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.

简介：EffectofLa-richrareearthoneutecticmicrostructureinA1-2%Fealloywasstudied.WhentheadditionofREissmall,a-A1phaseisintheformofcellulardendrite.WiththeincreaseoftheadditionofRE,thenucleationandgrowthofa-A1dendritearesuppressed,andeutecticAl3Fephaseisrefined.WhentheadditionofREgetsto0.6%(massfrac-tion),thesizeofeutecticAl3Feincreases.Inaddi-tion,mechanismoftheeffectofmixedREoneutecticmorphologyofA1-2%Fealloyisexplored.

简介：EffectofMnsubstitutionforFeincubicLavesZr0.1Tb0.9(Fe1-xMnx)2andY0.1Tb0.9(Fe1-xMnx)2com-poundsispresented.Similarresultsinbothsystemsareobtained:ThestructureandthemagnetismofTbFe2arebothinfluencedslightlybyasmallamountofYorZrsubstitutionforTb;Withincreasingxvalue,thelatticeconstantincreasesmonotonously;theCurietemperaturedecreaseslinearly;whilesaturationmagnetizationincreaseslinearly.ForthesmallamountofMnsubstitutionforFeinbothsystems,magnetostrictionissignificantlylargerthanthatinthepureironalloys.Thelargestmagnetostrictionof|γ‖-|γ|=2200×10-6atmagneticfieldof2×107/4πA/misobtainedforY0.1Tb0.9(Fe0.95Mn0.052.

简介：AseriesofCe-Fe-Zr-O(x)/MgO(xdenotesthemassfractionofCe-Fe-Zr-O,x=10%,15%,20%,25%,30%)complexoxideoxygencarriersforselectiveoxidationofmethanetosynthesisgaswerepreparedbytheco-precipitationmethod.ThecatalystswerecharacterizedbymeansofX-raydiffractionandH2-TPR.TheXRDmeasurementsshowedthatMgFeO4particleswereformedandFe2O3particleswelldispersedontheoxygencarriers.Thereactionsbetweenmethanedilutedbyargon(10%CH4)andoxygencarrierswereinvestigated.SuitablecontentofCeO2/Fe2O3/ZrO2mixedoxidescouldpromotethereactionbetweenmethaneandoxygencarriers.Therearemainlytwokindsofoxygenofcarriers:surfacelatticeoxygenwhichhadhigheractivitybutlowerselectivity,andbulklatticeoxygenwhichhadloweractivitybuthigherselectivity.Amongallthecatalysts,Ce-Fe-Zr-O(20%)/MgOexhibitedthebestcatalyticperformance.Theconversionofthemethanewasabove56%,andtheselectivityoftheH2andCOwerebothabove93%,theratioofH2/COwasstableandapproachedto2foralongtime.

简介：Awhitelong-lastingphosphorCa2MgSi2O7:Dy3+waspreparedbythesolid-statereaction.Astrongbandpeakedat260nmwasshownintheexcitationspectrumof578nmemission,whichmightbeattributedtotheoxygendeficiencyofthehost.Afterirradiatedwith254nmfor4min,thewhiteafterglowofthesamplecouldbeseenfor3h.Moreover,thedepthsandfrequencyfactorsoftrapcenterswerecal-culatedfromthethermo-luminescencecurveofthesample,whichindicatedthatthetrapcenterscorrespondingtothe414Kbandweremorehelpfultothelong-lastingphosphorescence.

简介：EffectsofNbandZrsubstitutionsonthecrystal]izationbehaviorsandmagneticpropertiesofmelt-spun(Nd,Pr)2Fe14B/α-Fealloyswerestudied.Theresultsshowthatfor(Nd0.4Pr0.6)8.5Fe85.5B6ribbons,themetastable(Nd,Pr)3Fe62B14precipitatesaftertheinitialcrystallizationofα-Feanddecomposesintothefinalmixtureof(Nd,Pr)2Fe14Bandα-Fe.For(Nd0.4Pr0.6)8.5Fe84.5Zr0.5Nb0.5B6ribbons,however,(Nd,Pr)2Fe14Bandα-Fephasesprecipitatesimultaneously.ThisindicatesthatbothNbandZrdopingcanavoidtheformationofmetastablephaseand!

简介：Loadedonthecordierite,therareearthdopedcompositecatalystwaspreparedbysol-gelmethodcombinedwithdippingtechnique.TakingOrthodichlorobenzeneasmodel,thecatalystwasusedtoremovethedioxinsofthewastegas.Theresultsshowedthatat280℃andgasspacevelocitybeing8000h-1,theorthodichlorobenzenecouldberemovedeffectivilybythepreparedCeO2-TiO2-V2O5compositecatalystwhoseactivitywasremarkablyenhancedbythedopingofCe,whiletheindustrialside-streamtestofdioxinsfromrefuseincinerationsmokeindicatedthatthedecompositionratecouldreachabove93%underthesameconditions.

