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Product Code M2250
Price £271.00 ex. VAT

TPT10 has a very similar structure to both Y6 and Y7 except that the peripheral end groups are mono-brominated instead of being either bis-fluorinated or chlorinated. With fewer bromine substitutes, TPT10 shows a better solubility in common solvents.

TPT10 has been successfully used with PTQ10 and PTQ11 to produce potentially low-cost high efficiency polymer organic solar cells with a reported PCE of 16.32%, a step closer for commercialisation of such devices.

Device structure: ITO/ZnO/PTQ11:TPT10 (1:1.2):0.5 % 1-CN/MO3/Ag

Thickness (nm) VOC (V) JSC (mA cm-2) FF (%) PCE (%)
110 0.88 24.79 74.8 16.32

General Information

Full name 2,2'- [[12,13-Bis(2-ethylhexyl)-12,13-dihydro-3,9-dinonylbisthieno[2'',3'':4',5']thieno[2',3':4,5]pyrrolo[3,2-e:2',3'-g][2,1,3]benzothiadiazole-2,10-diyl]bis[methylidyne(5 or 6-bromo-3-oxo-1H-indene-2,1(3H)-diylidene) ]]bis[propanedinitrile]
Synonyms BTP-2Br, BTIC-2Br-m
Chemical formula C82H88Br2N8O2S5
Molecular weight 1537.8 g/mol
CAS number 2414381-17-0
HOMO / LUMO HOMO = -5.52 eV, LUMO = -3.99 eV [1]
Solubility Chloroform, chlorobenzene and dichlorobenzene
Form Dark blue powder/crystal
Classification / Family BTP series NFAs, n-type non-fullerene electron acceptors, Organic semiconducting materials, Low band-gap small molecule, Small molecular acceptor, Organic photovoltaics, Polymer solar cells, NF-PSCs.

Chemical Structure

Chemical structure of TPT10, CAS# 2414381-17-0.

MSDS Documentation

TPT10 MSDS sheet


Batch Quantity Price
M2250A1 100 mg £271.00
M2250A1 250 mg £542.00
M2250A1 500 mg £944.00
M2250A1 1 g £1720.00
M2250A1 5 g / 10 g* Please contact us for details

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

Literature and Reviews

  1. High Efficiency Polymer Solar Cells with Efficient Hole Transfer at Zero Highest Occupied Molecular Orbital Offset between Methylated Polymer Donor and Brominated Acceptor, C. Sun et al., J. Am. Chem. Soc., 142, 1465−1474 (2020); DOI: 10.1021/jacs.9b09939.
  2. Volatilizable and cost-effective quinone-based solid additives for improving photovoltaic performance and morphological stability in non-fullerene polymer solar cells, Y. Zhang et al., J. Mater. Chem. A, 8, 13049-13058 (2020); DOI: 10.1039/D0TA04941G.
  3. Bromination: An Alternative Strategy for Non‐Fullerene Small Molecule Acceptors, H. Wang et al., Adv. Sci (Weinh), 7(9), 1903784 (2020); DOI: 10.1002/advs.201903784.

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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