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Merck

901058

Sigma-Aldrich

J51

greener alternative

Sinónimos:

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

Fórmula lineal:
(C72H93F2N3S6)n
Número de CAS:
UNSPSC Code:
12352103
NACRES:
NA.23

description

Band gap: 1.99 eV

Quality Level

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

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_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable


Certificados de análisis (COA)

Busque Certificados de análisis (COA) introduciendo el número de lote del producto. Los números de lote se encuentran en la etiqueta del producto después de las palabras «Lot» o «Batch»

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Visite la Librería de documentos

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)
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)
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.

Artículos

Novel biosensing devices, like bio-FET sensors, offer label-free analysis by detecting ionic and biomolecular charges, crucial for diagnostics and biological research.

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%.

Nuestro equipo de científicos tiene experiencia en todas las áreas de investigación: Ciencias de la vida, Ciencia de los materiales, Síntesis química, Cromatografía, Analítica y muchas otras.

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