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15 个结果
  • 简介:CO2photoreductionisanattractiveprocesswhichallowsthestorageofsolarenergyandsynthesisofsolarfuels.Manydifferentphotocatalyticsystemshavebeendeveloped,whilethealternativephoto-reactorsarestillinsufficientlyinvestigated.Inthiswork,photoreductionofCO2withH2OintoCH4wasinvestigatedinamodifiedconcentratingsolarreactor,usingTiO2andPt/TiO2asthecatalysts.TheTiO2andPt/TiO2sampleswereextensivelycharacterizedbydifferenttechniquesincludingpowderX-raydiffraction(XRD),N2adsorption/desorptionandUV–visabsorption.ThecatalyticperformanceoftheTiO2andPt/TiO2samplesinthegasphasewasevaluatedunderunconcentratedandconcentratedXe-lamplightandnaturesolarlightwithdifferentconcentratingratios.VariousparametersofthereactionsystemandthecatalystswereinvestigatedandoptimizedtomaximizethecatalyticperformanceofCO2reductionsystem.Comparedwiththenormallightirradiation,theTiO2andPt/TiO2samplesshowhigherphotocatalyticactivity(about6–7times)forreducingCO2intoCH4underconcentratedXe-lamplightandnaturesolarlight.Intherangeofexperimentallightintensity,itisfoundthattheconcentrationofthelightmakesitsuitableforthecatalyticreaction,andincreasestheutilizationefficiencyoftheTiO2andPt/TiO2sampleswhiledoesnotdecreasethequantumefficiency.

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  • 简介:在这研究,塑料闪烁器察觉者的不同参数被Geant4模拟工具箱调查。这些参数由PMT以及表面的半径,长度和位置组成了反射打并且完成选择。而且,二器官的塑料材料的反应时间分布被学习。结果显示收集光光子与PMT半径头一起有一种线性关系。另外,PMT的垂直地点与光光子收集有一种非线性的关系。然而,收集由增加PMT长度或动人的PMT头减少了水平位置。二塑料闪烁器材料的反应功能在对试验性的出版结果的好同意。另外,Geant4放射运输代码能模仿事件放射光子并且预言随后的事件到PMT头很好。结果显示BC-404有更快的焕发性质对BC-400器官的闪烁器材料。在Geant4产量之间的比较说明最好的反射镜材料和表面为光光子完成类型,这是地面TiO2。

  • 标签: GEANT4 塑料材料 光子 学习 水平位置 PMT
  • 简介:CrystallineTiO2(P25)andisolatedtitanatespeciesinaZSM-5structure(TS-1)weremodifiedwithAuandAg,respectively,andtestedinthegas-phasephotocatalyticCO2reductionunderhighpurityconditions.Thenoblemetalmodificationwasperformedbyphotodeposition.LightabsorbancepropertiesofthecatalystsareexaminedwithUV–Visspectroscopybeforeandaftertheactivitytest.Inthegas-phasephotocatalyticCO2reduction,itwasobservedthatthecatalystswithAgnanostructuresaremoreactivethanthosewithAunanostructures.Itisthusfoundthattheenergeticdifferencebetweenthebandgapenergyofthesemiconductorandthepositionoftheplasmonisinfluencingthephotocatalyticactivity.Potentially,plasmonexcitationduetovisiblelightabsorptionresultsinplasmonresonanceenergy,whichaffectstheexcitationofthesemiconductorpositively.Therefore,anoverlapbetweenbandgapenergyofthesemiconductorandmetalplasmonisneeded.

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  • 简介:Two-dimensional(2D)graphitecarbonnitride(g-C3N4)nanosheetshavebeensuccessfullyusedasasaturableabsorber(SA)inapassivelyQ-switchedNd:LLFlaserat1.3μmforthefirsttime,tothebestofourknowledge.Underanincidentpumppowerof9.97W,theshortestpulsedurationof275nswasacquiredwithoutputpowerof0.96Wandpulserepetitionrateof154kHz,resultinginapulseenergyof6.2μJ.Inaddition,thesaturableabsorptionbehaviorsofzero-dimensional12nmg-C3N4nanoparticles(g-C3N4-NPs)andthree-dimensionalorderedmesoporousg-C3N4(mpg-C3N4)werealsoobserved,althoughtheirmorphologyandstructurewerequitedifferentfrom2Dg-C3N4.Theexperimentalresultsintroducethepotentialapplicationofg-C3N4nanomaterialsasSAsinQ-switchedlasers.

