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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.

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简介：合成了一维绳梯链状双金属化合物[Ni(en)2]3[Fe(CN)6]2·2H2O,并对其变温穆斯堡尔谱进行了研究,结果表明该分子磁体中铁的电子态为低自旋Fe3+,而大的四极分裂值(QS)表明此化合物的[Fe(CN)6]3-单元对称结构发生了形变,低温时出现的磁弛豫谱,给出了在该温度点附近出现铁磁耦合相互作用的信息。

简介：ThegatedielectricthicknessdecreasesdramaticallywiththecontinuousscalingofMOSdevices,whichhasseriousconsequencesontheleakagecurrentandthepowerconsumptionoftheSiO2-basedMOSdevices.Hafniumdioxide(HfO2),asakindofhigh-kmaterial,arerecognizedasalternativestoSiO2forfutureadvancedgatedevicesandspaceapplications[1].Radiation-inducedeffectsonconventionalSiO2dielectricshavebeeninvestigated.Now,anenormousamountofeffortwasrequiredtoadaptthenewhigh-ksystemsforradiationhardapplication.

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简介：Chemical-loopingcombustion(CLC)isanovelcombustiontechniquewithinherentCO2separation.Magnetite(Fe3O4)wasselectedastheoxygencarrier.Shenhuacoal(InnerMongolia,China),strawcokeandnaturalcokewereusedasfuelsforthisstudy.Influencesofoperationtemperatures,coaltoFe3O4massratios,anddifferentkindsoffuelsonthereductioncharacteristicsoftheoxygencarrierwereinvestigatedusinganatmospherethermogravimetricanalyzer(TGA).Scanningelectronmicroscopy(SEM)wasusedtoanalysethecharacteristicofthesolidresidues.Experimentalresultsshownthatthereactionbetweenthecoalandtheoxygencarrierbecomestrongatatemperatureofhigherthan800℃.Astheoperationtemperaturerises,thereductionconversionrateincreases.Atthetemperaturesof850oС,900℃,and950℃,thereductionconversionrateswere37.1%,46.5%,and54.1%respectively.However,SEMimagesshowthatatthetemperatureofhigherthan950℃,theironoxidesbecomemeltedandsintered.Thepossibleoperationtemperatureshouldbekeptaround900℃.WhenthemassratiosofcoaltoFe3O4were5/95,10/90,15/85,and20/80,thereductionconversionrateswere29.5%,40.8%,46.5%,and46.6%respectively.Withtheincreaseofcoal,theconversionrategoesup.Butthereexistanoptimalratioaround15/85.Comparisonsbasedondifferentkindsoffuelsshowthatthesolidfuelwithahighervolatileandamoredevelopedporestructureisconducivetothereductionreactivityoftheoxygencarrier.

简介：Photocatalyticwatersplittingandcarbondioxidereductionprovideuscleanandsustainableenergyresources.Thecarbondioxidereductionisalsotheredemptionofthegreenhouseeffect.MoS3/TiO2photocatalystsbasedonTiO2nanoplateshavebeensynthesizedviaahydrothermalacidificationrouteforwaterandcarbondioxidereductionreactions.ThisfacileapproachgenerateswelldispersedMoS3withlowcrystallinityonthesurfaceofTiO2nanoplates.Theas-synthesizedMoS3/TiO2photocatalystshowedconsiderableactivityforbothwaterreductionandcarbondioxidereduction.ThethermaltreatmenteffectsofTiO2,theloadingpercentageofMoS3andthecrystallinephaseofTiO2havebeeninvestigatedtowardsthephotocatalyticperformance.TiO2nanoplatesynthesizedthroughhydrothermalreactionwiththepresenceofHFacidisanidealsemiconductormaterialfortheloadingofMoS3forphotocatalyticwaterandcarbondioxidereductionsimultaneouslyinEDTAsacrificialsolution.