简介：15%Ag-addedcubicperovskitesSr0.9La0.1TiO3andRuddlesden-Popper(RP)phasesSr2.7La0.3Ti2O7werefabricatedviahydrothermalsynthesis,coldpressingandhigh-temperaturesintering.Thestructureandthermoelectricpropertieswerealsoinvestigatedforallsamples.TheresultsindicatedthatAgprecipitatedasasecondphase.AgadditionmadeelectricalconductivityandabsoluteSeebeckcoefficientenhanced,asaresult,theZTvalueswereenhancedbothfortwoseries.Comparedwithcubicperovskite,RPphasewassubjectedtosmallerimpactbyAgaddition.ThereasonsforenhancingZTvalueandthedifferentimpactfortwoseriesbyAgadditionwerealsodiscussed.

简介：ＳｔｕｄｙｏｎｔｈｅＥａｓｙＤｉｒｅｃｔｉｏｎｏｆＭａｇｎｅｔｉｚａｔｉｏｎｏｆＳｍ０．８８Ｄｙ０．１２Ｆｅ２ＡｌｌｏｙＺｈｕＭｉｎｇｙｕａｎ（朱明源），ＺｈａｎｇＨｕｉｙｏｕ（张慧友），ＺｈｕＹｕｌｉａｎｇ（诸于良）ＪｉｎＨｏｎｇｍｉｎ?..

简介：FluorescencespectraofSm2+andEu2+→Sm2+energytransferwerestudiedinSrB4O7.Thereappearsonlyfluorescencefrom5D0transitionofSm2+at77K.Thevibroniclinesassociatedwith5D0→7F0transitionwereobserved.Thethermalpopulationtoupperstatesof5D1and4f5dlevelsfrom5D0givesriseto5D1→7FJand5d→4fradiativetransitionsofSin2+athighertemperature.

简介：

简介：新奇双1:11系列arsenotungstate，[CuI(phen)2]5H6[Sm(AsW11O39)2]

简介：Basedonthethermodynamicallyself-consistentanalysisandoptimizationofthreesub-binarysystemsoftheternarysystemPrCl3-CaCl2-MgCl2,thethermodynamicsofthisternarysystemhasbeenstudied.UsingHillertmodelandtakingMgCl2asanasymmetriccomponent,thePrCl3-CaCl2-MgCl2phasediagramhasbeencalculated.Theagreementbetweencalculatedandmeasuredcompositionsandtemperaturesatdeflectingpointsonliquidusisgood.Thesystemisasimpleeutecticonewithaeutecticpointat26.0mol%PrCl3,41.5mol%CaCl2,32.5mol%MgCl2;560℃（calculated）and26.0mol%PrCl3,39.4mol%CaCl2,34.6mol%MgCl2;546℃（measured）,respectively.

简介：Thenoveleomplexesofalkaliandrareearthmetalwithperiodatehavebeenpreparedforthefirsttime.ChemicalanalysisindicatesthatthecompositionofthecomplexesisM2LnIO6·xH2O（M=Li,Na,K;Ln=Pr,Tb）,andallofthecomplexeshavebeencharacterizedbyUV-Visible,IRspectroscopicstudies,susceptibilitymeasurementsandthermalanalysis.

简介：

简介：一系列立方的稀土元素sesquioxidesRE2O3的拉曼系列(RE=Eu，Gd，Dy，惊讶，嗯，Tm，Yb，陆，Sc和Y)被拉曼光谱学与532和785根nm激光线调查。丰富的另外的乐队由于激光激动的光被观察。为Eu2O3，Dy2O3，Ho2O3，Er2O3，Tm2O3和Yb2O3，，光主要为Gd2O3，Lu2O3，Sc2O3和Y2O3来自内在的三价的lanthanide离子，他们的光被归因于象Eu3+，Nd3+和Er3+那样的另外的光lanthanide离子的踪迹杂质。这调查为检测踪迹作为一个有用工具证实了拉曼光谱学光lanthanide杂质。

简介：在不同温度下对用金属锰法制得Ｍｎ３Ｏ４粉末和含有部分Ｍｎ（ＯＨ）２的Ｍｎ３Ｏ４粉末分别进行除气处理，然后用静态氮吸附法对其进行对比实验，测试其在各自温度处理后的比表面积。结果表明，在金属锰法制取高纯Ｍｎ３Ｏ４粉末时，应使部分Ｍｎ（ＯＨ）２保留下来，然后对其进行高温（如２００℃）处理，这样可以大大提高高Ｍｎ３Ｏ４粉末的比表面积。

简介：ThispaperistodiscussthesensingcharacteristicsofSnO2semiconductorcomponentsinwhichPr6O11isadded.Whenexperimentingunder11gasesofCH3COCH3,C2H5OH.C6H5CH3,H2,NH3,CO,CO2CH4,C4H10,n—C6H14andn—C7H16,wefindthatthecomponentshaveselectivitytoCH3COCH3,C2H5OHandthattheidealamountofPr6O11inthecomponentsisaboutI.Owt%.TheexperimentsalsoshowthatwiththeincreaseoftheamountofPr6O11,theidealworkingtemperature,theresponseandrestorationtimedecrease.

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：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.