简介:ZnOnanoconearrays(NCAs)decoratedwithblackTiO2nanoparticles(BTiO2NPs)wereuniformlyanchoredonthesurfaceofcarboncloth(CC)directlybyasimplyelectrochemicaldepositionmethod.ThusanovelB-TiO2NPs/ZnONCAs-CChierarchicalheterostructurewasformed.Itdisplayedsuperiorperformanceandachievedahigherphotocurrentover0.4mA·cm^-2beforetheonsetofthedarkcurrent,attributedtotheseparationofthephotogeneratedelectron-holepair.BasedontheB-TiO2NPs/ZnONCAs-CCheterostructure,thecatalystwasfabricatedforpromotingtheseparationofchargecarriers.Moreover,theintroductionofTi^3+andoxygenvacanciesonthesurfaceofTiO2NPsexpandedtheabsorptionbandedgeandenhancedtheelectricalconductivityaswellasthechargetransportationonthecatalyticsurface.ItindicatesthattheB-TiO2NPs/ZnONCAs-CCcompositeisbeneficialtotheimprovementofthephotoelectrochemical(PEC)activity.
简介:InorganicbufferlayerssuchasSiO2orTiO2andtransparentconductiveindium-tin-oxide(ITO)filmswerepreparedonpolyethyleneterephthalate(PET)substratesbyionassisteddeposition(IAD)atroomtemperature,andtheeffectsofSiO2andTiO2onthebendingresistanceperformanceofflexibleITOfilmswereinvestigated.TheresultsshowthatITOfilmswithSiO2orTiO2bufferlayerhavebetterresistancestabilitiescomparedtooneswithoutthebufferlayerwhentheITOfilmsareinwardsbentatabendingradiusmorethan1.2cmandwhentheITOfilmsareoutwardsbentatabendingradiusfrom0.8cmto1.2cm.ITOfilmswithSiO2bufferlayerhavebetterresistancestabilitiescomparedtooneswithTiO2bufferlayeraftertheITOfilmsarebentseveralhundredsofcyclesatthesamebendingradius,fortheadhesionofSiO2isstrongerthanthatofTiO2.ThecompressivestressresultedfrominwardbendingleadstotheformationofmoredefectsintheITOfilmscomparedwiththetensilestressarisingfromoutwardbending.SiO2andTiO2bufferlayerscaneffectivelyimprovethecrystallinityofITOfilmsin(400),(440)directions.
简介:Inthisstudy,titaniumdioxidesupportedbymulti-walledcarbonnanotubes(MWCNTs/TiO2)andCr-dopedTiO2supportedbyMWCNTs(MWNTs/Cr-TiO2)weresynthesizedbythesol-gelmethod.Thepreparedsampleswerecharacterizedbytransmissionelectronmicroscopy,X-rayphotoelectronspectroscopy,X-raydiffraction,theBrunauerEmmett-Telleranalysis,andtheRamanspectroscopy.TheoxidationandefficiencyforremovalofSO2inasimulatedfluegaswereinvestigatedexperimentallyinafixed-bedreactor.The15%MWCNTs/Cr-Ti02sampledisplayedexcellentadsorptionproperties,andaSO2removalrateequatingto30.4151mg/gfromthesimulatedfluegascontaining2300μg/gofSO2,8%of02,and5%ofH20wasachievedunderoptimalconditionscoveringatemperatureof333.15K,andaspacevelocityof1275h^-1.TheadsorptionprocesswasenhancedbecauseCrdopingmodifiedtheporestructureandinhibitedthegraingrowthofTiO2.Inaddition,theFreundlichandLangmuirmodelsrevealedthatSO2wasmainlyadsorbedthroughchemicaladsorptiononthesamplesurfaces,andthethermodynamicmodelanalysisindicatedthattheadsorptionwasaspontaneous,exothermic,andentropy-reducingprocess.TheadsorptionkineticsofSO2canbedescribedbythepseudosecond-orderkineticandtheBanghamdynamicsmodels.Thepossiblereactionmechanisminvolvedindesulfurizationprocesswasalsoproposed.
