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DPP-DTT, PDPP2T-TT-OD


Product Code M0311A6-100mg
Price $264.00 ex. VAT

DPP-DTT, high quality and high purity semiconducting polymer

High performance p-type polymer and donor material for BHJ photovoltaics


DPP-DTT is a high mobility p-type polymer, suitable for OFET and sensing and photovoltaic applications.

Ossila's DPP-DTT was used in a high impact paper

DPP-DTT from Ossila was used in the high-impact paper (IF 18.81), Stretchable Mesh-Patterned Organic Semiconducting Thin Films on Creased Elastomeric Substrates, S. Kim et al., Adv. Funct. Mater., 2010870 (2021); DOI: 10.1002/adfm.202010870.

Luminosyn™ DPP-DTT

Luminosyn™ DPP-DTT (also referred to as PDPP2T-TT-OD) is now available.

High molecular weight
Higher molecular weight offers higher charge mobility

High purity
DPP-DTT is purified via Soxhlet extraction with methanol, hexane and chlorobenzene under an argon atmosphere

Batch-specific GPC data
Have confidence in what you are ordering; batch-specific GPC data for your thesis or publications

Large quantity orders
Plan your experiments with confidence with polymers from the same batch

OFET and Sensing Applications

The exceptional high mobility of this polymer of up to 10 cm2/Vs [2] via solution-processed techniques, combined with its intrinsic air stability (even during annealing) has made PDPP2T-TT-OD of significant interest for OFET and sensing purposes.

While the highest mobilities require exceptional molecular weights of around 500 kD (and with commensurate solubility issues), high mobilities in the region of 1-3 cm2/Vs can still be achieved with good solution-processing at around 250 kD. As such, we have made a range of molecular weights available to allow for different processing techniques.

In our own tests, we have found that by using simple spin-coating onto an OTS-treated silicon substrate (using our prefabricated test chips), high mobilities comparable to the literature can be achieved  (1-3 cm2/Vs). Further improvements may also be possible with more advanced strain-inducing deposition techniques.

DPP-DTT OFET output characteristics DPP-DTT OFET transfer curves
DPP-DTT saturation mobility fit DPP-DTT OFET mobility
Example OFET characteristics for DPP-DTT (Batch M311, Mw = 87 kDa, PDI = 4.1) solution processed from chlorobenzene on a 300 nm SiO2 substrate treated with OTS. Output characteristic (top left), transfer curves (top right), mobility fitting (bottom left) and calculated mobility (bottom right).

Photovoltaic Applications

Although shown as a promising hole-mobility polymer for OFETs, when used as the donor material in a bulk heterojunction photovoltaic (with PC70BM as the acceptor), initial efficiencies of 1.6% were achieved for DPP-DTT [3]. The low device metrics were attributed to poor film morphology. However, a higher efficiency of 6.9% was achieved by using thicker film (220 nm) [4].

PDPP2T-TT-OD has also recently been used successfully as an active-layer dopant material in PTB7-based devices [5]. An improvement in device performance was observed, with average efficiencies increasing from 7.6% to 8.3% when the dopant concentration of DPP-DTT was 1 wt%. The use of DPP-DTT as a high-mobility hole-interface layer for perovskite hybrid devices has also been investigated [6].

Synthetic route

DPP-DTT synthesis: DPP-DTT was synthesised by following the procedures described in [2] and [3] (please refer to the following references):

With 2-thiophenecarbonitrile and dimethyl succinate as starting materials in t-amyl alcohol, it gave 3,6-Dithiophen-2-yl-2,5-dihydropyrrolo[3,4-c]pyrrole-1,4-dione. Alkylation of 3,6-Dithiophen-2-yl-2,5-dihydropyrrolo[3,4-c]pyrrole-1,4-dione with 2-octyldodecylbromide in dimethylformamide afforded 3,6-bis(thiophen-2-yl)-2,5-bis(2-octyldodecyl)pyrrolo[3,4-c]pyrrole-1,4(2H,5H)-dione. Further bromination gave 3,6-bis(5-bromothiophen-2-yl)-2,5-bis(2-octyldodecyl)pyrrolo[3,4-c]pyrrole-1,4(2H,5H)-dione (M1).

DPP-DTT synthesis procedure to achieve M1

Further reaction of M1 with 2,5-bis(trimethylstannyl)thieno[3,2-b]thiophene (M2) under Stille coupling conditions gave the target polymer DPP-DTT, which was further purified via Soxhlet extraction with methanol, hexane and then chloroform.

