简介：Eu3+/Sm3+codopedBiPO4黄磷与没有表面活化剂的环境经由一个灵巧的热水的方法被综合。X光检查衍射分析证明样品拥有了标准BiPO4单斜晶的结构。扫描电子显微镜学图象证明所有样品与像梭的形状分散得好的、测微计大小的晶体创作了。到Eu3+的从Sm3+的精力转移被光系列和Sm3+4G5/26H5/2排放的腐烂过程证实。橘子红光能在Eu3+/Sm3+codopedBiPO4黄磷被获得。Sm3+4G5/26H5/2排放的平均一生在BiPO4:0.03Sm3+在BiPO4:0.03Sm3+从2.70ms减少了到2.37ms，0.05Eu3+。在395nm附近的强壮、宽的吸收乐队，从Eu3+的7F05L6转变和Sm3+的6H5/24K11/2转变发源，资助BiPO4:Eu3+，有近紫外激动的white-light-emitting二极管的域里的潜在的应用程序的Sm3+黄磷。

简介：Ca3Y2(BO3)(4):Eu3+黄磷被高温度solid-statereaction方法综合，并且光特征被调查。排放光谱在相应于电的dipoleD-5(0)的613和621nm展出二强壮的红排出物在365nm刺激下面的Eu3+的-F-7(2)转变，原因是Eu3+代替forY3+在Ca3Y2(BO3)(4)的水晶结构占据非中心对称的位置。为613nm的Theexcitation光谱显示黄磷能是有效地激动的由紫外(紫外)(254nm，365nm和400nm)并且蓝色(470nm)光。Ca3Y2(BO3)(4)的排放紧张上的Eu3+集中的效果:Eu3+黄磷被测量，排放紧张与增加Eu3+集中增加的结果表演，然后减少。Ca3Y2(BO3)(4)的CIE颜色坐标:Eu3+黄磷是(0.639，0.357)在15mol%Eu3+。

简介：TheNaGd（WO_4）_2：Eu~（3＋）phosphorswerepreparedbythemicroemulsionmediatedhydrothermalmethod.ThemorphologyandsizeofthesamplescouldbedependentonthepHintheinitialsolution.Thesephosphorsobtainedhadastrongabsorptionat395nmmatchingwiththepopularemissionofnear-UVLEDchips,andcouldemitintenseredlightat616nm.Thesmallellipsoid-likeparticlesorshortrodswereprovidedwithlargeparametersofoscillatorstrength？_2andasymmetryratio.Comparedtotheellipsoid-likephosphors,therod-likephosphorstookonstrongeremission,longerlifetimeandlargerquantumefficiency.Thisworkdemonstratedthattheone-dimensionNaGd（WO_4）_2：Eu~（3＋）phosphorsmightbeamorefavorabledevicethanzero-dimensiononesforphotoluminescence.

简介：Eu-activatedCaMoO4phosphorswereco-precipitatedinanaqueoussolution,andNH3·H2O,NH4HCO3and(NH2)2COaspre-cipitatingaidagentswerecomparedbasedonthemorphologyandparticlesizedistributionofthephosphorsamples.Sm3+assensitizerionwasinvestigatedontheluminescenceofCaMoO4:Eu,anditcouldstrengthenthe406nmabsorptionofthisphosphor.Atlast,thescheeliteCaMoO4:EuandwolframiteZnMoO4:Euwereselectedtocomparetheirhostabsorption.TheresultshowedthatthescheelitemolybdatehostexhibitedstrongerUVabsorptionthanwolframiteone.

简介：Ternarycomplexesofeuropiumandterbiumwithbenzoicacidand1,10-phenanthroline[RE(BA)3phen](BA=benzoatephen=1,10-phenanthroline)wereintroducedintoasilicamatrixbysol-gelmethod.Thethermalstabilityandluminescencebehaviorofthecomplexesinsilicagelswerestudiedincomparisonwiththecorrespondingsolid-statecomplexesbythermaldecomposition,excitationandemissionspectra.Thethermalstabilityofthecomplexesisenhancedinsilicagelmatrixandtheluminescenceremainesunchanged.

