简介:BulknanocrystallineSmCo6FesinteredmagnetwaspreparedbySparkPlasmaSinteringtechnique(SPS).XRDpatternsshowthatthemagnetexhibitsastableTbCu7structure.TEMobservationindicatesthatthemicrostructureofthemagnetiscomposedofSmCo6Fesinglephasegrainswithanaveragegrainsizeof30nm.Magneticmeasurementshowsthatunder9Tmagneticfield,thecoercivityofthemagnetreaches1.12T;thesaturationmagnetizationandtheremanenceare1.13and0.67T,respectively.Themagnethasa(BH)maxof75.6kJ·cm-3.
简介:CeB6粉末被CeO2,B2O3和Mg作为反应物在被拿的高温度的自我繁殖的合成(SHS)准备。SHS反应的断热的温度和动力学被调查。SHS反应产品和沥滤的产品被X光检查衍射(XRD)和扫描电子显微镜学(SEM)描绘。结果比让反应由自己宣传的1800K,和明显的激活精力(Ea)和反应在微分扫描热量测定(DSC)曲线是的Mg-B2O3-CeO2上订发热的山峰的(n)的显示Mg-B2O3-CeO2反应系统的断热的温度相当高23.03kJ/mol并且1.31,分别地。明显的激活精力更低,因此反应容易发生了。SHS产品由MgO,CeB6和小Mg3B2O6组成了。沥滤的产品由单个CeB6阶段组成了,它的纯净比99.0%高,并且CeB6的平均粒子尺寸比150nm小。
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:Thenoveleomplexesofalkaliandrareearthmetalwithperiodatehavebeenpreparedforthefirsttime.ChemicalanalysisindicatesthatthecompositionofthecomplexesisM2LnIO6·xH2O(M=Li,Na,K;Ln=Pr,Tb),andallofthecomplexeshavebeencharacterizedbyUV-Visible,IRspectroscopicstudies,susceptibilitymeasurementsandthermalanalysis.
简介:AseriesofCeB6-dopedandCeO2-dopedCa1-xSiAlN3:xCe3+(denotedasCASN:Ce3+@CeB6andCASN:Ce3+@CeO2,respectively)weresynthesizedbyalloy-nitridationmethodunderhigh-puritynitrogenatmosphere.Themorphologies,crystalphases,andluminescencepropertieswereinvestigatedindetail.WithanincreaseintheconcentrationofCeB6,theunitcellvolumeofCASN:Ce3+@CeB6slightlyincreasesduetothesubstitutionbetweenions,whichleadstoachangeofmicrostructurearoundCe3+.CASN:Ce3+@CeB6efficientlyemitsyellow-orangelightwithamaximumemissionintensityataround550nmforthecontentxof0.01(beingincomparablesituation,CASN:Ce3+@CeO2isx=0.04)whenexcitedat460nm.ComparedwithCASN:Ce3+@CeO2,theredemissioncomponentofCe3+inCASN:Ce3+@CeB6ismuchstronger.Thisisascribedtoenergytransferofintra-Ce3+(withinoneCe3+ion)andinter-Ce3+(betweenCe3+andCe3+ions).Inaddition,thereplacementsofN3-(0.132nmforCN=4)andO2-(0.124nmforCN=4)byB2-(0.140nmforCN=4),whichcanleadtoamarkedexpansionofthehostlatticeandadecreaseoftheoxidationofsamples,arealsoresponsiblefortheincreaseofredemissioncomponent.Furthermore,CASN:Ce3+@CeB6phosphorhasanexcellentthermalstabilitybecauseofthepartialsubstitutionofCe-O(Ce-N)bondsbymorecovalentCe-B.Asaresult,theoutstandingluminescentpropertiesofCASN:Ce3+@CeB6phosphormakeitpracticaltouseinthesinglephosphor-coatedhigh-color-renderingpowerwhiteLED.
简介:AseriesofSm~(3+)dopedY_2MoO_6werepreparedthroughhightemperaturesolidstatereactiontechnique.Theirphasestructures,morphologiesandluminescencepropertieswereinvestigatedbyX-raydiffraction(XRD),scanningelectronmicroscopy(SEM)andphotoluminescencespectrometry.ThemostintenseabsorptionofY_2MoO_6hostoccurredat367nm.EnergytransferfromhostlatticetoSm~(3+)ionscouldbeobserved,andtheschematicdiagramofenergytransferwasconstructed.ThecriticalenergytransferdistanceandenergytransfermechanismbetweenSm~(3+)ionswerediscussedindetail.Consideringthehighcolorpurityandappropriateemissionintensity,Sm~(3+)dopedY_2MoO_6couldbeapromisingphosphorundernearultravioletlightexcitation.
