简介:Thenanomaterialsoftenexhibitveryinterestingelectrical,optical,magnetic,andchemicalproperties,whichcannotbeachievedbytheirbulkcounterparts[1-7].Thedevelopmentofuniformnanometersizedparticleshasbeenintensivelypursuedbecauseoftheirtechnologicalandfundamentalscientificimportance[8-15].Itissignificantthatnanostructuredmaterialscanbecontrollablyassembledintotherequiredgeometryontosubstrates,becomingthebasisofthenextgenerationofcomponentsanddevices[16-31].Thedevelopmentofnewmethodsandstrategiesfororganizingthenanoparticlebasicbuildingblocksintothedesiredstructuresisrequired.Superlatticesmadefromthesebuildingblocksgiveustheopportunitytostudynotonlythepropertiesoftheindividualbuildingblocks,butalsocollectiveeffects.Thesuperparamagneticironoxidenanocrystals(NCs)havebeenusedinthefieldsofbio-medicine,ferrofluids,refrigerationsystem,catalysis,particularlyinmagneticresonanceimaging,tissueengineering,anddrugdeliveryapplications[32-42].
简介:Graphitic碳氮化物(g-C3有向在可见轻照耀下面的4-nitrophenol的降级的高photocatalytic活动的N4)被蚀刻的HCl准备由氨中立化列在后面。准备样品的结构,形态学,表面区域,和photocatalytic性质被学习。在处理以后,g-C3N4从几测微计减少了到几百纳米,和g-C3N4从11.5 增加了;m2/g到115 ;m2/g。同时,g-C3N4显著地在可见的光下面向4-nitrophenol的降级在处理以后被改进照耀。小粒子g-C3N4是5.7次体积g-C3为水处理和环境补习为未来应用使它成为有希望的可见轻光催化剂的N4,。
简介:摘要院科技信用是科研活动正常规范进行的重要保障。构建科学的科技信用评价体系,是提高科技信用管理水平的重要手段。本文在对科技信用评价原则进行分析的基础上,提出了科技信用评价的“4C”模式,构建了科技信用评价指标体系,并对科技信用评价的具体流程进行了探讨。
简介:Highlychargedions(HCIs)carryingamountofpotentialenergywillproducesomenewphysicalphenomenabecausethepotentialenergywillbedepositedintoaverysmallvolumewithinaveryshorttime.WewouldapplythecalorimetricmethodtostudytheenergydepositionofHCIs[1;2].Hereinweintroducethenewsetupforcalorimetricmeasurementforthepotentialenergydepositionofhighlychargedionsat320kVHighlyChargedIonsPhysicsExperimentalPlatform.Thesetupwasconstructedby3parts:theDewar,theelectricaltemperaturecontrollerandthemainpart.ThediamondtargetwasconnectedtotheLN2cooledheatsinkby4copperwiresandaPlatinumtemperaturesensorwasgluedtotherearsideofthetarget.AsshowninFig.1.
简介:Two-dimensional(2-D)BiVO4nanosheets-graphene(GR)compositeswithdifferentweightadditionratiosofGRhavebeenpreparedviaafacilewetchemistryprocess.X-raydiffraction(XRD),Ramanspectra,X-rayphotoelectronspectra(XPS),UV-visdiffusereflectancespectra(DRS),field-emissionscanningelectronmicroscopy(FE-SEM),transmissionelectronmicroscopy(TEM),nitrogenadsorption-desorption,transientphotocurrentresponseandphotoluminescence(PL)spectrawereemployedtodeterminethepropertiesofthesamples.ItisfoundthatBiVO4nanosheetscouldpavewellonthesurfaceofgraphenesheets.BiVO4nanosheets-GRcompositeswithaproperadditionamountofGRexhibitedhigherphotocatalyticactivitythanbareBiVO4nanosheetstowardliquid-phasedegradationofrhodamineB(RhB)andmethylorange(MO)undervisiblelightirradiation.TheenhancementofphotocatalyticactivitiesofBiVO4nanosheets-GRcompositescanbeattributedtotheeffectiveseparationofphotoexcitedelectron-holepairs.Thisworknotonlyprovidesasimplestrategyforfabricatingspecific2-Dsemiconductor-2-DGRcomposites,butalsoopensanewwindowofsuch2-Dsemiconductor-2-DGRcompositesasvisiblelightphotocatalyststowardanimprovedvisiblelightphotoactivityinpurifyingpollutedwaterresources.
简介:Well-dispersedBaSO4nanoparticlesweresynthesizedinthepresenceofsodiumpolyacrylate(PAAS)byasimpleprecipitationmethod,withBaCl2and(NH4)2SO4asreactants.ThedifferentrolesperformedbyPAASinthesynthesisofBaSO4nanoparticleswereinvestigatedusingX-raydiffractometry,Fouriertransforminfraredspectroscopy,andtransmissionelectronmicroscopy.TheresultsindicatethattheassynthesizedBaSO4nanoparticlesweresphereswithanaveragediameterof30nmandthattheirsurfaceswereaffectedbythePAAS.Underatypicalprocedureemployed,PAASreactedwithBaCl2toyieldanintermediate,servingasacontrolreleasingagentandseparatingthenucleationandcrystalgrowthprocessesoftheBaSO4nuclei.DuringformationoftheBaSO4nanospheres,theintermediateslowlydissolvedandreleasedbariumandpolyacrylateions,inhibitingthegrowthandaggregationofnewlyformedBaSO4seedsandresultinginparticlesofnarrowdiameterdistributionandimproveddispersibility.Moreover,thesepolyacrylateionsfurthermodifiedthesurfacesoftheBaSO4nanoparticles.