
CaesiumLeadperovskiteQuantumdotsofchloride/bromide(450nm,blue),bromide(515nm,green)andiodide(685nm,red)arenowavailable.
Perovskitequantumdotsaresemiconductingnanocrystals.Comparedtometalchalcogenidequantumdots,perovskitequantumdotsaremoretoleranttodefectsandhaveexcellentphotoluminescencequantumyieldsandhighcolourpurity.ThesepropertiesarehighlydesirableforelectronicandoptoelectronicapplicationsandhenceperovskitequantumdotshavehugepotentialforrealworldapplicationsincludingLEDdisplaysandquantumdotsolarcells.
ossilasupplieshighquality,lowpriceperovskitequantumdotsfrom£200.00.

Whatisaquantumdot?
Aquantumdot(QD),orsemiconductingnanocrystal(NC),isasinglecrystalofasemiconductingmaterialmeasuringonlyafewnanometresindiameter.Whenexcited,thesmallsizeofthecrystalactsa‘quantumbox’andconfineselectronsandholesinanvolumesmallerthanthecorrespondingexcitonBohrrADIus.Thesmallerthedot,thegreatertheconfinementenergyandthehighertheenergyofphotonsthatareabsorbedoremitted.
Themostwell-studiedquantumdotsaremetalchalcogenidequantumdotsbasedonsemiconductorssuchascadmiumselenide,indiumphosphideorLead(II)sulfide.ThebandgapofsuchquantumdotscanbetunedthroughouttheentirevisIBLespectrumsimplybychangingtheirsizeduringchemicalsynthesis.
Forthehighestphotoluminescencequantumyields(PLQYs),acore/shellstructureisusuallyrequired.Inthisarrangement,asecondsemiconductorisusedtoencapsulatethenanocrystal(e.g.CdSe/CdS,InP/ZnS).Thismaterialpassivatessurfacedefectsoftheemissivecorewhichwouldotherwiseactasnon-radiativerecombinationsitesforexcitons.
DuetotheirhighPLQY,relativeeaseoffabricationandwideemission-colourtunABIlity,quantumdotshavingthistypeofstructureareespeciallysuitableforapplicationindisplayandimagingtechnologies-andarealreadyappearingincommercialproductssuchastelevisions.

Whatisaperovskitequantumdot?
Anewclassofquantumdotisemergingbasedonperovskites.ThesehavealreadybeenshowntohavepropertiesrivallingorexceedingthoseofmetalchalcogenideQDs.
Duetotheiroutstandingphotovoltaicperformance,perovskitesarereceivingsignificantattentionfromtheresearchcommunity.Recently,hasbeenshownthatreducingthedimensionsofaperovskitecrystaldowntoafewnanometresresultsinthecreationofquantumdotswithveryhighphotoluminescencequantumyieldsandexcellentcolourpurity(i.e.narrowemissionlinewidthsof~10nmforblueemittersand40nmforredemitters[1]).
Thesequantumdotsarehighlytoleranttodefects,astheyrequirenopassivationofthesurfacetoretaintheirhighPLQY.Althoughdefectandtrapsitesarepresent,theirenergiesarepositionedoutsidethebandgapandareeitherlocatedwithintheconductionorvalencebands[2].SuchperovskitenanocrystalsaresimpletosynthesiseinacolloidalsUSPensionandareeasilyintegratedintooptoelectronicdevicesusingreadilyavailableprocessingtechniques,makingthemastrongcontenderforfuturetechnologies.
Size,Properties,andStructure
- 99%puritywithPhotoluminescenceQuantumYieldof60–70%
- EmissionPeakat515nmandEmissionLinewidth(FWHM)of21nm
- Cubiccrystalstructurewithtypicalsize4-15nm
Formoreinformation,pleaseseethepropertiestab.
PerovskiteQuantumDotApplications
Perovskitequantumdotsarecurrentlylesswellresearchedthanothertypesofquantumdot.However,theyhaveshowngreat potentialforarangeofdifferentapplicationsinoptoelectronicsandnanotechnology.Forexample, perovskitequantumdotshavebeenusedtocreatesolarcellshavingpowerconversionefficienciesthatexceedthatofcomparabledevicesbasedonmoreconventionalsemiconductornanocrystalmaterials.