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  • 简介:One-potachievementofethyllevulinatefromcassavawasconductedinethanol-watersystemoverseveralsimplesulfatesaltcatalysts.Al2(SO4)3catalysthadthebestperformanceinsynthesizingethyllevulinatecomparingwiththoseofaseriesofsulfatesalts.Thehighestyieldsofethyllevulinatewasupto39.27%aswellas7.78%levulinateacidwhencassavawascatalyzedinethanolmediumbyadding10wt%water.13Cand1HNMRspectroscopicinvestigationsconfirmedthatisomerizationofglucosetofructoseoverAl2(SO4)3catalystisanimportantstepinproducingethyllevulinateandlevulinateacid.DuetoaggregationsofAl3+underhydrothermalconditions,tinyamountofAl3+weredetectedinfiltrateatthepercentageof0.32%evenifinabsolutewater.BronstedandLewisacidscouldimprovetheyieldofethyllevulinateandlevulinateacidbysynergisticeffect.AllresultssuggestedthatA12(SO4)3wasasimpleandefficientcatalystforethyllevulinateandlevulinateacidproduction.

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  • 简介:Ablackphosphorus(BP)saturableabsorber(SA)solutionwithdifferentconcentrations(1.0and0.5mg/ml)isfabricatedwiththeliquid-phaseexfoliationmethod.ByusingtheBP-SA,acompactdiode-pumpedpassivelyQ-switchedNd:YV04laserisdemonstrated.OnereflectingBragggratingsisusedastheoutputcouplerformodeselection.ByinsertingthoseBP-SAsolutionsinthelasercavity,themaximumsinglelongitudemode,Q-switchedoutputpowersof126mWat692.5kHzand149mWat630.3kHzareachievedatthepumppowerof8.0W,correspondingtothepulsedurationsof144nsand196ns,respectively.Moreover,longitudinal-modecharacteristicsofQ-switchedoutputlaserindifferentopticalcavitylengthsbasedontwo-kindBP-SAsolutionconcentrationsareinvestigated.OurresultsshowthatBP-SAcouldalsobedevelopedasaneffectiveSAfortheQ-switched,singlelongitudinalmodepulselaser.

  • 标签: A SINGLE-LONGITUDINAL-MODE Passively Q-SWITCHED Nd:YVO4 Laser
  • 简介:Nanostructuredmetaloxidesderivedfrommetalorganicframeworkshavebeenshowntobepromisingmaterialsforapplicationinhighenergydensitylithiumionbatteries.Inthiswork,porousnanostructuredZnCo2O4andCo3O4weresynthesizedbyafacileandcost-effectiveapproachviathecalcinationofMOF-74precursorsandtestedasanodematerialsforlithiumionbatteries.ComparedwithCo3O4,theelectrochemicalpropertiesoftheobtainedporousnanostructuredZnCo2O4exhibithigherspecificcapacity,moreexcellentcyclingstabilityandbetterratecapability.Itdemonstratesareversiblecapacityof1243.2mAh/gafter80cyclesat100mA/gandanexcellentrateperformancewithhighaveragedischargespecificcapacitiesof1586.8,994.6,759.6and509.2mAh/gat200,400,600and800mA/g,respectively.ThesatisfactoryelectrochemicalperformancessuggestthatthisporousnanostructuredZnCo2O4ispotentiallypromisingforapplicationasanefficientanodematerialforlithiumionbatteries.

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  • 简介:Wereportontheperformanceofacontinuous-waveNd:GdVO4laserin-banddiode-pumpedat912nmwithhighoutputpowerandexcellentbeamquality.Thelaserproducedanoutputpowerof19.8Wat1063nmwithanopticalefficiencyof59.3%andslopeefficiencyof62.7%.Thelaserthresholdwas2.04Woftheabsorbedpumppower,andthelaseroutputbeamqualitywas≤1.2inthehorizontalandverticaldirections.Thestrengthofthermallensingatfulloutputpower(33.4Wofabsorbedpower)wasmeasuredtobeanaverageof8.6diopters.Itisshownthatthermallensingisreducedbyafactorof2withrespecttotheNd:YVO4lasers,thusopeningawayforfurtheroutput-powerscaling.

