简介:Trivalentsamariumdopedbariummolybdate(BaMoO_4:Sm~(3+))redphosphorwassuccessfullysynthesizedbyhydrothermalmethod.Thecrystalstructure,morphologyandphotoluminescentpropertywerecharacterizedbyX-raydiffraction,fieldenvironmentalscanningelectronmicroscopyandphotoluminescencespectroscopy.TheresultsindicatedthatthesynthesizedBaMoO_4:Sm~(3+)phosphorconsistedofapurephasewithanoctahedralstructure.Themainexcitationpeakswerelocatedat362,404,445and477nm,respectively,andwereobviouslyobserved.Themainemissionpeakswerelocatedat533,566,602and646nm,respectively.Thephosphorsexhibitedaredperformanceat646nm,whichwasappropriatefortheultraviolet-lightemittingdiode(UV-LED)andblueLED.TheluminescentintensityofBaMoO_4:Sm~(3+)increasedwithanincreaseinthedopingamountofSm~(3+).Theluminescentintensityhadtheoptimalvalueforx=0.03.WhenthedopingamountofSm~(3+)wasfurtherincreased,theconcentrationquenchingphenomenonwasobserved.Monovalentlithium(Li+)cationwasusedasachargecompensator.TheluminescenceintensityfirstincreasedwithincreasingLi+dopingconcentration,andthendecreased.TheoptimalcontentofLi+wasabout2%.TheBaMoO_4:Sm~(3+)phosphorpreparedinthisstudycouldactassuperiorredphosphorforwhiteLEDs.
简介:黄磷(Bi1-xSmx)2ZnB2O7(x=0.01,0.03,0.05,0.07,和0.09)被常规稳固的州的反应综合。所有样品的纯净被X光检查粉末衍射(XRD)检查。XRD分析证明所有这些混合物具有Bi2ZnB2O7的一个单个阶段,显示在Bi2ZnB2O7的双性人(3+)能被没有晶体结构的变化的Sm(3+)部分代替。在房间温度的刺激和排放系列显示出Sm(3+)的典型4f-4f转变。主导的刺激线在404nm附近由于(6)H5/2→(4)K11/2和排放光谱在563,599,646,和704nm由一系列线组成由于(4)G5/2→(6)H5/2,(6)H7/2,(6)H9/2,并且(6)H11/2分别地。在Bi2ZnB2O7的Sm(3+)的最佳的集中关于3mol%(相对1mol双性人(3+))并且批评距离Rc作为2.1nm被计算。Bi1.94Sm0.06ZnB2O7的排放紧张的温度依赖在在100和450K之间的温度范围被检验。紧张下降了到起始的紧张的一半的熄灭的温度是280K。为在Bi1.94Sm0.06ZnB2O7的Sm(3+)的一生作为0.29和1.03ms的价值被适合。
简介:采用高分子网络凝胶法合成Sm^3+掺杂YPO4纳米荧光材料,利用X射线衍射(XRD)、透射电镜(TEM)、傅里叶红外光谱(FT-IR)和荧光光谱等对合成产物的晶体结构、颗粒尺寸、形貌和光学性能进行分析与测试,并研究Sm^3+掺杂浓度(n(Sm)/n(Y+Sm))的影响。结果表明,采用高分子网络凝胶法合成的YPO4:Sm^3+为单一的四方晶系磷钇矿结构的YPO4晶体,颗粒尺寸约为20nm。其激发光谱在405nm处有一最强激发带,属于Sm^3+的6H5/2-4K11/2跃迁,发射光谱在603nm^处有一最强峰,属于Sm3+的4G5/2-6H7/2跃迁。激发和发射光谱测试结果表明,Sm3+掺杂YPO4荧光材料可以被405nm波长的光有效地激发,发射出强烈的Sm3+特征橙红色光。当Sm3+掺杂浓度高于2%时观察到浓度猝灭现象,浓度猝灭机理为电多极-电多极相互作用。
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:ThephotocatalystsK4Nb6017andK4Nb6017dopedwithFe^3+andCr^3+werepreparedbysolidstatereactionandwerecharacterizedbypowderx-raydiffraction,UV-visdiffusivereflectanceandscanningelectronmicroscopy.ThephotocatalyticactivityofK4Nb6O17andK4Nb6O17dopedwithFe^3+,Cr^3+wereinvestigatedwithmethanolaselectrondonorandPtaspromotercatalystunder+400nmUVirradiation.Thedifferenceofphotocatalyticactivitybetweenthemwasalsodiscussed.TheindividualrateofhydrogenevolutionfortheK4Nb6O17,Fe-K4Nb6O17andCr-K4Nb6O17asphotocatalystsare5.35,5.00,6.25mmol·L^-1.h^-1respectively.
简介:Er~(3+)andLa~(3+)codopedY_2O_3nanocrystallinepowdersweresynthesizedbygelcombustionmethodandcharacterizedwiththermalanalysis,X-raydiffraction(XRD),transmissionelectronmicroscopy(TEM),high-resolutionTEM(HRTEM)techniquesandfluorescencespectroscopy.Afterbeingcalcinedat1200oC,the(Y_(1–x)La_x)_2O_3:Er~(3+)powderswereconfirmedtobecubicY_2O_3phasewiththecrystallinegrainsizeintherangeof20–40nm.TheEr~(3+)emissionat1.53μmfromthe~4I_(13/2)→~4I_(15/2)transitionwasobserved,whichwasfoundtobeenhancedbyintroducingLa~(3+)ions.SuchenhancementcouldbeattributedtotheadjustmentofEr~(3+)ions'localenvironmentbythecodopingofLa~(3+)ions,leadingtotheincreasedgroundstateabsorptioncrosssectionofEr~(3+)ions.
