoupledenergylevelsoftheEr3+andStarksublevelsoftheTm3+ionwasreported.Thedevelopedphosphorscouldbeusefulinthedisplaydevicesandopticalthermometricapplications.
简介:AdetailedstudyofthefluorescenceemissionpropertiesandenergytransfermechanisminEr3+/Tm3+co-dopedleadsilicateglasseswasreported.Enhancednearinfrared1.8μmandvisibleup-conversionemissionswereinvestigatedunder808and980nmexcitations,respectively.TheenergytransfermechanismbetweenEr3+andTm3+wasanalyzedaccordingtotheabsorptionspectra,theemissionspectraandthelevelstructuresofEr3+andTm3+.TheenergytransferefficiencybetweenEr3+andTm3+reached68.1%intheEr3+/Tm3+co-dopedleadsilicateglasseswhenpumpedby808nmlaserdiode.Basedontheabsorptionspectra,theJudd-Ofeltparameters,spontaneousemissionprobability,absorptionandemissioncrosssections,gaincoefficientswerecalculatedandanalyzed.Itwasfoundthatthecalculatedemissioncrosssectionandthemaximumgaincoefficientaround1.8μmwere4.9×10–21cm2and1.12cm–1,respectively.TheseresultsindicatedthattheEr3+/Tm3+co-dopedlead-silicateglasseshadpotentialapplicationinnearinfraredlasers.
简介:一系列立方的稀土元素sesquioxidesRE2O3的拉曼系列(RE=Eu,Gd,Dy,惊讶,嗯,Tm,Yb,陆,Sc和Y)被拉曼光谱学与532和785根nm激光线调查。丰富的另外的乐队由于激光激动的光被观察。为Eu2O3,Dy2O3,Ho2O3,Er2O3,Tm2O3和Yb2O3,,光主要为Gd2O3,Lu2O3,Sc2O3和Y2O3来自内在的三价的lanthanide离子,他们的光被归因于象Eu3+,Nd3+和Er3+那样的另外的光lanthanide离子的踪迹杂质。这调查为检测踪迹作为一个有用工具证实了拉曼光谱学光lanthanide杂质。