简介:ThepreparationofPT/PEK-cfilmsisreportedaswellastheirdielectricandopticalproperties.Thec-axisorientationratioofthefilmsis68%.Dielectricconstantandlossfactorat10kHzisabout4.023F/mand0.003,respectively.Therefractiveindicesofthefilms,neandno,are1.6573and1.6278at0.63μmwavelength,respectively.Theopticalband-gapofthefilmwithathicknessof2.33μmisfoundtobe3.06eV
简介:CarbonsupportedPt(Pt/C)electrocatalystswerepreparedwithglucoseasprotectionagentandNaBH4asreductant.ThePtnanoparticlesdepositedoncarbonsupportpresentedreducedsizeandwelldispersityattributedtotheprotectioneffectofglucose.GlucoseabsorbedontheparticlesurfacewasreadilyremovedbywaterwashingwithoutleadingtoagglomerationofthePtnanoparticles.Theas-preparedPt/Celectrocatalystsshowedimprovedmassactivityformethanolelectrooxidationcomparedtothecatalystpreparedwithoutglucoseprotection.TheimprovedperformanceisattributedtothelargerelectrochemicalactivesurfaceareathusincreasedactivesitesonthePt/Celctrocatalystspreparedundertheprotectionofglucose.
简介:大音阶的第五音胶化旋转涂层在Pt/Ti/SiO2/Sisubstrate上准备的Pb(Zr0.4Ti0.6)O-3电影作为最高的电极与磅或Ru被用于铁电体电容器。为thePt/PZT/Pt和Ru/PZT/Pt铁电体电容器,尽管与一样的铁电体他,不同最高的电极材料招致PZT电容器的不同性质例如疲劳,漏,残余、浸透的极化,除了PZTfilm的类似的水晶取向。在(10)10交换周期以后,Ru/PZT/Pt和Pt/PZT/Ptcapacitors的残余的极化分别地减少到70%和84%。在(8)10交换周期以后,后者的漏水流密度在积极偏爱显然增加,与前者相比。为最高的电极的Differentmaterials在PZT/top电极接口带不同条件。在PZT/electrode接口和在到充电注射的PZT/electrode接口的电极材料的氧化物的影响的氧空缺集中的Theinfluence能作为最高的电极与磅或Ru解释PZT电容器的性质的差别。
简介:APt-MoO3/Ccatalyst,aimedtoeliminatetheharmfuleffectofsulfurdioxide(SCb)ontheperformanceofPtnanoparticles(NPs)forcatalysisofoxygenreductionreaction(ORR)inprotonexchangemembranefuelcells(PEMFC),isdevelopedandcharacterizedbyTEM,XRDandXPS.TheresultsrevealthatPt-MoO3/Ccatalystexhibitsnotonlyahighercatalyticactivity,butalsoabetterSO2poisoningresistanceandabetterrecoveryperformancethanthecommercialPt/Ccatalystdoes.
简介:ThemetaloxidesCuMnCeandCeYwashcoatsoncordieritewerepreparedusinganimpregnationmethod,andthenusedassupportfortheactivePtcomponenttopreparethePt/CuMnCeandPt/CeYmonolithiccatalystsforthedeepoxidationofVOCs.IncomparisonwiththePt/CeY,CuMnCe,andCeYmonolithiccatalysts,thePt/CuMnCemonolithiccatalystshowsanexcellentperformancefortoluene,ethylacetate,andn-hexaneoxidationandtheT90%islowto216,200and260℃,respectively.TheactivecomponentsPt/PtOandCuMnCeresultinabettersynergeticinteraction,whichpromotethecatalystreducibility,increasetheoxygenmobility,andenhancetheadsorptionandactivationoforganicmolecules.
简介:Pt/WO3/CnanocompositeswithparallelWO3nanorodsweresynthesizedandappliedasthecathodecatalystforprotonexchangemembranefuelcells(PEMFCs).Electrochemicalresultsandsinglecelltestsshowthatanenhancedactivityfortheoxygenreductionreaction(ORR)isobtainedforthePt/WO3/CcatalystcomparedwithPt/C.ThehighercatalyticactivitymightbeascribedtotheimprovedPtdispersionwithsmallerparticlesizes.ThePt/WO3/Ccatalystalsoexhibitsagoodelectrochemicalstabilityunderpotentialcycling.Thus,thePt/WO3/CcatalystcanbeusedasapotentialPEMFCcathodecatalyst.