Potentialapplicationsforperovskitequantumdotsinclude:
- LightEmittingDiodes
- SolarCells
- SinglePhotonSources
- X-RayDetectors
- Lasers
- Photodetectors
- QuantumComputing
- Cellimaging
- Cancermapping
Formoreinformation,pleaseseetheapplicationstab.
TechnicalData
CsPbBr3PerovskiteQuantumDots
CASnumber | 15243-48-8 |
Chemicalformula | CsPbBr3 |
Molecularweight | 579.82 g/mol |
Fullname | Caesiumleadtribromidequantumdots |
Synonyms | Caesiumleadbromidequantumdots |
Classification/Family | Perovskitequantumdots, Perovskitenanocrystalsolutions, Cadmium-freequantumdots,Quantumdotsolutions,Greenemitter,QuantumdotLEDs(QDLEDs),PerovskiteLEDs(PeLEDs),Perovskitesolarcells(PvSCs) |
Purity | 99% |
Appearance | YellowLiquid |
EmissionPeak | 515nm |
EmissionLinewidth(FWHM) | 21nm |
PhotoluminescenceQuantumYield | 60-70% |
CsPbCl1.5Br1.5 PerovskiteQuantumDots
CASnumber | Notavailable |
Chemicalformula | CsPbCl1.5Br1.5 |
Molecularweight | 513.14 g/mol |
Fullname | Caesiumleadchloridebromidequantumdots |
Synonyms | Caesiumlead chloridebromidequantumdots |
Classification/Family | Perovskitequantumdots, Perovskitenanocrystalsolutions, Cadmium-freequantumdots,Quantumdotsolutions,Greenemitter,QuantumdotLEDs(QDLEDs),PerovskiteLEDs(PeLEDs),Perovskitesolarcells(PvSCs) |
Purity | 99% |
Appearance | Clear Liquid |
EmissionPeak | 450nm |
EmissionLinewidth(FWHM) | 20nm |
PhotoluminescenceQuantumYield | 30-40% |
CsPbI3 PerovskiteQuantumDots
CASnumber | 18041-25-3 |
Chemicalformula | CsPbI3 |
Molecularweight | 720.82 g/mol |
Fullname | Caesiumleadtriiodide quantumdots |
Synonyms | Caesiumlead iodide quantumdots |
Classification/Family | Perovskitequantumdots, Perovskitenanocrystalsolutions, Cadmium-freequantumdots,Quantumdotsolutions,Greenemitter,QuantumdotLEDs(QDLEDs),PerovskiteLEDs(PeLEDs),Perovskitesolarcells(PvSCs) |
Purity | 99% |
Appearance | DarkRed Liquid |
EmissionPeak | 688nm |
EmissionLinewidth(FWHM) | 39nm |
PhotoluminescenceQuantumYield | 60-70% |
PerovskiteQuantumDotSpectralData
CsPbBr3PerovskiteQuantumDotsAbsorptionSpectra
CsPbBr3PerovskiteQuantumDotsPhotoluminescenceSpectra
CsPbCl1.5Br1.5 PerovskiteQuantumDotsPhotoluminescenceSpectra
CsPbI3 PerovskiteQuantumDotsPhotoluminescenceSpectra
MSDS Documents
CsPbBr3PerovskiteQuantumDotsinToluene
CsPbBr3PerovskiteQuantumDotsinOctane
PropertiesofPerovskiteQuantumDots
PerovskiteQuantumDot Structure
Halideperovskitenanocrystalshaveacubiccrystalstructure withthechemicalformula A+Pb2+X-3.Theycanbeclassedasanorganic-inorganichybrid,where A isanorganiccationsuchasmethylammonium(MA)orformamidinium(FA),orfullyinorganic(A=Cs),andwhere X isahalogen(Cl,BrorI).Duetothelackofvolatileorganics,fully-inorganic nanocrystals tendtohavebetterstabilityandhigherPLQY(>90%)thanhybridorganic-inorganicmaterials[3].Mixedhalideperovskitescanalsobeproducedwhere X isamixtureofCl/BrorBr/I.
Forvisibleoptoelectronicapplications,thenanocrystalsaregenerallysynthesisedtohaveasizeof4-15nm(dependentonthehalogenatomandtherequiredopticalproperties).Theemissionwavelengthcanbetunedthroughtheentirevisiblespectrum(400-700nm [4])bychangingeitherthenanocrystalsizeorhalideratio(formixedhalidesystems).

