简介:以CH3COOLi·2H2O和锐钛矿型TiO2为原料,通过直接融盐法合成锂离子电池负极材料Li4/3Ti5/3O4,考察合成条件对材料性能的影响,并通过X射线衍射仪(XRD)和扫描电镜(SEM)对样品进行物相和形貌分析。结果表明,先在70℃保温5h或10h,再在800℃煅烧2h可得到纯相的Li4/3Ti5/304粉末,平均粒径在300nm左右,且粒径分布均匀。充放电测试表明在70℃保温5h、800℃煅烧2h得到的样品具有最优异的电化学性能。以0.1C倍率充放电,其首次放电容量达到172(mA.h)/g,接近理论容量,20次循环后,容量仍保持在140(mA·h)/g。与传统的固相法相比,用直接融盐法得到的材料具有较大的锂离子扩散速率、高倍率性能和循环可逆性。
简介:ThispaperistodiscussthesensingcharacteristicsofSnO2semiconductorcomponentsinwhichPr6O11isadded.Whenexperimentingunder11gasesofCH3COCH3,C2H5OH.C6H5CH3,H2,NH3,CO,CO2CH4,C4H10,n—C6H14andn—C7H16,wefindthatthecomponentshaveselectivitytoCH3COCH3,C2H5OHandthattheidealamountofPr6O11inthecomponentsisaboutI.Owt%.TheexperimentsalsoshowthatwiththeincreaseoftheamountofPr6O11,theidealworkingtemperature,theresponseandrestorationtimedecrease.
简介:Afacilecatalysis-freemethodwasutilizedtosynthesizefunctionalneodymiumhexaboride(NdB6)nanowiresofsinglecrystalusingNdpowdersandBCl3asstartingmaterials.TheXRDpatternconfirmedthatasinglephaseNdB6couldbeobtained.Raman-spectraelucidatedtheactivevibrationalmodesofthehexaborides.TheTEMimagesclearlyshowedthatthehexaboridesweresubmicroninsizewithacubicmorphology.Thefieldemissionoftheseone-dimensionalNdB6nanowiresshowedalowfieldemissionturn-on(5.55V/μmatacurrentdensityof10μA/cm2),andhighcurrentdensitywithafieldenhancementfactorof1037.TheemissioncurrentdensityandtheelectricfieldfollowedtheFowler-Nordheim(F-N)relationship.Thegoodperformanceforfieldemissionwasattributedtothesingle-crystallinestructureandthenanowiregeometry.
简介:MeltspinningtechnologywasusedtopreparetheMg2Ni-type(Mg24Ni10Cu2)100–xNdx(x=0,5,10,15,20)alloysinordertoobtainananocrystallineandamorphousstructure.TheeffectsofNdcontentandspinningrateonthestructuresandelectrochemicalhydrogenstorageperformancesofthealloyswereinvestigated.ThestructurecharacterizationsofX-raydiffraction(XRD),transmissionelectronmicroscopy(TEM)andscanningelectronmicroscopy(SEM)linkedwithenergydispersivespectroscopy(EDS)revealedthattheas-spunNd-freealloydisplayedanentirenanocrystallinestructure,whereastheas-spunNd-addedalloysheldananocrystallineandamorphousstructureandthedegreeofamorphizationvisiblyincreasedwiththerisingofNdcontentandspinningrate,suggestingthattheadditionofNdfacilitatedtheglassformingoftheMg2Ni-typealloy.TheelectrochemicalmeasurementsindicatedthattheadditionofNdandmeltspinningimprovedtheelectrochemicalhydrogenstorageperformancesofthealloyssignificantly.Thedischargecapacitiesoftheas-castandspunalloysexhibitedmaximumvalueswhenNdcontentwasx=10,whichwere86.4,200.5,266.3,402.5and452.8mAh/gcorrespondingtothespinningrateof0(As-castwasdefinedasthespinningrateof0m/s),10,20,30and40m/s,respectively.Thecyclestability(S20,thecapacitymaintainrateat20thcycle)oftheas-castalloyalwaysrosewiththeincreasingofNdcontent,andthoseoftheas-spunalloysexhibitedthemaximumvaluesforNdcontentx=10,whichwere77.9%,83.4%89.2%and89.7%,correspondingtothespinningrateof10,20,30and40m/s,respectively.
简介:采用气氛烧结技术制备NiFe2O4-xNiO复合陶瓷材料(x为复合陶瓷中NiO的质量分数,%。x=0、5、10、17、25),并以该材料作阳极进行960℃的铝电解实验。分析烧结体的显微结构和物相组成以及电解试样的表层形貌与成分,研究NiO的添加对NiFe2O4陶瓷烧结性能和电解腐蚀性能的影响,并对该材料的烧结机制和熔盐腐蚀行为进行探讨。结果表明:氮气气氛下1300℃烧结的NiFe2O4-NiO复合陶瓷存在NiO和NiFe2O4两种物相,NiO相含量高于理论值;NiFe2O4陶瓷的相对密度为98.54%,添加NiO后复合陶瓷材料的相对密度有所下降,但仍保持在95%以上;电解过程中阳极表面形成不含NiO相的致密保护层,阻止电解质熔盐的渗透;保护层厚50~80μm,为含Al的尖晶石NiFe2O4相;随着NiO含量增加,阳极表面的致密层变得越发不平整。
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简介:Thesimplemodelfor4f-5dtransitionsoflanthanideionsincrystalswasextendedtodealwiththecaseoftheoctahedralcrystalfield,whereforthet2componentof5dorbitalsthespin-orbitinteractioncouldnotbeneglectedduetoincompletequenchingofthe5dorbitalangularmomentum.Theenergylevelsforthe4fN-15dconfigurationandtherelativelinestrengthsforthe4fN4fN-15dtransitionwerecalculatedindetail.Theresultwasappliedtotheinterpretationofthelow-temperature4f-5dexcitationspectrumofCs2NaYCl6∶Tb3+.
简介:BulknanocrystallineSmCo6FesinteredmagnetwaspreparedbySparkPlasmaSinteringtechnique(SPS).XRDpatternsshowthatthemagnetexhibitsastableTbCu7structure.TEMobservationindicatesthatthemicrostructureofthemagnetiscomposedofSmCo6Fesinglephasegrainswithanaveragegrainsizeof30nm.Magneticmeasurementshowsthatunder9Tmagneticfield,thecoercivityofthemagnetreaches1.12T;thesaturationmagnetizationandtheremanenceare1.13and0.67T,respectively.Themagnethasa(BH)maxof75.6kJ·cm-3.