简介：FluorescencespectraofSm2+andEu2+→Sm2+energytransferwerestudiedinSrB4O7.Thereappearsonlyfluorescencefrom5D0transitionofSm2+at77K.Thevibroniclinesassociatedwith5D0→7F0transitionwereobserved.Thethermalpopulationtoupperstatesof5D1and4f5dlevelsfrom5D0givesriseto5D1→7FJand5d→4fradiativetransitionsofSin2+athighertemperature.

简介：Ca8Mg(SiO4)4Cl2:Eu2+phosphordopedwithSr2+cationforCa2+partially,wassynthesizedbysolid-statereactionathightemperatureunderreducingatmosphere,anditsluminescentpropertieswereinvestigated.TheexperimentalresultsindicatethattheemissionintensityofthephosphorincreasesafterbeingdopedwithafewamountofSr2+ion.Theemissionpeakofthephosphorblueshifttoabout464nmwhenthephosphorisdopedwithlargequantityofSr2+ions.TheexcitationspectrumindicatesthatthephosphorcanbewellexcitedbyUVandbluelightfrom300to460nm,andthephosphorwasfittedwellfortheexcitationbyUVorblue-LED.

简介：Organicsubstancesuchassolventandresin'seffectonluminescentcapabilityofSrAl2O4:Eu2+,Dy3+phosphorwasstudied.Someorganicsolventsandresinswereselectedforexperimentation.TheresultsindicatethatthoseorganicsolventswillnothavenegativeeffectontheappliedcapabilityofSrAl2O4:Eu2+,Dy3+phosphor.Adoptingtheorganicresinsandcoveringmethod,theafterglowluminanceofSrAl2O4:Eu2+,Dy3+phosphorwasincreasedby85.01%and82.51%.

简介：Eu2+andDy3+codoped(Ca,Sr)7(SiO3)6Cl2yellowphosphorsweresuccessfullysynthesizedbyself-fluxmethod.Thestructure,morphologyandphotoluminescencepropertieswereinvestigatedbyX-raydiffraction(XRD),scanningelectronmicroscopy(SEM)andphotoluminescencespectra.Theas-preparedphosphorshowedabroademissionspectrumcenteredat550nmforEu2+single-dopedphosphor,whilelocatedat548–544nmfortheEu2+,Dy3+codopedsamplesunderexcitationat380nmlight.TheemissionintensitywasgreatlyimprovedwhenDy3+wasdopedintothe(Ca,Sr)7(SiO3)6Cl2:Eu2+system.Thecomposition-optimizedsamplewith3mol.%ofDy3+andconstant10mol.%ofEu2+exhibiteda220%PLenhancementcomparedtothephosphorwith10mol.%Eu2+single-doped.Meanwhile,itwasfoundthatthequantumefficiencyofphosphornamely(Ca,Sr)7(SiO3)6Cl2:3mol.%Dy3+,10mol.%Eu2+couldgetupto24.6%.Thesynthesizedyellow-emitting(Ca,Sr)7(SiO3)6Cl2:Dy3+,Eu2+isapromisingcandidateashigh-efficiencyyellowphosphorforNUV-excitedwhiteLEDs.

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简介：Aseriesofnovelbluelong-lastingphosphorescencephosphorsSr6Al18Si2O37:Eu2+,RE3+(RE3+=Ho3+,Gd3+,Dy3+andPr3+)werepreparedbytheconventionalhigh-temperaturesolid-statereactioninareductiveatmosphere.TheirpropertiesweresystematicallyinvestigatedutilizingX-raydiffraction(XRD),photoluminescence,phosphorescenceandthermoluminescence(TL)spectra.ThephosphorsemittedbluelightthatwasrelatedtotheemissionofEu2+dueto5d-4ftransition.Brightbluelong-lastingphosphorescence(LLP)couldbeobservedaftertheexcitationsourcewasswitchedoff.Fortheoptimizedsample,thebluelong-lastingphosphorescencecouldlastfornearly4hinthelightperceptionofthedark-adaptedhumaneye(0.32mcd/m2).TheeffectsofRE3+ionsonphosphorescencepropertiesofthephosphorswerestudied,andtheresultsshowedthattheco-dopingofRE3+ionsgreatlyenhancedtheintensityofthepeakaround315Kwhichwasrelatedtothelonglastingphosphorescenceofthephosphorsatroomtemperatureandconsequentlyimprovedtheperformanceofthebluephosphorescencesuchasintensityandpersistenttime.

