简介:Inthiswork,asimpleandfacileone-potoleylaminesolvothermalsyntheticmethodwasdevelopedtosynthesizeCu_2ZnSnS_4(CZTS)nanocrystals.AndtheCu_2ZnSn(S,Se)_4(CZTSSe)thinfilmswerepreparedbyselenizingCZTSnanocrystals.TheobtainedCZTSnanocrystalsandCZTSSefilmswerestudiedusingX-raydiffraction(XRD),transmissionelectronmicroscopy(TEM),scanningelectronmicroscopy(SEM),energy-dispersiveX-rayspectroscopy(EDX),andultraviolet–visiblespectrophotometer(UV–Vis).TEMresultsshowthatthesphere–likeCZTSnanoparticleswithdiameterbetween12and35nmarepolydispersed.XRDstudiesindicatethatthepreparedCZTSnanocrystalsformkesteritecrystalstructure,andtheCZTSSefilmswithkesteritecrystalstructurearealsoobtainedattheannealingtemperaturesof500and550°C.Inparticularafterannealingat500°Cfor20min,theCZTSSefilmexhibitsasmooth,uniform,crack-free,andlarge-grainedtopographyandpossessesCu-poorandSn-richcomposition.Moreover,itshowsstrongopticalabsorptionfromvisibletonear-infrared(IR)region,anditsopticalbandgap(Eg)isfoundtobeabout1.44eV.
简介:ElectrocrystallizationMechanismofTungsteninMoltenKF-B_2O_3-K_2WO_4WenZhenhuanandLiGuoxun文振环,李国勋(GeneralResearchInstiiuteforNo...
简介:在H2SO4-Fe2(SO4)3体系中研究载金黄铁矿的浸出动力学,探讨反应温度、Fe3+浓度、硫酸浓度、搅拌速度等对黄铁矿浸出的影响规律。结果表明:在H2SO4-Fe2(SO4)3体系中,在30~75°C下黄铁矿浸出过程主要受化学反应控制Fe3+浓度与黄铁矿的浸出呈正相关,通过Arrhenius经验公式求得浸出表观活化能为51.39kJ/mol。EDS与XPS分析结果表明:黄铁矿氧化过程中硫的氧化经一系列中间形态,最终被氧化成硫酸根,并伴有部分元素硫生成,符合硫代硫酸根氧化路径机理。
简介:TheeffectofyttriaonthesolidreactionmechanismofaCaHPO4·2H2O+CaCO3systematdifferenttemperatureswasexperimentallystud-ied.Thesampleswithandwithoutyttriaweresubjectedtothermogravimetric/differentialscanningcalorimetrymeasurement.ThesampleswereheattreatedatthetemperaturescorrespondingtothepeaksontheDSCspectra,andtheresultedphasecompositionswereidentifiedbyX-raydiffraction.Thetransformationmechanismwasdeducedbycomparingthephasesobtainedatdifferenttemperatures.Theresultsshowthatthetransformationsatbelow1073Karenotaffectedbyyttria,butallthoseatabove1073Karecompletelyaltered.Theformationtem-peratureofhydroxyapatitedecreasesby134K,andthedecompositiontemperatureincreasesby38K.ThepolymorphoustransformationofCa3(PO4)2fromβphasetoαphaseincreasesby47K.Thethermodynamicpropertiesofthetransformationsatabove1073Karealsomodi-fiedbytheadditionofyttria;thatis,theendothermalpeaksaresubstitutedbyexothermalpeaks.
简介:Fe2O3和ZnO的粉末混合物是在一家高精力的行星的球工厂的milled综合ZnFe2O4和X光检查粉末diffractometry被用来获得阶段,雏晶尺寸和Fe2O3和ZnFe2O4的microstrain的相对内容。Fe2O3的格子常数被房间精炼方法获得。macrokinetics和事的结构进化被学习,结果证明ZnFe2O4的mechanochemical合成的动力学过程适合Avrami-Erofe'ev模型并且被成核生长机制,和结构的macrokinetics理论在燃烧合成研究控制区域能被用来也描述运动过程。
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:ThelongafterglowSrAl2O4:Dy,Euphosphorisliabletohydrolyzeinwaterwithdeteriorationoftheluminescentproperty.SrAl2O4:Dy,Euphosphorswerethereforeheatedat60-90℃inTEOSsoltoformasurfacegelandthenheat-treatedat400℃toobtainSiO2coatedphosphors.ObservationbyTransmissionElectronMicroscope(TEM)andX-rayphotoelectronspectroscopy(XPS)showsthatathinsilicafilmformsonthesurfaceofthephosphors.Thecoatingprocedurecanbeillustratedbyafour-stepprocessandthetransparentsilicafilmcansuppressthehydrolysisprocess,sothattheluminescentpropertiesofthephosphorsareunimpairedorevenbetter.
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:Nb-24Ti-18Si-2Al-2Hf-4CrandNb-24Ti-18Si-2Al-2Hf-8Cralloyswerepreparedbyarcmeltinginawater-cooledcrucibleunderargonatmosphere.Microstructuralcharacteristicsandoxidationresistanceofthealloysat1250℃wereinvestigated.Theresultsshowthat,whentheCrcontentis4at%,themicrostructuresconsistof(Nb,Ti)_(ss)andNb_5Si_3;asCrcontentincreasesto8at%,C14LavesphaseCr_2Nbisformed.Theisothermaloxidationtestsshowthattheoxidationkineticsofthetwoalloysfollowsimilarfeatures.Theweightgainsofthetwoalloysafteroxidationat1250℃for100hare235.61and198.50mg·cm~(-2),respectively.Duringoxidation,SiO_2,TiO_2,Nb_2O_5andCrNbO_4areformedatfirst.Then,Ti_2Nb_(10)O_(29)isformedafteroxidationfor20minandbeginstochangeintoTiNb_2O_7astheoxidationproceeds.SiO_2isformedassolidstateatfirstbutlaterevolvesintoglassystatetoimprovethecohesionofthescale.Afteroxidationfor100h,oxidationproductsconsistofSiO_2,TiNb_2O_7,Nb_2O_5andCrNbO_4.
