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简介：Liquid-phase-exfoliationtechnologywasutilizedtopreparelayeredMoS2,WS2,andMoSe2nanosheetsincyclohexylpyrrolidone.Thenonlinearopticalresponseofthesenanosheetsindispersionswasinvestigatedbyobservingspatialself-phasemodulation（SSPM）usinga488nmcontinuouswavelaserbeam.ThediffractionringpatternsofSSPMwerefoundtobedistortedalongtheverticaldirectionrightafterthelasertraversingthenanosheetdispersions.Thenonlinearrefractiveindexofthethreetransitionmetaldichalcogenidesdispersionsn2wasmeasuredtobe10-7cm2W-1,andthethird-ordernonlinearsusceptibilityχ（3）10-9esu.TherelativechangeofeffectivenonlinearrefractiveindexΔn2e∕n（2e）oftheMoS2,WS2,andMoSe2dispersionscanbemodulated0.012–0.240,0.029–0.154,and0.091–0.304,respectively,bychangingtheincidentintensities.Ourexperimentalresultsimplynovelpotentialapplicationoftwo-dimensionaltransitionmetaldichalcogenidesinnonlinearphasemodulationdevices.

简介：Inthiswork,theinfluenceofCO2onthestructuralvariationandcatalyticperformanceofNa2WO4/Mn/SiO2foroxidativecouplingofmethanetoethylenewasinvestigated.ThecatalystwaspreparedbyimpregnationmethodandcharacterizedbyXRD,RamanandXPStechniques.AppropriateamountofCO2inthereactantgasesenhancedtheformationofsurfacetetrahedralNa2WO4speciesandpromotedthemigrationofOinMOx,Na,Wfromthecatalystbulktosurface,whichwerefavorableforoxidativecouplingofmethane.WhenthemolarratioofCH4/O2/CO2was3/1/2,enrichedsurfacetetrahedralNa2WO4speciesandhighsurfaceconcentrationofOinMOx,Na,Wweredetected,andthenhighCH4conversionof33.1%andhighC2H4selectivityof56.2%wereobtained.WithfurtherincreaseofCO2inthereagentgases,thecontentofactivesurfacetetrahedralNa2WO4speciesandsurfaceconcentrationofOinMOx,Na,Wdecreased,whilethatofinactivespecies(MnWO4andMn2O3)increaseddramatically,leadingtolowCH4conversionandlowC2H4selectivity.ItcouldbespeculatedthatNa2WO4crystalwastransformedintoMnWO4crystalwithexcessiveCO2addedunderthereactionconditions.PretreatmentofNa2WO4/Mn/SiO2catalystbymoderateamountofCO2beforeOCMalsopromotedtheformationofNa2WO4species.

简介：Aseriesofoxygenpermeabledual-phasecompositeoxides60wt%Ce0.8Gd0.2O2-δ-40wt%LnBaCo2O5+δ(CGO-LBCO,Ln=La,Pr,Nd,Sm,GdandY)weresynthesizedthroughasol-gelrouteandeffectsoftheLn3+cationsontheirphasestructure,oxygenpermeabilityandchemicalstabilityagainstCO2wereinvestigatedsystemicallybyXRD,SEM,TG-DSCandoxygenpermeationexperiments.XRDpatternsrevealthatthelargerLn3+cations(La3+,Pr3+andNd3+)successfullystabilizedthedouble-layeredperovskitestructureofsinteredLBCO,whilethesmallerones(Sm3+,Gd3+,andY3+)resultedinthepartialdecompositionofLBCOwithsomeimpuritiesformed.CGO-PBCOyieldsthehighestoxygenpermeationflux,reaching2.8×10-7mols-1cm-2at925?Cwith1mmthicknessunderair/Hegradient.TheTG-DSCprofilesin20mol%CO2/N2andoxygenpermeabilityexperimentswithCO2assweepgasshowthatCGO-YBCOdemonstratesthebestchemicalstabilityagainstCO2,possiblyduetoitsminimumbasicity.ThestableoxygenpermeationfluxofCGO-YBCOunderCO2atmosphererevealsitspotentialapplicationintheoxy-fuelcombustionrouteforCO2capture.

