简介:Magnetoplasmonicsensorsareattractivecandidatesforultrasensitivechemicalandbiomedicalsensorapplications.Avarietyofferromagneticmetalthinfilmshavebeenusedformagnetoplasmonicdeviceapplications,yetthedependenceofsensorperformanceontheopticalandmagneto-opticalpropertiesofferromagneticmetalmaterialshasbeenrarelystudied.Inthiswork,wereportthestudyofenhancedmagneto-opticalKerreffect(MOKE)andsensingperformanceinAu∕FexCo1-xbilayermagneto-opticalsurfaceplasmonresonance(MOSPR)transducers.TheopticalconstantsofFexCo1-x(x=0,0.29,0.47,0.65,and1)inasputter-depositedAu∕FexCo1-xdevicearecharacterizedbytheattenuatedtotalinternalreflection(ATR)method.FexCo1-xthinfilmsshowdifferentMOKEsasafunctionofthechemicalconcentration,withthehighesttransverseMOKEsignalobservedinFe0.7Co0.3.Indexsensingperformanceiscloselyrelatedtothematerial’sopticalandmagneto-opticalconstants.BystudyingthesensingperformanceintheparameterspaceoftheAu∕FexCo1-xbilayerthicknesses,thehighestsensitivityisfoundtobe0.385(theoretical)and0.306RIU-1(experimental)intheAu∕Fe0.7Co0.3MOSPRdevices.OurresearchhighlightstheinfluenceoftheopticalpropertiesofferromagneticmaterialtodevicesensitivityinMOSPRtransducers.ThehighsensitivityinAu∕FexCo1-xMOSPRdevicesmakethesestructuresattractivecandidatesforchemicalandbiomedicalsensingapplications.
简介:AseriesofRbxCs1-xAg4I5(x=0-1)thinfilmsweregrownbyvacuumevaporationonNaCIcrystalsubstratesat350K.Theabsorptionspectraofthesefilmsweremeasuredat80Kinthewavelengthrangefrom240nmto400nm.ItisshownthatsuperionicconductorthinfilmsofquaternarycompoundRb0.5Cs0.5Ag4I5andternarycompoundRbAg415canbeobtainedatx=0.5-0.6andx=0.7-1,respectively.Atx=0.65,thecombinedcompoundfilmofthemixtureof30mol%RbAg4I5and70mol%Rb0.5Cs0.5Ag4I5ispresented.Then,basedonthespectralpositionsoftheA1andA2peaks,wedeterminedthattheRb0.5Cs0.5Ag4I5excitoncouplingenergyRexis0.21eV,theforbiddenzonewidthEgis3.82eVandtheexcitonradiusaexis0.70hm.Furthermore,theionicconductivitiesofsuperionicconductorthinfilmsofRbAg4I5andRb0.5Cs0.5Ag4I5andtheirmixturefilmareinvestigated,respectively,inthetemperaturerange303K-393K.
简介:Asupramolecular1Dferromagneticsystemwasstudiedexperimentallyaswellastheoretically.Hybriddensityfunctionaltheory(DFT)calculationswerebasedontheX-rayanalysis.TheresultsofDFTcalculationsandMcConnellmechanismhavecontributedtotheunderstandingofthefactorsgoverningtheexchangecouplingofmagnetisminthecrystalpacking.Boththeexperimentalevidenceandtheoreticalcalculationindicatethatspindensityin2-iodonitronylnitroxide(INN)radicalsconfirms1Dferromagneticchainwithinter-chainantiferromagneticinteraction.
简介:Inthispaper,adetailedLiesymmetryanalysisofthe(2+1)-dimensionalcouplednonlinearextensionofthereaction-diffusionequationispresented.Thegeneralfinitetransformationgroupisderivedviaasimpledirectmethod,whichisequivalenttoLiepointsymmetrygroupactually.Similarityreductionandsomeexactsolutionsoftheoriginalequationareobtainedbasedontheoptimalsystemofone-dimensionalsubalgebras.Inaddition,conservationlawsareconstructedbyemployingthenewconservationtheorem.
