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简介：(Y,Gd)BxV1-xO4-x:Eu3+phosphorswerepreparedbysolidstatereaction.Theredemissioncolorpurityof(Y,Gd)BxV1-xO4-x:Eu3+phosphorismuchbetterthanthatoftherecentwidely-usedcommercialredemittingphosphor(Y,Gd)BO3:Eu3+anditsrelativeemissionintensityis84%ofthecommercialphosphor(Y,Gd)BO3:Eu3+.Itisexpectedthat(Y,Gd)BxV1-xO4:Eu3+phosphorwillbeapromisingcandidateforPDP(plasmadisplaypanels)application.

简介：ThereactionofNdCl3withlithiummethylnaphthalenein1:2moleratioinTHFgeneratesblackpowder.Thepowderreactswithcyclooctatetraene（COT）inTHFtoformthetitlecomplex.[Li（THF）4Nd（C8H8）2]·2THFcrystallizesinthemonoclinicspacegroupP2/cwithunit-celldimensionsa=1.7858（7）nm,h=1.3243（4）nm,c=1.8086（6）nm.β=106.52（4）°,V=4.10nm3andDc=1.268g/cm3forZ=4.F（000）=1660,R=0.0774,Rn=0.0733.Thecomplexconsistsofdiscreteion-pairandtwoTHFmoleculesadduct.Intheanion,theneodymiumatomiscoordinatedbytwoCOTrings.ThestructureofthecationshowsthatthelithiumatomisattachedwithTHFmoleculesonly.

简介：Tobreakthroughthebottle-neckofquantumyieldinupconversion(UC)core-shellsystem,weelucidatedthattheenergytransferefficiencyincore-shellsystemhadanevidentcontributionfromthechargetransferofinterfacewithrelatedtotwofactors:(1)bandoffsetsand(2)bindingenergyareadensity.Thesetwovariablesweredeterminedbymaterialintrinsicpropertiesandcore-shellthicknessratio.Wefurtherunraveledthemechanismofnon-radiativeenergytransferbychargetransferinduceddipoleattheinterface,basedonaquasi-classicalderivationfromF?rstertyperesonantenergytransfer(FRET)model.Withstablebondingacrosstheinterface,thecontributionsonenergytransferinbothradiativeandnon-radiativeenergytransfershouldalsobeaccountedtogetherinAuzel'senergytransfer(ETU)modelincore-shellsystem.Basedonthediscussionaboutinterfacebonding,bandoffsets,andformationenergies,wefiguredoutthesignificanceofinterfacebondinginducedgapstates(IBIGS)thatplayedasignificantroleforinfluencingthechargetransferandradiativetypeenergytransfer.Theinterfacebandoffsetswereakeyfactorindominatingthenon-radiativeenergytransfer,whichwasalsocorrelatedtocore-shellthicknessratio.Wefoundthattheenergyareadensitywithrelatedtocore/shellthicknessratiofollowedthetrendofBoltzmansigmoidalgrowthfunction.Bythephysicaltrend,thisworkcontributedareferencehowthemulti-layeredcore-shellstructurewasformedstartingfromtheverybeginningwithinminimumsize.Aroutewaspavedtowardsasystematicstudyoftheinterfacetounveiltheenergytransfermechanismincore-shellsystems.

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简介：Thesynthesis,compositionoptimization,VUVPhotoluminescence(PL)spectra,andopticalproperties,of(Y,Gd)(V,P)O4∶Eu3+phosphorswereinvestigatedbysynchrotronradiation.TheVUVPLEspectraandthecorrelationamongVUVPLintensity,λem,andEu3+,Gd3+,andP-contentwereestablished.ThePLEspectralstudiesshowedthat(Y,Gd)(V,P)O4∶Eu3+exhibitedsignificantabsorptionintheVUVrange.TheVUVPLintensitywasfoundtoenhancewithPO43-andGd3+-doping.Furthermore,thechromaticitycharacteristicsof(Y,Gd)(V,P)O4∶Eu3+werealsofoundtobe(0.6614,0.3286)andcomparedagainst(Y,Gd)BO3∶Eu3+asareference.Basedonthecharacterizationresults,wearecurrentlyimprovingandevaluatingthepotentialapplicationof(Y,Gd)(V,P)O4∶Eu3+asanewred-emittingPDPphosphor.

简介：Whitelight-emittingYVO_4：1mol.%Dy~（3＋）,xmol.%Eu~（3＋）phosphorpowderswithordermorphologyandwellcrystallizationwerehydrothermallysynthesizedat180°C.Themicrostructure,white-lightemission,andlight-emittingmechanismofthepowderswerecarefullystudiedusingX-raydiffractometry,scanningelectronmicroscopyandphotoluminescencespectra.TheexcitationandemissionspectraofthephosphorpowdersindicatedthecoexistenceofefficientenergytransferfromEu~（3＋）toDy~（3＋）andinefficientenergytransferfromDy~（3＋）toEu~（3＋）besidestheenergytransferfromVO_4~（3–）toEu~（3＋）.IncreasingtheEu~（~（3＋））concentrationinitiallyenhancedandthenweakenedtheluminescentintensityofDy~（3＋）.Thewhite-lightemissionsofYVO_4：1mol.%Dy~（3＋）,xmol.%Eu~（3＋）phosphorpowderswerebothrelatedtotheenergytransferbetweenVO_4~（3–）andDy~（3＋）/Eu~（3＋）,aswellasbetweenEu~（3＋）andDy~（3＋）.TheinefficientenergytransferfromDy~（3＋）toEu~（3＋）wasfirstfound.

简介：Reactionof(MeC5H4)3LnwithHOCH2CH2NMe2intetrahydrofuran(THF)givesthenewcomplexes[(MeC5H4)2Ln(μ-OCH2CH2NMe2)]2(Ln=Sm,Y,Nd)withnitrogenfunctionalizedμ-alkoxideligand.ThecomplexeswerecharacterizedbyelementalanalysisandIR,and[(MeC5H4)2Sm(μ-OCH2CH2NMe2)]2wasstructurallycharacterizedbytheX-raydiffractiontobeadimerformedbytwounsymmetricoxygenbridges.ThecomplexhasatricyclicskeletonwiththeadditionaltwoSm-NbondsviaintramolecularcoordinationofOCH2CH2NMe2.ThecoordinationnumberofthecentralmetalSmisnine.Thetitlecomplexesshowgoodcatalyticactivityforring-openingpolymerizationofε-caprolactone.