简介：CO2methanationhasbeenahottopicbecauseofitsimportantapplicationinthespacecraftandpotentialutilizationofcarbondioxide.Nickelcatalystisactiveforthisreaction.However,itsactivitystillneedstobeimproved.Dielectricbarrierdischarge(DBD)plasma,initiatedatambientconditionandoperatedat~150°C,hasbeenemployedinthisworkfordecompositionofnickelprecursortoprepareNi/MgAl2O4.Theplasmadecompositionresultsinhighdispersion,uniquestructure,enhancedreducibilityofNiparticlesandpromotedcatalyst-supportinteraction.AnimprovedactivityofCO2methanationwithahigheryieldofmethanehasbeenachievedovertheplasmadecomposedcatalyst,comparedtothecatalystpreparedthermally.Forexample,themethaneyieldoftheplasmapreparedcatalystis71.8%at300°Cbutitis62.9%overthethermalpreparedcatalyst.ThecatalystcharacterizationconfirmedthatCO2methanationovertheDBDplasmapreparedcatalystfollowspathwayofCOmethanation.

简介：IntheinterlayerexpansionofthelayeredzeoliteprecursorCOK-5,aSn,salt,bis(2,4-pentanedionate)-dichlorotin[Sn(acac)2Cl2],insteadofasilylatingagentwasusedtolinkthelayersat180°C.Theobtainedmaterial,whichisdesignedasSn-COE-5,showsashiftofthefirstXRDreflection,whichisverysimilartothatofCOK-5interlayerexpandedwithdichlorodimethylsilane(DCDMS),indicatinganincreaseininterlayerdistance.X-raydiffraction(XRD),N2sorptionisotherms,inductivelycoupledplasma(ICP),andX-rayphotoelectronspectroscopy(XPS)supporttheincorporationofisolatedSnsitesinthesample.Intheconversionofglucosetolevulinicacid,Sn-COE-5exhibitsmuchhigheractivitythanCOK-5,whichisduetothepresenceofLewisacidicsitesintheSn-COE-5.

简介：Lifetimemeasurementsoflow-lyingexcitedstatesin87Zrand87Nbhavebeenperformedviaandcoincidences.The124MeV32SbeamwasdeliveredfromtheSector-FocusingCyclotron(SFC)oftheHeavyIonR-esearchFacilityinLanzhou(HIRFL).Theparentnuclei87Nband87Mowereproducedbytherespectivereactions58Ni(32S,3p)and58Ni(32S,2p1n),atabeamenergy100MeVthroughthe8mAldegrader.

简介：Amolybdenumdisulfide（MoS2）saturableabsorberwasfabricatedbythermallydecomposingtheammoniumthiomolybdate.ByusingtheMoS2absorber,acompactdiode-pumpedpassivelyQ-switchedTm:GdVO4laserhasbeendemonstrated.AstableQ-switchedlaserwithrepetitionratesfrom25.58to48.09kHzwasachieved.Maximumaverageoutputpowerwas100mWwiththeshortestpulsedurationof0.8μs.Maximumpulseenergyis2.08μJatcenterof1902nm.

简介：Theroleofpulseparametersonnanoparticlepropertyisinvestigatedself-consistentlybasedonacoupleoffluidmodelandaerosoldynamicsmodelinacapacitivelycoupledparallel-plateacetylene(C2H2)discharge.Inthismodel,themasscontinuityequation,momentumbalanceequation,andenergybalanceequationforneutralgasaretakenintoaccount.Thus,thethermophoreticforceariseswhenagastemperaturegradientexists.Thetypicalresultsofthismodelarepositiveandnegativeiondensities,electronimpactcollisionsrates,nanoparticledensity,andchargedistributions.Thesimulationisperformedfordutyratio0.4/0.7/1.0,aswellaspulsemodulationfrequencyfrom40kHzto2.7MHzforpureC2H2dischargesatapressureof500mTorr.Wefindthatthepulseparameters,especiallythedutyratio,haveagreataffectonthedissociativeattachmentcoefficientandthenegativedensity.Moreimportantly,bydecreasingthedutyratio,nanoparticlesstarttodiffusetothewall.Undertheactionofgasflow,nanoparticledensitypeakiscreatedinfrontofthepulseelectrode,wherethegastemperatureissmaller.

