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901097

Sigma-Aldrich

PDBT-T1

greener alternative

Sinônimo(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

Fórmula linear:
(C72H78O2S10)n
Número CAS:
1701403-91-9
Número MDL:
MFCD00133992
Código UNSPSC:
12162002
NACRES:
NA.23

descrição

Band gap: 1.93 eV

Nível de qualidade

100

Formulário

solid

peso molecular

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

características do produto alternativo mais ecológico

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

sustainability

Greener Alternative Product

pf

>200 °C

solubilidade

soluble (hot o-dichlorobenzene)

Energia orbital

HOMO -5.36 eV 
LUMO -3.43 eV 

categoria alternativa mais ecológica

, Enabling

Categorias relacionadas

Descrição geral

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.

Código de classe de armazenamento

11 - Combustible Solids

Classe de risco de água (WGK)

WGK 3

Ponto de fulgor (°F)

Not applicable

Ponto de fulgor (°C)

Not applicable

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Certificados de análise (COA)

Lot/Batch Number

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Highly Efficient Parallel-Like Ternary Organic Solar Cells.
Tao L, et al.
Chemistry of Materials, 29(7), 2914-2920 (2017)
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)
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%.
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 =

Artigos

Progress for High Performance Tandem Organic Solar Cells

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%.

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