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简介：水晶的Au5Si2/Si异质接面nanowires(Au5Si2/SiNWs)被热蒸发的SiO粉末在一个低真空系统在厚黄金涂的硅底层上获得。生产Au5Si2/Si异质接面的结构分析被采用一台传播电子显微镜(TEM)和一个选择区域执行电的衍射计。化学作文被纳入TEM的一个精力散的X光分光镜学习。一个二拍子的圆舞生长模型被建议描述Au5Si2/SiNWs的形成。在第一步期间，水晶的SiNWs经由在相对高的温度把帮助氧化物的生长过程与vapour-liquid-solid模型相结合的生长机制被形成。在第二步，preformedSiNWs的温度减少和减少片断与残余Au反应由一个solid-liquid-solid过程形成单个水晶的Au5Si2nanowires。现在的工作应该基于nanowires为未来合成和高质量的金silicidenanowires和微电子设备的研究是有用的。

简介：本文考察了稀土氧化物，合金和氧化锆对ＡｌＰＯ４５载体和Ｆｅ／ＡｌＰＯ４５催化剂的影响。结果表明，Ｌａ、Ｃｅ和Ｙ稀士氧化物的引入可有效地促进硝酸铁丙酮溶液中制备的Ｆｅ／ＡｌＰＯ４５催化剂在ＣＯ加氢反应中的催化活性；负载不同合金的ＡｌＰＯ４５催化剂具有明显不同的催化反应结果；ＺｒＯ可调变ＡｌＰＯ５载体的表面性能，削弱活性组份和载体间的相互作用，使在硝酸铁水溶液中制备的催化剂在合成气转化中具有一定的催化活性。更多还原

简介：Severecapacityfadingandpoorhighrateperformanceoflithiumsulfur(Li-S)batterycausedby"shuttleeffect"andlowconductivityofsulfurhampersitsfurtherdevelopmentsandapplications.Li4Ti50i2(LTO)possesseshigh1whiumionconductivity,anditisalsocanbeusedasanactiveadsorbentforpolysulfide.Herein,fineLTOparticlecoatedcarbonnanofibers(CNF)werepreparedandaconductivenetworkbothforelectronandlithiumionwasbuilt,whichcangreatlypromotetheelectrochemicalconversionofpolysulfideandimprovetherateperformanceofLi-Sbatteries.Meanwhile,aquantityofadsorptionsitesisconstructedbydefectsofthesurfaceofLTO-CNFmembranetoeffectivelyimmobilizepolysulfide.ThemultifunctionalLTO-CNFinterlayercouldimpedetheshuttleeffectandenhaneecomprehensiveelectrochemicalperformanceofLi-Sbatteries,especiallyhighrateperformanee.WithsuchLTO-CNFinterlayer,theLi-Sbatterypresentsaspecificcapacityof641.9mAh/gat5Crate.After400cyclesat1C,acapacityof618.0mAh/gisretained.ThisworkprovidesafeasiblestrategytoachievehighperformanceofLi-Sbatteryforpracticalutilization.

简介：做Si的Ge(2)sb(2)Te(5)电影被dc劈啪作响magnetronco与Ge2Sb2Te5和Si目标准备了。在在两结晶化温度和阶段转变温度fromface-centred-cubic(fcc)的增加的Te(5)电影结果分阶段执行到的Ge(2)sb(2)的Si的增加六角形(十六进制)阶段。Ge2Sb2Te5电影的抵抗力显示出重要增加，Si做。当在这部电影做Si的11.8at.%时，在退火的460度C以后的抵抗力与undopedGe2Sb2Te5电影相比从64～99终止从1～11m终止(.)厘米和动态抵抗增加增加。这对写阶段变化随机存取记忆的当前的减小很有用。

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简介：NanosizedGa-containingZSM-5zeoliteswerepreparedviaisomorphoussubstitutionandimpregnationfollowedbycharacterizedusingvarioustechniques.Thecatalyticperformanceofthezeolitesforthearomatizationof1-hexenewasinvestigated.TheresultsindicatethatisomorphoussubstitutionpromotestheincorporationofGaheteroatomsintotheframeworkalongwiththeformationofextra-frameworkGaO+species（[GaO+]a）thathavestrongerinteractionswiththenegativepotentialoftheframework.Inaddition,basedonthePy-IRresultsandcatalyticperformance,the[GaO+]aspecieswithstrongerLewisacidsitesproducedabettersynergismwithmoderateBr?nstedacidsitesandthusimprovedtheselectivitytoaromaticcompounds.However,theimpregnationresultsintheformationofGa2O3phaseandsmallamountsofGaO+speciesthataremainlylocatedontheexternalsurface（[GaO+]b）,whichcontributetoweakerLewisacidsitesduetoweakerinteractionswiththezeoliteframework.During1-hexenearomatization,thenanosizedGaisomorphouslysubstitutedZSM-5zeolitesamples（Gax-NZ5）exhibitedbettercatalyticperformancecomparedtotheimpregnatedsamples,andthehighestaromaticyield（i.e.,65.4wt%）wasachievedovertheGa4.2-NZ5sample,whichcontainedwiththehighestGacontent.