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:有一致形态学的新奇红射出的K2(Ge,Si)F6:Mn4+黄磷被一起沉淀方法综合。纯K2有P636阶段>除P3m1空间组以外的mc空间组就被Si的加入在K2在房间温度的GeF6根据XRD描述。薄片状的显示出的SEM图象和为K2GeF6:Mn4+和K2(Ge,Si)F6:Mn4+黄磷分别地。光致发光刺激(PLE)和光致发光(PL)在K2GeF6:Mn4+和K2(Ge,Si)F6:Mn4+系统。并且K2有Si的GeF6:Mn4+显示出一座强壮的山峰。同时水晶的地包围Mn4+变化能在这个氟化物系统影响腐烂时间。带的设备的颜色范围基于K2(Ge,Si)F6:Mn4+和K2分别地,GeF6:Mn4+到达了多达94.58%NTSC(国家电视标准委员会)和94.386%NTSC那基于氮化物红黄磷比那高得多。在K2(Ge,Si)F6:Mn4+黄磷的所有这些原来的特征作为为改善灯光和常规白LEDs的显示质量的红黄磷为潜在的应用是合乎需要的。
简介:Pt-freecounterelectrode(CE)composedofLa2MoO6(La2O3-MoO3)wassuccessfullysynthesizedbysimplepyrolysisoflanthanumacetate(C6H9O6La·xH2O)andhexaammoniumheptamolybdatetetrahydrate((NH4)6Mo7O24·4H2O).Furthermore,threeproportionscompositescatalystsofLa2MoO6@MWCNTsbasedonLa2MoO6andmultiwallcarbonnanotubes(MWCNTs)werepreparedandcharacterizedasPtfreecatalystforCEindye-sensitizedsolarcells(DSSCs).ThemorphologyandstructureofLa2MoO6@MWCNTscompositesweredeterminedbyscanningelectronmicroscopy,transmissionelectronmicroscopeandX-raydiffraction.TheelectrochemicalperformanceofLa2MoO6@MWCNTscompositecatalystsforCEswasdeterminedbyphotocurrent-voltagemeasurements,cyclicvoltammetry,electrochemicalimpedancespectroscopy,andTafelpolarization.Thepowerconversionefficienciesof4.68%,4.87%and5.06%areobtainedforLa2MoO6:MWCNTswiththemassratiosof5:1,3:1and1:1towardsthereductionofI3-toI-underthesameconditions,respectively,whicharesuperiortothoseofMWCNTs(3,94%)andLa2MoO6(1.71%)electrodes.TheexperimentalresultsrevealthatthepresenceofMWCNTsresultsinanaugmentedactivecatalyticsurfaceareaandenhancedchargetransferfromCEtotheelectrolyte.
简介:Eu2+andDy3+codoped(Ca,Sr)7(SiO3)6Cl2yellowphosphorsweresuccessfullysynthesizedbyself-fluxmethod.Thestructure,morphologyandphotoluminescencepropertieswereinvestigatedbyX-raydiffraction(XRD),scanningelectronmicroscopy(SEM)andphotoluminescencespectra.Theas-preparedphosphorshowedabroademissionspectrumcenteredat550nmforEu2+single-dopedphosphor,whilelocatedat548–544nmfortheEu2+,Dy3+codopedsamplesunderexcitationat380nmlight.TheemissionintensitywasgreatlyimprovedwhenDy3+wasdopedintothe(Ca,Sr)7(SiO3)6Cl2:Eu2+system.Thecomposition-optimizedsamplewith3mol.%ofDy3+andconstant10mol.%ofEu2+exhibiteda220%PLenhancementcomparedtothephosphorwith10mol.%Eu2+single-doped.Meanwhile,itwasfoundthatthequantumefficiencyofphosphornamely(Ca,Sr)7(SiO3)6Cl2:3mol.%Dy3+,10mol.%Eu2+couldgetupto24.6%.Thesynthesizedyellow-emitting(Ca,Sr)7(SiO3)6Cl2:Dy3+,Eu2+isapromisingcandidateashigh-efficiencyyellowphosphorforNUV-excitedwhiteLEDs.
简介:Aseriesofnovelbluelong-lastingphosphorescencephosphorsSr6Al18Si2O37:Eu2+,RE3+(RE3+=Ho3+,Gd3+,Dy3+andPr3+)werepreparedbytheconventionalhigh-temperaturesolid-statereactioninareductiveatmosphere.TheirpropertiesweresystematicallyinvestigatedutilizingX-raydiffraction(XRD),photoluminescence,phosphorescenceandthermoluminescence(TL)spectra.ThephosphorsemittedbluelightthatwasrelatedtotheemissionofEu2+dueto5d-4ftransition.Brightbluelong-lastingphosphorescence(LLP)couldbeobservedaftertheexcitationsourcewasswitchedoff.Fortheoptimizedsample,thebluelong-lastingphosphorescencecouldlastfornearly4hinthelightperceptionofthedark-adaptedhumaneye(0.32mcd/m2).TheeffectsofRE3+ionsonphosphorescencepropertiesofthephosphorswerestudied,andtheresultsshowedthattheco-dopingofRE3+ionsgreatlyenhancedtheintensityofthepeakaround315Kwhichwasrelatedtothelonglastingphosphorescenceofthephosphorsatroomtemperatureandconsequentlyimprovedtheperformanceofthebluephosphorescencesuchasintensityandpersistenttime.