硅负极材料的相关应用介绍课件

寿命寿命硅负采材料

Silicon

anode

with

life

cycle

lifeProf.XinpingQiuDepartmentofChemistry,TsinghuaUniversityBeijing,100084,China寿命寿命硅负采材料

Siliconanodewithl8/13/2023DifficultiesforsiliconanodeapplicationLargevolumeexchangeleadtostructuralfailureofelectrodeRelativelowconductivityandrateperformanceElectronnumberEnergydensityMolecularmassSi:4200mAh/g1Multielectronreactionmaterials8/1/2023Difficultiesforsilic8/13/2023J.R.Dahn,Electrochem.Solid-StateLett.,2001,4,A137.J.R.Dahn,J.Electrochem.Soc.2003,150,A1457.2ColossalvolumechangeChangein(a)length+andwidthx,(b)height,and(c)volumeofthea-Sitowercomparedto(d)voltagevs.AFMscannumber.SchematicdiagramoftheinsituAFMapparatus.OpticalmicrographofaLi-alloyfilmafterexpansion8/1/2023J.R.Dahn,Electrochem8/13/2023Y.Cui,Nat.Nanotechnol.,2008,3,31.|Y.Cui,NanoLett.2011,11,2949.|G.Yushin,Nat.Mater.,2010,9,353.|G.A.Ozin,Adv.Funct.Mater.2009,19,1999.|X.J.Huang,Adv.Mater.2011,23,4938.|X.P.Qiu,Electrochem.Commun.,2007,5,930.|S.M.Lee,Electrochim.Acta,2008,53,4500.|J.G.Zhang,J.Electrochem.Soc.,2010,7,A765.|J.R.Dahn,Electrochem.Solid-StateLett.,2007,10,A17.

|G.Yushin,ACSAppl.Mater.Inter.,2010,11,3004.|G.Yushin,Science,2011,334,75.SibasedanodeNanomaterialsSiarrayCurrentcollectorBinder3Strategiesforsiliconanodes8/1/2023Y.Cui,Nat.NanotechnParticlepulverization

“Astrongsizedependenceoffractureinsiliconmaterialwasdiscoveredthatthereexistsacriticalparticlesizeof∼150nmbelowwhichcrackingdidnotoccur.”

[2]Sizeeffect[1]HZhang,NanoLetters2012,12,2778.;[2]XHLiu,ACSNano.2012,2,1522–15318/13/20234ElectrodeElectroniccontactInterfaceStabilityofSEIfilmParticleFractureandPulverizationCurrentcollector;Binder;ArrayStabilityinSi-basedmaterial?[1]Particlepulverization“AstrLiinsertionLiextractionLongcycles8/13/20235TheexposedactivesurfaceduetothevolumechangecausecontinualformationofSEIfilmsandlowcoulombicefficiency(CE).ResearchroutesReducetheparticlesizetoaccommodateSEIfilmDesignporousorhollowstructuretobufferthevolumeexpansionCompositewithCorMetal(Cu)toincreaseelectronicconductivityandmodifytheinterfacebetweenSiandelectrolyte.InvestigatenewbinderandelectrolyteadditivessystemforSi-basedanodematerialsStabilityofSEIfilmLiinsertionLiextractionLong65%SiH4+95%Ar5%H2&95%Ar450

C,1h-2.5hCalcination2N2atmosphere900C,4hN2atmosphere225C,1h500C,2hHeatingunderstirringPorouscarbon80C,solventevaporationCalcination1RemovetemplateHClSiCVDPorousSi-C

NanoCaCO3

SucrosesolutionDepositedsiliconCarbonframeworkafter1stand2ndcalcination8/13/2023PorousSi/CcompositeSynthesisProcess65%SiH4+95%ArCalcination8/13/2023Morphology7in1bold,1ePorousstructureofcarbonsubstratecanbeobservedfromTEMimagesAfterCVD,siliconparticlesadheretotheframeworkandporousstructurewasmaintained.Particlesizeofsiliconis~10nmandhomogeneouslydispersed.ThedepositedsiliconinPorousSi-Cisamorphous,asindicatedbytheabsenceofcrystallitesandbroaddiffuseringsintheSAEDpatterns.Incontrast,whencompositeisheatedto700°Cfor0.5h,alatticefringecorrespondingtod111=0.31nmforsiliconisseeninPorousSi-C-700.ResultsandanalysisSEMandTEMimages8/1/2023Morphology7in1bold8/13/20238in1bold,1eObviouscharacteristicpeakofcrystalsiliconafterheattreatmentat700C

