简介:Glasseswiththecompositionof65GeO212Ga2O3-10BaO-8Li2O-5La2O3(molarratio)dopedwith1.526wt.%,3.006wt.%,5.836wt.%,11.028wt.%,and15.678wt.%Tm2O3,respectively,werefabricatedbyconventionalmeltingmethod.AccordingtotheabsorptionspectraandtheJudd-Ofelttheory,theJ-Ostrengthparameters(Ω2,Ω4,Ω6)werecalculated,withwhichtheradiativetransitionprobabilities,branchingratiosandradiativelifetimeswereobtained.Theinfraredemissionspectra(with808nmLDexcitation)at~1.47and~1.8μmofvariousconcentrationsofTm3+-dopedglasseswerestudied.Theemissionintensityat~1.8μmreachedtothemaximumwhentheTm2O3-dopingconcentrationwasneartobe~3.006wt.%(1.0mol.%),andthendecreasedasdopingconcentrationincreasedfurther.Themechanismofthefluorescenceintensitychangewasexplainedwiththecross-relaxationeffectandtheconcentrationquenchingeffectofTm3+.Meanwhile,accordingtoMcCumbertheory,theabsorptionandemissioncross-sectionscorrespondingtothe3F4→3H6transitionsofTm3+at1.8μmwasobtained.ForTm3+-dopedgermanateglasses,themaximumemissioncross-sectionreachedavaluehigherthanthatre-portedforfluorozircoaluminateglasses.Itisexpectedtobeafavorablecandidatehostfor~2.0μmmid-inflatedlaserbecausetheglassshowsfavorableopticalspectra.
简介:TheeuropiumionsdopedMMoO_4(M=Sr,Ba)nanophosphorsweresuccessfullysynthesizedviaafacilehydrothermalmethodusingisopropanol.Therelationshipbetweenphosphorcrystallinephase,morphology,photoluminescentpropertiesandhexadecyltrimethylammoniumbromide(CTAB)concentration,pHvalueinprecursorsolutionwasinvestigated.TheresultsindicatedthatthemorphologyandphotoluminescentpropertieswerestronglyinfluencedbyCTABconcentrationandpHvalueinprecursorsolution.InSrMoO_4:Eu~(3+)hosts,thephosphorsurfacetendedtobecomesmootherastheconcentrationofCTABwasincreased;whileparticlestendedtoagglomerateasincreasingpHvalue.TherelativeintensityratioofchargetransferbandtoEu~(3+)characteristicemissionpeaksofMMoO_4:Eu~(3+)(M=Sr,Ba)waschangedasCTABconcentrationandpHvaluechanged.TheemissionspectraofMMoO_4:Eu~(3+)(M=Sr,Ba)couldbeadjustedbyCTABconcentrationandpHvalueduetotheirimpactsonthestructure.ItwasimportantthatthedifferentmorphologiesandphotoluminescentpropertiesofMMoO_4:Eu~(3+)(M=Sr,Ba)couldbeobtainedbythefacilehydrothermalmethodandmodulatedbychangingCTABconcentrationandpHvalue.
简介:Thenoveleomplexesofalkaliandrareearthmetalwithperiodatehavebeenpreparedforthefirsttime.ChemicalanalysisindicatesthatthecompositionofthecomplexesisM2LnIO6·xH2O(M=Li,Na,K;Ln=Pr,Tb),andallofthecomplexeshavebeencharacterizedbyUV-Visible,IRspectroscopicstudies,susceptibilitymeasurementsandthermalanalysis.
简介:TheLa-CosubstitutedSr_(1–x)La_xFe_(12–x)Co_xO_(19)(x=0–0.5)ferriteswithappropriateBi_2O_3additivewerepreparedbyconventionalsinteringmethodandmicrowavesinteringmethodatlowsinteringtemperaturescompatiblewithLTCC(lowtemperatureco-firedceramics)systems,andtheirsinteringbehaviorwaschieflyinvestigated,includingthecrystalstructure,saturationmagnetizationMs,magneticanisotropyfieldHa,intrinsiccoercivityHci,andCurietemperatureTC.ExperimentresultsclearlyshowedthatthepureM-typecrystalphasewassuccessfullyobtainedwhentheLa-Cosubstitutionamountxdidnotexceed0.3.However,thesingleM-typephasestructuretransformedtomultiphasestructurewithfurtherincreasedx,wheretheM-typephasecoexistedwiththenon-magneticphasesuchasα-Fe_2O_3phase,La_2O_3phase,andLaCoO_3phase.AppropriateLa-CosubstitutionimprovedtheMs(〉62emu/g),Ha(〉1400kA/m),andHci(〉320kA/m)fortheferriteswithxvaryingfrom0.1to0.3,buttheTCdecreasedwithincreasingsubstitutionamount.Moreover,themicrowavesinteredferritescouldprovidelargerHciandsimilarMscomparedwiththeconventionalsinteredferrites.
简介:La公司代替了M类型钡铁酸盐(欺骗)由传统的稳固的状态被准备在低温度(1173K)的方法和sintered。X光检查衍射(XRD),扫描电子显微镜学(SEM)和颤动的样品磁强计(VSM)被采用在样品的结构和磁性上调查La公司的影响。由在为在空中的6h的1173K的sintering,有Ba(LaCo)xFe122xO19(x=0.00.5)的化学作文的单个阶段M类型钡铁酸盐被形成。M-H曲线证明钡铁酸盐的磁性被La公司替换显然完成。浸透磁化(女士)和coercivity(Hc)分别地到达了65.15Am2/kg和4165Oe的最大的价值。这行为被归因于La公司替换和粒子尺寸的地点。SEM表明铁酸盐粒子的形状被La公司替换影响。