简介:Er^3+-dopedSrBi4Ti4O15-Bi4Ti3O12(SBT-BIT-xEr^3+,x=0.00,0.05,0.10,0.15and0.20)inter-growthceramicsweresynthesizedbythesolid-statereactionmethod.Structural,electricalandup-conversionpropertiesofSBT-BIT-xEr^3+wereinvestigated.Allsamplesshowedasinglephaseoftheorthorhombicstructure.RamanspectroscopyindicatedthattheEr^3+substitutionforBi^3+atAsitesofthepseudo-perovskitelayerincreasesthelatticedistortionofSBT-BIT-xEr^3+ceramics.ThesubstitutionofBi^3+byEr^3+leadstoadecreaseofdielectriclosstanδandanincreaseofconductivityactivationenergy.Piezoelectricconstantd33wasslightlyimproved,butdielectricconstantwasdecreasedwiththeEr^3+doping.TheSBT-BIT-xEr^3+ceramicwithx=0.15exhibitstheoptimizedelectricalbehavior(d33~17pC/N,tanδ~0.83%).Moreover,twobrightgreen(532and548nm)andonered(670nm)emissionbandswereobservedunderthe980nmexcitation.Optimizedemissionintensitywasalsoobtainedwhenx=0.15fortheSBT-BIT-xEr^3+ceramic.Therefore,thiskindofceramicsoughttobepromisingcandidatesformultifunctionaloptoelectronicapplications.
简介:WereportQ-switchedandmode-lockederbium-dopedall-fiberlasersusingternaryReS2(1-x)Se2xassaturableabsorbers(SAs).ThemodulationdepthandsaturableintensityofthefilmSAare1.8%and0.046MW∕cm2.InQ-switchedmechanismoutput,thepulsewascenteredat1531.1nmwithmaximumpulseenergyandminimumpulsewidthof28.29nJand1.07μs,respectively.Inmode-lockedoperation,thepulsewascenteredat1561.15nmwithpulsewidthof888fs,repetitionrateof2.95MHz,andmaximumpulseenergyof0.275nJ.Tothebestofourknowledge,thisisthefirstreportonthemode-lockedEr3+-dopedfiberlaserusingternarytransitionmetaldichalcogenides.Thisworksuggestsprospective2D-materialSAscanbewidelyusedinversatilefieldsduetotheirattractiveoptoelectronicandtunableenergybandgapproperties.
简介:摘要 : 随着 LTE-V2X 车联网技术及标准的研究应用,将大幅提升车辆智能化水平,并有效增强交通运输的安全性。在 LTE-V2X 技术及标准研究中,相关部门及企业应增大研究力度,使该技术及标准不断优化,切实推进其实际应用,进而促进智能汽车等行业的发展。
简介:TheapplicationofXzeoliteintheareasforproducingpara-xylenebyadsorptiveseparation,N2/O2separation,etc.,wasreviewed,andtheframeworkSiO2/Al2O3molarratio,thecationsandthewatercontentofXzeolitesignificantlyaffecteditsselectivityandcapacity.Astheactivecomponentofpara-xyleneadsorbent,theXzeolitewithaframeworkSiO2/Al2O3molarratioof2.2-2.4coupledwithcationsofBa^2+andK^+,aswellasawatercontentof4.0%-5.0%exhibitedhigherpara-xyleneselectivity.ForN2/O2separation,higherN2capacityandN2/O2separationfactorwereachievedwhentheXzeolitehadaframeworkSiO2/Al2O3molarratioof2.0coupledwithLi^+cations.TheintroductionofanothercationinXzeolitecouldfurtherincreasetheN2/O2separationfactor,whiletheadsorptionofwater,however,couldleadtoaremarkabledecreaseofN2capacity.Besides,theXzeolitecouldbeusedinadsorptiveseparationofhighlypureHeandselectiveadsorptionofCO2,CO,CH4,N2,Ar,andH2.