简介:PolycrystallineNd3+andLa3+co-dopedyttriananopowderNd3+:Y1.90La0.10O3fortransparentceramicswassynthesizedbyco-precipitationmethodusingoxalateacidastheprecipitantand(NH4)2SO4astheelectricalstabilizerunderultrasonicradiation.Nanopowderscalcinedatdifferenttemperatureswerecharacterizedwiththermalgravimetric-differentialthermalanalysis(TG/DTA),X-raydiffraction(XRD),transmittingelectronmicroscopy(TEM),energydispersivespectrometry(EDS)andspectralanalysistechniques.Th...
简介:Ternarycomplexesofeuropiumandterbiumwithbenzoicacidand1,10-phenanthroline[RE(BA)3phen](BA=benzoatephen=1,10-phenanthroline)wereintroducedintoasilicamatrixbysol-gelmethod.Thethermalstabilityandluminescencebehaviorofthecomplexesinsilicagelswerestudiedincomparisonwiththecorrespondingsolid-statecomplexesbythermaldecomposition,excitationandemissionspectra.Thethermalstabilityofthecomplexesisenhancedinsilicagelmatrixandtheluminescenceremainesunchanged.
简介:Er3+/Yb3+codopedzincateBaGd2ZnO5phosphorsweresynthesizedviaatraditionalsolidstatereaction.ThecrystalstructureandphasepuritywerecheckedbymeansofX-raydiffraction(XRD),andtheresultsshowedthatpurephaseBaGd2ZnO5phosphorswithvariousEr3+,Yb3+concentrationswereobtained.TheinfluenceofEr3+andYb3+dopingconcentrationsonthegreenandredupconversionemissionswasstudied.Itwasfoundthatbothgreenandredupconversionemissionsunder980nmexcitationweretwo-photonprocessesindependentfromtherareearthdopingconcentrations.However,theupconversionluminescenceintensitiesgreatlydependedontherareearthdopingconcentration.Furthermore,thepopulationprocessesofupconversionluminescenceandthequenchingmechanismswereanalyzed.Thetemperature-dependentgreenupconversionluminescencewasstudied,andthetemperaturequenchingprocessoftwogreenupconversionemissionswasmodeled.Thethermalquenchingprocessesofthegreenupconversionemissionscouldbewellexplainedbythemodelweproposed.
简介:
简介:TheLa3+-loadedadsorbentwaspreparedbythereactionbetweenLa3+andethanolamine-modifiedvegetabletannicextract,totreatF--containingwastewater.TheproblemsofheavycolorcausedbyvegetabletannicextractandofturbiditycausedbyreactionbetweenLa3+andF-weresolved.Whenotherconditionswerenotchanged,pH,temperature,stirringtime,anddosewerechangedrespectivelyandtheadsorbancewastestedrespectively.Theresultsshowthatthisadsorbentpossesseshighsaturatedadsorptivecapacity(18.86mg·g-1)whenpHis5~6,T≤80℃,0.2gdosage,and180minagitatingtime,andtheadsorbancereachesthehighest(98.5%).Theadsorbentcanbeeasilyregeneratedwith0.5mol·L-1NaOHatpH12.
简介:Calciumtitanatedopedwithpraseodymiumwaspreparedthroughsolidstatereactionanditexhibitedintenseredemissionat612nm.Phosphorswerecharacterizedforphotoluminescence,thermo-luminescenceandafterglowemissions.Studyofeffectsofrareearthsonphotoluminescenceaswellasafterglowintensitywasreported.Presenceofgadoliniumenhancedluminescence.Presenceofsomemonovalentionsenhancedbothafterglowandphotoluminescenceemission.Thermo-luminescenceglowcurveswereanalyzedand...
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: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:SphericalYAG:Ce3+phosphorparticleswithnarrowsizedistributionwerepreparedbyspraypyrolysis.Theeffectsoftheconcentrationofsolution,theflowrateofcarriergasandtheannealingtemperatureonthephosphormorphologywerestudied.Theproductivityofprecursorparticlesshowsatrendofdropafterrisingwiththeincreaseofconcentration.Raisingtheflowrateofnitrogencanimprovetheproductivityoftheprecursorparticles.Phosphorpreparedbyspraypyrolysishasobviouslyhigheremissionintensitythanthatsynthesizedbysolidstatereaction,spraypyrolysismakesCe3+ionswelldistributedinthecrystallatticeastheluminescentcenters,andphosphorparticleshaveregularsphericityandnarrowsizedistribution.
简介:Differentfluxeswereusedtosynthesizelongpersistencephosphors,calciumsulfidesactivatedbyEu2+andTm3+,byconvenientsolid-statemethod.ThephosphorusingNH4Fasafluxhasgoodcrystallinityandlargeparticlesize,itsstabilityagainstwaterandotheratmosphericcomponentsisenhanced,anditsafterglowislongerandfluorescentintensityismoreintensethanthoseofthephosphorusingNH4Clasflux.TheirPLintensitiesvariedwithtimeinmoistairweremeasured,noremarkablechangewasfoundforthosepreparedwithNH4FfluxincontrastwithNH4Clasflux.SousingNH4Fasfluxisagoodmethodtoenhancethestabilityofalkalineearthsulfides.