简介:有一致的杆形状的单斜晶的LaPO4nanostructures被一个简单大音阶的第五音胶化方法成功地综合了。过程包含形成同类,透明,metal-citrate-EDTA胶化先锋,由锻烧列在后面支持胶化先锋的热分解产出LaPO4nanoparticles。他们的形态学和结构被XRD,TEM,TG-DSC和HRTEM描绘。结果显示单个单斜晶的阶段LaPO4nanorods乐意地在800点被获得吗?在3h以内。而且,做Eu3+的LaPO4nanocrystals的光致发光(PL)描述被执行。在PL性质上做内容的锻烧温度和Eu3+的效果详细被详细描述。房间温度光致发光(PL)描述表明光亮度以及到5D0-7F2的5D0-7F1的紧张比率高度依赖于锻烧温度,并且Eu0.05La0.95PO4nanophosphor与最强烈的排放显示出相对有希望的PL表演。
简介:InordertoimprovethehydrogenstoragepropertiesofLiBH_4-MgH_2composite,twodifferentkindsofNb-basedcatalysts,NbCandNbF_5,wereaddedtoLiBH_4-MgH_2compositebyballmilling,andtheeffectofcatalystsonhydrogenstoragepropertiesofthemodifiedLiBH_4-MgH_2systemwasinvestigated.TheexperimentalresultsshowthatLiBH_4-MgH_2compositeisatwo-stepdehydrogenationprocess,andNb-basedcompoundscanremarkablyenhanceitsdehydrogenationkinetics.Forthecompositewithoutadditionofcatalysts,thestartingdecompositiontemperatureforthefirstdehydrogenationstepisaround320℃,andthereisalongperiodofincubationtime(around220min)fortheoccurrenceoftheseconddecompositionstepevenathightemperatureof450℃.Itneedsmorethan10htocompletethedecompositionprocessandreleasearound9wt%H_2.Afteradditionof5mol%NbF_5,thestartingdecompositiontemperatureforthefirstdehydrogenationstepisaround150℃,thereisnoincubationtimefortheseconddecompositionstep,andittakesaround40mintocompletethesecondstepandreachesatotaldehydrogenationcapacityof9.5wt%.NbF_5hasbettercatalyticeffectthanNbC.Basedonthehydrogenation/dehydrogenationbehaviorsandstructuralvariation,themechanismofcatalyticeffectwasdiscussed.
简介:CastingtitaniumalloyTC4(ZTC4)afterhotisostaticpressing(HIP)isoneofthepreferredmaterialsinthefieldofaerospacemanufacturing.Inthispaper,HIPZTC4afteralong-termthermalexposurewasinvestigated.Inordertoevaluatethevariationofmechanicalpropertieswithservicetime,thetensilepropertiesofthisalloyafterexposureat400°Cfor100,500,and1,000hwereinvestigated.Microstructureofsampleswasobservedbythemeansofopticalmicroscopy(OM),scanningelectronmicroscopy(SEM),andtransmissionelectronmicroscopy(TEM).Tensiletestwascarriedoutunderdifferenttesttemperaturesandfractureappearancewasstudied.Theresultsshowthatthestrengthincreaseswithexposuretimeduetothehardera2(Ti3Al)phaseprecipitatedintheaphaseandsuperficialoxygenlayerformed,whichresultsinthefactthattheresistanceofcrackpropagationcouldbeincreasedandcracksfirstinitiatebetweensurfaceoxidationandthematrix.Besides,thetensiletemperaturealsohasasignificanteffectonthemechanicalpropertiesofHIPZTC4.Theyieldstrengthandtensilestrengthdecreasewiththeincreaseoftensiletemperature,whilethetotalelongationincreases.
简介:Carbon-coatedlithiummanganesesilicate(Li2MnSiO4/C)nanoparticlesweresynthesizedbypolyolprocess.X-raydiffraction(XRD)patternsoftheobtainedmaterialsexhibitagoodfitwiththatoftheLi2MnSiO4phase.Fieldemissionscanningelectronmicroscopy(FESEM)imagesoftheobtainedsamplesshowthattheparticlesizeisonlytensofnanometers.Thehighresolutiontransmissionelectronmicroscopy(HRTEM)analysisshowsthattheLi2MnSiO4nanoparticlesaresurroundedbyaverythinfilmofamorphouscarbon.Thecompositepreparedthroughpolyolprocessshowsgoodperformanceascathodematerialsinlithiumcellsatroomtemperature.ThechargecapacityoftheLi2MnSiO4/Csamplesis219mAh/g(about1.3Li+perunitformulaextracted),andthedischargecapacityis132mAh/g(about0.8Li+perunitformulainserted)inthefirstcycleinthevoltagerangeof1.5-4.8V.Agoodcapacitycyclingmaintenanceof81.8%after10cycleswasobtained.
