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.

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简介：ThemeasurementsoftemperaturedependenceofthemagneticsusceptibilityofLa1-xSrxCoO3perovskiteoxidesatdifferentSrdoping(0≤x≤0.5)andannealingtemperaturewerepresented.Forthesamplewithx=0.1,ashoulderwasobservedaround150K,andapeakwhichisonefeatureofspinglassappearedaround50Kinthecurveofsusceptibilityversustemperature.Thehigh-temperature(250～420K)susceptibilityfitswellwithCurie-Weisslawforallsamples.WeissconstantandeffectivemagneticmomentweredeterminedandtheirvariationswithSrdopingandoxygenannealingconditionwereobtained.TheWeissconstantincreasesmonotonouslywithSrcontentforx>0.2.Thevaluesofeffectivemomentswereinterpretedwiththespinstateofcobaltions.Studiesonthesusceptibilitiesofthesampleswithx=0.2underdifferentpreparationtemperaturesandannealingtemperaturesshowthattherisingofsinteringtemperatureandannealingtemperaturewillincreasethepara-ferromagnetictransitiontemperature,andreducetheeffectivemomenttonormalvalue.OurresultshowsthatbothCo3+andCo4+ionsshouldbeinISstateafterannealingandtheoxygenannealingcausesthetransitionofCo3+spinstatefromHStoIS.

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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：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.

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：Thesolutionreactionmechanisms,composition,donoratoms,propertiesofcoordinatelinkandstabilityofthecomplexesonthesystemsofadrenalinewithNa3+,Gd3+andTm3+havebeenstudiedbypH-potentiometrictitrationandelectronicspectroscopy.Adrenalineperturbsthef-felectronictransitionofNd3+andTm3+sothattheabsorptionspectraoftheircomplexesareshiftedtowardlongerwavelengths.Theabsorptionspectraofthecomplexesformedbythethreef-blockelementionswithadrenalineareshiftedtowardshorterwavelengthswiththeincreaseofPHinΔγ=350～650nm

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：Theeffectofanexternalelectricfieldonthecrystallizationbehaviorofamorphous(Nd0.1Fe0.9)3Balloywasinvestigated.ThecrystallizationproductofNd2Fe23B3phasewasobtainedforthisamorphousalloyannealedat923Kfor300sinthepresenceofanexternalelectricfieldof300kV·m-1(50Hz);whilethecrystallizationproductsareNd1.1Fe4B4,α-Fe,andFe3Bphasesunderthesameannealingconditionexceptforfree-electricfield.Ontheotherhand,thesampleswereannealedat1023K,whichishigherthanthedecompositiontemperatureofmetastableNd2Fe23B3phase,for600s.Inthecaseofthepresenceofanexternalelectricfield,themetastableNd2Fe23B3phase,asamainphase,isstillstayedinthesample.ThisfactsuggeststhattheexternalelectricfieldenhancesthestabilizationofthemetastableNd2Fe23B3phase.Theeffectoftheexternalelectricfieldonthephaseselectionandstabilizationwasexplainedintermsofthespecificconductancedifferencebetweenthecrystallizationproducts.

简介：YbAl3(BO3)4crystalofgoodopticalqualitywasgrownbythefluxmethod.ThestructureofYbAl3(BO3)4crystalwasdeterminedbysingle-crystalX-raydiffraction.TheexperimentshowsthatYbAl3(BO3)4belongstothedoubleborateswithatrigonalstructure.ThespacegroupisR32anditsunitcellconstantsweremeasuredtobea=0.92965nm,c=0.72129nm,V=0.53673nm3,Z=3.Thetransmittancespectraweremeasured.Thecut-offofYbAl3(BO3)4crystalis216nm,andtherearetwoabsorptionpeakslocatedat940and975nmfrom190nmto2600nm.ThethermalpropertiesofYbAl3(BO3)4crystalwerestudiedforthefirsttime.Theaveragethermalexpansioncoefficientsweredeterminedtobe2×10-6/℃,9.5×10-6/℃alonga-andc-direction.ThespecificheatofYbAl3(BO3)4crystalwasmeasuredtobe0.6695J·(g·℃)-1atroomtemperature.AllresultsindicatethattheYbAl3(BO3)4crystalisanexcellentstoichioimetriclasermaterial.

简介：Er3+-Tm3+-Yb3+tri-dopedBaMoO4phosphorsweresynthesizedbyco-precipitationtechniqueandcharacterizedbyX-raydiffractionanalysis,absorptionstudyandfieldemissionscanningelectronmicroscopyanalysis.Upconversionaswellasdownconversionluminescencestudieswereperformedbyusingnearinfrared（980nm）andultraviolet（380nm）excitations.Energyleveldiagram,pumppowerdependenceandcolourcoordinatestudywereutilizedtodescribethemulticolorupconversionemissionproperties.Undersingle980nmdiodelaserexcitationthedualmodesensingbehaviourisrealizedviaStarksublevelsandthermallycoupledenergylevelsoftheTm3+andEr3+ionsinthepreparedtri-dopedphosphors.AcomparativefluorescenceintensityratioanalysisforintegratedemissionintensitiesarisingfromtheStarksublevels{1G4（a）and1G4（b）}andthermallycoupledenergylevels{2H11/2and4S3/2}oftheTm3+andEr3+ions,respectivelywascarriedoutinthepreparedtri-dopedBaMoO4phosphors.ThemaximumsensitivityforthermallycoupledenergylevelsoftheEr3+andStarksublevelsoftheTm3+ionwasreported.Thedevelopedphosphorscouldbeusefulinthedisplaydevicesandopticalthermometricapplications.

