简介:Tungstenisregardedasanimportantcandidateofplasmafacingmaterialininternationalthermonuclearexperimentalreactor(ITER),sothedeterminationandmodelingofspectraoftungstenplasma,especiallythespectraathightemperaturewereintenselyfocusedonrecently.Inthiswork,usingtheatomicstructurecodeofCowan,acollisionalradiativemodel(CRM)basedonthespin-orbit-split-arraysisdeveloped.Basedonthismodel,thechargestatedistributionoftungstenionsisdeterminedandthesoftX-rayspectrafromhighchargedionsoftungstenatdifferenttemperaturesarecalculated.Theresultsshowthatboththeaverageionizationchargeandlinepositionsarewellagreedwithotherscalculationsandmeasurementswithdiscrepanciesoflessthan0.63%and1.26%,respectively.Thespectraathighertemperaturesarealsoreportedandtherelationshipbetweenionabundanceandtemperatureispredictedinthiswork.
简介:LetL~2([0,1],x)bethespaceoftherealvalued,measurable,squaresummablefunctionson[0,1]withweightx,andlet■_nbethesubspaceofL~2([0,1],x)definedbyalinearcombinationofJ_0(μ_kx),whereJ_0istheBesselfunctionoforder0and{μ_k}isthestrictlyincreasingsequenceofallpositivezerosofJ_0.Forf∈L~2([0,1],x),letE(f,■_n)betheerrorofthebestL~2([0,1],x),i.e.,approximationoffbyelementsof■_n.Theshiftoperatoroffatpointx∈[0,1]withstept∈[0,1]isdefinedbyT(t)f(x)=(1/π)∫_0~πf((x~2+t~2-2xtcosθ)~(1/2))dθ.Thedifferences(1-T(t))~(r/2)f=∑_(j=0)~∞(-1)~j(_j~(r/2))T~j(t)foforderr∈(0,∞)andtheL~2([0,1],x)-modulusofcontinuityω_r(f,τ)=sup{||(I-T(t))~(r/2)f||:0≤t≤τ}oforderraredefinedinthestandardway,whereT~0(t)=Iistheidentityoperator.Inthispaper,weestablishthesharpJacksoninequalitybetweenE(f,■_n)andω_r(f,τ)forsomecasesofrandτ.Moreprecisely,wewillfindthesmallestconstant■_n(τ,r)whichdependsonlyonn,r,andτ,suchthattheinequalityE(f,■_n)≤■_n(τ,r)ω_r(f,τ)isvalid.
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简介:GrazingincidentX-raydiffractionatdifferentgrazinganglesforself-organizedGedotsgrownonSi(001)arecarriedoutandlatticeconstantexpansionsof1.2?paralleltothesurfaceascomparedwiththeSilatticearefoundwithintheGedots.A3.1?latticeexpansionoftheGedotsalongthegrowthdirectionisalsofundbyordinaryX-ray(004)diffraction.AccordingtothePoissonequationandtheVegardlaw,ourresultsinferthattheGedotshouldbeapartiallystrainrelaxedSiGealloywithGecontentofabuot55?2001ElsevierScienceB.V.Allrightsreserved.
简介:WereportQ-switchedandmode-lockederbium-dopedall-fiberlasersusingternaryReS2(1-x)Se2xassaturableabsorbers(SAs).ThemodulationdepthandsaturableintensityofthefilmSAare1.8%and0.046MW∕cm2.InQ-switchedmechanismoutput,thepulsewascenteredat1531.1nmwithmaximumpulseenergyandminimumpulsewidthof28.29nJand1.07μs,respectively.Inmode-lockedoperation,thepulsewascenteredat1561.15nmwithpulsewidthof888fs,repetitionrateof2.95MHz,andmaximumpulseenergyof0.275nJ.Tothebestofourknowledge,thisisthefirstreportonthemode-lockedEr3+-dopedfiberlaserusingternarytransitionmetaldichalcogenides.Thisworksuggestsprospective2D-materialSAscanbewidelyusedinversatilefieldsduetotheirattractiveoptoelectronicandtunableenergybandgapproperties.
