简介:用微波高温固相法合成了Er^3+单掺Lu2O3,Li^+与Er^3+共掺Lu2O3及Li^+,Zn^2+,Mg^2+掺杂Lu2O3∶Er^3+的荧光粉。实验表明金属离子Li^+、Zn^2+、Mg^2+、Er^3+掺杂Lu2O3,不影响Lu2O3的立方晶相。扫描电子显微镜测量表明,Li^+掺杂可以有效改善粉体的分散性和形貌,Li^+,Zn^2+,Mg^2+共掺杂获得的粉体颗粒分布更加均匀,粒径范围为80~100nm。379nm激发下,Li^+与Er^3+共掺样品发光较单掺Er^3+样品在565nm处的发光增强了4.5倍,而Li^+、Zn^2+、Mg^2+与Er^3+共掺样品较其发光增强5.3倍。980nm激发下,Li^+与Er^3+共掺样品,Li^+、Zn^2+、Mg^2+与Er^3+共掺样品的发光分别比单掺Er^3+样品在565nm处发光增强23倍与39倍,在662nm处发光强度分别增强20倍与43倍。379nm激发下,较单掺Er3+的样品,掺杂Li^+的样品和Li^+,Zn^2+,Mg^2+和Er^3+共掺的样品荧光寿命均有所增加,而Zn^2+、Er^3+共掺及Mg^2+、Er^3+共掺样品的荧光寿命则有所缩短。
简介:TheroleoftemperatureontheoxidationdynamicsofCu2OonZnO(0001)wasinvestigatedduringtheoxidationofCu(111)/ZnO(0001)byusingoxygenplasmaastheoxidant.AtransitionfromsinglecrystallineCu2O(111)orientationtomicro-zonephaseseparationwithmultipleorientationswasrevealedwhentheoxidationtemperatureincreasedabove300°C.TheexperimentalresultsclearlyshowtheeffectoftheoxidationtemperaturewiththeassistanceofoxygenplasmaonchangingthemorphologyofCu(111)filmandenhancingthelateralnucleationandmigrationabilitiesofcuprousoxides.Averticaltop-downoxidationmodeandalateralmigrationmodelwereproposedtoexplainthedifferentnucleationandgrowthdynamicsofthetemperature-dependentoxidationprocessintheoxidationofCu(111)/ZnO(0001).
简介:描述表面在nanocrystals熄灭孤立的离子中心的一个模型基于在做的离子和熄灭中心的nanocrystalline表面之间的精力转移被建议。熄灭的率在nanocrystal取决于离子的位置,在非选择的刺激下面的因此腐烂曲线通常是非指数的。与这个模型一起计算的腐烂曲线在对T-4(1)的好同意>(6)在ZnS的A(1)排放:Mn2+nanocrystals。
简介:研究了YBaCu3O6~7超导催化剂上CO2的加氢制醇反应。考察了温度、压力和空速等条件对催化剂反应性能的影响。反应的主要产物是甲醇、CO和少量甲醚。利用XPS、XRD和AFM等技术对催化剂的结构、铜的存在状态和反应活性位进行表征发现,在反应过程中,YBa2Cu3O6~7由orthombic相转变为tetragonal相。反应活性位可能是Cu(I)物种。反应后催化剂颗粒的分散程度明显提高
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:AnefficientprocessfortheconversionofdimethyloxalateintoethyleneglycolwithhighselectivityandhighyieldoverCu2Owasinvestigated.InsituformedCuasatruecatalyticallyactivespeciesshowedagoodcatalyticperformanceforDMOconversiontoproduceEGin95%yield.
简介:CO2conversionviaphotocatalysisisapotentialsolutiontoaddressglobalwarmingandenergyshortage.PhotocatalysiscandirectlyutilizetheinexhaustiblesunlightasanenergysourcetocatalyzethereductionofCO2tousefulsolarfuelssuchasCO,CH4,CH3OH,andC2H5OH.Amongstudiedformulations,CubasedphotocatalystsarethemostattractiveforCO2conversionbecausetheCu-basedphotocatalystsarelow-costandabundancecomparingnoblemetal-basedcatalysts.Inthisliteraturereview,acomprehensivesummaryofrecentprogressonCu-basedphotocatalystsforCO2conversion,whichincludesmetalliccopper,copperalloynanoparticles(NPs),copperoxides,andcoppersulfidesphotocatalysts,canbefound.Thisreviewalsoincludedadetaileddiscussiononthecorrelationsofmorphology,structure,andperformanceforeachtypeofCu-basedcatalysts.Thereactionmechanismsandpossiblepathwaysforproductionsofvarioussolarfuelswereanalyzed,whichprovideinsightintothenatureofpotentialactivesitesforthecatalysts.Finally,thecurrentchallengesandperspectivefutureresearchdirectionswereoutlined,holdingpromisetoadvanceCu-basedphotocatalystsforCO2conversionwithmuch-enhancedenergyconversionefficiencyandproductionrates.
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:Thethird-ordernonlinearopticalpropertiesofwater-solubleCu2-xSenanocrystalsarestudiedinthenearinfraredrangeof70-980nmusingafemtosecondpulsedlaserbytheZ-scantechnique.ItisobservedthatthenonlinearopticalresponseofCu2-xSenanocrystalsissensitivelydependentontheexcitationwavelengthandexhibitstheenhancednonlinearitycomparedwithotherselenidessuchasZnSeandCdSe.TheW-shapedZ-scantrace,amixtureofthereversedsaturatedabsorptionandsaturatedabsorption,isobservedneartheplasmonresonancebandofCu2-xSenanoerystals,whichisattributedtothestate-fillingoffreecarriersgeneratedbycoppervacancies(self-dopingeffect)ofCu2-xSenanoerystalsaswellasthehotcarrierthermaleffectuponintensefemtosecondlaserexcitation.ThelargenonlinearopticalresponseandtunableplasmonicbandmakeCu2-xSenanocrystalspromisingmaterialsforapplicationsinultra-fastall-opticalswitchingdevicesaswellasnonlinearnanosensors.
