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:Synchrotronradiationsmall-angleX-rayscattering(SAXS)andtheviscositytechniquewereusedtoinvestigatetheeffectofdissolvedCO2intolueneontheconformationofpolystyrene(PS)inthesolution.TheviscosityofPSsolutiondecreasesfasterwithincreasingantisolventCO2pressurethanthatofthesolventintheabsenceofthepolymer.theintrinsicviscosity[η]calculatedusingthewellknownHugginsequationdecreaseswithantisolventpressure.ItwasfoundthatthesecondvirialcoefficientA2andtheapparentmean-squareradiusofgyration^1/2decreaseswithpressureofantisolventCO2.AllthesephenomenacanbeattributedtotheshrinkofPSchaininthecourseofaddingthegasantisolventbecausetheintercationbetweenthepolymerandsolventbecomesweaker.Thevalues^1/2atdifferentpressuresobtainedfromSAXSdataagreereasonablywiththosecalculatedfromFlorytheoryusingtheviscositydatadeterminedinthiswork.ThisimpliesthatFlorytheory,whichhasbeenusedwidelyforthesolutionsofpolymersinliquidsolvents,isalsoapplicabletothepolymersolutionwithgasantisolvent.
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简介:Veryrecently,BelleannouncedtheirobservationofΥ(5S)!bJ!(J=0;1;2),indicatingthattheΥ(5S)!bJ!decaysalsohavelargedecaywidths,i.e.,themeasuredbranchratiosofΥ(5S)!bJ!are<3:410??3,(1:640:23+0:30??0:22)10??3,and(0:570:220:07)10??3withJ=0;1;2,respectively[1].ItshouldbenoticedthateventhoughthetreelevelcontributionstoΥ(5S)!bJ!(J=0;1;2)shouldbestronglysuppressedduetotheOkubo-Zweig-Iizuka(OZI)rule,suchlargedecaywidthsareobserved,whichagaininspiresourinterestinunderstandingsuchquantities.Inthiswork,weproposethatthecontributionfromthehadronicloopshouldbeconsideredinstudyingΥ(5S)!bJ!.
简介:Inthisarticle,wetaketheX(5568)asthediquark-antidiquarktypetetraquarkstatewiththespin-parityJ~P=0~+,constructthescalar-diquark-scalar-antidiquarktypecurrent,carryouttheoperatorproductexpansionuptothevacuumcondensatesofdimension-10,andstudythemassandpoleresidueindetailswiththeQCDsumrules.WeobtainthevalueM_X=(5.57±0.12)GeV,whichisconsistentwiththeexperimentaldata.ThepresentpredictionfavorsassigningtheX(5568)tobethescalartetraquarkstate.
简介:ThispaperconstructstheinteractionpotentialoftheSH(X2Π)radicalbyusingthecoupled-clustersinglesdoubles-approximate-triplestheorycombiningthecorrelation-consistentquintuplebasissetaugmentedwiththediffusefunctions,aug-cc-pV5Z,inthevalencerange.Employingthepotential,itaccuratelydeterminesthespectroscopicparameters.ThepresentDe,Re,ωe,ωeχe,αeandBevaluesareof3.7767eV,0.13424nm,2699.846cm?1,47.7055cm-1,0.2639cm-1and9.4414cm-1,respectively,whichareinexcellentagreementwiththoseobtainedfromthemeasurements.Atotalof19vibrationalstateshasbeenfoundwhenJ=0bysolvingtheradialSchrdingerequationofnuclearmotion.Thecompletevibrationallevels,classicalturningpoints,initialrotationandcentrifugaldistortionconstantswhenJ=0arereportedforthefirsttime,whichareingoodaccordwiththeexperimentalresults.Thetotalandvariouspartial-wavecrosssectionsarecomputedfortheelasticcollisionsofsulfurandhydrogenintheirgroundstatesatlowtemperatureswhentwoatomsapproacheachotheralongtheSH(X2Π)potentialenergycurve.Overtheimpactenergyrangefrom1.0×10-11to1.0×10-4a.u.,eightshaperesonanceshavebeenfoundinthetotalelasticcrosssections.Foreachshaperesonance,theresonantenergyisaccuratelycalculated.Carefulinvestigationshavepointedoutthattheseresonancesresultfromthel=0,1,2,3,4,6,7,8partial-wavecontributions.
简介:TheelectronicpropertiesandtopologicalphasesofThXY(X=Pb,Au,Pt,PdandY=Sb,Bi,Sn)compoundsinthepresenceofspin–orbitcoupling,usingdensityfunctionaltheoryareinvestigated.TheThPtSncompoundisstableintheferromagneticphaseandtheotherThXYcompoundsarestableinnonmagneticphases.Bandstructuresofthesecompoundsintopologicalphases(insulatorormetal)andnormalphaseswithingeneralizedgradientapproximation(GGA)andEngel–Voskogeneralizedgradientapproximation(GGAEV)arecompared.TheThPtSn,ThPtBi,ThPtSb,ThPdBi,andThAuBicompoundshavetopologicalphasesandtheotherThXYcompoundshavenormalphases.Bandinversionstrengthsandtopologicalphasesofthesecompoundsatdifferentpressurearestudied.Itisseenthatthebandinversionstrengthsofthesecompoundsaresensitivetopressureandforeachcompoundasecond-orderpolynomialfittedonthebandinversionstrengths–pressurecurves.
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