简介:AsystematicinvestigationofthemagneticandtransportpropertiesofTidopedLa0.67Ca0.33MnO3wasreported.TheTisubstitutionforMnionsresultsinareductioninferromagnetismandconductivity.Themetal-insulatortransitiontemperatureisclosetoCurietemperaturewhichdecreasesfrom274to82Kasxincreasesfrom0to0.17.ThemostimportanteffectofTidopingistointroducespinclustersinthesamplesduetothedistortionoflocallatticeandtheinhomogeneousmagneticstructureinducedprimarilybytherandomdistributionofMnions.Amaximummagnetoresistanceratioaslargeas90%in1Tat122Kwasobtainedforthesamplewithx=0.055,whichisfourtimeslargerthanthatobtainedforLCMOsampleat272K.Thereisaremarkablefield-historydependentMRinthecoolingprocessforthedopedsampleswhilesuchphenomenondisappearsinthewarmingrun.Theresistivityfollowswellthevariablerangehoppingbehaviorinparamagneticstate.Boththesizeeffectandspindependenthoppingofcarriersbetweenthespinclustersshouldbeconsideredinthissystem.
简介:Thenanosizedparticlematerialsofdoped-TiO2withY2O3werepreparedbymeansofsol-geltechniqueforuseinelectrorheological(ER)fluids,andtheircrystalstructuresweremeasuredbyX-raydiffraction(XRD)analysis.TocomparewiththepureTiO2,adistinctenhancementintheshearstressunderdcelectricfieldwasfoundbyusingsuchmaterials.Thiscanbeexplainedbytheincreaseofthedielectriclossanddielectricconstantatlowfrequency.TheeffectsofthecrystalstructureoftheparticlesonthedielectricpropertyandERperformanceofmaterialswereinvestigated.
简介:用柠檬酸溶胶-凝胶工艺制备出了LiV3O8化合物,并检测了其作为热电池阴极材料时的放电性能,干凝胶210℃焙烧所得的粉末颗粒疏松多孔,300℃时可变成结晶岩状,低温焙烧时出现了Li0.3V2O5和LiV2O5相,经650℃长时间保温后可转变为LiV3O8,模拟Li-B/LiCl-KCl/LiV3O8(或V2O5)热电池500℃放电试验表明,LiV3O8因具有良好的电子导电体和较低的Li+扩散极化,其放电较V2O5平稳,虽峰值电压略有降低,但可利用的比容量(电压降至峰值电压的75%或2.0V)均不低于V2O5;LiV3O8中掺入8%的P2O5时可提高小电流放电时的电压。
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简介:ThephotoluminescencepropertiesofBiTaO4∶Pr3+andBiTaO4atroomtemperaturewerestudied,andtheinfraredtransmissionanddiffusionreflectionspectraofBiTaO4weremeasured.ThephotoluminescencespectrumofBiTaO4peaksatabout420,440and465nm.Therehasanobviousexcitationbandfrom330to370nm.ThephotoluminescencespectrumofBiTaO4∶Pr3+consistsofthecharacteristicemissionofPr3+,anditsmainpeakisat606nmfrom3P0→3H6transitionofPr3+.Itsexcitationspectrumconsistsofthewidebandwithmaximumat325nm,thewidebandintherangeof375~430nm,andthecharacteristicexcitationofPr3+.Thebandsat325nmand375~430nmmaybefromtheabsorptionofthechargetransfertransitionofthetantalategroupanddefectenergylevelsinitsforbiddenband,respectively.ThereisenergytransferfromhosttoPr3+.BecauseboththehostdensityandphotoluminescencepeakintensityofBiTaO4∶Pr3+aresuperiortoPbWO4,BiTaO4∶Pr3+maybeapotentialheavyscintillator.
简介:VariousaffectingfactorsanddegradationmechanismwerestudiedonultrasonicdegradationofmethylorangeadoptingY2O3dopinganataseTiO2catalystpreparedinlaboratory.Intheexperiment,theUV-VISspectrophotometerwasusedtofollowandinspectthedegradationprocessofmethylorange.TheresultsindicatethattheultrasonicdegradationratiosofmethylorangeinthepresenceofanataseTiO2catalystaremuchbetterthanthosewithoutcatalyst.Moreover,thecatalyticperformanceofY2O3dopinganataseTiO2catalystisobviouslyhigherthanthatofanataseTiO2catalystwithoutdoping.TheoptimalconditionswereadoptedinthisworkandthedegradationandCODeliminationratioofmethylorangegotto98%and99.0%in90min,respectively.