for0.5hThreeobviousdiffractionpeaksaround28°,47°and56°arefoundafterheattreatment,whichcorrespondverywelltothe(111),(220)and(311)peaksofsiliconwithoutanyimpuritypeaks.Thepeakat520cm-1(indicativeofcrystallinesilicon)isnotdetectedaftersiliconCVD.Thebandscenteredaround155,474cm-1andtheweakshoulderat400cm-1aretypicalfeaturesofamorphoussiliconvibrationmodes[1].ResultsandanalysisStructuralcharacterization[1]D.Aurbach,J.Phys.Chem.C,2007,111,11437.XRDpatternsandRamanspectra8/1/20238in1bold,1eResultN2sorptionisothermsPoresizedistributionBothporouscarbonandporousSi-CshowtypeIVisotherm,whichistypicalcharacteristicofmesoporousstructureObviousdecreaseofspecificsurfacearea(SSA)andporevolumeafterSiCVDPorouscarbon:650m2/g,1.32cc/gPorousSi-C:150m2/g,0.39cc/gPoreswithdiameterof~3nmgeneratedby

decompositionofsucrosePoreswithdiameterof10~40nmduetotheremovalofCaCO3template,whichwerereducedafterSiCVDPorousStructure8/13/20239N2sorptionisothermsPoresizeCharge-DischargecurvesCyclingperformance1)2ndchargecapacity;2)VC:vinylenecarbonate8/13/202310Electrochemicalperformance1stdchcapacity:2404mAh/g1stchcapacity:1541mAh/g1stcoulombicefficiency:64.1%Reversiblecapacity1:1504mAh/gCapacityretention:67%after200cyclesRecipe:PorousSi-C:CB:binder(PAA)=6:2:2;Electrolyte:1MLiPF6inEC-DMC-EMC(1:1:1vol%)with2wt%VC2;loading:0.61

mg/cm2.Capacityisonlybasedonactivematerial.Currentdensity:0.1A/gfor1-2cycle,then0.5A/g;Voltage:0.05–2.0Vvs.LiCharge-DischargecurvesCyclingRatecapabilityIncreasecurrentdensityfrom0.1to2Ag-1,thespecificcapacityofSi/Ccompositeisstillabove500mAhg-1,whenthecurrentdensitychangesbackto0.1Ag-1,morethan92%ofthecapacityatthefirsttencyclesisrecoverable.8/13/202311CurrentDensity(A/g)Dischargecapacity(mAh/g)Chargecapacity(mAh/g)Coulombicefficiency(%)0.192386293.40.562962699.51.046146099.72.03113111000.176675798.9ResultsandanalysisRatecapabilityIncreasecurrenNyquistplotofSi-Ccompositeattheendofdischargeafterdifferentcyclesin1bold,1eElectrochemicalimpedancespectra(EIS)measurementina5.0mVACvoltagesignalinthe105-0.02Hzfrequencyrange.BeforeeachEIStest,theelectrodesweredischargedto0.01Vgalvanostaticallyandthenremainedatopen-circuitforatleast2htostabilizetheirpotential.Theconstancyofthecharacteristicfrequency(20Hz,from30-60cycles)suggeststhatthekineticsofthechargetransferreactiondoesnotvaryuponcycling.Evolutionoftheresistanceinmid-frequencyregion(inset)showsanincreaseinfirst5cyclesthenreduceandmaintainaround40Ohminlatercycles.Resultsandanalysis8/13/202312EIStest[1]D.Guyomard,J.Mater.Chem.,2011,21,6201.NyquistplotofSi-CcompositeSEIfilmwithcyclingSuperficialandcross-sectionalSEMimagesofourcompositeaftera),b)10cycles;c),d)20cycles;e),f)50cyclesandg),h)commercialSimaterialafter50cycles.a)b)d)c)h)g)f)e)PorousstructureofoursynthesizedcompositestillmaintainsaftercyclingandSEIfilmisonlyobservedattheexternalsurfaceofthesiliconparticlewithoutobviousincrassation.

IncommercialSimeasurements,excessiveSEIfilmisfoundafter50cycles,whichisunabletobedistinguishedfromSinanoparticles.8/13/202313SEIfilmwithcyclingSuperficiMaterialsaftercycling[1]Y.Cui,NanoLett.10(2010)1409Si/Cafter50cyclesa)SEMandb)TEMimageofSi/Ccompositeattheendof50th

cycle;

thecorrespondingelementalmappingofc)carbonandd)silicon.1mMofaceticacidwasusedtoremovetheSEIfilm[1].Porouscarbonstructureismaintained,nanosiliconparticlesaround10nmdoesnotshowaggregationandrupture.Resultsandanalysisa)b)c)d)C-KSi-K8/13/202314Materialsaftercycling[1]Y.SEIconfinementSchematic8/13/202315SEIfilmformsinsidetheporesduetothelowelectrochemicalpotentialoflithiuminsertioninfirstfewcycles.Whentheporesarefullfilled,SEIfilmisconfinedbythewallofcarbonsubstrate,whichpreventtheinternalsiliconparticlefrombeingexposedintheelectrolyte.ResultsSEIconfinementSchematic8/1/208/13/202316SchematicofsynthesisAdvantage:1.EasytosynthesisandregulateaccordingtocommercialCaCO3template2.Hollowstructurewithreservevolumecanaccommodatelargevolumechanges3.Interconnectednanosiliconmeansmoreactiveconductivecontact.NanoCaCO3SiliconlayerLegend:HollowsiliconPurificationbyHFacid(10wt%)5%SiH4+95%Ar400-500

