简介:ThetransportpropertieswerestudiedforrareearthmanganeseoxideLa0.67Cao.33Mn1-xFexO3(x=0-O.3)systems.ItisfoundthatwithincreasingFe^3+-dopingcontentx,theresistanceincreasesandtheinsulator-metaltransitiontemperature(T1M)shiftstolowertemperature.Ifthedopingcontentissmall,thetransportpropertiesmanifestmetalliccharacteristicsinthetemperaturerangeofT<T1M,whiletheywillobeyathermalactivationmodelinthetemperaturerangeofT>T1M.SuchabehaviormaybeattributedtotheFe^3+-dopingandpossibleMnionsscatteringtoelectrons.TheFe^3+dopingmayleadtotheformationofFe^3+-O^2--Mn^4+channels,whichcouldterminatethedoubleexchangeMn^3+-O^2--Mn^4+channels.TheantiferromagneticclustersofFeionsmayinducetheMnionstoscettertotheelectrons.
简介:InordertoimprovethehydrogenationanddehydrogenationperformancesoftheMg2Ni-typealloys,MgwaspartiallysubstitutedbyLainthealloy,andmeltspinningtechnologywasusedforthepreparationoftheMg20-xLaxNi10(x=0,2,4,6)hydrogenstoragealloys.ThestructuresofthealloyswerestudiedbyX-raydiffraction(XRD),scanningelectronmicroscopy(SEM)andhigh-resolutiontransmissionelectronmicroscopy(HRTEM).Itwasfoundthatnoamorphousphaseformedintheas-spunLa-freealloy,buttheas-spunalloyscontainingLaheldamajoramorphousphase.WhenLacontentx≤2,themajorphaseintheas-castalloyswasMg2Niphase,butwithfurtherincreaseofLacontent,themajorphaseoftheas-castalloyschangedintoLaNi5+LaMg3phase.Thermalstabilityoftheas-spunalloyswasstudiedbydifferentialscanningcalorimetry(DSC),showingthatspinningratewasanegligiblefactoronthecrystallizationtemperatureoftheamorphousphase.Thehydrogenabsorptionanddesorptionkineticsoftheas-castandas-spunalloysweremeasuredusinganautomaticallycontrolledSievertsapparatus,confirmingthatthehydrogenabsorptionanddesorptioncapacitiesandkineticsoftheas-castalloysclearlyincreasedwithrisingLacontent.ForLacontentx=2,theas-spunalloydisplayedoptimalhydrogendesorptionkineticsat200°C.
简介:Duetotheremarkablemagnetoresistance(MR)effectonperovskite-typemanganite,magnetoelectronicsandspintronicshavebecomeattractivesubjectsofexperimentalandtheoreticalinvestigationsfortheapplicationpurpose.(La0.9Nd0.1)2/3Ca1/3Mn1-xFexO3(x=0,x=0.05)werepreparedsuccessfullybysol-gelmethod.Thestructure,magneticproperties,andtransportpropertiesofthecompoundswereinvestigated.Themagnetoresistanceeffectdependsonthecompositionandthetemperature.XRDpatternsshowthatthecompoundisasinglephasepolycrystalwithpseudocubicstructure.Alargenegativeisotropicmagnetoresistanceeffectinthesampleswereobservedatlowtemperatureregion.ThemaximumMRofthesampleswas77%and97%,respectively.Itwasmostlikelyduetothescatteringorthetunnelingtransportofspin-polarizedcarriersinlatticeunderstrongmagneticfield.
简介:采用元胞自动机模型建立了05Cr17Ni4Cu4Nb不锈钢固溶过程的二维模型,模拟了固溶过程中的晶粒形核生长以及化合物相的扩散溶解,模拟结果动态地再现了固溶过程的微观组织特征。通过该模型分析了固溶温度和固溶时间对固溶处理后微观组织的影响。
简介:NominalcompositionofCa1-xZnxTiO3:0.002Pr3+(x=0.000~0.200)phosphorswerepreparedbyconventionalsolidreactionroute.XRDandPLmeasurementswereusedtoinvestigatethesolid-solutionstructureandluminescencepropertiesofZn-dopedCa1-xZnxTiO3:0.002Pr3+phosphors.Theeffectofsolid-solutionstructureformedbysubstitutionbetweenCa2+andZn2+ionsontheluminescentpropertieswasanalyzed.Theresultsrevealthat,withtheincreaseofZnsubstitutioncontentbelow0.010,latticeparametersandtheintensityofexcitationpeakatboth260and330nmaswellasthecorresponding610nmemissionintensityaremonotonouslydecreasedquicklyinasimilartendency.Also,theevolutionofluminescenceintensityandcrystalcellparametersagainstZndopingconcentrationareingoodagreement.AboveresultsarecloselyrelatedwiththestructurechangewithinCa1-xZnxTiO3:0.002Pr3+solid-solutionphaseformedbytheZnionssubstitutionfortheCasites.Presentstudyrevealsthatthesolid-solutionstructureformedbysubstitutionbetweenCa2+andZn2+ionshassignificanteffectontheluminescencepropertiesofsinglephaseCa1-xZnxTiO3:0.002Pr3+phosphors.
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.