简介：Themassesofneutron-defcientnuclidesplayacriticalroleinthecalculationofastrophysicalrapidproton-captureprocesses[1].Neutron-defcientnuclideswithmassnumber∧around80arethelastsetofnuclideswithunknownmassesonthepathwayofvp-process[2].Themassmeasurementofnuclideswouldbeveryuseful.In2016,massesofneutron-defcientnuclides79Y,81Zr,82Zr,83Nband84Nbnucleiwerepreciselymeasureddirectlybytheexperimentalstorage-ringCSReatLanzhou.

简介：Thesuppressionoftherecombinationofelectronsandholes(e–h)andtheenhancementofthelightabsorptionofsemiconductorsaretwokeypointstowardefficientphotocatalyticdegradation.Here,wereportafew-layerg-C3N4/α-MoO3nanoneedles(flg-C3N4/α-MoO3NNs)all-solid-stateZ-schememechanismphotocatalystsynthesizedviaatypicalhydrothermalmethodinacontrolledmanner.Therecombinationofthephoto-inducede–hpairscouldbeeffectivelyrestrainedbytheZ-schemepassagewaybetweentheflg-C3N4andα-MoO3NNsinthecomposite,whichcouldalsopromiseahighredoxabilitytodegradepollutants.Anditbecamepossibleforthepreparedphotocatalysttoabsorblightinawiderangeofwavelengths.Thedetailedmechanismwasstudiedbyelectronspin-resonancespectroscopy(ESR).Thelow-dimensionalnanostructureofthetwoconstituents(α-MoO3NNswithone-dimensionalstructureandflg-C3N4withtwo-dimensionalstructure)endowedthecompositewithvarietiesofexcellentphysicochemicalproperties,whichfacilitatedthetransferanddiffusionofthephotoelectronsandincreasedthespecificsurfaceareaandtheactivesites.The10wt%flg-C3N4/α-MoO3NNsshowedthebestphotocatalyticperformancetowardRhBdegradation,therateofwhichwas71.86%,~2.6timeshigherthanthatofα-MoO3NNs.

简介：AnewlayeredCu-basedoxychalcogenideBa3Fe2O5Cu2S2hasbeensynthesizedanditsmagneticandelectronicpropertieswererevealed.Ba3Fe2O5Cu2S2isbuiltupbyalternativelystacking[Cu2S2]2-layersandironperovskiteoxide[（FeO2）（BaO）（FeO2）]2-layersalongthecaxisthatareseparatedbybariumionswithFe3+fivefoldcoordinatedbyasquare-pyramidalarrangementofoxygen.Fromthebondvalencearguments,weinferredthatinlayeredCuCh-based（Ch=S,Se,Te）compoundsthe+3cationinperovskiteoxidesheetprefersasquarepyramidalsite,whilethelowervalencecationprefersthesquareplanarsites.Thestudiesonsusceptibility,transport,andopticalreflectivityindicatethatBa3Fe2O5Cu2S2isanantiferromagneticsemiconductorwithaNe′eltemperatureof121Kandanopticalbandgapof1.03eV.Themeasurementofheatcapacityfrom10Ktoroomtemperatureshowsnoanomalyat121K.TheDebyetemperatureisdeterminedtobe113K.TheoreticalcalculationsindicatethattheconductionbandminimumispredominantlycontributedbyO2pand3dstatesofFeionsthatantiferromagneticallyarrangedinFeO2layers.TheFe3dstatesarelocatedatlowerenergyandresultinanarrowbandgapincomparisonwiththatoftheisostructuralSr3Sc2O5Cu2S2.

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：Directconversionoffructose-basedcarbohydratesto5-ethoxymethylfurfural(EMF)catalyzedbyLewisacidinethanolwasinvestigated.ItwasfoundthatBF3(Et)2Owasfavorablefor5-hydroxymethylfurfural(HMF)etherificationtoEMF.BF3(Et)2OcombinationwithAlCl36H2Owiththemolarratioof1wasaneffectivecatalystsystemforsynthesisofEMFfromfructose-basedcarbohydrates.55.0%,45.4%and23.9%ofEMFyieldswereobtainedfromfructose,inulinandsucroseunderoptimizedconditions,respectively.

简介：InthispaperweusedMOF-5andCu3(BTC)2toseparateCO2/CH4andCH4/N2mixturesunderdynamicconditions.Bothmaterialsweresynthesizedandpelletized,thusallowingforameaningfulcharacterizationinviewofprocessscale-up.ThematerialswerecharacterizedbyX-raydiffraction(XRD)andscanningelectronmicroscopy(SEM).Byperformingbreakthroughexperiments,wefoundthatCu3(BTC)2separatedCO2/CH4slightlybetterthanMOF-5.BecausethecrystalstructureofCu3(BTC)2includesunsaturatedaccessiblemetalsitesformedviadehydration,itpredominantlyinteractedwithCO2moleculesandmoreeasilycapturedthem.Conversely,MOF-5withasuitableporesizeseparatedCH4/N2moreefficientlyinourbreakthroughtest.

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.