简介:采用2步水热法合成了LaPO4∶Eu3+-Fe3O4复合材料.在LaPO4∶Eu3+-Fe3O4复合材料中,LaPO4∶Eu3+为单斜晶相,呈纳米棒状,纳米棒的直径和长度分别为20-100nm和0.2-1μm;Fe3O4为正交晶相、呈20-30nm的颗粒状,Fe3O4粒子紧紧附着在LaPO4∶Eu3+纳米棒的表面;样品的磁性和发光性质研究表明所合成的LaPO4∶Eu3+—Fe3O4复合材料既具有发光性质又具有磁性.
简介:Li4Ti5O12(LTO)/carbonnanotubes(CNTs)compositematerialissynthesizedbasedonasolid-statemethodbysand-milling,spray-dryingandcalciningat8508CunderN2flow.TheLTO/CNTssampleswith1wt%and3wt%weightratioofCNTsadditionandthepristineLTOsampleareprepared.TherateperformanceandthethermalstabilityofthesesamplesareinvestigatedbasedonLiMn2O4(LMO)/LTOfull-cell.TheresultsshowthattheweightratioofCNTsadditionhasdistincteffectonLTOperformances.ThecompositematerialsofLTOcompositedCNTshavebetterperformanceathigh-rateduetotheintercalationenhancementbyconductivenetworkofCNTs.Atsecond,theoverchargingtemperatureresponseofthecell’ssurfacewith1wt%CNTsadditionisthelowest.Theparticlesizedistributionismeasuredandthemostuniformparticlesareobtainedwith1wt%CNTsaddition.ThistrendcouldexplainthatthemediumquantityofCNTsisoptimaltoimprovetheheatandmasstransferandpreventtheproblemsofcrystallitegrowinginterferenceandaggregationduringthecalcinationprocess.
简介:Three-dimensional(3D)flowerlikehierarchicalZn2GeO4andMn2+-dopedZn2GeO4microstructureshavebeenpreparedbyafacilehydrothermalapproach.X-Raydiffraction(XRD),fieldemissionscanningelectronmicro-scopy(FESEM),transmissionelectronmicroscopy(TEM)andphotoluminescence(PL)spectrometrywereemployedtocharacterizethesamples.SuchflowerlikehierarchicalZn2GeO4microstructureswithanaveragediameterof3―4μmwerefoundtobeconstructedbyabundantsinglecrystallinenanorodsofabout90nmindiameter.TheluminescentpropertiesofZn2GeO4:xMnphosphorswithdifferentcontentsofMn2+asanactivatorwereinvestigated.TheMn2+-dopedsamplesshowedgreenluminescencecorrespondingtothed-dtransitionofMn2+undertheirradiationofUVlight.Theredshift(from531nmto538nm)inλemwithincreasingMn2+contentwasobservedintheluminescentspectra,whichshouldbeattributedtoaweakcrystalfieldbecauseofthesubstitutionofZn2+byMn2+atadistortedtetrahedrallatticesite.
简介:Pureandneodymium-dopedgadoliniumcalciumoxoboratecrystalsofhighqualityweregrownbytheCzochralskimethod.Theorientationofcrystalwaspreciselydetermined,andthesamplesformeasurementswereprepared.Throughsynchrotronx-raytopographyandhigh-resolutionx-raydiffractometry,thetwinstructurewasdiscovered.Somepropertiessuchasthefigureofmeritvalue,anddielectric,piezoelectric,andelasticconstantsweremeausuredalongwithadiscussionoftheanisotropyofthelaserproperties.
简介:
简介:Highlyefficientsheet-likeBiPO4/zeoliteandball-flower-likeBiPO4/zeolitehadbeensuccessfullysynthesizedbyastandardhydrothermalmethod.Theadditionofassistantreagentinthehydrothermalsystemispromisingtoobtainspecialmorphology.Theassistantreagent(EDTA)actsasagrowthmodifierofcrystal.Thepossibleformationmechanismsofsheet-likeBiPO4/zeoliteandball-flower-likeBiPO4/zeolitewereschematicallydiscussed.Adetailedstudyofsheet-likeBiPO4/zeoliteandball-flower-likeBiPO4/zeoliteimpactedonthephotodecolorationmethyleneblue(MB)solutionshowedthatthecompositehadahighlyreusableandstablepropertyforlong-runphotocatalyticapplication.