简介：Wereportanovelapproachtoobtainingaclassicalblue-greenexcitableCaS:Eu2+phosphorwithdesiredredemissionbymicrowave(MW)firingprocedureintheabsenceofaddingelementalsulphur.ThedisturbingeffectofMWelectromagneticfieldondecompositionofCaSO4intoCaSactivatedbyeuropiumisdistinctlyobservedtogivepurehostphasewithoutaddinganyelementalsulphurandcarbon.ThehostphaseevolutionisobservedtobehighlydependentonthevariationofappliedMWpowerfromX-raydiffraction(XRD)patternsandthecorrespondingphotoluminescence(PL),andamaximumPLintensityat1100WofMWpowerisacquiredfortheobtainedpurerhostphase.Thenon-thermalandnon-equilibriumeffectsbyMWarerevealedtocorrelatewiththeinteractionbetweenpolarstructureofthehostandappliedelectromagneticfield.Theresultsdemonstrateanoptionalproceduretopreparethisred-emittingphosphorinaneffective,environment-friendlyandscalableapproachforphosphorproductionintheapplicationofbio-illuminationforplantcultivationandartificialphotosynthesis.

简介：Ca-dopedBaMgAl10O17:Eu2+,Mn2+(BAM)bluephosphorsweresynthesizedbyfluxassistedsolid-statereactionmethodusingCaF2andBaF2asco-flux.GooddispersityandparticlesizehomogenizationofhexagonalpurephaseBAMwereobtainedbysinteringat1400℃.TheeffectsoftheCa2+ionscontentonthestructure,morphologyandphotoluminescencepropertiesofthephosphorswerestudied.TheresultsindicatedthattheincorporationofCacoulddecreasethelatticeconstant,improvethehomogeneityanddispersityandenhancethephotoluminescence(PL)intensityofthephosphoreffectively.TheoptimumBa0.86Ca0.04Mg0.97Al10O17:0.1Eu2+,0.03Mn2+PLintensitywasenhancedforabout30%andrelativebrightnesswasimprovedabout4%.Furthermore,thesynthesizedBAMandcommercialBAMphosphorswereannealedfor30minat600oCinair.TheCa-dopedphosphorshadstrongeremissionintensity,higherbrightnessandbetterchromaticitystabilitythanthatofthecommercialphosphor.TheseresultsindicatedthatCa-dopedbluephosphorshadgoodpotentialapplicationsinthecommercialtricolorfluorescentlampsaswellasinotherdisplayandlamps.

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简介：XunwuRareEarthCorporationhasintroducedP507reductionextractionprocessfromAnhuiRe-searchInstituteofMetallurgytoprepareeuropiumoxideoffluorescentgradeinonestep.Theprocesshasbeenemployedinaproductionlineinthecorpo-ration.Andafterthreemonthsindustrialexperi-ment,allthetechnicalindexesreachedthedesigned

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简介：本文观察到BaF2:Gd，Eu通过下转换过程实现可见光发射的量子剪裁过程。Gd3+吸收一个VUV光子，通过交叉弛豫过程把能量传递给两个Eu3+，从而发射出两个可见光光子，实现量子剪裁过程。通过光谱结果的计算，其量子剪裁效率可达194％。

简介：Differentfluxeswereusedtosynthesizelongpersistencephosphors,calciumsulfidesactivatedbyEu2+andTm3+,byconvenientsolid-statemethod.ThephosphorusingNH4Fasafluxhasgoodcrystallinityandlargeparticlesize,itsstabilityagainstwaterandotheratmosphericcomponentsisenhanced,anditsafterglowislongerandfluorescentintensityismoreintensethanthoseofthephosphorusingNH4Clasflux.TheirPLintensitiesvariedwithtimeinmoistairweremeasured,noremarkablechangewasfoundforthosepreparedwithNH4FfluxincontrastwithNH4Clasflux.SousingNH4Fasfluxisagoodmethodtoenhancethestabilityofalkalineearthsulfides.

简介：Lastyear'seconomicgrowthintheEuropeanUnion,renewaloftheFranco-Germanaxis,andEUcohesioninresponsetoDonaldTrumpandBrexitoughttobehealthysignsofrecovery,butpopulism'srestraintaffectsEUintegration.IfthefalloutfromBrexitisanymeasureofthefuture,inconsistentleadershipwillbeforcedtododgeinternalandexternalcomplicationsforsometime,astheEUfacesintractablepoliticalandeconomicpressurefrommultipleparties.Althoughseparationandintegrationneednotremaindiametricalpoles,thedestiny,internationalstatus,andinfluenceoftheEUandmemberstateshasbeenpredicatedonintegration.Givencurrenteconomicanddemographicfactors,enhancingtheUnion'sattractivenesswhilehandlingotherissueswillmaketheEUaweakglobalactor.Lackingconfidence,strategiccohesionandprotectivedefenses,theEUinforthcomingyearscouldwitnessnosignificantprogress.EUmemberstatesarehauntedbypopulism,terrorism,extremismandeconomicinequality.Sino-EUrelationswillseecontinuedcooperationwithariskofturbulence.