C,1h-2.5hSiCVDTemplateremovalbyHClacid(2wt%)8/1/202316Schematicofsynthes8/13/202317ImagesandpatternsMorphologyResultsa)TEMimagesofnanoCaCO3template;b)SEMimagesofHSA-10(insetisatlowmagnification);TEMimagesofc)HSA-10,e)HSA-15,f)HSA-20;d)thecorrespondingSAEDpatternofHSA-10.Amorphoushollowsiliconmaterialwithdifferentshellthicknesswaspreparedabcdef8/1/202317ImagesandpatternsM8/13/202318ImagesandpatternsStructuralcharacterizationbcCharacteristicpeaksofcrystallinesilicon(PDF#65-1060)around28°,47°and56°areabsent,whichcorroboratethestatementofsiliconisamorphous.Thefirstmain3/2-1/2doublet(thespin-orbitsplittingis0.6eVandtheintensityratiois3:1),locatedat99.1-99.7eVcorrespondstoSi0(75%content).Thecomponentlocatedathigherbindingenergy(100.0eV)isassociatedwithSiOxformedatthesurfaceofHSAwithaproportionof25%.Resultsandanalysis8/1/202318ImagesandpatternsS8/13/202319ResultsandanalysisThenitrogenadsorption/desorptionisothermsofHSAsamplesshowasharpcapillarycondensationstepathighrelativepressures(P/P0=0.85-0.99),indicatingtheexistenceoflargepores.Correspondingporesizedistributesmainlyintherangeof20nmand100nm,whichisattributedtotheremovalofsite-occupyingnanoCaCO3.IsothermandPoresizedistributionPorousStructureSampleSpecificsurfacearea(m2g-1)Porevolume(ccg-1)HSA-1050.40.983HSA-1538.60.221HSA-2032.70.0918/1/202319Resultsandanalysis8/13/202320CyclingperformanceCycleperformanceTestconditionsRecipe:HS:CB:binder(PAA)=6:2:2Electrolyte:1MLiPF6inEC-DMC-EMC(1:1:1vol%)with2wt%VC;Loading:0.4-0.6mgcm-2

Currentdensity:0.1A/gfor1-3cycle,then0.4A/g;Voltage:0.02–1.50Vvs.LiResultsHSA-10givesthehighestcapacityretention(91%)in100cyclesandcorrespondingreversiblecapacityis~980mAhg-1.Whenincreasetheshellthicknessofsilicon,reversiblecapacityincreases(980mAhg-1ofHSA-15and1133mAhg-1ofHSA-20after100cycles)butthecapacityretentiondecreasesobviously(76%ofHSA-15and73%ofHSA-20)Electrochemicalperformance8/1/202320CyclingperformanceCMaterialsaftercycling[1]Y.Cui,NanoLett.10(2010)1409HAS-10after50cyclesa)SEMimageofHSA-10after100cycles;b)SEMimageofHSA-10after100cycleswithoutSEIfilm;c),d)TEMimageofHSA-10after100cycleswithoutSEIfilmatdifferentmagnification.Aggregatedsecondaryparticles(Fig.c)and~10nmsiliconshellstructure(Fig.b&d)weremaintainedwithoutfractureofthehollowspheres.Resultsandanalysis8/13/202321abcdMaterialsaftercycling[1]Y.EIStest8/13/202322StableinterfaceandsmallerresistanceNyquistplotofSi-Ccompositeattheendofdischargeafterdifferentcyclesin1bold,1eElectrochemicalimpedancespectra(EIS)measurementina5.0mVACvoltagesignalinthe105-0.02Hzfrequencyrange.BeforeeachEIStest,theelectrodesweredischargedto0.01Vgalvanostaticallyandthenremainedatopen-circuitforatleast2htostabilizetheirpotential.Evolutionoftheresistanceinmid-frequencyregionmaintains~20OhmduringcyclingwhichislowerthanSi/CcompositeandnanoSimaterial.ResultsandanalysisEIStest8/1/202322StableinterDSCTest8/13/202323StableSEIstructureofsiliconfoamDSCheatingcurvesin1bold,1eCurrentdensityaround0.1mA/gwasappliedtolithiatetheSiactivematerial.Afterthevoltagereached1mV,thecellswereremainedatopen-circuitfor2hthencarefullyopenedinaglovebox.TheelectrodewassoakedinDMCandthendriedundervacuumovernight.MeasurementswereconductedwithaDSC1(METTLERTOLEDO)atatemperaturerampof2◦Cmin-1(30-300◦C)