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简介：Thecrackingandaromatizationofn-hexaneoverH-ZSM-5modifiedbyvariousrareearthswereinvestigatedbymeansofcontinuousflowmicro-reactor.ThesurfacepropertiesofmodifiedH-ZSM-5catalystswereobtainedfromIR,XRDandXPS.Theresultsshowthattherareearthsenhancethearomatizingpropertiesofthecatalystswhicharepreparedbymechanicalmixturemethod.Theresultsofn-hexanecrackingandaromatizationarecorrelatedwiththeacidity.TheBrnstedacidicsitesaretheactivesitesofn-hexanearomatization,whileLewisacidsiteplaysanimportantroleinn-hexanecracking.

简介：Silicawasused,asacatalystcarrier,toloadceroussulfateforcatalyzingthesynthesisofn-butylacetate.Themainpurposeofthisresearchwastoexplorethefeasibilityofsilicainimprovingthedecentralityandactivityofthecatalyst.Theeffectsofmolarratioofbutylalcoholtoaceticacid,theceroussulfateloadingsandthereactiontimeontheconversionofaceticacidwerestudiedbysinglefactorexperimentmethodandorthogonalexperimentmethodrespectively.Therefractiveindex(n20D)andmolecularstructureofthepreparedn-butylacetateweremeasuredbyAbbeRaefractometerandFourierTransformInfraredspectroscope,respectively.Thecomparisonsofthesilicaloadedandunloadedcatalystsforcatalyzingthesynthesisofn-butylacetateweremade.Theresultsshowedthatthesuitableconditionsforsynthesizingn-butylacetatewere:molarratioofbutylalcoholtoaceticacidof1.4∶1,uselevelofloadedceroussulfateof0.30gandreactiontimeof50min,respectively.Themaximumconversionofaceticacidforthesilicaloadedcatalystreached98.62%whichwas12.32%and16.43%higherthanthosefortheunloadedcatalystsreportedinliteratures,buttheuselevelofceroussulfatefortheformerwasmuchlessthanthoseforthelattersundersimilaroptimaltechnicalconditions.Thesilicawasprovedtobeagoodcatalystcarrierforenhancingdecentralityandactivityofthecatalystandincreasingtheconversionofaceticacid.Therepentanceofthesilicaloadedceroussulfatewasalsoinvestigatedintheexperiment.

简介：SeveralREEdatasetswerecollectedinCoreDD2andEC2005intheinnershelfofEastChinaSea,CoreY127inthenorthernOkinawaTrough,CoreNT1,C9247andC92169inthesouthYellowSeatochecktheapplicabilityoftheδEuN-ΣREEsmodelforquantita-tivelydistinguishingsedimentsfromtheYangtzeRiverandtheYellowRiver.Bycomparison,severalsedimentsincoresDD2,EC2005,Y127aregenerallyinaccordancewiththismodel.ThecoresNT1,C9247andC92169,whichhavebeeninfluencedbytheYangtzeRiverandtheYellowRivertogether,however,wereinconsistentwiththeδEuN-ΣREEsmodel.TheδEuN-ΣREEsplotanditscorrespondingregressionequation,whichcouldbeusedtodistinguishsediments＂intuitivelyandquantitatively＂fromtheYangtzeRiver,andtheYellowRivershouldbereconsideredorreassessed.

简介：二高度光的铕(III)和铽(III)的准备有succinimide(SI)和N-hydroxysuccinimide(NHSI)的建筑群被报导，它进一步通过元素的化学分析，热分析，英尺红外，粉末X光检查衍射，SEM和荧光光谱学被调查。通过这些分析收集的数据揭示了Eu(III)的形成，有上面的Tb(III)建筑群对ligand在金属提及ligands(M:L)1:3的臼齿的比率。光中心从photoluminescent系列调查被保留的关于通过lanthanide的协作地点的有效促进感受性的有趣的结论。当时，强壮的光排放在Eu(III)-SI和Tb(III)-NHSI建筑群的情况下被观察-SI建筑群展出了的相应Eu(III)-NHSI和Tb(III)没有相片光性质。最新获得的光lanthanide建筑群可能具有为在光电子的各种各样的应用的特别兴趣。

简介：本文采用高温团相反应合成TCaTiO3∶Pr3+红色发光材料、报道了Pr3+激活的CaTiO3的光谱特征及长余辉特性，并与CaS∶Eu的光谱特性及长余辉进行了比较。CaTiO3∶Pr3+将是一种具有广泛用途的新材料