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  • 简介:Bysimultaneouslyemployingbothanelectro-opticmodulatorandcarbonnanotubesaturableabsorber(CNT-SA)inadual-lossmodulator,asubnanosecondsinglemode-lockingpulseunderneathaQ-switchedenvelopewithhighpeakpowerwasgeneratedfromadoublyQ-switchedandmode-locked(QML)Nd:Lu0.15Y0.85VO4laserat1.06μmforthefirsttime,toourknowledge.CNTswithdifferentwallstructures—single-walledCNTs(SWCNTs),double-walledCNTs(DWCNTs),andmulti-walledCNTs(MWCNTs)—wereusedasSAsintheexperimenttoinvestigatethesinglemode-lockingpulsecharacteristics.Atpumppowerof10.72W,themaximumpeakpowerof1.312MWwasobtainedwiththeDWCNT.

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  • 简介:LiMn2O4andLiNixAlyMn2-x-yO4(x=0.50;y=0.05-0.50)powdershavebeensynthesizedviafacilesolgelmethodusingBehenicacidasactivecheiatingagent.Thesynthesizedsamplesaresubjectedtophysicalcharacterizationssuchasthermogravimetricanalysis(TG/DTA),X-raydiffraction(XRD),Fouriertransforminfraredspectroscopy(FT-IR),field-emissionscanningelectronmicroscopy(FESEM),transmissionelectronmicroscopy(TEM)andelectrochemicalstudiesviz.,galvanostaticcyclingproperties,electrochemicalimpedancespectroscopy(EIS)anddifferentialcapacitycurves(dQ/dE).FingerprintXRDpatternsofLiMn2O4andLiNixAlyMn2-x-yO4fortifythehighdegreeofcrystallinitywithbetterphasepurity.FESEMimagesoftheundopedpristinespinelillustrateuniformsphericalgrainssurfacemorphologywithanaverageparticlesizeof0.5μmwhileNidopedparticlesdepictthesphericalgrainsgrowth(50nm)withice-cubesurfacemorphology.TEMimagesofthespinelLiMn2O4showstheuniformsphericalmorphologywithparticlesizeof(100nm)whilelowlevelofAl-dopingspinel(LiNio.5Alo.05Mn1.45O4)displayingcloudyparticleswithagglomeratedparticlesof(50nm).TheLiMn2O4samplescalcinedat850℃deliverthedischargecapacityof130mAh/ginthefirstcyclecorrespondsto94%coiumbicefficiencywithcapacityfadeof1.5mAh/g/cycleovertheinvestigated10cycles.Amongallfourdopantcompositionsinvestigated,LiNi0.5Al0.05Mn1.45O4deliversthemaximumdischargecapacityof126mAh/gduringthefirstcycleandshowsthestablecyclingperformancewithlowcapacityfadeof1mAh/g/cycle(capacityretentionof92%)overtheinvestigated10cycles.ElectrochemicalimpedancestudiesofspinelLiMn2O4andLiNi0.5Al0.05Mn1.45O4depictthehighandlowrealpolarizationof1562and1100Ω.

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  • 简介:我们在Mn50Ni40SnSbx(x=1,2,3,和4)合金。所有准备样品在房间温度与空间组一起展出B2类型结构。Sb的替换增加原子价电子集中并且减少联合起来的房间体积。作为结果,当x增加,magnetostructural转变向更高的温度很快变。在在不同磁场变化下面的磁性的熵的变化在这转变附近被探索。等温的磁化曲线展出典型metamagnetic行为,显示magnetostructural转变能被一个磁场导致。悦耳的martensitic转变和磁性的熵变化建议那Mn50Ni40SnSbx合金是应用在的吸引人的候选人固态制冷。

  • 标签: 马氏体相变 Sb掺杂 磁热效应 Mn 合金 磁熵变化