简介:
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:以硝酸锶、七钼酸铵、氧化镨为原料,采用低温燃烧法合成白光发光二极管(whitelightemittingdiode,简称WLED),用新型红色荧光粉SrMoO4:Pr3+,并研究其光谱性质。结果表明,SrMoO4:Pr3+激发光谱中Pr3+在449nm处有一最强3H4->3P0激发峰,其激发范围与蓝光LED芯片相匹配,能被蓝光有效激发;发射光谱在644nm处有最强峰,属于Pr3+的3P0->3F2跃迁,发红光,说明SrMoO4:Pr3+荧光粉是1种潜在的白光LED用蓝光激发的红色荧光粉。同时还研究了燃烧温度、尿素用量、稀土Pr3+掺杂量对荧光粉发光强度的影响,得出制备SrMoO4:Pr3+的最佳条件为:燃烧温度600℃,尿素用量为理论尿素用量的3倍,稀土Pr3+离子掺杂摩尔分数为2%。
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.
简介:采用包埋-刷涂法在C/C复合材料表面制备SiC/ZrSiO4复合涂层,借助X射线衍射(XRD)、扫描电镜(SEM)和能谱分析(EDS)等测试手段分析该复合涂层的微观结构,并研究SiC单涂层和SiC/ZrSiO4复合涂层在1500℃静态空气中的抗氧化性能。结果表明:包埋法制备的SiC内涂层结构疏松,具有较好的抗氧化性能,氧化55h后质量损失率仅为0.5%,但氧化58h后,涂层内部形成大孔洞并产生贯穿孔隙,导致涂层失效,质量损失率迅速增加到2.1%。SiC/ZrSiO4复合涂层由非均质镶嵌式结构的ZrSiO4涂层紧密覆盖在SiC内涂层表面而成,具有优异的抗氧化性能,氧化198h后质量仅增加0.5%,并且基本不再随时间延长而增加;复合涂层不仅能自愈合外涂层的缺陷和裂纹,还能抑制氧化过程中大孔洞的形成,避免贯通孔隙的产生。
简介:以六水合氯化钴(CoCl2·6H2O)和水合三氯化钌(RuCl3·3H2O)为前驱体,采用胶体法制备超级电容器用(RuO2/Co3O4)·nH2O复合薄膜电极材料。用X射线衍射仪以及CHl660C电化学工作站对该复合薄膜的物相结构及电化学性能进行表征。结果表明:当COCl2'6H20和RuCl3·3H2O的物质的量比n(Co):n(Ru)为2:1时,于350℃下热处理2.5h制备的复合薄膜电极具有优良的性能,在浓度为0.5mol/L的H2S04电解液中其比电容达到512F/g,500次充放电循环后比电容量保持在充放电循环前的96.1%;充放电电流为0.01A时,内阻为1.2Ω。
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:采用浓HNO3/浓H2SO4混合酸在60℃超声环境下对T300碳纤维进行表面氧化处理,并以其为增强体制备碳纤维/环氧树脂复合材料。利用X射线光电子能谱仪、拉曼光谱仪、扫描电镜、原子力显微镜对表面氧化前后的碳纤维形态与表面化学性质进行表征,研究氧化时间对纤维的表面形貌与表面性质以及碳纤维/环氧树脂基复合材料力学性能的影响。结果表明,氧化初期,碳纤维表面生成S—、N—含氧基团,以及—OH和—C=O;后期形成—COOH,氧化时间为15min时,—COOH的浓度达到最大值。碳纤维/环氧树脂复合材料的强度随混合酸氧化时间延长而不断增强,氧化15min时强度达到峰值,相比于未氧化处理的样品,复合材料层剪切强度从16.3MPa提高到38.8MPa,抗弯强度从148.3MPa提高到379.7MPa。
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.