简介:采用溶胶一凝胶法制备SO4^2-/TiO2催化剂的基体,用不同浓度的硫酸对催化剂基体进行浸渍,考察催化剂性能。选出制备催化剂的硫酸浓度。考察反应温度、甲醇流量对催化剂性能的影响;探讨了催化剂失活的原因。实验结果表明,催化剂S10活性最好;甲醇制烯烃的反应温度为410-430℃,具有98.8%的甲醇转化率和90.65%的乙烯选择性:反应时甲醇的流量为0.05mol·s^-1。
简介:Toimprovetheharvestingofvisiblelightandreducetherecombinationofphotogeneratedelectronsandholes,Ti3+self-dopedTiO2nanoparticlesweresynthesizedandassembledintophotoanodeswithhighvisiblelightphotoelectrochemicalproperties.X-raydiffraction,transmissionelectronmicroscopy,X-rayphotoelectronspectra,electronresonancespectroscopyandenergydispersiveX-rayspectrawereusedtocharacterizethestructure,crystallinity,morphologyandotherpropertiesoftheobtainednanoparticles.UV–visiblediffusereflectancespectrashowedthattheTi3+self-dopedTiO2nanoparticleshadastrongabsorptionbetween400and800nm.Moreover,whenhydrothermaltreatmenttimewasprolongedto22h,theheterogeneousjunctionwasformedbetweentheanataseandrutileTiO2,wheretheanataseparticlesexposedhighlyactive{001}facets.Undervisiblelightirradiation,theTi3+self-dopedTiO2electrodeexhibitedanexcellentphotoelectrocatalyticdegradationofrhodamineB(RhB)andwatersplittingperformance.Intriguingly,byselectinganappropriatehydrothermaltime,thehighphotoconversionefficiencyof1.16%wasachieved.
简介:CdSe/CdS半导体量点共同敏化TiO2nanorod数组在透明的传导性的做氟的符号的听氧化物(FTO)上被制作使用热水、连续的离子的层吸附和反应(SILAR)过程的底层。样品的结构、词法的性质被X光检查描绘衍射(XRD),地排放扫描电子显微镜学(FESEM),和传播电子显微镜学(TEM)。结果显示CdSe/CdSQD在TiO2nanorods的表面上是一致地涂的。轻吸收边的移动被拿紫外可见的吸收系列监视。与TiO2nanorod数组的吸收系列相比,CdSe/CdSQD的免职转移吸收边到更高的波长。当在量点的co-sensitizers敏化太阳能电池(QDSSC),在CdSe/CdS/TiO2nanorod数组的可见光的区域的提高的轻吸收显示CdSe/CdS层能行动。由优化CdSe层免职周期,5.78mA/cm2的光电流,0.469V的开的电路photovoltage和变换,1.34%的效率在100mw/cm2的照明下面被获得。
简介:以TiC14为源物质采用常压化学气相沉积法制备了TiO2薄膜。用紫外光谱测定了膜的透过率,进而计算出折光率、消光系数、光学带隙能等光学参数。结果发现,在不同气流量、沉积温度为100~250℃的条件下制备的TiO2膜,其折射率在2.16~2.82范围内,消光系数在0.04×10-3~6.70×10-3范围内,光学带隙能在2.8~3.08eV范围内。在光催化作用下,TiO2膜用于处理苯酚溶液,苯酚的转化率高达54.05%。关键词##4化学气相沉积(CVD);沉积率;折光率;消光系数;光催化更多还原
简介:Aunanoparticles(AuNPs)wereelectrodepositedatthehighlyorderedanataseTiO2nanotubearray(TiO2NA)electrodeundersonicating,andtheAuNP-TiO2NAsensorwascharacterizedbyscanningelectronmicroscope(SEM),X-rayphotoelectronspectroscopy(XPS),X-raydiffraction(XRD).ThephotoelectrochemicalexperimentsindicatetheAuNP-TiO2NAsensorhaslowerphotoelectro-resistance,higherphotoelectrocatalyticalactivityandstabilitythanthatofpureTiO2NAsensorunderthesameconditions.Theas-preparedsensorcanbeusedforthedeterminationofchemicaloxygendemand(COD)inrealsamples,andtheobtainedresultsarecomparablewellwiththoseofbystandardK2Cr2O7method.Themethodproposedissimple,fast,costeffective,andenvironmentallyfriendly.
简介:采用油的酸的一条简单solvothermal途径被开发了与不同形状准备锐钛矿TiO2nanocrystals,它被从0~0.5mmol增加NaF的数量从nanorods调节到nano椭圆体,并且光乐队差距因此从3.47eV减少了到3.29eV。不管多么当氟化物被改变到NH4F,结果的TiO2nanocrystals拥有了一个锐钛矿阶段,但是由小尺寸的nanocrystals组成并且nanorods,和乐队差距被增加到3.53eV。X光检查光电子光谱学(XPS)结果与NaF的增加的数量说明了氟的符号内容的增加为形状和光乐队的变化的报道能TiO2nanocrystals豁开。而且,氟的符号内容的缺席引起了形状的更少的变化,产品的光乐队差距的增加面对NH4F。这结果可以提供另一个方法与氟化物的帮助改变形状和金属氧化物nanocrystals的乐队差距。