PerovskiteQuantumDotSynthesis
Thefirsthybridorganic-inorganicperovskitequantumdotcolloidalsynthesisofMAPbBr3 wasreportedbySchmidtetal.usingahotinjectionmethod(similartothatusedtosynthesisemetalchalcogenideQDs [4]).Amixtureofmethylaminebromideandleadbromidewasinjectedintoanoctadecenesolutioncontainingoleicacidandalongchainalkylammoniumbromide.ThePLQYoftheresultingQDswas~20%,andwasstableforseveralmonthsduetothestabilisingandcappingeffectsoftheammoniumbromideandoleicacid.Byoptimisationofthereactantmolarratios,thePLQYwasincreasedtoover80% [5],andlaterto~100%bychangingthecappingligand [6].

Hotinjectionwasagainusedforthecolloidalsynthesisofinorganicmetal-halideperovskitequantumdots,firstreportedbyProtesescuetal [1].Thatrecipedevelopedwasasfollows:
- ThecaesiumprecursorCs-oleateisfirstpreparedbymixingcaesiumcarbonate(Cs2CO3)andoleicacid(OA)inoctadecene(ODE),andheatingundernitrogenuntiltheCs2CO3 hasreactedwiththeOA.Thissolutionmustbekeptabove100°CtopreventprecipitationoftheCs-oleate.
- Aleadhalideprecursorispreparedbymixingaleadhalide(PbCl2,PbI2,PbBr2 oramixtureofthese)inODEat120°Cundernitrogen,alongwithOAandoleylamine(OLA)thatactasstabilisingagents.Oncetheleadhalidehasdissolved,thetemperatureisincreasedtobetween140-200°C(dependingontherequirednanocrystalsize).
- Thecaesiumprecursoristheninjected.After5seconds,themixtureisrapidlycooledinanicebath,withthequantumdotsbeingisolatedthroughcentrifuging.
TheresultingnanocrystalshavesurfaceligandscomprisedofOAandOLA [3].SuchnanocrystalswerefoundtohavePLQYsupto~90%,withthesmallestcrystals(4nmdiameter)havinganemissionlinewidth(fullwidthhalfmaximum)of12nmatanemissionwavelengthof410nm,withthelargestquantumdots(15nmdiameter)havingalinewidthof42nmat700nm.
Mixed-halidePerovskiteQuantumDots
Anadvantagethatperovskitequantumdotshaveovertheirmetalchalcogenidecounterpartsisthesimplicitybywhichtheiremissionpropertiescanbemodified.Inadditiontotuningtheemissionwavelengthduringsynthesisthroughreactiontemperature(andultimately,nanocrystalsize),itcanalsobechangedpost-synthesisthroughananion-exchangereaction [7,8].Bymixingadonorhalidesourcesuchasoctadecylammonium(ODA-Y),chloro-oleyalmine-oleylammoniumchloride(OLAM-Y)ortetrabutylammonium(TBA-Y)halide(whereYisCl,BrorI)withasolutionofCsPbX3 nanocrystals,thechemicalcompositionofthenanocrystalscanbetunedcontinuouslyovertherangeCsPb(X1-Z:YZ),where0≤Z≤1.

Anionexchangeisfollowedbylatticereconfiguration,givingamixedhalidestructure.Thisresultsinasingleemissionpeakatanenergysomewhereinbetweenthoseoftheconstituentnanocrystals,therebyretainingthenarrowlinewidthneededforcolorpurity.HoweverithasbeenfoundthatdirectconversionbetweenCsPbI3 andCsPbCl3 isnotpossiblebecauseofthelargemismatchinthesizeofthehalideions.
Ithasalsobeendemonstratedthatthisanionexchangeprocesscanbeeasilyaccomplishedbysimplymixingdifferentstocksolutionsofthenanocrystalconstituentsatdifferentvolumeratios(e.g.CsPbBr3 andCsPbI3 toobtainCsPb(Br1-Z:IZ)3 [7,9]).BothmethodsallowthenanocrystalemissiontobetunedovertheentirevisiblerangewhileretainingahighPLQYandcolorpurity.Theanionexchangeprocesscanhoweverbesuppressedbyaddingpolyhedraloligomericsilsesquioxane(POSS)tothesolution.Thiscreatesaprotectivecagearoundthenanocrystals,andallowsmixingofdifferenthalidecompositionswhileretainingthephotoluminescent propertiesoftheconstituentnanocrystals.Italsohastheaddedeffectofprotectingthenanocrystalsfromwater [10].

