简介:La1.5Mg17Ni0.5hydrogenstoragematerialswerepreparedbyhydridingcombustionsynthesis(HCS)andmechanicalalloying(MA)methodrespectively.TheexperimentalresultsshowthatthehydrogenabsorptionpropertiesofLa1.5Mg17Nio.5preparedbyMAarebetterthanthatbyHCS.La1.5Mg17Nio.5preparedbyMAcanabsorb6.73mass%hydrogenat523Kwithin1min,and4.92mass%hydrogenat423K.TheimprovementofhydridingpropertiesofLa1.5Mg17Ni0.5alloypreparedbyMAcanbeascribedtotheformationofnano-crystallineanddefectsduringthemechanicalalloying.
简介:
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: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:有一致形态学的新奇红射出的K2(Ge,Si)F6:Mn4+黄磷被一起沉淀方法综合。纯K2有P636阶段>除P3m1空间组以外的mc空间组就被Si的加入在K2在房间温度的GeF6根据XRD描述。薄片状的显示出的SEM图象和为K2GeF6:Mn4+和K2(Ge,Si)F6:Mn4+黄磷分别地。光致发光刺激(PLE)和光致发光(PL)在K2GeF6:Mn4+和K2(Ge,Si)F6:Mn4+系统。并且K2有Si的GeF6:Mn4+显示出一座强壮的山峰。同时水晶的地包围Mn4+变化能在这个氟化物系统影响腐烂时间。带的设备的颜色范围基于K2(Ge,Si)F6:Mn4+和K2分别地,GeF6:Mn4+到达了多达94.58%NTSC(国家电视标准委员会)和94.386%NTSC那基于氮化物红黄磷比那高得多。在K2(Ge,Si)F6:Mn4+黄磷的所有这些原来的特征作为为改善灯光和常规白LEDs的显示质量的红黄磷为潜在的应用是合乎需要的。
简介:Metalsilver(Ag)wasaddedintoSm0.5Sr0.5CoO3(SSC)bynitratepyrolysismethodtoobtainporouscathodematerial(SSC-Agx)forSOFC.ThecompositephasesinthesematerialsofSSC-AgxwereidentifiedbyX-raydiffraction.ThemicrostructureofanelectrodeonCe0.sSm0.2O1.9intermediatetempera-tureelectrolytebyspraymethod,polarizationcurveandtheimperaturepedancespectraatlowandintermediate(500-800℃)wereinvestigated.Theresultsshowthatthematerialcontaining20%Agexhibitsthebestelectrochemicalproperties,itstotalimpedanceofcathodeisonly1/11ofSSCat600℃,andaquarterofSSCsat750℃.Thecompositetech-niqueofcathodeSm0.5Sr0.5CoO3addedwithAgisanefficientmethodtoimprovethecathodeperformanceofSOFCsoperatingintherangeofintermediatetempera-ture.
简介:采用高温固相法合成尖晶石LiMn2O4,并以化学沉积方式对其进行包覆氧化钴的表面处理。通过X射线衍射(XRD)、扫描电镜(SEM)等技术对表面处理前后的LiMn2O4进行表征,分析了表面处理后LiMn2O4物理特性的变化,并结合电化学性能测试,研究了表面处理及其工艺和条件对LiMn2O4电化学容量与循环性能的影响。结果表明,表面处理后LiMn2O4循环性能显著提高。随氧化物含量的增加,循环性能提高,容量降低。未经表面包覆的LiMn2O4首次充放电容量为108.13mAh/g,50次循环充放电后容量衰减26.3%。500℃加热处理的表面包覆0.5%、2%氧化钴的LiMn2O4首次循环放电容量各为118.38mAh/g、115mAh/g,经过50次充放电循环后,容量分别降低8%、7%。
简介:
简介:ThephotocatalystsK4Nb6017andK4Nb6017dopedwithFe^3+andCr^3+werepreparedbysolidstatereactionandwerecharacterizedbypowderx-raydiffraction,UV-visdiffusivereflectanceandscanningelectronmicroscopy.ThephotocatalyticactivityofK4Nb6O17andK4Nb6O17dopedwithFe^3+,Cr^3+wereinvestigatedwithmethanolaselectrondonorandPtaspromotercatalystunder+400nmUVirradiation.Thedifferenceofphotocatalyticactivitybetweenthemwasalsodiscussed.TheindividualrateofhydrogenevolutionfortheK4Nb6O17,Fe-K4Nb6O17andCr-K4Nb6O17asphotocatalystsare5.35,5.00,6.25mmol·L^-1.h^-1respectively.
简介:FluorescencespectraofSm2+andEu2+→Sm2+energytransferwerestudiedinSrB4O7.Thereappearsonlyfluorescencefrom5D0transitionofSm2+at77K.Thevibroniclinesassociatedwith5D0→7F0transitionwereobserved.Thethermalpopulationtoupperstatesof5D1and4f5dlevelsfrom5D0givesriseto5D1→7FJand5d→4fradiativetransitionsofSin2+athighertemperature.
简介:Organicsubstancesuchassolventandresin'seffectonluminescentcapabilityofSrAl2O4:Eu2+,Dy3+phosphorwasstudied.Someorganicsolventsandresinswereselectedforexperimentation.TheresultsindicatethatthoseorganicsolventswillnothavenegativeeffectontheappliedcapabilityofSrAl2O4:Eu2+,Dy3+phosphor.Adoptingtheorganicresinsandcoveringmethod,theafterglowluminanceofSrAl2O4:Eu2+,Dy3+phosphorwasincreasedby85.01%and82.51%.
简介:Ca-dopedBaMgAl10O17:Eu2+,Mn2+(BAM)bluephosphorsweresynthesizedbyfluxassistedsolid-statereactionmethodusingCaF2andBaF2asco-flux.GooddispersityandparticlesizehomogenizationofhexagonalpurephaseBAMwereobtainedbysinteringat1400℃.TheeffectsoftheCa2+ionscontentonthestructure,morphologyandphotoluminescencepropertiesofthephosphorswerestudied.TheresultsindicatedthattheincorporationofCacoulddecreasethelatticeconstant,improvethehomogeneityanddispersityandenhancethephotoluminescence(PL)intensityofthephosphoreffectively.TheoptimumBa0.86Ca0.04Mg0.97Al10O17:0.1Eu2+,0.03Mn2+PLintensitywasenhancedforabout30%andrelativebrightnesswasimprovedabout4%.Furthermore,thesynthesizedBAMandcommercialBAMphosphorswereannealedfor30minat600oCinair.TheCa-dopedphosphorshadstrongeremissionintensity,higherbrightnessandbetterchromaticitystabilitythanthatofthecommercialphosphor.TheseresultsindicatedthatCa-dopedbluephosphorshadgoodpotentialapplicationsinthecommercialtricolorfluorescentlampsaswellasinotherdisplayandlamps.