简介：Differentrareearth(RE)ionsdopantswereaddedintotheSrAl2SiO7:Eu2+phosphorsinordertoenhancethephosphorescenceproperties,andtheeffectoftheREionsincludingYb3+,Ce3+,Nd3+,Dy3+andTm3+,wascomparativelyinvestigated.ItwasfoundthatNd3+additionimprovedthephosphorescencepropertiesobviouslyamongallthestudiedREions.Therefore,Sr1.96–xAl2SiO7:xEu2+,yNd3+phosphorswerestudiedindetail,andtheoptimumEu2+andNd3+concentrationsweredeterminedwiththeafterglowtimeofabout20min.Thephasestructures,photoluminescence(PL)properties,long-lastingphosphorescence(LLP)properties,afterglowdecaycurvesandthermo-luminescence(TL)fortheselectedphosphorsduringthecorrespondingstudywereinvestigated.AllthephosphorsexhibitedgreenPLemissionandLLPemission.ThereweretwoTLbandslocatedatabout325and380Kforthestudiedsamples,andtherelationshipbetweenREadditionandphosphorescencepropertieswasdiscussed.

简介：ThephaseandmorphologytransformationduringthehydrothermaltreatingprocessofY2O3wasevaluatedwithX-raydiffcrcnce(XRD),scanningelectronmicroscopy(SEM),transmissionelectronmicroscopy(TEM),particlesizeandspecificsurfaceareadetermination.TheresultsshowedthatthecubicY2O3didnottransferintohexagonalY(OH)3inpurewater.Therefore,purehexagonalY(OH)3withnanotubeandmicrorodmorphologieswereobtainedbyhydrothermaltreatingY2O3at150℃for12hin15mlof2mol/LNaOHsolutionwithandwith-outPVAorPEGItwassuggestedthatthecharacteristicpreferentialgrowthofY(OH)3wasattributedtothestructureanisotropyofhexahedronY(OH)3.TheadditionofPVAorPEGcouldpromotetheformingprocessofnanotubesbyselectiveadsorptionondifferentcrystalplanes,whichalteredthegrowthratealongdifferentdirectionsandresultedinthediffusionlimitofconstructingionsinthecentertopofrods.Finally,Y(OH)3:EuandY2O3:Eunanotubeswerealsosynthesizedbyusingthismethod,andtheirphotoluminescencepropertieswereevaluated.

简介：Anisotropicstructures,nanoneedles,andnanospindlesofrareearthhydroxychloride(RE(OH)2Cl)andoxychloride(REOCl)(rareearth=EuandTb)weresynthesized.Therareearthhydroxychloridenanostructureswereformedviaathermallyassistedhydrolysisoftherare-earthsesquioxidenanocrystals.Themorphologicalevolutionofthenanostructureswasstudiedusinghigh-resolutiontransmissionelec-tronmicroscopyandscanningelectronmicroscopy,whilethestructuralevolutionwasinvestigatedusingX-raydiffractiontechniques.Thethermalstabilityoftherareearthhydroxychlorideswasinvestigatedusingthermogravimetricanalysis.Therareearthoxychloridenanospin-dlesweresynthesizedviaasimpleheat-treatmentofrareearthhydroxychloridenanospindles.

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简介：Longlastingstrontiumaluminatephosphorsweresynthesizedbymeansofcoatedprecipitationintheexperiment.SrA12O4monoclinicphasewithlongafterglowwassynthesizedat1100℃withtheaidofH3BO3,andthesynthetictemperaturedecreasedabout100℃-150℃thaninsolidstatereaction.TheprocessofheattreatmentwasstudiedbyTG-DTA.ThephasecompositionsofpowderswereanalyzedbyXRD.ThemicrographsofthesampleswereinvestigatedbySEMandtheluminescentpropertieswereresearchedbyopticalspectrum.TheeffectsofH3BO3onthephasecompositionandmicrostructureofthecalcinedpowderswereinvestigated.TheresultsindicatedthatH3BO3acceleratedtheformationofSrAl2O4byconsumingtheintermediatephase.TheadditionofDy2O3stimulatedtheafterglowpropertyduetotheincreaseinthedepthofthetrapcenterinthematerials.