ApplicationsofPerovskiteQuantumDots
Perovskitequantumdotshavehugepotentialforarangeofapplicationsinelectronics,optoelectronicsandnanotechnology.Currently,thefieldisnotwellresearched,butinitialresultsareextremelypromising.Detailsonaselectionoftheapplicationsthathavebeeninvestigatedaregivenbelow.
QuantumDotSolarCells
Currently,reportsofperovskitequantumdotsolarcellsarestilllimited,especiallywhencomparedtobulkand2-dimensionalperovskites.Thisislikelyduetothelimitedtimethatsuchmaterialshavebeenavailable.However,recentresults suggestthatperovskitequantumdotscouldplayarolefuturephotovoltaicdevices.
Thefirstuseofperovskitequantumdotsinsolarcellswasin2011byImetal.,whereMaPbI3 nanocrystalsactedasalight-sensitiserinastructureresemblingadye-sensitisedsolarcell [16],withapowerconversionefficiencyof6.5%reported.Thisresultpredatedthesynthesisofcolloidalperovskitequantumdots,andthenanocrystalswereinsteadformedthroughsurfaceinteractionswhenamixtureofmethylammoniumiodideandleadiodidewasspincastontoaTiO2 surface.
Atroomtemperature,bulkCsPbI3 formsanorthorhombiccrystallatticewithalargebandgapof~2.8eV.Thecubicphaseisfarmoresuitableforphotovoltaicapplicationsasaresultofanarrowerbandgap(1.73eV).However,thisphaseonlyformsinbulkCsPbI3 attemperaturesabove300°C.Duetotheelevatedtemperatureandtheeffectofreducedsurfacearea,allCsPbX3 nanocrystalscrystalliseintothecubicphaseduringsynthesis.IncontrastCsPbCl3 andCsPbBr3 quantumdotsarephase-stableinthecubicpolymorphoverlongperiods,howeverCsPbI3 willconvertbacktoanorthorhombicconfigurationoverafewdaysinambientconditions.
Swarnkaretal.showedthattreatingspincastCsPbI3 quantumdotfilmswithmethylacetatestabilisesthecubicstructure [17].Thiswasachievedby changingthesurfaceenergy viatheremovalofunreactedprecursors-withoutcausingtheaggregationofthedots.Theresultingfilmwasstableformonthsunderambientconditions,andhadexcellentoptoelectronicproperties.Indeed,whenfabricatedintosolarcells,suchfilmsachievedaPCEofover10%andhadalargeopen-circuitvoltageof1.23V.FurThermore,LEDsincorporatingstabilisedCsPbI3 nanocrystalsastheactivelayerdisplayedalowturn-onvoltageof<2V.
Itwaslaterdemonstratedthatcoatingthenanocrystalsin A+X- (where A isformamidinium,methylammoniumorCs,and X isIorBr)furtherimprovescharge-carriermobilityofthenanocrystalfilms.ThisallowedsolarcellshavingaPCEof13.4%tobefabricated–thehighestefficiencyphotovoltaicsbasedonquantumdotsofanykind [18].Thisresultispromisingforthedevelopmentofperovskitetandemsolarcells;hereabulkperovskitefilmperformstheroleofthelowbandgapabsorber,withtheperovskitequantumdotlayeractingasacomplementarywidebandgapabsorber [19].
Light-EmittingDiodes(LEDs)
Metalchalcogenidequantumdotsalreadyplayaroleinconsumerdisplayproducts-sotheincreasedPLQY,easeofsynthesis,excellentcolourpurity,andwidecolourtunabilityofperovskitequantumdotssuggestthattheyshouldbewell-suitedtosuchapplications.However,chargeinjectionandtransportinnanocrystalfilmsmustbeoptimisedinordertoachievehigh-efficiencydevices.
FirstdevicesbySongetal.usedanITO/PEDOT:PSS/PVK/CsPbX3/TPBi/LiF/Alstructuretodemonstrateblue,green,andorangeLEDs [11].Whiletheemissionlinewidthswerenarrow,thebrightnessoftheLEDswasmodest(<1000cdm-2),andtheexternalquantumefficiencies(EQE)werelimitedto~0.1%.
