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鈣鈦礦材料 DPP-DTT

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簡(jiǎn)要描述：Luminosyn DPP-DTT （also referred to as PDPP2T-TT-OD） is now available featuring

詳細(xì)介紹

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

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 - so you have confidence in what you are ordering. Also, GPC data is always convenient for your thesis and publications

Large quantity orders - so you can plan your experiments with polymer from the same batch

價(jià)格

Batch	Quantity	Price
M315	100 mg	4800.45
M315	250 mg	8011.45
M315	500 mg	12635.29
M315	1g	20871.50
M315	2g	36926.50

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

Batch Details

Batch	Mw	Mn	PDI
M314	292,200	74,900	3.90
M315	278,781	76,323	3.65

General Information

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)]
CAS number	1260685-66-2 (1444870-74-9)
Chemical formula	(C60H88N2O2S4)n
HOMO/LUMO	HOMO = -5.2 eV, LUMO = -3.5 eV [2]
Solubility	Chloroform, chlorobenzene and dichlorobenzene
Classification/Family	Bithiophene, Thienothiophene, Organic semiconducting materials, Low band-gap polymers, Organic photovoltaics, Polymer solar cells, OFETs

Chemical structure and product image of DPP-DTT, CAS No. 260685-66-2.

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.

Example OFET characteristics for DPP-DTT (M313) 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).

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.