简介:pH价值和Y2Y23-SiO2(Y-Si)泥浆>为Ti-6Al-4V投资扔的脸上衣的O3粉末和硅石大音阶的第五音被测量。Y-Si脸上衣系统做的壳的热行为被微分扫描热量计(DSC)调查,热gravimetric(TG)分析与集体spectrometry(MS)结合了,并且阶段转变被X光检查衍射(XRD)决定。热力量,剩余力量,线性扩大系数,和壳的穿的抵抗性能也被测试。微观结构和相互作用层的元素分发被分别地扫描电子显微镜(SEM)和精力散的分光计(版本)学习。microhardness测试者被申请microhardness。结果证明泥浆为至少60是稳定的?h。YZrO3的很小的数量低于1050被形成?普牯慭?楦汥?桴潥祲?畢?畯?敲?瑬?灡汰?畱污瑩瑡癩汥?潴愠眠摩牥挠慬獳漠?睴?楤敭獮潩慮?楤慬潴?牧癡瑩?桴潥楲獥?潆?慥档琠灹?景猠汯瑵潩獮眠?数晲牯?潨潬牧灡楨?敲潮浲污穩瑡潩?挠浯異吗??
简介:InordertocontrolthesizeanddistributionofthehighconductiveFe2PinLiFePO4/Fe2Pcomposite,twodifferentcoolingrates(Fast:15℃·min-1,Slow:2℃·min-1)wereemployedaftermechanicalalloying.Thedischargecapacityofthefastcooledwas83mAh·g-1andtheslowcooled121mAh·g-1.TheparticlesizeofthesynthesizedpowderwasexaminedbytransmissionelectronmicroscopyanddistributionofFe2Pwascharacterizedusingscanningelectronmicroscopy(SEM).Inaddition,two-stepheattreatmentwascarriedoutforbetterdistributionofFe2P.X-raydiffraction(XRD)andRietveldrefinementrevealthatLiFePO4/Fe2Pcompositeconsistsof95.77%LiFePO4and4.33%ofFe2P.
简介:LayeredcathodematerialLiCo1/3Ni1/3Mn1/3O2wassynthesizedbyPechiniprocess,andinvestigatedusingX-raydiffraction(XRD),scanningelectronmicroscopy(SEM)andgalvanostaticcharge/dischargecycling.Thesampleiswell-crystallizedandhasaphase-purea-NaFeO2structure.Theparticlesizesareuniform,anddistributedintherangeof20-200nm.TheinitialdischargecapacityoftheLi/LiCo1/3Ni1/3Mn1/3O2cellwasabout149mAh·g-1whenitwascycledatavoltagerangeof4.5-2.3Vwithaspecificcurrentof0.25mA.Theresultisbetterincomparisonwithsolid-statesolutionmethod.Thesyntheticprocedurewasdiscussed.Threemajorreactions:chelation,esterification,andpolymerizationsuccessivelyoccurred.
简介:Aseriesoftheelectrochemicalandlong-termcorrosiontestswascarriedoutina3.5wt%Na2SO4solutiononthermal-sprayedWC-17CoandWC-10Co-4Crcermetcoatingsinordertoexaminetheeffectofcompositionofbindermaterialsonthecorrosionbehavior.TheresultsrevealthattheoverallcorrosionresistanceoftheWC-17CocoatingisinferiortothatoftheWC–Co–CrcoatingsduetothecorrosionofbindermaterialswhichinduceWCparticlestofalloff.CoOandWO3oxidefilmsformonthesurfaceofWC-17CocoatinginNa2SO4solutionelectrochemicalcorrosionprocess,whichwillprotectthecoatingintheprocessofcorrosion.Cr2O3oxidefilmformedontheWC-10Co-4Crcoatingsurfacehasastronghinderedroletocorrosion.ThecorrosionmechanismofWC-17CocoatinginNa2SO4solutionisentirecorrosionofComatrix,whileitisfilm-holecorrosionmechanismforWC-10Co-4Crcoating.
简介:WehavecalculatedtheelectronicstructuresofCo2FeAl1-xSix(101)surfaceusingfirst-principlesmethodbasedonthedensityfunctionaltheory.Becauseofthesurfaceeffect,theminorityspinbandgapattheFermileveldisappearsatthesurfaceofbulkCo2FeAl1-xSix.However,beneaththesurface,theminorityspingapopensattheFermilevel,whichindicatesthattheelectronicstructuresofCo2FeAl1-xSix(101)be-comeclosetothatofbulkphase.Accordingly,theCo2FeAl1-xSix(101)surfaceisacompositetri-layerstructurethatcorrespondstotheweakeningofhalf-metallicpropertyinCo2FeAl1-xSixfilms.Eventhough,thespinpolarizationofCo2FeAl1-xSix(101)surfaceisstilllargerthanthatofCo2FeAlorCo2FeSimaterials,makingCo2FeAl1-xSixapromisingspintronicsmaterial.