Lietal.showedtheimportanceofnanocrystalsurfacechemistry;heretheEQEofCsPbBr3 nanocrystalLEDswasincreasedby50x(0.12%to6.27%)throughtheoptimisationofdevicecharge-transportlayersandsurfaceliganddensitycontrol(achievedthroughtheuseofawashingprocedureusinghexaneandethylacetate [3]).Whileligandsareneededtopassivatethequantumdotsurfaceandpreventaggregation(leadingtohighPLQYandgreaterstability),anexcessivedensityofsurfaceligandscaninhibitelectricalinjectionandtransport.Bytuningtheliganddensity,abrightnessof>15,000cdm-2 wasobtainedthatwasaccompaniedbyhighcolourpurity(20nmemissionlinewidthusing~8nmnanocrystals).
Oneproposalthatbypassestheelectricalpropertiesofnanocrystalfilmsistousethemasdown-convertersforinorganicblueorUVLEDs.Pathaketal.dissolvedhybridorganic-inorganicperovskitequantumdotsofvariousmixedhalidecompositions(emittinggreenorredluminescence)intoapolystyrenepolymersolutionwhichwasthenspincastintoathinfilm[12].Thepolystyrenepolymeractedasaninsulatingmatrixthatpreventedanionexchange,therebypreservingtheindividualemissionpeaksoftheconstituentnanocrystalsandallowingthegenerationofwhitelightwhenilluminatedwithacommercialblueLED.
Lasers
Amplifiedspontaneousemission(ASE)hasbeenobservedindropcastfilmsofCsPbBr3,andmixedCsPb(Br/I)3 andCsPb(Cl/Br)3 nanocrystals.Pumpthresholdscanbeaslowas5µJcm-2 [13];avaluethatcomparesveryfavourablywithothercolloidalQDsystems(e.g.anorderofmagnitudelowerthanspectrallysimilarCdSeQDs).TheASEemissionintensityis extremelystableinair,droppingbyonly10%afterseveralhoursofirradiationand~107 shotsinambientconditions.ThisperformancealsocomparesextremelywelltochalcogenideQDs [14]. Thestimulatedemissionhasbeenidentifiedasresultingfromtherecombinationofbiexcitons(whicharemorestableatroomtemperaturethanexcitons),withred-shiftedemissionleadingtoreducedself-absorption(andhencelowlasingthresholds).TheASEwavelength canalsobetunedthroughouttheentirevisiblespectrumviamixingthehalidecomposition.
Lasingwasobservedinawhisperinggallerymodeconfiguration.ItwaslatershownthatstimulatedemissioncouldbeobservedinCsPbBr3 nanocrystalfilmsfollowingtwo-photonabsorption [15].Here,itwasfoundthatthetwo-photonabsorptioncross-sectionwas2ordersofmagnitudelargerthanthatofsimilarmetalchalcogenidequantumdots,leadingtoastimulatedemissionthresholdofgreen-emittingCsPbBr3 nanocrystalsof2.5mJcm-2.Thisisfarlowerthancore-shellmetalchalcogenidequantumdots.Thisnon-linearstimulatedemissioncouldalsobetunedacrossthevisiblewavelengthsbyvaryingthemixedhalidecomposition.GreenstimulatedemissionfromCsPbBr3 quantumdots(followingthree-photonabsorption)wasalsoobserved–afirstforanytypeofquantumdot.Forthisreason,perovskitequantumdotspresentanexcitingProspectforthedevelopmentofnext-generationlasers.
SinglePhotonSources
Singlephotonsourcesarerequiredfornewlight-basedquantuminformationsystems.Here,currenteffortsmainlyfocusontheuseofepitaxially-grownquantumdots,diamondcolourcentersandcolloidalnanocrystals.Ofthese,colloidalNCsarethemostpromisingforroom-temperaturevisibleoperation [20].
DiluteCsPbX3 (X=Br,IorBr/I)NCsolutionshavebeenspincasttocreatespatially-separatedindividualQDs [20,21].Imagingthe photoluminescence fromindividualNCsshowedtheblinkingbehaviour thatischaracteristicofsingleemitters.Photoncoincidencecountingrevealedlowg(2) valuesof~6%,demonstratingtherealisationofanefficient,anti-bunchedsinglephotonsourceatroomtemperature–allofwhicharedesirablecharacteristicsforemergentquantumtechnologies.
IncomparisonwithmetalchalcogenideQDs,metalhalideperovskiteQDsdisplayshorterfluorescencelifetimesandhigherabsorptioncoefficientsandarethereforefasterandmoreefficientsourcesofsinglephotons.
