Skip to Content
MilliporeSigma
All Photos(1)

Documents

772380

Sigma-Aldrich

DTS(FBTTh2)2

Synonym(s):

7,7′-[4,4-Bis(2-ethylhexyl)-4H-silolo[3,2-b:4,5-b′]dithiophene-2,6-diyl]bis[6-fluoro-4-(5′-hexyl-[2,2′-bithiophen]-5-yl)benzo[c][1,2,5]thiadiazole], F-DTS, p-DTS(FBTTh2)2

Sign Into View Organizational & Contract Pricing


About This Item

Empirical Formula (Hill Notation):
C64H72F2N4S8Si
Molecular Weight:
1219.89
MDL number:
UNSPSC Code:
12352103
PubChem Substance ID:
NACRES:
NA.23

form

solid

solubility

chlorobenzene: 0.3-0.5% at 80 °C
dichlorobenzene: 0.3-0.5% at 80 °C
chloroform: soluble(lit.)
dichlorobenzene: soluble(lit.)

λmax

590 nm in chloroform

SMILES string

CCCCCCc1ccc(s1)-c2ccc(s2)-c3cc(F)c(-c4cc5c(s4)-c6sc(cc6[Si]5(CC(CC)CCCC)CC(CC)CCCC)-c7c(F)cc(-c8ccc(s8)-c9ccc(CCCCCC)s9)c%10nsnc7%10)c%11nsnc3%11

InChI

1S/C64H72F2N4S8Si/c1-7-13-17-19-23-41-25-27-49(71-41)51-31-29-47(73-51)43-33-45(65)57(61-59(43)67-77-69-61)53-35-55-63(75-53)64-56(79(55,37-39(11-5)21-15-9-3)38-40(12-6)22-16-10-4)36-54(76-64)58-46(66)34-44(60-62(58)70-78-68-60)48-30-32-52(74-48)50-28-26-42(72-50)24-20-18-14-8-2/h25-36,39-40H,7-24,37-38H2,1-6H3

InChI key

LNMKMESEJYZMDZ-UHFFFAOYSA-N

General description

DTS(FBTTh2)2 is a conductive polymer that can be used as a donor molecule. It has a narrow band gap and shows a maximum power conversion efficiency of 7.0%. Its photostability is more than that of P3HT.

Application

DTS(FBTTh2)2 can be used as a conjugating polymer that forms a donor-acceptor system with acceptor molecules such as perylene diimide, PC71BM and other fullerenes for the fabrication of bulk-heterojunction based solar cells.
Narrow band gap material for high-efficiency organic solar cells (OPVs) application
OPV Device Structure: ITO/MoOx/DTS(PTTh2)2: PC70BM/Al
  • JSC = 12.8 mA/cm2
  • VOC = 0.81 V
  • FF = 0.68
  • PCE = 7.0%

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable


Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Enhanced Efficiency Parameters of Solution-Processable Small-Molecule Solar Cells Depending on ITO Sheet Resistance
Wang DH, et al.
Advanced Energy Materials, 3(9), 1161-1165 (2013)
Relationship between photostability and nanostructures in DTS (FBTTh2) 2: fullerene bulk-heterojunction films
Yamane S, et al.
Solar Energy Materials and Solar Cells, 151, 96-101 (2016)
A High-Performing Solution-Processed Small Molecule: Perylene Diimide Bulk Heterojunction Solar Cell
Sharenko A, et al.
Advanced Materials, 25(32), 4403-4406 (2013)
Effects of Solvent Additives on Morphology, Charge Generation, Transport, and Recombination in Solution-Processed Small-Molecule Solar Cells
Kyaw AKK, et al.
Advanced Energy Materials, 4(7), 1301469-1301469 (2014)
Barium: an efficient cathode layer for bulk-heterojunction solar cells
Gupta V, et al.
Scientific reports, 3, 1965-1965 (2013)

Articles

Solution-processed organic photovoltaic devices (OPVs) have emerged as a promising clean energy generating technology due to their ease of fabrication, potential to enable low-cost manufacturing via printing or coating techniques, and ability to be incorporated onto light weight, flexible substrates.

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service