简介：

简介：

简介：ThreeseriesofCeO2/CuOsampleswerepreparedbyimpregnationmethodandcharacterizedbyXRD,N2adsorption-desorption,temperatureprogrammedreduction(TPR),XPSandTEMtechniques.IncomparisonwiththesamplespreparedwithCuOasinitialsupport,thesampleswithCu(OH)2asinitialsupporthavehigherreducibilitiesandsmallerrelativeTPRpeakareas,andalsolargerspecificsurfaceareasatcalcinationtemperaturesof400℃–600℃.Asaresult,Cu(OH)2isbetterthanCuOasinitialsupportforpreferentialoxidationofCOinexcessH2(CO-PROX).Thebestcatalyticperformancewasachievedonthesamplecalcinedat600℃andwithanatomicratioofCe/Cuat40%.XPSanalysesindicatethatmoreinterfacelinkagesCe-O-Cucouldbeformedwhenitwascalcinedat600℃.AndtheatomicratioofCe/Cuat40%ledtoaproperreducibilityforthesampleasillustratedbytheTPRmeasurements.

简介：ThemorphologyeffectofZr-dopedCeO2wasstudiedintermsoftheiractivitiesintheselectiveoxidationofstyrenetostyreneoxideusingtert-butylhydroperoxideastheoxidant.Inthepresentwork,ZrdopedCeO2nanorodsexhibitedthehighestcatalyticperformance（yieldofstyreneoxideandTOFvalue）followedbynanoparticlesandnanocubes.FortheZr-dopedCeO2nanorods,theapparentactivationenergyis56.3kJ/mol,whichismuchlowerthanthevaluesofcatalystssupportedonnanoparticlesandnanocubes（73.3and93.4kJ/mol）.Thehighresolutiontransmissionelectronmicroscopyresultsindicatedthat（100）and（110）crystalplanesarepredominantlyexposedforZr-dopedCeO2nanorodswhile（100）and（111）fornanocubes,（111）fornanoparticles.TheremarkablyincreasedcatalyticactivityoftheZrdopedCeO2nanorodsismainlyattributedtothehigherpercentageofCe3+speciesandmoreoxygenvacancies,whichareassociatedwiththeirexposed（100）and（110）crystalplanes.Furthermore,recyclingstudiesprovedthattheheterogeneousZr-dopedCeO2nanorodsdidnotloseitsinitialhighcatalyticactivityafterfivesuccessiverecycles.

简介：CuO-CeO2catalystswerepreparedbyaureaprecipitationmethodfortheoxidativesteamreformingofethanolatlow-temperature.Thecatalyticperformancewasevaluatedandthecatalystswerecharacterizedbyinductivelycoupledplasmaatomicemissionspectroscopy,X-raydiffraction,temperature-programmedreduction,fieldemissionscanningelectronmicroscopyandthermo-gravimetricanalysis.OverCuOCeO2catalysts,H2withlowCOcontentwasproducedinthewholetestedtemperaturerangeof250–450C.Thenon-noblemetalcatalyst20CuCeshowedhigherH2productionratethan1%Rh/CeO2catalystat300–400Candtheadvantagewasmoreobviousafter20htestingat400C.TheseresultsfurtherconfirmedthatCuO-CeO2catalystsmaybesuitablecandidatesforlowtemperaturehydrogenproductionfromethanol.