简介：Wereporteddiversesolitonoperationsinathulium/holmium-dopedfiberlaserbytakingadvantageofataperedfiber-basedtopologicalinsulator（TI）Bi2Te3saturableabsorber（SA）.TheSAhadanonsaturablelossof53.5%andamodulationdepthof9.8%.Stablefundamentallymode-lockedsolitonsat1909.5nmwithdistinctKellysidebandsontheoutputspectrum,apulserepetitionrateof21.5MHz,andameasuredpulsewidthof1.26pswereobservedinthework.Byincreasingthepumppower,bothbunchedsolitonswithsolitonnumberupto15andharmonicallymode-lockedsolitonswithharmonicorderupto10wereobtained.Toourknowledge,thisisthefirstreportofbothbunchedsolitonsandharmonicallymode-lockedsolitonsinafiberlaserat2μmregionincorporatedwithTIs.

简介：Thispaperreportsonthelongevityofglycerol-dry(CO2)reformingoverthelanthanum(La)promotedNi/Al2O3catalysts.TheXRDresultsshowedthattheNiparticlewaswell-dispersedinthepresenceofLapromoter.Inaddition,viatheNH3-TPDanalysis,itwasfoundthattheLapromoterhasreducedtheacidityofNicatalystwhichmayhaveexplainedthemitigationofcarbonlaydown.Itwasdeterminedthatthe3.0wt%La-promotedNi/Al2O3catalystpossessedthelargestBETspecificsurfaceareaof97m2g-1.Consequently,ityieldedthebestcatalyticlongevityperformancewithconversionattainedmorethan90%,evenafter72hofreactionduration.Significantly,itcanbeconfirmedthatthepresenceofCO2duringtheglyceroldryreformingwasessentialinreducingcarbondeposition,mostlikelyviagasificationpathway.Thishasensuredastabilityofcatalyticactivityforalongreactionperiod(72h).

简介：Depositionoftwo-dimensional（2D）MoS2materialsonthetaperedfiberallowsvariousphotonicapplicationsincludingsaturableabsorbersandfour-wavemixing.Ethanolcatalyticdeposition（ECD）ofMoS2ontheopticaltaperedfiberwasproposedanddemonstratedinthiswork.Differentfromtheconventionalopticaldrivendepositionusingwaterororganicsolvent,theECDmethodutilizedthehighvolatilityoftheethanolsolvent,whichsignificantlyincreasedthemovementspeedoftheMoS2nanosheetsandthusboostedthedepositionrateandreducedtheminimumpowerthresholdtodrivethedeposition.WebelievetheECDmethodshouldbeabletobeappliedtoothersimilar2Dmaterialssuchasothertypesoftransitionmetalchalcogenides.

简介：WejoinedtheSEASTAR(ShellEvolutionAndSearchfor2+energiesAtRIBF)collaborationatRIKENandareanalyzingthedataofn-richVandMnisotopeswithN40.Three-raysineachof63;65;67Mnareidentified.The??coincidencerelationshipsarebeinganalyzedforestablishingtheirlevelschemes.TheprogressinthedataanalysisispresentedinRef.[1].