简介:QuantumdynamicscalculationsforthetitlereactionH(2S)+S2(X3-Σg)→SH(X2Π)+S(3P)areperformedbyusingagloballyaccuratedoublemany-bodyexpansionpotentialenergysurface[J.Phys.Chem.A1155274(2011)].TheChebyshevrealwavepacketpropagationmethodisemployedtoobtainthedynamicalinformation,suchasreactionprobability,initialstate-specifiedintegralcrosssection,andthermalrateconstant.Itisfoundnotonlythatthereisareactionthresholdnear0.7eVinbothreactionprobabilitiesandintegralcrosssectioncurves,butalsothatboththeprobabilityandcrosssectionincreasefirstlyandthendecreaseasthecollisionenergyincreases.Theexistenceoftheresonancestructureinboththeprobabilityandcrosssectioncurvesisascribedtothedeeppotentialwell.Thecalculationoftherateconstantrevealsthatthereactionoccurringonthepotentialenergysurfaceoftheground-stateHS2isslowtotakeplace.
简介:Poly(methylmetacrylate)(PMMA)/Y0.0025Si0.025Ba0.9725(Ti(0.9)Sn0.1)O3(YBTS)composites在YBTS的不同重量比率被准备(0wt%,5wt%,10wt%和20wt%YBTS)招待以便在PMMA的电、光的性质上调查YBTS增加的效果。电的性质(阻抗,绝缘的经常的绝缘的损失和交流电导率)在频率范围被学习10kHz-1MHz并且在温度范围20鈥?0掳C。在增加YBTS的内容之上陶器,我们在在绝缘的经常的、绝缘的损失和PMMA的交流电导率的阻抗和增加观察了减小主人。我们也发现在高YBTS内容的松驰过程由于在离子的传导性的松驰。吸收系数(伪)在波长范围被决定了230鈥?在为所有YBTS-PMMAcomposites的房间温度的00nm。而且,YBTS的增加陶器高度特别在300nm下面提高PMMA主人的紫外吸收。对PMMA主人陶器的20wt%YBTS的增加减少从5eV的光精力差距到3.41eV。关联在之间电,光并且SEM结果被报导。关键词电-光-PMMA,陶器-铁电体-Composites
简介:Bysimultaneouslyemployingbothanelectro-opticmodulatorandcarbonnanotubesaturableabsorber(CNT-SA)inadual-lossmodulator,asubnanosecondsinglemode-lockingpulseunderneathaQ-switchedenvelopewithhighpeakpowerwasgeneratedfromadoublyQ-switchedandmode-locked(QML)Nd:Lu0.15Y0.85VO4laserat1.06μmforthefirsttime,toourknowledge.CNTswithdifferentwallstructures—single-walledCNTs(SWCNTs),double-walledCNTs(DWCNTs),andmulti-walledCNTs(MWCNTs)—wereusedasSAsintheexperimenttoinvestigatethesinglemode-lockingpulsecharacteristics.Atpumppowerof10.72W,themaximumpeakpowerof1.312MWwasobtainedwiththeDWCNT.
简介:Thecopolymersofchloroethylmethacrylate(CMA),glycidylmethacry-late(GMA),andmethylmethacrylate(MMA)weresynthesizedinbenzenesolution.Theirbreadthsofthemolecularweightdistributionsare2.1and2.3,respectivelyThether-malstabilityofP(GMA-CMA)issuperiortothatofP(CMA-MMA).TheresolutionsofP(CMA-MMA)andP(GMA-CMA)photoresistswerefoundtobe0.1~0.16μmand0.17~0.2μm,respectively.
简介:Synchrotronradiationsmall-angleX-rayscattering(SAXS)andtheviscositytechniquewereusedtoinvestigatetheeffectofdissolvedCO2intolueneontheconformationofpolystyrene(PS)inthesolution.TheviscosityofPSsolutiondecreasesfasterwithincreasingantisolventCO2pressurethanthatofthesolventintheabsenceofthepolymer.theintrinsicviscosity[η]calculatedusingthewellknownHugginsequationdecreaseswithantisolventpressure.ItwasfoundthatthesecondvirialcoefficientA2andtheapparentmean-squareradiusofgyration^1/2decreaseswithpressureofantisolventCO2.AllthesephenomenacanbeattributedtotheshrinkofPSchaininthecourseofaddingthegasantisolventbecausetheintercationbetweenthepolymerandsolventbecomesweaker.Thevalues^1/2atdifferentpressuresobtainedfromSAXSdataagreereasonablywiththosecalculatedfromFlorytheoryusingtheviscositydatadeterminedinthiswork.ThisimpliesthatFlorytheory,whichhasbeenusedwidelyforthesolutionsofpolymersinliquidsolvents,isalsoapplicabletothepolymersolutionwithgasantisolvent.