Ossila材料PTB7 CAS:1266549-31-8 PTB7_材料-深圳市泽拓生物科技有限公司

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产品简介 产地类别 进口     Ossila材料PTB7 CAS:1266549-31-8 PTB7
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详细介绍 Batch InformationBatch No.MwPDStock InfoM21118,0001.75Sold outM212 40,0002.0Sold outM21385,0002.0In stock

Ossila材料PTB7 CAS:1266549-31-8 PTB7

Applications

PTB7 for high-performance organic photovoltaics.

Poly[[4,8-bis[(2-ethylhexyl)oxy]benzo[1,2-b:4,5-b ]dithiophene-2,6-diyl][3-fluoro-2-[(2-ethylhexyl)carbonyl]thieno[3,4-b]thiophenediyl]], more commonly known as PTB7.

In stock now for immediate dispatch worldwide.

PTB7 gives some of the highest reported efficiencies for polymer:fullerene solar cells due to its extended absorption into the near infra-red and lower HOMO level. Together with our complete package of processing information, PTB7 becomes a quick and easy way to improve device efficiencies. This represents a cost-effective method to increase performance and impact of devices and data for a wide range of OPV related research.

At typical concentrations for spin-coated devices of 10 mg/ml, a standard batch of 100 mg will produce 10 ml of ink - enough to coat 200 of Ossila s standard sized substrates even assuming 50% ink loss during preparation and filtration. At concentrations of 1 mg/ml (more typical for ink-jet printing and spray coating) up to 100 ml of ink can be produced.

In a standardised reference architecture (using a PEDOT:PSS hole interface and Ca/Al electron interface) we have shown this batch to give a PCE of 6.8% (see data sheet below) and up to 7.4% using PFN. By using new interface materials and architectures PTB7 has been shown to reach efficiencies of 9.2% PCE in the literature [1,2].

The high solubility in a wide range of solvents makes ink preparation and filtration simple, and PTB7 is one of the easiest materials we have ever worked with (simply shake it to dissolve). This also makes it an excellent candidate for a variety of coating techniques including ink-jet printing, spray coating and blade coating.

For information on processing please see our specific fabrication details for PTB7, general fabrication video, general fabrication guide, optical modelling paper on our standard architecture [3], or us for any additional help and support.

References (please note that Ossila has no formal connection to any of the authors or institutions in these references):

[1] Enhanced power-conversion efficiency in polymer solar cells using an inverted device structure Zhicai He et al., Nature Photonics, V 6, p591 595 (2012).[2] Simultaneous Enhancement of Open-Circuit Voltage, Short-Circuit Current Density, and Fill Factor in Polymer Solar Cells Zhicai He et al., Advanced Materials, V 23, p4636 4643 (2011).[3] Optimising the efficiency of carbazole co-polymer solar-cells by control over the metal cathode electrode Darren C. Watters et al., Organic Electronics, V 13, p1401 1408 (2012)[4] Designing ternary blend bulk heterojunction solar cells with reduced carrier recombination and a fill factor of 77%, N. Gasparini et al, Nat. Energy, 16118 (2016); doi:10.1038/nenergy.2016.118 (Ossila PTB7 was featured in this paper).

Ossila材料PTB7 CAS:1266549-31-8 PTB7

Datasheet

Chemical structure of PTB7; Chemical formula (C41H53FO4S4)n.

SpecificationsFull namePoly[[4,8-bis[(2-ethylhexyl)oxy]benzo[1,2-b:4,5-b ]dithiophene-2,6-diyl][3-fluoro-2-[(2-ethylhexyl)carbonyl]thieno[3,4-b]thiophenediyl]]SynonymsPTB7CAS number1266549-31-8Absorption670 nm (CH2Cl2), 682 nm (film)SolubilityChloroform, Chlorobenzene, o-DCB

 

Usage DetailsInverted Reference Devices

Reference device were made on batch M211 to assess the effect of PTB7:PC70BM active layer thickness on OPV efficiency using an inverted architecture with the below structure. These consisted of the below structure and were fabricated under inert atmosphere (glovebox) before encapsulation and measurement under ambient conditions.

Glass / ITO (100 nm) / PFN (6.5 nm) / PTB7:PC70BM (1:1.5) / MoOx (15 nm) / Al (100 nm)

For generic details please see the general fabrication guide and video. For specific details please see the below condensed fabrication report which details the optical modelling and optimisation of the multilayer stack.

Previously it has been shown that PFN of around 6.5 nm gives optimum performance [1-3,P021] while modelling has shown that an Al back cathode gives higher performance than Ag when used with MoOx [4].

