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Merck
CN

901097

PDBT-T1

greener alternative

Synonym(s):

Poly[[5,10-bis(5-octyl-2-thienyl)dithieno[2,3-d:2′,3′-d′]benzo[1,2-b:4,5-b′]dithiophene-2,7-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]-2,5-thiophenediyl]

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About This Item

Linear Formula:
(C72H78O2S10)n
CAS Number:
MDL number:
NACRES:
NA.23
UNSPSC Code:
12162002
Form:
solid
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description

Band gap: 1.93 eV

form

solid

mol wt

Mw 20,000-50,000 (GPC, PS standard)

greener alternative product characteristics

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

sustainability

Greener Alternative Product

mp

>200 °C

solubility

soluble (hot o-dichlorobenzene)

orbital energy

HOMO -5.36 eV , LUMO -3.43 eV 

greener alternative category

Quality Level

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.

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable


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Highly Efficient Parallel-Like Ternary Organic Solar Cells.
Tao L, et al.
Chemistry of Materials, 29(7), 2914-2920 (2017)
Yuze Lin et al.
Advanced materials (Deerfield Beach, Fla.), 29(3) (2016-11-20)
Five polymer donors with distinct chemical structures and different electronic properties are surveyed in a planar and narrow-bandgap fused-ring electron acceptor (IDIC)-based organic solar cells, which exhibit power conversion efficiencies of up to 11%.
High-Performance Electron Acceptor with Thienyl Side Chains for Organic Photovoltaics.
Lin Y, et al.
Journal of the American Chemical Society, 138(14), 4955-4961 (2016)
Highly Efficient Parallel-?Like Ternary Organic Solar Cells.
Tao L, et al.
Chemistry of Materials, 29(7), 2914-2920 (2017)
Yuze Lin et al.
Journal of the American Chemical Society, 138(14), 4955-4961 (2016-03-26)
We develop an efficient fused-ring electron acceptor (ITIC-Th) based on indacenodithieno[3,2-b]thiophene core and thienyl side-chains for organic solar cells (OSCs). Relative to its counterpart with phenyl side-chains (ITIC), ITIC-Th shows lower energy levels (ITIC-Th: HOMO = -5.66 eV, LUMO =

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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.

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