简介：Co(II)-salenwasencapsulatedinMIL-100(Cr)metalorganicframeworkby"shipinabottle"tosynthesizeanewelectrocatalyst,Cosalen@MIL-100(Cr).ThematerialwascharacterizedbyXRD,FT-IR,UV-VisandN2-adsorption.TheCosalen@MIL-100(Cr)modifiedglassycarbonelectrodeexhibitsawell-definedreductionpeakatthepotentialof–0.21Vtowardtheoxygenreductionreaction(ORR)bycyclicvoltammetry(CV)inpH=6.84phosphatebuffer.Almost400mVpositiveshiftofpotentialatCosalen@MIL-100(Cr)modifiedelectrodeforORRcomparedwiththatatbareglassycarbon,indicatesthatCosalen@MIL-100(Cr)possessesexcellentelectrocatalyticactivity.ThetransferrednumberofelectronsforORRwasdeterminedbychronocoulometry.TheresultsuggeststhattheintroductionofCo(II)-salencomplexintoMOFincreasestheelectrocatalyticactivityviaafour-electronreductionpathway.Furthermore,thiselectrocatalystexhibitsgoodstabilityandreproducibility.

简介：Variousmesoporouschromiaaluminacatalystswerepreparedbyfivedifferentmethodsbasedonametal-organicframeworkMIL-101andtheircatalyticperformancesoverisobutanedehydrogenationwereinvestigated.ThehighlydispersedchromiumspecieswereproducedoncatalystKCrAl-I1withlargestspecificsurfaceareaof198m2g-1preparedwithaluminiumisopropoxide(Al(i-OC3H7)3)byultrasonicimpregnationmethod.However,thecatalystKCrAl-I2synthesizedbystirringimpregnationpossessedcrystallineα-Cr2O3phase,whichwaspoorlydispersed.TwotypesofCr-richandAl-richCrxAl2-xO3solidsolutions,designatedasCrAl-IandCrAl-IIphase,wereformedoverthecatalystsKCrAl-I3(preparedbyAl(i-OC3H7)3withnitricacidregulation),KCrAl-C4(preparedbyaluminiumchloridehexahydrate)andKCrAl-N5(preparedbyaluminiumnitratenonahydrate).CatalyticevaluationresultsrevealedthatKCrAl-I1exhibitedthehighisobutaneconversionduetoitshighlydispersedchromiumspecies.However,KCrAl-I3,KCrAl-C4andKCrAl-N5showedthehigherisobuteneselectivity(95.2%-96.4%)onaccountoftheformationofchromiaaluminasolidsolutionsinthecatalysts.Moreover,thesolidsolutionoverthechromiaaluminacatalystscouldgreatlysuppressthecokeformation.

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