简介:Broadband(1.6–18THz)terahertztime-domainspectroscopy(THz-TDS)andtime-resolvedterahertzspectroscopy(TRTS)wereperformedona54μmthickchalcogenideglass(As30Se30Te40)samplewithatwo-colorlaser-inducedairplasmaTHzsystemintransmissionandreflectionmodes,respectively.Twoabsorptionbandsat2–3and5–8THzwereobserved.TRTSrevealsanultrafastrelaxationprocessofthephotoinducedcarrierresponse,welldescribedbyarateequationmodelwithafiniteconcentrationofmid-bandgaptrapstatesforself-trappedexcitons.ThephotoinducedconductivitycanbewelldescribedbytheDrude–Smithconductivitymodelwithacarrierscatteringtimeof12–17fs,andweobservesignificantcarrierlocalizationeffects.Afastrefractiveindexchangewasobserved100fsbeforetheconductivityreacheditsmaximum,with2ordersofmagnitudelargeramplitudethanexpectedfortheopticallyinducedTHzKerreffect,indicatingthatfreecarriersareresponsibleforthetransientindexchange.
简介:Herein,wereportthevictorioussynthesisofmetal-organicframeworks(MOFs)onTiO2nanotubes(NTs)usingalayer-by-layer(LbL)approach.HighlycrystallineandhomogenousthinfilmsofMOFsweregrownandcharacterizedusingXRD,SEM,FT-IRandUV/Visspectroscopy.Moreover,theutilizationoftheMOFfilmsassensitizerswasprobedinbespokeGraetzeltypeliquidjunctionsolarcells.TheconstructedcellperformancerevealedanIscof1.16mAcm–2,Vocof0.63V,FFof0.33,andEffof0.42%.Further,pumpprobetransientlaserspectroscopywasperformedtoinvestigatetheenergyandchargetransferdynamicsoftheMOFs/TiO2NTsinterface.Theresultsindicated86%injectionefficiency.Theultrafastpump-probespectroscopyallowstheinvestigationofthisprocessandthedifferencesbetweenMOFs.ItalsoshowedthattherelaxationoftheMOFchromophoresisincompetitionwithelectroninjectionintheTiO2motif.Thusthisstudyprovidesanewinsightintoelectrontransferfromphotoexcitedmetal-organicframeworks(MOFs)intotitaniumdioxide.
简介:Thenatureofresistivetransitionofhigh-qualitycrystallinethinfilmsofYBa2Cu3O7-δhasbeenstudiedundermagneticfields(H)appliedalongthecdirectionoverawiderangeofdopedholes,p,intheCuO2planes.Thefield-andtemperature-dependentin-planeresistivity,ρab(T,H),hasbeenanalyzedwithinthethermallyassistedflux-flow(TAFF)formalism.Thefluxactivationenergy,U(T,H),hasbeenextractedfromthisanalysis.Thelow-Tpartoftheρab(T,H)datacanbedescribedbyanactivationenergyhavingthefunctionalformofU(T,H)=(1-t)m(H-0/H)β,wheret=T/Tc(reducedtemperature),andH0isafieldscalethatprimarilydeterminesthemagnitudeofU(T,H).Thetemperatureexponent,m,showsasystematicvariationwithp,whereasthefieldexponent,β,isinsensitivetothepvaluesandisclosetounity.TheH0,ontheotherhand,changesrapidlyaspisvaried.U(T,H)islinkedtothepinningpotentialandconsequentlyonthesuperconductingcondensationenergy.Sincethenormalstatepseudogapdirectlyaffectssuperconductingcondensationenergy,aclearcorrespondencebetweenH0andthePGenergyscale,εg,isfound.Possibleimplicationsoftheseresultsarediscussed.
简介:古典分子的动力学模拟被执行学习高温度(在300K上面)体积水的动态行为,明确地散开系数,氢契约,和近邻居的一生的行为。二个水潜力被比较:最近建议的全球性最佳的点费用(OPC)模特儿和著名TIP4P-Ew当模特儿。由考虑计算反的散开系数和旋转松驰常数的Arrhenius阴谋,到有增加温度的一个线性趋势的从VogelFulcherTammann行为的一条转线路分别地是为OPC和TIP4P-Ew模型的检测atT*309和T*285K。试验性地,转线路点是以前观察的atT*3155K。我们也为热扩大P(T,P),等压的P(T)曲线十字在大约一样的T*是在实验。水氢契约并且最近的邻居的一生被评估并且被发现穿过nearT*,在一生是大约1ps的地方。为T
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.