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Documenti

901097

Sigma-Aldrich

PDBT-T1

greener alternative

Sinonimo/i:

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

Formula condensata:
(C72H78O2S10)n
Numero CAS:
Codice UNSPSC:
12162002
NACRES:
NA.23

Descrizione

Band gap: 1.93 eV

Livello qualitativo

Forma fisica

solid

PM

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

Caratteristiche più verdi

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

sustainability

Greener Alternative Product

Punto di fusione

>200 °C

Solubilità

soluble (hot o-dichlorobenzene)

Energia dell’orbitale

HOMO -5.36 eV 
LUMO -3.43 eV 

Categoria alternativa più verde

Descrizione generale

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.

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable


Certificati d'analisi (COA)

Cerca il Certificati d'analisi (COA) digitando il numero di lotto/batch corrispondente. I numeri di lotto o di batch sono stampati sull'etichetta dei prodotti dopo la parola ‘Lotto’ o ‘Batch’.

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

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Contatta l'Assistenza Tecnica.