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。

简介：PolycrystallineNd3+andLa3+co-dopedyttriananopowderNd3+:Y1.90La0.10O3fortransparentceramicswassynthesizedbyco-precipitationmethodusingoxalateacidastheprecipitantand(NH4)2SO4astheelectricalstabilizerunderultrasonicradiation.Nanopowderscalcinedatdifferenttemperatureswerecharacterizedwiththermalgravimetric-differentialthermalanalysis(TG/DTA),X-raydiffraction(XRD),transmittingelectronmicroscopy(TEM),energydispersivespectrometry(EDS)andspectralanalysistechniques.Th...

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简介：分别采用液-固和液-液掺杂方式向钼粉中引入氧化镧，用粉末冶金方法烧结出Mo合金。通过透射电镜和扫描电镜研究了不同掺杂方式制备的Mo—La2O3材料中第二相颗粒的粒度分布、形貌，以及钼合金的断口形貌。试验结果表明液-液掺杂方法有利于细化、分散La2O3；液-液掺杂试样的断裂韧性优于液-固掺杂试样。并通过位错塞积理论讨论了La2O3的粒度分布对钼合金性能的影响。

简介：TwonovelwashcoatsCe0.8Zr0.15La0.05OδandCe0.8Zr0.2O2waspreparedbyanimpregnationmethod,whichactedasahostfortheactivePdcomponenttopreparePd/Ce0.8Zr0.15La0.05Oδ/substrateandPd/Ce0.8Zr0.2O2/substratemonolithiccatalystsfortoluenecombustion.ThewashcoatswascharacterizedbyX-raydiffraction(XRD),Ramanspectroscopy,Brunauner-Emmett-Teller(BET),andH2-temperature-programmedreduction(H2-TPR).Theresultindicatedthatboththewashcoatshadstrongvibration-shockresistanceaccordingtoultrasonictest.DopingLa3+intoCeO2-ZrO2solidsolutioncouldgeneratemoreoxygenvacancies,andcouldinhibitthesinterofCeO2-ZrO2solidsolutionwhencalcinedathightemperatures(800,900and1000°C).ThewashcoatCe0.8Zr0.15La0.05Oδhadmuchbetterredoxproperties.ThereductivetemperatureofCe4+speciesshiftedtolowtemperatureby60°Cwhenthewashcoatscalcinedathightemperatures(800,900and1000°C).ThePd/Ce0.8Zr0.15La0.05Oδ/substratemonolithiccatalystcalcinationat500°Chadthebestcatalyticactivityandthe95%tolueneconversionatatemperatureaslowas190°C.Whencalcinedatlowtemperature(500and700°C),thecatalyticactivityhaslittleimprovement,however,whencalcinedathightemperature,thecatalyticactivityofPd/Ce0.8Zr0.15La0.05Oδ/substratemonolithiccatalystshadsignificantimprovement.Ascatalystwashcoat,theCe0.8Zr0.15La0.05OδhadbetterthermalstabilitythanthewashcoatCe0.8Zr0.2O2,thedevelopedPd/Ce0.8Zr0.15La0.05Oδ/substratemonolithiccatalystinthisworkwaspromisingforeliminatingVolatileorganiccompounds.

简介：ThestructureandhydridingperformanceofLa0.6Nd0.4Ni4.8Mn0.2Cux(x=0～0.4)alloyswereinvestigatedinordertodevelopsuitablematerialsformetalhydrideairconditioner.TheeffectofCuadditiononthecrystalstructure,equilibriumpressure,hydrogencapacityandhysteresisaswellashydrogenabsorption/desorptionkineticsweresystematicallystudiedbyusingthemeasurementofP-Cisotherms,X-raydiffractionandscanningelectronmicroscopy.AstheamountofCuincreases,theplateaupressureincreasesandhydrogenabsorption/desorptionkineticsisimproved,buttheeffectivehydrogenstoragecapacitydecreases.Itisshownthatvariationsinthebasalplaneparameteracanbeusedasanindicationfortheplateaupressurechanges.Withtheincreaseofparametera,theplateaupressuredecreases.ForLa0.6Nd0.4Ni4.8Mn0.2Cux(x=0～0.4)alloysthereisarelationshipbetweentheeffectivehydrogenstoragecapacitiesandtheratiosoftheirunitcellparameterscanda.Theeffectivehydrogenstoragecapacitydecreaseswithincreaseofa/c.

