简介：Sn-dopedTiO_2nanoparticleswithhighsurfaceareaof125.7m~2·g~(-1)aresynthesizedviaasimpleone-stephydrothermaimethodandexploredasthecathodecatalystsupportforprotonexchangemembranefuelcells.ThesynthesizedsupportmaterialsarestudiedbyX-raydiffractionanalysis,energydispersiveX-rayspectroscopyandtransmissionelectronmicroscopy.Itisfoundthattheconductivityhasbeengreatlyimprovedbytheadditionof30mol%SnandPtnanoparticlesarewelldispersedonTi_(0.7)Sn_(0.3)O_2supportwithanaveragesizeof2.44run.ElectrochemicalstudiesshowthattheTi_(0.7)Sn_(0.3)O_2nanoparticleshaveexcellentelectrochemicalstabilityunderahighpotentialcomparedtoVulcanXC-72.Theas-synthesizedPt/Ti_(0.7)Sn_(0.3)O_2exhibitshighandstableelectrocatalyticactivityfortheoxygenreductionreaction.ThePt/Ti_(0.7)Sn_(0.3)O_2catalystreservesmostofitselectrochemicallyactivesurfacearea(ECA),anditshalfwavepotentialdifferenceis11mV,whichislowerthanthatofPt/XC-72(36mV)under10hpotentialholdat1.4Vvs.NHE.Inaddition,theECAdegradationofPt/Ti_(0.7)Sn_(0.3)O_2is1.9timeslowerthancommercialPt/XC-72under500potentialcyclesbetween0.6Vand1.2Vvs.NHE.Therefore,theassynthesizedPt/Ti_(0.7)Sn_(0.3)O_2canbeconsideredasapromisingalternativecathode,catalystforprotonexchangemembranefuelcells.

简介：Usingsevenworkingfluids,asystematicexperimentalstudywasperformedtoinvestigatethelocalconvectiveheattransferfromverticalheaterstoimpingingcircularsubmergedjetsintherangeofReynoldsnumberbetween1.17×10^2and3.69×10^4withtheemphasisplacedontheexaminationofPrandtlnumberdependence.Heattransfercoefficientsatthestagnationpointwerecollectedandcorrelatedwiththeplateheldwithinandbeyondthepotentialcore.Radialdistributionofthelocalheattransfercoefficientwasmeasuredwithfivetestliquids.Basedonthemeasuredprofilesofthelocalheattransfer,acorrelationwasdevelopedtocovertheentirerangeoftheadialdistance.Basidesthepresentdata,thecorrelationsdevelopedinthisworkwerealsocomparedwithalargequantityofavailabledataofcircularairjets.Generalagreementwasobservedbetweentheairdataandthecorrelations.

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简介：Ba1.0Co0.7Fe0.2Nb0.1O3-δ(BCFN)oxidewithperovskitecubicstructurewassynthesizedbysolidstatereactionmethod.CO2corrosionofBCFNmembranewasinvestigatedbyX-raydiffraction(XRD),scanningelectronmicroscopy(SEM),diffusereflectanceinfraredFouriertransformedspectroscopy(DRIFT)andX-rayabsorptionfinestructurespectroscopy(XAFS).Cobalt(Co)K-edgeabsorptionspectraofBCFNannealedinCO2revealthattheoxidationstatesofCoinallthesampleswerelargerthan+3andtheydecreasedwiththeincreaseofcalcinationtime.At800℃,1%CO2introducedintoHecouldspeedupthereductionofCocationsincomparisonwithpureHe.Inaddition,sulfateionsinthebulkofBCFNmembranepreferredtomigratetothesurfaceunderCO2calcinationandformmonoclinicBa(CO3)0.9(SO4)0.1besidesorthorhombicwitherite.Moreover,SEMresultsindicatethatthenucleationandgrowthofcarbonatesgrainsstartedatthegrainboundaryofthemembrane.