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简介：Inthispaper,carbonmicrospherepreparedbyhydrothermaltreatmentwasactivatedbyKHCO3athightemperature,andemployedasthecatalystforVO2+/VO2+redoxreactionforvanadiumredoxflowbattery(VRFB).CarbonmicrospherecanbeetchedbyKHCO3duetothereactionbetweenthepyrolysisproductsofKHCO3andcarbonatoms.Moreover,KHCO3activationcanbringmanyoxygenfunctionalgroupsoncarbonmicrosphere,furtherimprovingthewettabilityofcatalystandincreasingtheactivesites.Theelectrocatalyticpropertiesofcarbonmicrospherefromhydrothermaltreatmentareimprovedbyhightemperaturecarbonization,andcanfurtherbeenhancedbyKHCO3activation.Amongcarbonmicrospheresamples,theVO2+/VO2+redoxreactionexhibitsthehighestelectrochemicalkineticsonKHCO3activatedsample.ThecellusingKHCO3activatedcarbonmicrosphereasthepositivecatalystdemonstrateshigherenergyefficiencyandlargerdischargecapacity,especiallyathighcurrentdensity.TheresultsrevealthatKHCO3activatedcarbonmicrosphereisanefficient,low-costcarbon-basedcatalystforVO2+/VO2+redoxreactionforVRFBsystem.

简介：WehavecomprehensivelyinvestigatedthefrustratedJ1-J2-J3Heisenbergmodelonasimplecubiclattice.Thismodelallowsthreeregimesofmagneticorder,viz.,(π;π;π),(0;π;π)and(0;0;π),denotedasAF1,AF2,andAF3,respectively.Theeffectsoftheinterplayofneighboringcouplingsonthemodelarestudiedintheentiretemperaturerange.Thezerotemperaturemagneticpropertiesofthismodelarediscussedutilizingthelinearspinwave(LSW)theory,nonlinearspinwave(NLSW)theory,andGreen’sfunction(GF)method.ThezerotemperaturephasediagramsevaluatedbytheLSWandNLSWmethodsareillustrated,andareobservedtoexhibitdifferentparameterboundaries.Incertainregionsandalongtheparameterboundaries,thepossiblephasetransformationsdrivenbytheparametersarediscussed.TheresultsobtainedusingtheLSW,NLSW,andGFmethodsarecomparedwiththoseobtainedusingtheseriesexpansion(SE)method,andareobservedtobeingoodagreementwhenthevalueofJ2isnotclosetotheparameterboundaries.ThegroundstateenergiesobtainedusingtheLSWandNLSWmethodsareclosetothatobtainedusingtheSEmethod.Atfinitetemperatures,onlytheGFmethodisemployedtoevaluatethemagneticproperties,andthecalculatedphasediagramisobservedtobeidenticaltotheclassicalphasediagram.Theresultsindicatethatattheparameterboundaries,atemperature-drivenfirst-orderphasetransitionbetweenAF1andAF2mayoccuralongtheboundaryline.AlongtheAF1-AF3andAF2-AF3boundarylines,AF3islessstablethanAF1andAF2.OurcalculatedcriticaltemperatureagreeswiththatobtainedusingMonteCarlosimulationsandpseudofermionfunctionalrenormalizationgroupscheme.