Photodetectors
ThehighabsorptioncoefficientofperovskiteQDsoverawidespectralrangemaymakethemsuitablecandidatesforuseinlight-detectiondevices.Panetal.havereportedthefabricationofaphototransistorbasedonFAPbBr3 quantumdotsandgraphene [22].TheQDswhichactasthelightabsorber,aredepositedontoamonolayerofgraphenethattransportsphotoexcitedchargestothesource/drain.Suchphototransistorshaveabroadresponsespanningthevisiblespectrum,althoughtheyhavereducedresponsetophotonshavingenergiesbelowthesemiconductorbandgap(540nm).Here,aphotoresponsivityof1.15×105 AW-1 wasobservedat520nm;avaluethatisamongstthehighestofanygraphene-basedphotodetectors.
PricingTable
Perovskite | Solvent | Concentration | Volume | ProductCode | Price |
CsPbBr3 | Toluene | 10mg.ml-1 | 5ml | M2124A1 | £200.00 |
CsPbBr3 | Toluene | 10mg.ml-1 | 10ml | M2124A1 | £350.00 |
CsPbBr3 | Toluene | 10mg.ml-1 | 25ml | M2124A1 | £700.00 |
CsPbBr3 | Octane | 10mg.ml-1 | 5ml | M2124B1 | £200.00 |
CsPbBr3 | Octane | 10mg.ml-1 | 10ml | M2124B1 | £350.00 |
CsPbBr3 | Octane | 10mg.ml-1 | 25ml | M2124B1 | £700.00 |
Shippingisfreeforqualifyingordersplacedviaoursecureonlinecheckout.
Literature
References
- NanocrystalsofCesiumLeadHalidePerovskites(CsPbX3,X=Cl,Br,andI):NovelOptoelectronicMaterialsShowingBrightEmissionwithWideColorGamut,L.Protesescuetal.,NanoLett., 15 (6),3692–3696(2015)
- LeadHalidePerovskiteNanocrystalsintheResearchSpotlight:StabilityandDefectTolerance,Huangetal.,ACSEnergyLett.,2 (9),2071–2083(2017)
- 50‐FoldEQEImprovementupto6.27%ofSolution‐ProcessedAll‐InorganicPerovskiteCsPbBr3 QLEDsviaSurfaceLigandDensityControl,Lietal.,Adv.Mater.,29(5),1603885(2017)
- NontemplateSynthesisofCH3NH3PbBr3 PerovskiteNanoparticles,L.Schmidtetal.,Am.Chem.Soc.,136(3),850–853(2014)
- MaximizingtheemissivepropertiesofCH3NH3PbBr3 perovskitenanoparticles,S.Gonzalex-Carreroetal.,J.Mater.Chem.A,3,9187-9193(2015)
- TheLuminescenceofCH3NH3PbBr3 PerovskiteNanoparticlesCreststheSummitandTheirPhotostabilityunderWetConditionsisEnhanced,Gonzalex-Carreroetal.,Small,12(38),5245-5250(2016)
- FastAnion-ExchangeinHighlyLuminescentNanocrystalsofCesiumLeadHalidePerovskites(CsPbX3,X=Cl,Br,I),N.Nedelcuetal.,NanoLett., 15 (8),5635–5640(2015)
- TuningtheOpticalPropertiesofCesiumLeadHalidePerovskiteNanocrystalsbyAnionExchangeReactions,Akkermanetal.,J.Am.Chem.Soc., 137 (32),10276–10281(2015)
- Room-TemperatureConstructionofMixed-HalidePerovskiteQuantumDotswithHighPhotoluminescenceQuantumYield,C.Bietal.,J.Phys.Chem.C,122(9),5151–5160(2018)
- WaterresistantCsPbX3 nanocrystalscoatedwithpolyhedraloligomericsilsesquioxaneandtheiruseassolidstateluminophoresinall-perovskitewhitelight-emittingdevices,H.Huangetal.,ChemSci.,7(9),5699–5703(2016)