The PTB7:PC70BM solution was made in chlorobenzene at 25 mg/ml before being diluted with 3% diiodooctane (DIO) to promote the correct morphology.

Active layer thicknesses of 75 nm, 90 nm and 105 nm were chosen corresponding to the lower, middle and upper end of the "thin film" absorption peak of a typical stack as predicted by optical modelling [1]. For each of these thickness a total of four substrates was produced, each with 4 pixels and the data presented below represents a non-subjective (no human intervention) analysis of the best 75% of pixels by PCE (12 pixels for each condition).

An additional two substrates were also prepared with a methanol wash to help remove the DIO as has been reported in the literature to help improve performance[5].

Overall, the maximum efficiency of 7.2% average PCE (7.4% maximum) was found at 75 nm film thickness.

 

 Figure 1: PCE, Jsc, Voc and FF for inverted architecture devices at different spin speeds. Data shown is averaged with max and min overlaid with filled circles (please see note of Dektak measurements). As previously reported [1,2,3], films of approximay 90 nm give the highest performance with greater Jsc and only minor loss in fill factor.

 

Figure 2: The JV curve for the best performing device - inverted architecture.

 

Note 1: Dektak Thickness calibration

We normally calibrate thin films by use of a Dektak surface profiler, however the use of DIO results in an enhanced level of uncertainty in the film as the DIO will take several hours to fully dry under normal conditions and is likely to undergo some slight further shrinkage when placed in vacuum. The DIO can also be removed by baking the substrate on the hotplate at 80 C for about 10 mins which can be useful for doing quick measurements but also drives excess phase separation between the polymer and PCBM making it unsuitable for device work.

Note 2: Effect of epoxy

Due to the very high solubility of the PTB7 it was noted during fabrication that the film changed colour when in contact with the EE1 encapsulation epoxy in liquid form for extended periods indicating that there was some miscibility. Inspection of the active areas underneath the top cathode indicated that the epoxy had not seeped into the active area before curing and device metrics indicate that this did not appear to affect performance. However, we would recommend minimising contact time between the epoxy and PTB7 films before UV curing.

 

Fabrication

Substrates and cleaning

Pixelated Cathode substrates (S173)5 mins sonication in hot Hellmanex III(1 ml in beaker)2x boiling water dump rinses5 mins sonication in warm IPA2x dump rinses5 mins sonication in hot NaOHDump rinse in boiling waterDump rinse in waterStored in DI water overnight and until use

PFN Solution

Dissolved at 2 mg/mlAcetic acid dissolved 1:9 in methanol to make stock solution2 l/ml of acetic added to solutionStirred for 30 minsFiltered through 0.45 m PVDF filter

PFN Test Films

PFN Test film initially spun at 500 rpm and gave 20 nmSecond test film spun at 1000 rpm and gave 16 nmThickness was extrapolated to 6.5 nm at 6000 rpm

Active Layer Solution

Fresh stock solutions of PTB7 (Ossila M211) made on at 10 mg/ml in CB and dissolved with stirbar for 1 hourMixed 1:1.5 with dry Ossila 99% C70 PCBM to make overall concentration of 25 mg/ml and dissolved with stirbar for 1 hourOld stock solution of 1,8 Diiodooctane mixed 1:1 with CB to make measuring out small quantities easierDIO/CB mixture added to solution to give overall DIO amount of 3%

Active Layer Test Films

Test film spun at 1000 rpm for 2 mins using unfiltered solution and dried using methanol before Dektak1000 rpm gave approximay 85 nm

Active layers

Devices spun using 30 l dynamic dispense (20 l gave only moderate wetting/coverage)Non methanol devices spun for 2 minsMethanol devices spun for 30 seconds, then coated with 50 l methanol by static dispense then spun at 2000 rpm for 30 seconds.Cathode wiped with CBVacuum dried in glovebox antichamber for 20 mins

Evaporation

Left in chamber over the weekend and evaporated with the below parameters.

15 nm MoOx at 0.2 Å/s100 nm Al at 1.5 Å/sDeposition pressure

Encapsulation

As standard using Ossila EE1, 30 mins UV in MEGA LV101

Measurements

JV sweeps taken with Keithley 237 source-meterIllumination by Newport Oriel 9225-1000 solar simulator with 100 mW/cm2 AM1.5 outputNREL certified silicon reference cell used to calibrateLamp current: 7.8 ASolar output at start of testing: 1.00 suns at 25 CSolar output at end of testing: 1.00 suns at 25 CAir cooled substratesRoom temperature at start of testing: 25 CRoom temperature at end of testing: 25 CCalibrated aperture mask of size 0.256 mm2

 

Standard (Non-inverted) Reference Devices

Reference device were made on batch M211 using a standardised architecture for comparative measurements using Ossila standard substrates and materials. These consisted of the below structure and were fabricated under inert atmosphere (glovebox) before encapsulation and measurement under ambient conditions.