简介:Cu-Fecompositeoxideswerepreparedbyco-precipitationmethodandtestedforhigheralcoholsynthesisfromsyngas.TheselectivitytoC2+OHandC6+OHinalcoholdistributionwasveryhighwhilethemethaneproductfractioninhydrocarbondistributionwasratherlow,demonstratingapromisingpotentialinhigheralcoholssynthesisfromsyngas.ThedistributionofalcoholsandhydrocarbonsapproximatelyobeyedAnderson-Schulz-Florydistributionwithsimilarchaingrowthprobability,indicatingalcoholsandhydrocarbonsderivedfromthesameintermediates.TheeffectsofCu/Femolarratio,reactiontemperatureandgashourlyspacevelocity(GHSV)oncatalyticperformancewerestudiedindetail.ThesamplewithaCu/Femolarratioof10/1exhibitedthebestcatalyticperformance.Higherreactiontemperatureacceleratedwater-gas-shiftreactionandledtolowertotalalcoholsselectivity.GHSVshowedgreateffectoncatalyticperformanceandhigherGHSVincreasedthetotalalcoholselectivity,indicatingthereexistedvisibledehydrationreactionofalcoholintohydrocarbon.
简介:WeinvestigatethesurfacestructureandcompositionofaYBa2Cu3Oy(YCO)thinfilmodifiedbyCF4plasmafluorination.Inadditiontotheabsorptionofhydrocarbons,chemicalreactionsoftheYBCOsurfacetakeplaceduringCF4plasmatreatment.Variousx-rayphotoelectronspectroscopicdataarereportedanddiscussed.Theexistenceofathinbarrierisconfirmed,whichhomogeneouslycoverstheedgeofthebaseYBCOfilminourinterfaceengineeringJosephsonjunction.MeasurementsofAugerelectronspectroscopicdataandtheresistanceversustemperatureindicatethatthebarrierisacontrollable-insulatinglayer.
简介:在传统的利用化爆和二级轻气炮作为驱动源的状态方程阻抗匹配实验中,为了考核不同标准材料的可信度,采用了标准材料交叉检验技术。即依次利用这些标准材料作为测量某个待测材料测量雨贡纽线的标准材料,通过比较待测材料雨贡纽线数据的一致性实现对这些标准材料的检验。2004年在神光-Ⅱ装置上完成的二倍频激光Al-Cu和Cu-A1阻抗匹配实验,是一种交叉实验。这两类实验不仅铝、铜二者互为标准材料和待测材料,而且实验包含了正反阻抗匹配两种类型:铝-铜正阻抗匹配实验中冲击波由低阻抗铝进入高阻抗待测材料铜,铜-铝反阻抗匹配实验中冲击波由高阻抗铜进入低阻抗待测材料铝中。
简介:Adoubleactivecentersystem,namelySalen-Cu(Ⅱ)@MIL-101(Cr),wassuccessfullysynthesizedviathe“shipinabottle”approach,whichactedasabifunctionalmaterialforbothcaptureandconversionofCO2inasingleprocess.Forthefirsttime,Salen-Cu(Ⅱ)@MIL-101(Cr)catalystwasdevelopedforthesynthesisofpropylenecarbonatefromCO2andpropyleneoxideunderroomtemperatureandambientpressurewithayieldof87.8%over60h.Furthermore,thereactionmechanismwasalsodiscussed.
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:Anovelgas-phaseelectrocatalyticcellcontainingalow-temperatureprotonexchangemembrane(PEM)wasdevelopedtoelectrochemicallyconvertCO2intoorganiccompounds.TwodifferentCu-basedcathodecatalysts(CuandCu-C)werepreparedbyphysicalvapordepositionmethod(sputtering)andsubsequentlyemployedforthegas-phaseelectroreductionofCO2atdifferenttemperatures(70-90℃).ThepreparedelectrodesCuandCu-CwerecharacterizedbyX-raydiffraction(XRD),X-rayphotoemissionspectroscopy(XPS)andscanningelectronmicroscopy(SEM).Asrevealed,CuispartiallyoxidizedonthesurfaceofthesamplesandtheCuandCu-Ccathodiccatalystswerecomprisedofaporous,continuous,andhomogeneousfilmwithnanocrystallineCuwithagrainsizeof16and8nm,respectively.Theinfluenceoftheappliedcurrentandtemperatureontheelectro-catalyticactivityandselectivityofthesematerialswasinvestigated.Amongthetwoinvestigatedelectrodes,thepureCucatalystfilmshowedthehighestCO2specificelectrocatalyticreductionratesandhigherselectivitytomethanolformationcomparedtotheCu-Celectrode,whichwasattributedtothehigherparticlesizeoftheformerandlowerCuO/Curatio.Theobtainedresultsshowpotentialinterestforthepossibleuseofelectrical「enewableenergyforthetransformationofCO2intovaluableproductsusinglowmetalloadingCubasedelectrodes(0.5mgCucm2)preparedbysputtering.