简介：La15Fe77B8hydrogenstoragealloyswerepreparedusingavacuuminduction-quenchingfurnace.TheresultsofX-raydiffraction(XRD)andscanningelectronmicroscopy(SEM)suggestedthatLa15–xSmxFe2Ni76Mn5B2(x=0,2,4,6)alloyshadmultiphasestructureincludingthemainLaNi5phase,La3Ni13B2phaseand(Fe,Ni)phase.WiththeincreasingsubstitutionofSmforLa,themainphasestructureofalloysdidnotchange,whiletheunitcellvolumesdecreased,thecyclestabilitywasimprovedandthemaximumdischargecapacitydecreased,butthelowtemperaturemaximumdischargecapacityofthesamesubstitutionalloywasgraduallyapproachingthemaximumdischargecapacityatroomtemperature,whichshowedthatLa15Fe77B8hydrogenstoragealloysofthepartialsubstitutionofSmforLahadbetterlow-temperaturedischargeability(LTD).Forthesamesubstitutionalloys,self-dischargecharacteristicsandcyclestabilityatlowtemperaturewerebetterthanthatatroomtemperature.Furthermore,thehigh-ratedischargeability(HRD)andtheexchangecurrentdensityI0firstincreasedandthendecreasedwiththeincreasingofSmcontent,whereasthehydrogendiffusioncoefficientDinalloybulkdecreasedgradually,whichindicatedthatappropriatesubstitutionofSmforLaimprovedtheelectrochemicalkineticspropertiesofthealloys.TheHRDwasmainlydominatedbythecharge-transferrateonthealloysurface.

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：Er~（3＋）andLa~（3＋）codopedY_2O_3nanocrystallinepowdersweresynthesizedbygelcombustionmethodandcharacterizedwiththermalanalysis,X-raydiffraction（XRD）,transmissionelectronmicroscopy（TEM）,high-resolutionTEM（HRTEM）techniquesandfluorescencespectroscopy.Afterbeingcalcinedat1200oC,the（Y_（1–x）La_x）_2O_3：Er~（3＋）powderswereconfirmedtobecubicY_2O_3phasewiththecrystallinegrainsizeintherangeof20–40nm.TheEr~（3＋）emissionat1.53μmfromthe~4I_（13/2）→~4I_（15/2）transitionwasobserved,whichwasfoundtobeenhancedbyintroducingLa~（3＋）ions.SuchenhancementcouldbeattributedtotheadjustmentofEr~（3＋）ions＇localenvironmentbythecodopingofLa~（3＋）ions,leadingtotheincreasedgroundstateabsorptioncrosssectionofEr~（3＋）ions.

简介：采用溶胶喷雾干燥-煅烧还原方法制备超细/纳米W-La2O3复合粉末，将粉末压制成形后在1950℃烧结，制备La2O3弥散强化钨合金，检测合金的密度与强度，并采用SEM对超细粉末形貌、合金的组织结构、断口形貌进行分析，结果表明：随La2O3加入量增加，粉末颗粒显著细化，W-0.7%La2O3复合粉末的粒径仅为0.1μm；制备的W-La2O3超细/纳米复合粉末具有很高的烧结活性，烧结后，合金最高相对密度达到99.1%；La2O3均匀弥散分布于钨晶界，抑制钨合金的晶粒长大，提高材料的强度，W-0.7%La2O3合金中钨平均晶粒尺寸仅为8.7μm，抗弯强度达到548MPa；合金的断裂形式表现为穿晶-沿晶共有的复合断裂形式。

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简介：Duetotheremarkablemagnetoresistance(MR)effectonperovskite-typemanganite,magnetoelectronicsandspintronicshavebecomeattractivesubjectsofexperimentalandtheoreticalinvestigationsfortheapplicationpurpose.(La0.9Nd0.1)2/3Ca1/3Mn1-xFexO3(x=0,x=0.05)werepreparedsuccessfullybysol-gelmethod.Thestructure,magneticproperties,andtransportpropertiesofthecompoundswereinvestigated.Themagnetoresistanceeffectdependsonthecompositionandthetemperature.XRDpatternsshowthatthecompoundisasinglephasepolycrystalwithpseudocubicstructure.Alargenegativeisotropicmagnetoresistanceeffectinthesampleswereobservedatlowtemperatureregion.ThemaximumMRofthesampleswas77%and97%,respectively.Itwasmostlikelyduetothescatteringorthetunnelingtransportofspin-polarizedcarriersinlatticeunderstrongmagneticfield.

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简介：近日，内蒙古科技厅组织专家组对包头稀土研究院承担的一项科技型中小企业技术创新基金项目“高功率La-Fe-B系贮氢电极合金的应用开发研究”进行了验收，

简介：采用电磁感应悬浮炉制备La0.55Pr0.05Nd0.15Mg0.25Ni3.5-xCoxAl0.25（x=0,0.1,0.2,0.3,0.4）系列合金,研究Co含量对合金的相结构、吸放氢性能和电化学性能的影响。研究结果表明,该系列合金主要由LaNi5、Nd2Ni7相组成。当Co含量大于0.2时,合金中出现La2Ni7相。压强-吸氢量-温度（Pressure-Content-Temprature）测试显示在303K温度下,合金具有良好的吸氢性能,当x=0.4时合金的最大吸氢量为1.29（质量分数,%）。电化学测试表明：随x值变化,合金电极的最大放电容量分别为340.0（x=0.0）、346.6（x=0.1）、370.0（x=0.2）、320.0（x=0.3）和346.6（mA.h）/g（x=0.4）;随Co含量增加,合金电极容量保持率不断增加,高倍率放电性能先增加后减小,循环伏安曲线、氢在合金体中的扩散系数D共同反映了合金电极的动力学特性。