Glass / ITO (100 nm) / PEDOT:PSS (30 nm) / PTB7:PC70BM (variable) / Ca (2.5 nm) / Al (100 nm)

For generic details please see the fabrication guide and video. For specific details please see the below condensed fabrication report and also Watters et al. [3] which details the optical modelling and optimisation of the multilayer stack.

For this standard reference architecture an average PCE of 6.6% was achieved for the optimised thickness with a peak efficiency of 6.8%. Note that no other optimisation was performed (blend ratio, DIO concentration, drying conditions etc) and so further small improvements may be obtained by varying these conditions and significant improvements obtained by using alternative interface materials [1,2].

   Figure 3: PCE, Jsc, Voc and FF for standard architecture devices at different spin speeds. Data shown is averaged with max and min overlaid with filled circles (please see note of Dektak measurements). As previously reported [1,2,3], films of approximay 90 nm give the highest performance with greater Jsc and only minor loss in fill factor.

 

Figure 4: The JV curve for the best performing device - standard architecture.

 

Note 1: Dektak Thickness calibration

We normally calibrate thin films by use of a Dektak surface profiler, however the use of DIO results in an enhanced level of uncertainty in the film as the DIO will take several hours to fully dry under normal conditions and is likely to undergo some slight further shrinkage when placed in vacuum. The DIO can also be removed by baking the substrate on the hotplate at 80 C for about 10 mins which can be useful for doing quick measurements but also drives excess phase separation between the polymer and PCBM making it unsuitable for device work.

Note 2: Effect of epoxy

Due to the very high solubility of the PTB7 it was noted during fabrication that the film changed colour when in contact with the EE1 encapsulation epoxy in liquid form for extended periods indicating that there was some miscibility. Inspection of the active areas underneath the top cathode indicated that the epoxy had not seeped into the active area before curing and device metrics indicate that this did not appear to affect performance. However, we would recommend minimising contact time between the epoxy and PTB7 films before UV curing.

 

Fabrication

Substrates and cleaning

Pixelated Cathode substrates (S173)5 mins sonication in hot Hellmanex (1 ml in beaker)2x boiling water dump rinses5 mins sonication in warm IPA2x dump rinses5 mins sonication in hot NaOHDump rinse in boiling waterDump rinse in waterStored in DI water overnight and until use

PEDOT:PSS layer preparation

Clevios AI 4083Filtered into vial using Whatman 0.45 m PVDF filterSpun 6000 rpm for 30 seconds (30 nm)Dynamic dispense of 20 l using pipettorIPA cathode strip wipe and labelledPut straight onto hotplate at 160 C as soon as cathode wiped and labelledTransferred to glovebox when all samples spun.Baked in glovebox at 150 C for 1 hour

Active layer Solution Preparation

Fresh stock solutions of PTB7 at 10 mg/ml in CB and shaken to dissolveMixed 1:1.5 with dry Ossila 99% C70 PCBM to make overall concentration of 25 mg/ml1,8 Diiodooctane mixed 1:1 with CB to make measuring out small quantities easierDIO/CB mixture added to solution to give overall DIO amount of 3%

Active layer spin casting

Devices spun for 2 mins using 25 l dynamic dispenseCathode wiped with chlorobenzeneLeft to dry in glovebox for 2 hours but colour indicated they were still slightly wetDried in vacuum in glovebox antichamber for 10 mins to remove DIO

Evaporation

Left in chamber over the weekend and evaporated with the below parameters.

MaterialCabase pressure8.0 E-8 mbarDep start pressure1.7 E-7 mbarMax pressure2.7 E-7 mbarThickness2.5 nmRate0.2 Å/sMaterialAlbase pressure7.0 E-8 mbarDep start pressure6.0 E-7 mbarMax pressure7.0 E-7 mbarThickness100 nmRate1.0 Å/s

 Encapsulation

As standard using Ossila EE1, 30 mins UV in MEGA LV101

Measurements

JV sweeps taken with Keithley 237 source-meterIllumination by Newport Oriel 9225-1000 solar simulator with 100 mW/cm2 AM1.5 outputNREL certified silicon reference cell used to calibrateLamp current: 7.8 ASolar output at start of testing: 0.99 suns at 25 CSolar output at end of testing: 1.00 suns at 25 CAir cooled substratesRoom temperature at start of testing: 21 CRoom temperature at end of testing: 21 CCalibrated aperture mask of size 0.256 mm2

 

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