简介:ThisstudyshowsthepreparationofaTiO_2coatedPt/C(TiO_2/Pt/C)byatomiclayerdeposition(ALD),andtheexaminationofthepossibilityforTiO_2/Pt/Ctobeusedasadurablecathodecatalystinpolymerelectrolytefuelcells(PEFCs).CyclicvoltammetryresultsrevealedthatTiO_2/Pt/Ccatalystwhichhas2nmprotectivelayershowedsimilaractivityfortheoxygenreductionreactioncomparedtoPt/Ccatalystsandtheyalsohadgooddurability.TiO_2/Pt/Cpreparedby10ALDcyclesdegraded70%after2000Accelerateddegradationtest,whilePt/Ccorroded92%inthesameconditions.TiO_2ultrathinlayerbyALDisabletoachieveagoodbalancebetweenthedurabilityandactivity,leadingtoTiO_2/Pt/CasapromisingcathodecatalystforPEFCs.ThemechanismoftheTiO_2protectivelayerusedtopreventthedegradationofPt/Cisdiscussed.
简介:Electrolysisofammoniainalkalineelectrolytesolutionwasappliedfortheproductionofhydrogen.BothPt-loadedNifoamandPt-IrloadedNifoamelectrodeswerepreparedbyelectrodepositionandservedasanodeandcathodeinammoniaelectrolyticcell,respectively.TheelectrochemicalbehaviorsofammoniainKOHsolutionwereindividuallyinvestigatedviacyclicvoltammetryonthreeelectrodes,i.e.bareNifoamelectrode,Pt-loadedNifoamelectrodeandPt-IrloadedNifoamelectrode.ThemorphologyandcompositionofthepreparedNifoamelectrodewereanalyzedbyscanningelectronmicroscopy(SEM)andX-raydiffraction(XRD).Effectsoftheconcentrationofelectrolytesolutionandtemperatureofelectrolyticcellontheelectrolysisreactionwereexaminedinordertoenhancetheefficiencyofammoniaelectrolysis.Thecompetitionofammoniaelectrolysisandwaterelectrolysisinthesamealkalinesolutionwasfirstlyproposedtoexplainthechangesofcellvoltagewiththeelectrolysisproceeding.Atvaryingcurrentdensities,differentcellvoltagescouldbeobtainedfromgalvanostaticcurves.Thelowcellvoltageof0.58V,whichislessthanthepracticalelectrolysisvoltageofwater(1.6V),canbeobtainedatacurrentdensityof2.5mA/cm2.Basedonsomeexperimentalparameters,suchastheappliedcurrent,theresultingcellvoltageandoutputofhydrogengas,thepowerconsumptionpergramofH2producedcanbeestimated.
简介:Thisworkreportsafeasiblesynthesisofhighly-dispersedPtandPt-Fenanoparticlessupportedonmultiwallcarbonnanotubes(MWCNTs)withoutFeandmultiwallcarbonnanotubeswithiron(MWCNTs-Fe)whichappliedaselectrocatalystsformethanolelectrooxidation.APtcoordinationcomplexsaltwassynthesizedinanaqueoussolutionanditwasusedasprecursortopreparePt/MWCNTs,Pt/MWCNTs-Fe,andPt-Fe/MWCNTsusingFeCl24H2OasironsourcewhichwerenamedS1,S2andS3,respectively.Thecoordinationcomplexofplatinum(TOA)2PtCl6wasobtainedbythechemicalreactionbetween(NH4)2PtCl6withtetraoctylammoniumbromide(TOAB)anditwascharacterizedbyFT-IRandTGA.ThematerialswerecharacterizedbyRamanspectroscopy,SEM,EDS,XRD,TEMandTGA.TheelectrocatalyticactivityofPt-basedsupportedonMWCNTsinthemethanoloxidationwasinvestigatedbycyclicvoltammetry(CV)andchronoamperometry(CA).Pt-Fe/MWCNTselectrocatalystsshowedthehighestelectrocatalyticactivityandstabilityamongthetestedelectrocatalystsduetothattheadditionof'Fe'promotestheOHspeciesadsorptionontheelectrocatalystsurfaceatlowpotentials,thus,enhancingtheactivitytowardthemethanoloxidationreaction(MOR).