简介:TheextendedRiccatimappingapproachisfurtherimprovedbygeneralizedRiccatiequation,andcombineitwithvariableseparationmethod,abundantnewexactcomplexsolutionsforthe(2+1)-dimensionalmodifieddispersivewater-wave(MDWW)systemareobtained.Basedonaderivedperiodicsolitarywavesolutionandarationalsolution,westudyatypeofphenomenonofcomplexwave.
简介:AnefficientprocessfortheconversionofdimethyloxalateintoethyleneglycolwithhighselectivityandhighyieldoverCu2Owasinvestigated.InsituformedCuasatruecatalyticallyactivespeciesshowedagoodcatalyticperformanceforDMOconversiontoproduceEGin95%yield.
简介:Atacertainhightemperature,thiscyclewillbedominantandendtherp-processtoheavierregion[2].Itprovidesanuppertemperaturelimitforrp-processalongtheprotondriplinetoproducenuclidesbeyondA=84,includingthelightpnuclidesof92;94Mo,96;94Ru.TheexistenceofZr-Nbcycleisanimportantquestioninrp-process[2].α-separationenergy(Sα)of84Moplaysanimportantroleintheformationofthiscycle.Astrongenhancementof83Nb(p,α)reactionrateisduetoaverylowSαof84Mo[1].
简介:PhotocatalyticH2productionhasemergedasoneofthemostcleanandpromisingrenewableenergysources.InspiteoftheeffortstoobtainefficientphotocatalystsabletoproduceH2fromSunlightandwater,thereisstilltheneedtopreparecheaperandenvironmentalfriendlierphotocatalysts.Phosphatebasedmaterialscouldbegoodcandidatestofulfilltheserequirements.InthismanuscriptwehavepreparedasetofmixedTi3+/Ti4+valence,open-frameworktitaniumphosphates(of-TiPO4)andmixedtitaniumoxide/phosphatederivatives(cr-TiP),correlatingtheirstructureandcompositionwiththephotocatalyticactivityforH2production.Wedeterminedthatmixedtitaniumoxide/phosphatecrystallinephasesproducedenhancedH2evolutionunderSunsimulatedlightirradiationthanmixedTi3+/Ti4+valence,open-frameworktitaniumphosphatesandtitaniumoxidephases.
简介:Recentadvancesontheuseofnanocarbon-basedelectrodesfortheelectrocatalyticconversionofgaseousstreamsofCO2toliquidfuelsarediscussedinthisperspectivepaper.Anovelgas-phaseelectrocatalyticcell,differentfromthetypicalelectrochemicalsystemsworkinginliquidphase,wasdeveloped.Thereareseveraladvantagestoworkingasphase,e.g.noneedtorecovertheproductsfromaliquidphaseandnoproblemsofCO2solubility,etc.Operatingundertheseconditionsandusingelectrodesbasedonmetalnanoparticlessupportedovercarbonnanotube(CNT)typematerials,longC-chainproducts(inparticularisopropanolunderoptimizedconditions,butalsohydrocarbonsuptoC8-C9)wereobtainedfromthereductionofCO2.Pt-CNTaremorestableandgiveinsomecasesahigherproductivity,butFe-CNT,particularusingN-dopedcarbonnanotubes,giveexcellentpropertiesandarepreferabletonoble-metal-basedelectrocatalystsforthelowercost.ThecontrolofthelocalizationofmetalparticlesattheinneroroutersurfaceofCNTisanimportactfactorfortheproductdistribution.ThenatureofthenanocarbonsubstratealsoplaysarelevantroleinenhancingtheproductivityandtuningtheselectivitytowardslongC-chainproducts.TheelectrodesfortheelectrocatalyticconversionofCO2arepartofaphotoelectrocatalytic(PEC)solarcellconcept,aimedtodevelopknowledgeforthenewgenerationartificialleaf-typesolarcellswhichcanusesunlightandwatertoconvertCO2tofuelsandchemicals.TheCO2reductiontoliquidfuelsbysolarenergyisagoodattempttointroducerenewablesintotheexistingenergyandchemicalinfrastructures,havingahigherenergydensityandeasiertransport/storagethanothercompetingsolutions(i.e.H2).
简介:IntercalationcompoundFePS3(CoCp2)0.40(CoCp2=cobaltocene)wassynthesized,andthecrystalstructureandmagneticpropertieswerestudiedbyx-raydiffraction,magneticsusceptibilitymeasurement,andMSssbauerspectroscopy.Thecrystalstructurewasindexedtomonoclinicunitcellwitha=5.996^。A,b=10.106^。A,c=12.511^。A,β=105.916°,andabout5.6^。Aexpansionatthec-directioncomparedtopureFePS3.TheMSssbauerspectraindicatethattherearethreekindsofdivalentionswithhighspinstateintheintercalationcompound,whichimplieschargetransferfromguesttotheFe-Se^*ganti-bondingorbitsofthehostlattice.Nocationicvacanciesareformedintheintercalationcompound.Theferromagnetismatlowtemperatureoriginatesfromthespincantingofdivalentions.