简介:UsingtheaveragingtheoryoffirstandsecondorderwestudythemaximumnumberoflimitcyclesofgeneralizedLinarddifferentialsystems{x=y+εhl1(x)+ε2hl2(x),y=-x-ε(fn1(x)y2p+1+gm1(x))+∈2(fn2(x)y2p+1+gm2(x)),whichbifurcatefromtheperiodicorbitsofthelinearcenterx=y,y=-x,whereεisasmallparameter.Thepolynomialshl1andhl2havedegreel;fn1andfn2havedegreen;andgm1,gm2havedegreem.p∈Nand[·]denotestheintegerpartfunction.
简介:Inordertodeepentheunderstandingoftherelationshipbetweenfundamentalproperties(including:microstructureandcomposition)andphotocatalyticperformance,fourbismuthatecompounds,including:LiBiO3,NaBiO3,KBiO3,andAgBiO3,areregardedasresearchexamplesinthepresentwork,becausetheyhaveparticularcrystalstructuresandsimilarcompositions.Usingdensityfunctionaltheorycalculations,theirstructural,electronic,andopticalpropertiesareinvestigatedandcomparedsystematically.Firstofall,thecalculatedresultsofcrystalstructuresandopticalpropertiesareinagreementwithavailablepublishedexperimentaldata.Basedonthecalculatedresults,itisfoundthatthetunneledorlayeredmicro-structuralpropertiesleadtothestrongerinteractionbetweenbismuthandoxygen,andtheweakerinteractionbetweenalkaline-earthmetaland[BiO6]octahedron,resultinginthefeatureofmulti-bandgapsinthecasesofLiBiO3,NaBiO3,andKBiO3.ThisconclusionissupportedbythecaseofAgBiO3,inwhichthefeatureofmulti-bandgapsdisappears,duetothestrongerinteractionbetweenthenoblemetaland[BiO6]octahedron.Thesepropertieshavesignificantadvantagesinthephotocatalyticperformance:absorbinglowenergyphotons,rapidlytransferringenergycarriers.Furthermore,thefeaturesofelectronicstructuresofbismuthatecompoundsarewellreflectedbytheabsorptionspectra,whichcouldbeconfirmedbyexperimentalmeasurementsinpractice.Combinedwiththecalculatedresults,itcouldbeconsideredthatthecrystalstructuresandcompositionsofthephotocatalystdeterminetheelectronicstructuresandopticalproperties,andsubsequentlydeterminethecorrespondingphotocatalyticperformance.Thus,anovelBi-basedphotocatalystdrivenbyvisible-lightcouldbedesignedbyutilizingspecificcompositionstoformfavorableelectronicstructuresorspecificmicro-structurestoformabeneficialchannelforenergycarriers.
简介:Mg–9Li–3Al–1.6Yalloyswerepreparedthroughmixturemethod.Themicrostructure,mechanicalproperties,andcorrosionresistanceoftheas-castandasextrudedalloyswerestudiedbyopticalmicroscopy(OM),scanningelectronicmicroscopy(SEM),X-raydiffraction(XRD),mechanicalpropertiestesting,andelectrochemicalmeasurement.Theas-castMg–9Li–3Al–1.6Yalloywiththeaveragegrainsizeof325lmiscomposedofb-Limatrix,blocka-Mg,andgranuleAl2Yphases.Afterextrusion,thegrainsizeoftheas-castalloyisobviouslyrefinedandreachesto75lm;thestrengthandelongationoftheextrudedalloyareenhancedby17.20%and49.45%,respectively,owingtotheirfinemicrostructureandreductionofcastingdefects.Theas-extrudedalloyshowsbettercorrosionresistancecomparedtotheas-castone,whichmayberelatedtothelowstoredenergyanddislocationdensityintheextrudedalloy,alsothehomogenizationtreatmentbeforeextrusion.
简介:ThecapacitytocaptureCO2wasdeterminedinseveralstoichiometriccompositionsintheLi2O–Bi2O3system.Thecompounds(Li7BiO6,Li5BiO5,Li3BiO4andLiBiO2phases)weresynthesizedviasolid-statereactionandcharacterizedbyX-raydiffraction,scanningelectronmicroscopyandN2adsorptiontechniques.Thesampleswereheat-treatedattemperaturesfrom40to750°CundertheCO2atmospheretoevaluatethecarbonateformation,whichisindicativeofthecapacityofCO2capture.Moreover,Li7BiO6showsanexcellentCO2capturecapacityof7.1mmol/g,whichisconsiderablyhigherthanthoseofotherpreviouslyreportedceramics.Li7BiO6isabletoreactwithCO2from240°Ctoapproximately660°CshowingahighkineticreactionevenatCO2partialpressurevaluesaslowas0.05.
简介:通过Cu纳米颗粒掺杂制备了Li[(Ni0.6Co0.2Mn0.2)1-xCux]O2三元正极材料,并通过调节Cu的掺杂量,讨论了Cu的掺入对Li[(Ni0.6Co0.2Mn0.2)1-xCux]O2三元正极材料晶体结构、表面形貌、电化学性能和循环性能等一系列性能的影响,铜掺杂量为x=0.01时,在0.2C倍率下的首次放电比容量达到了219.1mAh/g,经过50次充放电循环之后,剩余比容量为115.4mAh/g。最终结果为Li[(Ni0.6Co0.2Mn0.2)1-xCux]O2中Cu的掺入量为x=0.01时,所得正极材料的电化学性能和循环性能最为优异。
简介:Athree-dimensionalfew-layerreducedgrapheneoxide-wrappedmesoporousLi4Ti5O12(m-LTO@FLRGO)electrodeisproducedusingasimplesolutionfabricationprocess.WhentestedasananodeforLiionbatteries,them-LTO@FL-RGOcompositeexhibitsexcellentratecapabilityandsuperiorcyclelife.Thecapacityofm-LTO@FL-RGOreaches165.4mAhg-1after100cyclesbetween1and2.5Vatarateof1C.Evenatarateof30C,ahighdischargecapacityof115.1mAhg-1isstillobtained,whichisthreetimeshigherthanthepristinemesoporousLi4Ti5O12(m-LTO).Thegraphenenanosheetsareincorporatedintothem-LTOmicrosphereshomogenously,whichprovideahighconductivenetworkforelectrontransportation.