简介：我们在一个Y3Ga5O12(YGG)主人系统调查Bi3+和RE3+(RE=Tb或Eu)的光性质。Bi3+的另外的做能在这位主人提高Tb3+或Eu3+的光。到Tb3+和Eu3+的从Bi3+的精力转移被观察，精力转移的机制被调查。自从Bi3+排放乐队或Eu3+刺激乐队，转移能作为电的多极相互作用被解释的精力的机制重叠，当Tb3+或Eu3+的紧张随Tb3+或Eu3+集中的增加增加时，Bi3+排放紧张减少。因此，Bi3+离子是到在Y3Ga5O12主人的Tb3+和Eu3+使活跃之物的一种有效sensitizer。

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简介：ThepreparationofhybridmesoporousMCM-48graftedbyvinylgroupviapost-graftingprocesswasreportedandstudiedbyX-raydiffraction,BETand29SisolidMASNMR.Anorganicβ-diketonateEuropiumcomplexthecorrespondingluminescencepropertywascharacterized.

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.

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简介：Europium（Ⅲ）-dopedYF3ispreparedbyahydrothermalprocessat200℃.X-raydiffraction（XRD）patternidentifiestheformationofYF3phasewithoutdetectableimpurity.Environmentscanningelectronmicroscopy（ESEM）imageshowstheevensizedistributionofthesampleswithcubicmorphology.TheexcitationandemissionspectraoftherareearthionsdopedYF3areinvestigatedbyfluorescencespectrophotometer.Theexcitationspectrumfor591nmemissionhasseveralexcitationbandsat320,365,386,397and467nm,andthemainpeakvaluewas397nm.TypicalEu3+emissionpeaksat591nm（5D0→7F1）and612nm（5D0→7F2）areobservedwhenexcitedby397nm,andthestrongestemissionis591nm,demonstratingthattherareearthionsoccupythecentrosymmetricalsitesinYF3.

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

简介：Calciumtitanatedopedwithpraseodymiumwaspreparedthroughsolidstatereactionanditexhibitedintenseredemissionat612nm.Phosphorswerecharacterizedforphotoluminescence,thermo-luminescenceandafterglowemissions.Studyofeffectsofrareearthsonphotoluminescenceaswellasafterglowintensitywasreported.Presenceofgadoliniumenhancedluminescence.Presenceofsomemonovalentionsenhancedbothafterglowandphotoluminescenceemission.Thermo-luminescenceglowcurveswereanalyzedand...

简介：Inthepresentwork,theLEDchipwasirradiatedbyusing59.6MeVNionsinaterminalchamberoftheSector-focusedcyclotron(SFC)intheNationalLabortaryofHeavy-ionAcceleratorsinLanzhou.The63MeVNionspenetratedthroughagoldfoilandscatteredinalargearea.Theenergyofionwasreducedto59.6MeVafterscatteringofthegoldfoil.TheLEDwasprovidedbytheSemiconductorLightingCenterinInstituteofSemiconductorinBeijing.TheluminencesoftheLEDbefore/afterirradiationweretestedthroughaintegratingsphereinSemiconductorLightingCenterinInstituteofSemiconductorinBeijing.Theluminancewastestedunderacurrentof350mA.Fig.1showstherelationshipbetweentheluminencesandtheirradiationfluences.Theirradiationledto

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。

简介：Eu3+activatedSr1–xEuxZrO3(x=0.01–0.04)phosphorwithperovskitestructurewassuccessfullysynthesizedbyusingcombustionmethod.Thestructure,morphologyandopticalpropertiesofthematerialwerecharacterizedbyX-raydiffraction,scanningelectronmicroscopyandfluorescencespectrometry.TheXRDresultsindicatedthatcrystalsofSrZrO3:Eu3+belongstotetragonalperovskitesystem.ThephosphorcouldbeeffectivelyexcitedbyUVlightandtheemissionspectraresultsindicatedthatreddish-orangeluminescenceofSrZrO3:Eu3+duetomagneticdipoletransition5D0→7F1at593nmwasdominant.Thus,thepreparedphosphorshowedremarkableluminescentpropertieswhichfindapplicationsinfieldemissiondisplay(FED)andplasmadisplaypanel(PDP)devices.

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