简介：Thesuppressionoftherecombinationofelectronsandholes(e–h)andtheenhancementofthelightabsorptionofsemiconductorsaretwokeypointstowardefficientphotocatalyticdegradation.Here,wereportafew-layerg-C3N4/α-MoO3nanoneedles(flg-C3N4/α-MoO3NNs)all-solid-stateZ-schememechanismphotocatalystsynthesizedviaatypicalhydrothermalmethodinacontrolledmanner.Therecombinationofthephoto-inducede–hpairscouldbeeffectivelyrestrainedbytheZ-schemepassagewaybetweentheflg-C3N4andα-MoO3NNsinthecomposite,whichcouldalsopromiseahighredoxabilitytodegradepollutants.Anditbecamepossibleforthepreparedphotocatalysttoabsorblightinawiderangeofwavelengths.Thedetailedmechanismwasstudiedbyelectronspin-resonancespectroscopy(ESR).Thelow-dimensionalnanostructureofthetwoconstituents(α-MoO3NNswithone-dimensionalstructureandflg-C3N4withtwo-dimensionalstructure)endowedthecompositewithvarietiesofexcellentphysicochemicalproperties,whichfacilitatedthetransferanddiffusionofthephotoelectronsandincreasedthespecificsurfaceareaandtheactivesites.The10wt%flg-C3N4/α-MoO3NNsshowedthebestphotocatalyticperformancetowardRhBdegradation,therateofwhichwas71.86%,~2.6timeshigherthanthatofα-MoO3NNs.

简介：ThisworkismainlytostudytheeffectofheavyionirradiationonthedamageofsinglelayerMoS2.ThenumberoflayersofMoS2preparedbyCVD(chemicalvapordeposition)methodwasdeterminedbyopticalmicroscopyandRamanspectroscopy.ThemonolayerMoS2preparedbyCVDunderhighenergy209BiionirradiationwasanalyzedbyRamananalysisandAFMobservation.AndtheresultsarecomparedandanalyzedbeforeandafterthebeamirradiationofsinglelayerMoS2preparedbymechanicalstrippingmethod.

简介：TheinteractionprocessofionsandplasmasisanimportanttopicinIon-Beam-DrivenHighEnergyDensityPhysicsandInertialConfinementFusionresearch.Duetothestrongnon-lineareffectsandthespecialimportanceinICFresearch,moreandmoreemphasishasbeengiventotheinvestigationsforionbeaminlowenergyrangeand/orforplasmawithhighintensity[1;2].Here,weaddressthenewlymeasuredresultsoftheenergylossbyslowionspenetratingthefullyionizedhydrogenplasmatarget.

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简介：Fe_(3–x)O_4raspberryshapednanostructures/graphenenanocompositesweresynthesizedbyaone-steppolyol-solvothermalmethodtobetestedaselectrodematerialsforLi-ionbattery(LIB).Indeed,Fe_(3–x)O_4raspberryshapednanostructuresconsistoforiginalorientedaggregatesofFe_(3–x)O_4magnetitenanocrystals,ensuringalowoxidationstateofmagnetiteandahollowandporousstructure,whichhasbeeneasilycombinedwithgraphenesheets.TheresultingnanocompositepowderdisplaysaveryhomogeneousspatialdistributionofFe_(3–x)O_4nanostructuresatthesurfaceofthegraphenesheets.TheseoriginalnanostructuresandtheirstronginteractionwiththegraphenesheetsresultedinverysmallcapacityfadinguponLi+ionintercalation.Reversiblecapacity,ashighas660mAh/g,makesthismaterialpromisingforanodeinLi-ionbatteriesapplication.

简介：Two-dimensional（2D）graphitecarbonnitride（g-C3N4）nanosheetshavebeensuccessfullyusedasasaturableabsorber（SA）inapassivelyQ-switchedNd:LLFlaserat1.3μmforthefirsttime,tothebestofourknowledge.Underanincidentpumppowerof9.97W,theshortestpulsedurationof275nswasacquiredwithoutputpowerof0.96Wandpulserepetitionrateof154kHz,resultinginapulseenergyof6.2μJ.Inaddition,thesaturableabsorptionbehaviorsofzero-dimensional12nmg-C3N4nanoparticles（g-C3N4-NPs）andthree-dimensionalorderedmesoporousg-C3N4（mpg-C3N4）werealsoobserved,althoughtheirmorphologyandstructurewerequitedifferentfrom2Dg-C3N4.Theexperimentalresultsintroducethepotentialapplicationofg-C3N4nanomaterialsasSAsinQ-switchedlasers.