Skip to Content
Merck
All Photos(2)

Key Documents

901099

Sigma-Aldrich

PBDB-T

greener alternative

Synonym(s):

Poly[[4,8-bis[5-(2-ethylhexyl)-2-thienyl]benzo[1,2-b:4,5-b′]dithiophene-2,6-diyl]-2,5-thiophenediyl[5,7-bis(2-ethylhexyl)-4,8-dioxo-4H,8H-benzo[1,2-c:4,5-c′]dithiophene-1,3-diyl]] polymer

Sign Into View Organizational & Contract Pricing


About This Item

Linear Formula:
(C68H78O2S8)n
CAS Number:
UNSPSC Code:
12162002
NACRES:
NA.23

description

Band gap: 1.8 eV
Limited solubility in CHCl3

Quality Level

form

powder

mol wt

Mw >50,000 by GPC (GPC standard: PS)

greener alternative product characteristics

Design for Energy Efficiency
Learn more about the Principles of Green Chemistry.

sustainability

Greener Alternative Product

mp

>200 °C

solubility

chlorobenzene: soluble
dichlorobenzene: soluble

Orbital energy

HOMO -5.28 eV 
LUMO -3.48 eV 

PDI

<3.0

greener alternative category

General description

We are committed to bringing you Greener Alternative Products, which adhere to one or more of The 12 Principles of Greener Chemistry. This product belongs to Enabling category of greener alternatives thus aligns with "Design for energy efficency". Hole transport organic materials allow perfect energy level alignment with the absorber layer and therefore efficient charge collection, are prone to degradation in ambient conditions.Click here for more information.

Application

PBDB-T, a conjugated push-pull medium bandgap polymeric donor, can be used as a donor molecule that can be used in polymeric solar cells (PSCs). It can also be used in the fabrication of organic thin-film transistors (OTFTs).

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable


Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Already Own This Product?

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

Visit the Document Library

Customers Also Viewed

Slide 1 of 3

1 of 3

Energy-Level Modulation of Small-Molecule Electron Acceptors to Achieve over 12% Efficiency in Polymer Solar Cells.
Li S, et al.
Advanced Materials, 28(42), 9423-9429 (2016)
Design, Application, and Morphology Study of a New Photovoltaic Polymer with Strong Aggregation in Solution State.
Qian D, et al.
Macromolecules, 45(24), 9611-9617 (2012)
Reducing the confinement of PBDB-T to ITIC to improve the crystallinity of PBDB-T/ITIC blends
Liang Q, et al.
Journal of Material Chemistry A, 6(32), 15610-15620 (2018)
Wenchao Zhao et al.
Advanced materials (Deerfield Beach, Fla.), 29(2) (2016-11-05)
Ternary polymer solar cells are fabricated based on one donor PBDB-T and two acceptors (a methyl-modified small-molecular acceptor (IT-M) and a bis-adduct of Bis[70]PCBM). A high power conversion efficiency of 12.2% can be achieved. The photovoltaic performance of the ternary
The influence of air and temperature on the performance of PBDB-T and P3HT in organic thin film transistors
Brixi S, et al.
Journal of Material Chemistry C, 6(44), 11972-11979 (2018)

Articles

The emerging organic photovoltaic (OPV) technology is very promising for low-cost solar energy production. OPV devices can be produced using high-throughput, large-volume printing methods on lightweight and flexible plastic substrates, making them easy to deploy and use in innovative ways.

The emerging organic photovoltaic (OPV) technology is very promising for low-cost solar energy production.

Professor Chen (Nankai University, China) and his team explain the strategies behind their recent record-breaking organic solar cells, reaching a power conversion efficiency of 17.3%.

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