简介:Dynamicsinpartialtransientliquidphasebonding(PTLPbonding)ofSi3N4ceramicwithTi/Cu/Timulti-interlayerwassystematicallystudiedthroughmicro-analysisofjointinterfaces.Theresultsshowthatgrowthofreactionlayerandisothermalsolidificationprocessiondoatthesametime.GrowthofreactionlayerandmovingofisothermalsolidificationinterfaceobeytheparaboliclawgovernedbythediffusionofparticipatingelementsduringthePTLPbonding.Coordinationoftheabovetwodynamicsprocessisdonethroughtimeandtemperature.Whenreactionlayerthicknessissuitableandisothermalsolidificationprocessisfinished,thehighbondingstrengthatroomtemperatureandhightemperatureareobtained.
简介:石墨材料为一节所有钒氧化还原作用流动电池被用作电极,并且电极被转变修改提高它的电气化学的行为的金属性的离子。合成电极高有的一块多孔的石墨比表面区域和高电流密度。金属性的离子改进了的转变修改的电极能催化V的催化作用行为(Ⅱ)-V(Ⅴ)氧化还原作用反应由周期的voltammograms出现了。这篇文章由电气化学的阻抗光谱学(EIS)学习了修改电极的阻抗,并且同意电极由Co~(2+)和Mn~(2+)修改了,这比修改thenon的电极有一个更低的电嗬转移电阻。平均粒子尺寸分发的效果在Warburg阻抗的斜坡被大粒子尺寸分发减少的更低的频率。Co~(2+)的电压效率修改了电极测试房间是81.5%,它比修改thenon的电极的高。
简介:SphericalLiFePO4andLiFePO4/Ccompositepowdersforlithiumionbatteriesweresynthesizedbyanovelprocessingrouteofco-precipitationandsubsequentcalcinationsinanitrogenandhydrogenatmosphere.TheprecursorsofLiFePO4,LiFePO4/CcompositeandtheresultantproductswerecharacterizedbyX-raydiffraction(XRD),scanningelectronmicroscope(SEM),andtheelectrochemicalperformanceswereinvestigatedbygalvanostaticchargeanddischargetests.TheprecursorscomposedofamorphousFe3(PO4)2·xH2OandcrystallineLi3PO4obtainedintheco-precipitationprocessinghaveasphere-likemorphology.ThesphericalLiFePO4derivedfromthecalcinationsoftheprecursorat700℃for10hinareductionatmosphereshowsadischargecapacityof119mAh·g-1attheC/10rate,whiletheLiFePO4/Ccompositewith10wt.%carbonadditionexhibitsadischargecapacityof140mAh·g-1.TheelectrochemicalperformancesindicatethattheLiFePO4/CcompositehasahigherspecificcapacityandamorestablecyclingperformancethanthebareolivineLiFePO4duetothecarbonadditionenhancingtheelectronicconductivity.
简介:采用溶胶-凝胶法,添加不同比例的Li3PO4助熔剂,合成Li1.3Al0.3Ti1.7(PO4)3锂离子固体电解质烧结片,采用X射线衍射、扫描电子显微镜研究合成产物的结构与形貌,采用循环伏安及交流阻抗技术研究添加不同摩尔分数的Li1.3Al0.3Ti1.7(PO4)3固体电解质烧结片的结构、氧化-还原电位、离子电导率和活化能。结果表明:添加与未添加Li3PO4助熔剂的Li1.3Al0.3Ti1.7(PO4)3烧结片具有相似的X射线衍射结果。添加Li3PO4的Li1.3Al0.3Ti1.7(PO4)3烧结片的空隙率较小,更为致密。添加Li3PO4对Li1.3Al0.3Ti1.7(PO4)3的氧化-还原电位影响不大。在所有添加Li3PO4助熔剂的Li1.3Al0.3Ti1.7(PO4)3烧结片中,添加1%(摩尔分数)Li3PO4的烧结片具有最高的离子电导率6.15×10-4S/cm和最低的活化能0.3142eV。
简介:3.基板白边白角(接上期)3.4解决方法如上面所说,造成基板白边角的因素很多,所以要防止基板白边角的产生,需采取综合性的措施,才能收到较好的效果。其中以控制粘结片的树脂流动性,选择合适的层压菜单最为关键。3.4.1控制粘结片的树脂流动性与粘结片的流动性密切相关的技术参数有:粘结片的树脂流动度、粘结片的树脂凝