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901058

Sigma-Aldrich

J51

greener alternative

Synonym(s):

Poly[(5,6-difluoro-2-octyl-2H-benzotriazole-4,7-diyl)-2,5-thiophenediyl[4,8-bis[5-(2-hexyldecyl)-2-thienyl]benzo[1,2-b:4,5-b′]dithiophene-2,6-diyl]-2,5-thiophenediyl]

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About This Item

Linear Formula:
(C72H93F2N3S6)n
CAS Number:
1393529-03-7
MDL number:
MFCD00155450
UNSPSC Code:
12352103
NACRES:
NA.23

description

Band gap: 1.99 eV

Quality Level

100

form

solid

mol wt

Mw 40,000-80,000 by 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

organic solvents: soluble (Soluble in chlorobenzene and dichlorobenzene, Limited solubility in CHCl3)

Orbital energy

HOMO -5.29 eV 
LUMO -3.3 eV 

PDI

2.0‑3.0

greener alternative category

Enabling,

Related Categories

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 Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

JAN Code

901058-100MG:
901058-BULK:
901058-VAR:

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Certificates of Analysis (COA)

Lot/Batch Number
MKCF3031

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Indacenodithienothiophene-naphthalene diimide copolymer as an acceptor for all-polymer solar cells.
Xue L, et al.
Journal of Material Chemistry A, 4(16), 5810-5816 (2016)
Mapping Polymer Donors toward High-Efficiency Fullerene Free Organic Solar Cells.
Lin Y, et al.
Advanced Materials, 29(3) (2017)
Liang Gao et al.
Advanced materials (Deerfield Beach, Fla.), 28(37), 8288-8295 (2016-07-09)
A nonfullerene polymer solar cell with a high efficiency of 9.26% is realized by using benzodithiophene-alt-fluorobenzotriazole copolymer J51 as a medium-bandgap polymer donor and the low-bandgap organic semiconductor ITIC with high extinction coefficients as the acceptor.
Conjugated Side-Chain-Isolated D-A Copolymers Based on Benzo[1,2-b:4,5-b']dithiophene-alt-dithienylbenzotriazole: Synthesis and Photovoltaic Properties.
Min J, et al.
Chemistry of Materials, 24(16), 3247-3254 (2012)

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