DPP-DTT synthesis procedure - reaction of M1 and M2 to achieve DPP-DTT

General Information

CAS number 1260685-66-2 (1444870-74-9)
Chemical formula (C60H88N2O2S4)n
HOMO / LUMO HOMO = -5.2 eV, LUMO = -3.5 eV [2]
Synonyms
  • PDBT-co-DTT
  • PTT-DTDPP
  • PDPP-DTT
  • DPPT-TT
  • DPP-TTT
  • PDPP2T-TT
  • PDPP2T-TT-OD
  • DPPDTT
  • Poly[2,5-(2-octyldodecyl)-3,6-diketopyrrolopyrrole-alt-5,5-(2,5-di(thien-2-yl)thieno [3,2-b]thiophene)]
Solubility Chloroform, chlorobenzene and dichlorobenzene
Classification / Family Bithiophene, Thienothiophene, Organic semiconducting materials, Low band-gap polymers, Organic photovoltaics, Polymer solar cells, OFETs
dpp-dtt, PDPP2T-TT-OD, PDBT-co-DTT, 1260685-66-2, 1444870-74-9
Chemical structure and product image of DPP-DTT, CAS 1260685-66-2

MSDS Documentation

DPP-DTT MSDSDPP-DTT MSDS sheet

Pricing

Batch Quantity Price
M0311A 100 mg £240
M0311A 250 mg £480
M0311A 500 mg £800
M0311A 1 g £1450
M0311A 2 g £2600
M0311A 5 g / 10 g* Please enquire

*For 5 - 10 grams order quantity, the lead time is 4-6 weeks.

Batch information

Batch Mw Mn PDI Stock info
M314 292,200 74,900 3.90 Discontinued
M315 278,781 76,323 3.65 Discontinued
M316 ≥30,000 ≤3 Discontinued
M317 290,668 143,039 2.03 Discontinued
M0311A1 183,332 37,335 4.91 Discontinued
M0311A2 203,956 66,065 3.09 Discontinued
M0311A3 110,111 44,529 2.47 Discontinued
M0311A4 152,923 55,143 2.77 Out of stock
M0311A5 100,105 39,080 2.56 Discontinued
M0311A6 87,278 37,778
2.31 In Stock

References

  1. A High Mobility P-Type DPP-Thieno[3,2-b]thiophene Copolymer for Organic Thin-Film Transistors, Y. Li et al., Adv. Mater., 22, 4862-4866 (2010)
  2. A stable solution-processed polymer semiconductor with record high-mobility for printed transistors, J. Li et al., Nature Scientific Reports, 2, 754, DOI: 10.1038/srep00754 (2012)
  3. Synthesis of low bandgap polymer based on 3,6-dithien-2-yl-2,5-dialkylpyrrolo[3,4-c]pyrrole-1,4-dione for photovoltaic applications, G. Zhang et al., Sol. Energ. Mat. Sol. C., 95, 1168-1173 (2011)
  4. Efficient small bandgap polymer solar cells with high fill factors for 300 nm thick films, Li W et al., Adv Mater., 25(23):3182-3186 (2013); doi:10.1002/adma.201300017.
  5. Enhanced efficiency of polymer solar cells by adding a high-mobility conjugated polymer, S. Liu et al., Energy Environ. Sci., 8, 1463-1470 (2015)
  6. Electro-optics of perovskite solar cells, Q. Lin et al., Nature Photonics, 9, 106-112 (2015)
  7. A Vertical Organic Transistor Architecture for Fast Nonvolatile Memory, X. She et al., adv. Mater., 29, 1604769 (2017); DOI: 10.1002/adma.201604769.
  8. Solvent-Free Processable and Photo-Patternable Hybrid Gate Dielectric for Flexible Top-Gate Organic Field-Effect Transistors, J. S. Kwon et al., ACS Appl. Mater. Interfaces, 9 (6), 5366–5374 (2017); DOI: 10.1021/acsami.6b14500.

To the best of our knowledge the information provided here is accurate. However, Ossila assume no liability for the accuracy of this page. The values provided are typical at the time of manufacture and may vary over time and from batch to batch. All products are for laboratory and research and development use only, and may not be used for any other purpose including health care, pharmaceuticals, cosmetics, food or commercial applications.

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