简介:TheGroupofEnergyMaterials(GEM)inIMPisengagedintheirradiationresponseofmaterialscandidatetoadvancednuclearenergysystems(GenIV,fusionreactors).Themajorprogressofresearchinourgroupin2016isintheirradiationhardening/embrittlementofoxide-dispersion-strengthened(ODS)ferriticsteelsandVanadiumalloys,andinthemechanismsunderlyingdamageproductioninsiliconcarbide(SiC)fibers.Abriefdescriptionisgivenasfollows.1.EffectoftheoxidenanoparticlesontheirradiationhardeningofODSferriticsteelsTheinfluenceofoxidenanoparticlesontheirradiationresistanceofODSferriticsteelsisacrucialissuefortheupgradeofODSsteels.
简介:Asafundamentalpropertyofnuclei,atomicmassesarewidelyusedinmanydomainsofscienceandengineering.Areliableatomicmasstablederivedfromtheexperimentaldata,wheretheatomicmassesandtherelevantexperi-mentalinformationcanbefoundconveniently,isinhighdemandbytheresearchcommunity.Tomeetthedemands,theAtomicMassEvaluation(AME)wasinitiatedin1950'sandaseriesofAMEmasstableshavebeenpublishedeversince.CurrentlytheAMEservestheresearchcommunitybyprovidingthemostreliableandcomprehensiveinformationrelatedtotheatomicmasses.ThenewatomicmassevaluationAME2016waspublishedintheMarchissueofChinesePhysicsCastwocom-plementarypapers[1;2].
简介:Poly(β-carboxyethylmethylsiloxane)-LiClO4andpoly(β-alkoxylethylmethylsiloxane)-LiClO4crosslinkedfllmshavebeenprepared.Theionicconductivityofthefilmsdependsonthepolymerspecies,concentrationoflithiumperchlorate,temperatureandcontentofcrosslinkingagent.Theeffectofhighpolarorganicsolvent1,4-butyrolactoneontheionicconductivityandmechanicalpropertiesofpoly(β-carhoxyethylmethylsiloxane)-LiClO4systemwasalsoinvestignied.
简介:Ionicconductivityvaluesforsegmentedpolyetherpolyurethaneurea(PEUU)complexeswithLiClO4weredeterminedandvaluesashighas~1.1×10-4S·cm-1at353Kand~1.0×10-5S·cm-1at306Kwereachieved.TheionicconductivitydatawereanalyzedusingtheVTF(Vogel-Tamman-Fulcher)equationandWLF(Williams-Landel-Ferry)typeequation.Valueshavebeenestimatedforthe"apparent"activationenergiesofiontransportfromVTFequationandtheylieintherange2.70—5.53kJ·mol-1.
简介:Anovelseriesofcalix[4]azacrownderivativeswiththereactionbetweencalix[4]azacrownandthedifferentfluorophorederivatives,whichmaybeusefulfluorescentreceptors,havebeensynthesizedandstructurallycharacterizedbyIR,~1HNMR,~(13)CNMRandMS.Fromtheiranalysisdata,itwasfoundthosecompoundsadoptedaconeconformation.
简介:LetMbeapositivequaternionicKhlermanifoldofdimension4m.Wealreadyshowedthatifthesymmetryrankisgreaterthanorequalto[m/2]+2andthefourthBettinumberb_4isequaltoone,thenMisisometrictoHP~(m).Thegoalofthispaperistoreportthatwecanimprovethelowerboundofthesymmetryrankbyoneforhighereven-dimensionalpositivequaternionicKahlermanifolds.Namely,itisshowninthispaperthatifthesymmetryrankofMwithb_4(M)=1isgreaterthanorequaltom/2+1form≥10,thenMisisometrictoHP~m.OneofthemainstrategiesofthispaperistoapplyamoredelicateargumentofFrankeltypetopositivequaternionicKhlermanifoldswithcertainsymmetryrank.
简介:Anovelquaternarymetalselenide,K_2CdSnSe_4,wassynthesizedviaamolten-saltreactionat550℃.Thecompoundhasaone-dimensionalstructurecontainingachainof_∞~1[CdSnSe_4]~(2-)anionsseparatedbyK~+cations.ThecrystalbelongstothespacegroupI-42m,withtheunitcellparametersa=0.80298(11)nm,b=0.80298(11)nm,c=0.69217(14)nm,α=β=γ=90°.Areflectancespectroscopystudyrevealsthenatureofthesemiconductorwithanenergygapof1.7eVforthecompoundandithasastrongopticalabsorptioninarangeof2—5eV.