简介:Polyolefinsthatbearachiralsidechain(typicallyanisobutylgroup)experienceaso-calledmacromolecularamplificationofchirality:thechiralside-chaininducesaslightpreferenceforeithertgortg-mainchainconformation.Thisslightconformationalbiasisamplifiedcooperativelyalongthechain,andresultsinpreferredchiralityofthemainchainhelicalconformations.Asaresult,thesepolymersdisplayaliquid-crystal(LC)phasebothinsolutionand,inthemeltasatransientphaseonthewaytocrystallization.Theexistenceoftwoprocesses(melt-LCandLC-crystaltransitions)resultsinunconventionalbehaviorsthatwerefirstanalyzedbyPinoandcollaboratorsbackin1975.Thesepolymersalsoofferameanstotestthestructuralconsequencesofrecentlyintroducedcrystallizationschemes.Theseschemespostulatetheformationofatransientliquid-crystalphaseasageneralschemeforpolymercrystallization.
简介:Thesynthesisofanewtypeofhetero-macrocyclicpolyether2,3-henzo-1,4,7,13-tetraoxa-10-selenacyclopentadeca-2-eneisdeseribed.
简介:Ceria-zirconiasolidsolutionhasbeenpreparedbytheureagrindcombustionandcitricacidsol-gelmethodsforcatalyticapplicationsasoxygenstorage/releasematerialsinthisstudy.Thepropertiesandoxygenstorage/releasecapacitiesofsampleswithdifferentZrcontentswerecharacterizedandevaluatedbyX-raydiffraction(XRD),N2adsorption,scanningelectronmicroscopy(SEM),Ramanspectroscopy,andinsituCO–CO2loopingtest.Theresultsdemonstratethatthesamplespreparedbytwomethodsareallofexcellentlattice[O]release/storagepropertiesandmaintaingoodlong-termcyclestability.ButthepreparationmethodsignificantlyimpactsthehomogeneityofsamplesrelatedtotheirredoxpropertiesandthecontentofZrover20%,whichgreatlychangedthepropertiesofceria-zirconiasolidsolutionsandcausedtheirchangingofcrystallinesymmetryfromcubictotetragonal.Thesamplespreparedbycitricacidsolgelmethodareofmorehomogeneousparticlesizesandhigherspecificsurfaceareasthanthatbyureagrindcombustionmethod,whichisbenefittotheoxygenreleaseratherthanoxygenstorage.ThebulkoxygenamountmigratedtosurfaceincreaseswiththeincreasingZrcontent,however,theamountoflatticeoxygenmigrationdecreaseswhenZrcontentisover20%.WhenZrcontentis20%,thedifferencesofstorage/releasecapacitiesfromtwodifferentpreparationmethodsarereducedathightemperatureinthelong-termloopreaction.
简介:Thepresentworkisconcernedwithapenny-shapedDugdalecrackembeddedinaninfinitespaceofone-dimensional(1D)hexagonalquasicrystalsandsubjectedtotwoidenticalaxisymmetrictemperatureloadingsontheupperandlowercracksurfaces.ApplyingDugdalehypothesistothermo-elasticresults,theextentoftheplasticzoneatthecracktipisdetermined.Thenormalstressoutsidetheplasticzoneandcracksurfacedisplacementarederivedintermsofspecialfunctions.Forauniformloadingcase,thecorrespondingresultsarepresentedbysimplifyingtheprecedingresults.Numericalcalculationsarecarriedouttoshowtheinfluenceofsomeparameters.
简介:标题化合物(C24H16N4S)以噻吩-2-甲醛、苯甲酰乙腈和3-甲基-1-苯基-1H-吡唑-5-胺为原料,在离子液体[bmim]Br溶剂中,在80℃搅拌合成得到.其结构通过单晶X射线衍射法确定,晶体属于三斜晶系,空间群P-1,相对分子质量Mr=392.47,晶胞参数a=0.93612(8)nm,b=1.03063(12)nm,c=1.16624(16)nm,V=0.96853(19)nm3,Z=2,晶胞密度Dc=1.346g/cm3,吸收系数μ=0.185mm-1,单胞中电子的数目F(000)=408.晶体结构用直接法解出,经全矩阵最小二乘法对原子参数进行修正,最终的偏离因子R=0.0585,wR=0.1337.在晶体结构中新形成的吡啶环与吡唑环近似于共平面结构.