简介：Theoccurrencemodesofalkaliandalkaline-earthmetals(AAEMs)incoalrelatetotheirreleasebehaviorandashformationduringcombustion.TobetterunderstandthetransformationofAAEMs,thereleasebehaviorofwater-soluble,HCl-soluble,HCl-insolubleAAEMsduringShenmucoal(SMcoal)oxy-fuelcombustioninthepresenceofSO2andH2Oinadrop-tubereactorwasinvestigatedthroughserialdissolutionusingH2OandHClsolutions.TheresultsshowthatthereleaseratesofAAEMsincreasewithanincreaseintemperatureunderthethreeatmospheresstudied.ThehighreleaseratesofMgandCafromSMcoalaredependentonthehighcontentofsolubleMgandCainSMcoal.SO2inhibitsthereleaseratesofAAEMs,whileH2Opromotesthem.TheeffectsofSO2andH2OontheNaandKspeciesaremoreevidentthanthoseonMgandCaspecies.AllthreetypesofAAEMsincoalcanvolatilizeinthegasphaseduringcoalcombustion.TheW-typeAAEMsreleaseexcessively,whereasthereleaseratesofI-typeAAEMsarerelativelylower.DifferenttypesofAAEMmayinterconvertthroughdifferentpathwaysundercertainconditions.BothSO2andH2Opromotethetransformationreactions.TheeffectofSO2wasrelatedtosulfateformationandthepromotionbyH2OoccursbecauseofadecreaseinthemeltingpointofthesolidaswellasthereactionofH2O.

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简介：TheGroupofNuclearStructureResearchatIMPhasdevotedmuchefforttothelifetimemeasurementsoflowlyingexcitedstatesvia??fasttimingcoincidence.Twoexperimentswereperformedin2015attheradioactivebeamlineRIBLL[1]andgas-filledrecoilseparatorSHANS[2].

简介：WithMoS2assaturableabsorber,passiveQ-switchingandQ-switchedmode-lockingoperationsofaTm-dopedcalciumlithiumniobiumgalliumgarnet（Tm:CLNGG）laserwereexperimentallydemonstrated.TheQ-switchedlaseremittedamaximumaverageoutputpowerof62mWandhighestpulseenergyof0.72μJ.Q-switchedmodelockingwasalsoobtainedintheexperiment.TheresearchresultswillopenupapplicationsofMoS2atthemid-infraredwavelength.

简介：WehaveexploitedagreenapproachtopreparelayeredtitanateNa2-xHxTi2O5·H2OnanosheetarraysonFTOsubstratebyhydrothermalhydrolysisoftitanium(IV)isopropoxide(TTIP)withaidsofNa2EDTAandTEOAasco-coordinationagents,whichwerethentreatedbyHNO3toreplaceNa+byH+,followedbyacalcinationat450℃totopotacticallytransformintoanataseTiO2nanosheetarrays.SEM,TEM,XRD,andRamanspectroscopyhavebeenemployedtocharacterizethenanosheetfilms.TheTiO2nanosheetarrayswerefurtherappliedaselectrontransportmaterialsofCH3NH3PbI3perovskitesolarcells,achievingpowerconversionefficiencyof6.99%.

简介：Wehavefoundthattheexcitedenergyfromthegroundstatewith1f7=2configurationtothefirstexcitedstatewith2p3=2configurationin37SisobviouslylowercomparedwiththatinnearbyN=21isotones35Si,39Arand41Ca(seeFig.1,Theinsertindicatestherelevantsingle-particleorbitsofprotonandneutron).ThisinterestingphenomenonmayresultfromthecollapseofN=28closure,whichgivesthesufficientvalencespaceforcollectivedeformationwhichcanbeenrevealedfromtheB(E2)value.Therefore,toobtaintheB(E2),weperformtheexperimentsformeasuringthelifetimeofthefirstexcitedstatein37S.

简介：Inthispaper,theClarkson–Kruskaldirectapproachisemployedtoinvestigatetheexactsolutionsofthe2-dimensionalrotationalEulerequationsfortheincompressiblefluid.Theapplicationofthemethodleadstoasystemofcompletelysolvableordinarydifferentialequations.Severalspecialcasesarediscussedandnovelnonlinearexactsolutionswithrespecttovariablesxandyareobtained.Itisofinteresttonoticethatthepressurepisobtainedbythesecondkindofcurvilinearintegralandthecoefficientsofthenonlinearsolutionsaresolitarywavetypefunctionsliketanh(kt/2)andsech(kt/2)duetotherotationalparameterk=0.SuchphenomenonneverappearintheclassicalEulerequationswhereintheCoriolisforcearisingfromthegravityandEarth’srotationisignored.Finally,illustrativenumericalfiguresareattachedtoshowthebehaviorsthattheexactsolutionsmayexhibit.