- Quantumdotlight-emittingdiodesbasedoninorganicperovskitecesiumleadhalides(CsPbX3),J.Songetal.,Adv.Mater.,27,7162-7167(2015)
- PerovskiteCrystalsforTunableWhiteLightEmission,S.Pathaketal.,Chem.Mater.,27(23),8066–8075(2015)
- Low-thresholdamplifiedspontaneousemissionandlasingfromcolloidalnanocrystalsofcaesiumleadhalideperovskites,S.Yakuninetal.,Nat.Comm.,6,8056(2015)
- All‐InorganicColloidalPerovskiteQuantumDots:ANewClassofLasingMaterialswithFavorableCharacteristics,Y.Wangetal.,Adv.Mater.,27(44),7101-7108(2015)
- NonlinearAbsorptionandLow-ThresholdMultiphotonPumpedStimulatedEmissionfromAll-InorganicPerovskiteNanocrystals,Wangetal.,NanoLett., 16 (1),448–453(2016)
- 6.5%efficientperovskitequantum-dot-sensitizedsolarcell,JH.Imetal.,Nanoscale,3,4088-4093(2011)
- Quantumdot–inducedphasestabilizationofα-CsPbI3perovskiteforhigh-efficiencyphotovoltaics,A.Swarnkaretal.,Science,354(6308),92-95(2016)
- EnhancedmobilityCsPbI3quantumdotarraysforrecord-efficiency,high-voltagephotovoltaiccells,E.Sanehiraetal.,ScienceAdvances27Oct2017:Vol.3,no.10,eaao4204
- PerovskiteQuantumDots:ANewAbsorberforPerovskite-PerovskiteTandemSolarCells:Preprint,J.Christiansetal.,NationalRenewableEnergyLaboratory.NREL/CP-5900-71593(2018)
- SuperiorOpticalPropertiesofPerovskiteNanocrystalsasSinglePhotonEmitters,F.Huetal.,ACSNano,9(12),12410–12416(2015)
- RoomTemperatureSingle-PhotonEmissionfromIndividualPerovskiteQuantumDots,YS.Parketal.,ACSNano, 9(10),10386–10393(2015)
- Photodetectors:High‐ResponsivityPhotodetectorsBasedonFormamidiniumLeadHalidePerovskiteQuantumDot–GrapheneHybrid,R.Panetal.,Particle,35(4),1700304(2018)
Tothebestofourknowledgethetechnicalinformationprovidedhereisaccurate.However,Ossilaassumenoliabilityfortheaccuracyofthisinformation.Thevaluesprovidedherearetypicalatthetimeofmanufactureandmayvaryovertimeandfrombatchtobatch.
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LOQ-定量限LOD-检测限
1.模板提取(一般为RNA):Trizol、氯仿、异丙醇、无水乙醇、DEPC处理水
2.模板浓度测定:分光光度计或NanoDrop
3.逆转录:逆转录试剂盒(或者一步法试剂盒),这一步可以用普通PCR做,也可以用水域做。
4.荧光定量PCR试剂:通常有用SYBR Green Mix做的,但是这里建议你用EvaGreen做,灵敏度和平行性都要好于SYBR Green,并且如果你那是ABI或者Stratagene的PCR如果用SYBR Green还需要加一步Rox很麻烦。
5.其他:除了以上的那些还需要离心管、PCR管或板(Axygen反应比较好)、移液枪等,暂时就想到这么多。
1.步骤简单,45分钟内完成测定,比经典Lowry法快4倍而且更加方便。
2.灵敏度高,检测浓度下限达到25μg/ml,最小检测蛋白量达到0.5μg,待测样品体积为1-20μl 。
3.BCA法测定蛋白浓度不受绝大部分样品中的去污剂等化学物质的影响,可以兼容样品中高达5%的SDS,5%的Triton X-100,5%的Tween 20,60,80。
4.在20-2000μg/ml浓度范围内有良好的线性关系。
5.检测不同蛋白质分子的变异系数远小于考马斯亮蓝法蛋白定量。
临床实验室对商品定量试剂盒分析性能的验证.pdf(17431.6k)
加入荧光标记探针,巧妙地把核算扩增、杂交、光谱分析和实时检测技术结合在一起,借助于荧光信号来检测PCR产物。一方面提高了灵敏度,另一方面还可以做到PCR每循环一次就收集一个数据,建立实时扩增曲线,准确地确定CT值,从而根据CT值确定起始DNA的拷贝数,做到真正意义上的DNA定量。另外由于CT值是一个完全客观的参数,CT值越小,模版DNA的起始拷贝数越小。因此,利用CT值确定DNA拷贝数实时PCR方法比普通终点定量方法更加准确

