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简介:P-typenitrogen-dopedZnOfilmsarepreparedsuccessfullybyin-situthermaloxidationofZn_3N_2films.Thepreparedfilmsarecharacterizedbyx-raydiffraction,non-Rutherfordbackscattering(non-RBS)spectroscopy,xrayphotoelectronspectroscopy,andphotoluminescencespectrum.TheresultsshowthattheZn_3N_2filmsstarttotransformtoZnOat400°Candthetotalnitrogencontentdecreaseswiththeincreasingannealingtemperature.Thep-typefilmsareachievedat500℃withalowresistivityof6.33Ω·cmandahighholeconcentrationof+8.82×10~(17)cm~(-3),aswellasalowlevelofcarboncontamination,indicatingthatthesubstitutionalnitrogen(N_O)isaneffectiveacceptorintheZnO:Nfilm.ThephotoluminescencespectrashowclearUVemissionsandalsoindicatethepresenceofoxygenvacancy(V_O)defectsintheZnO:Nfilms.Thep-typedopingmechanismisbrieflydiscussed.
简介:A60%Fe/Al2O3catalystwaspreparedbytheco-precipitationmethod.ItwasreducedbyH2toproducemetallicFe,whichwasthensulfidedbyCS2toFe0.96SandFe3S4orphosphidedbytriphenylphosphine(PPh3)inliquidphasestoFe2PandFeP.Itwasfoundthattheironsulfides(Fe0.96SandFe3S4)exhibitedthelowactivityforthehydrodesulfurization(HDS)reactions.TheHDSactivitywasalsolowontheFe(metal)/Al2O3andFe2P/Al2O3catalystssincetheywereconvertedintoFe0.96SandFe3S4duringtheHDSreactions.Incontrast,theFeP/Al2O3wasfoundtobestableandactivefortheHDSreactions.Inparticular,FeP/Al2O3possessedsignificantlysmallerFePparticlesthanFeP/C,leadingtothesignificanthigherHDSactivityofFeP/Al2O3thanFeP/C.
简介:TypeIX-rayburstsarethemostfrequentthermonuclearexplosionsinnature,resultingfromthermonuclearrunawayonthesurfaceofanaccretingneutronstar[1].Thebreakoutreaction14O(α,p)17FfromthehotCNOcyclemayhaveaprominentimpactontheburstlightcurveandburstashes[2].However,insufficientexperimentalinformationisavailabletocalculateareliable,preciserateforthisreaction[3].Weproposedtoaddresstheexperimentalinvestigationofthe14O(α,p)17FusingTimeProjectionChamber(TPC)[4].
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.