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Merck

906980

Sigma-Aldrich

PFN-Br

greener alternative

Synonim(y):

OS0995, PFN-P2, Poly(9,9-bis(3’-(N,N-dimethyl)-N-ethylammoinium-propyl-2,7-fluorene)-alt-2,7-(9,9-dioctylfluorene))dibromide

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100 MG
1430,00 zł

1430,00 zł


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100 MG
1430,00 zł

About This Item

Wzór liniowy:
(C56H80N2.Br2)n
Numer CAS:
Kod UNSPSC:
12162002
NACRES:
NA.23

1430,00 zł


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Formularz

solid

masa cząsteczkowa

Mw 30,000-50,000 by GPC

charakterystyka ekologicznej alternatywy

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

sustainability

Greener Alternative Product

kolor

beige to yellow

mp

>200 °C

rozpuszczalność

DMF: soluble
DMSO: soluble
alcohol: soluble
chloroform: insoluble
water: soluble

PDI

2‑3.2

kategoria ekologicznej alternatywy

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Opis ogólny

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". Electron transport organic materials have the chemical functionality to transport electrons and are used as electron transport layer in OLED devices. Click here for more information.

Zastosowanie

PFN-Br is a solution processible, conjugated polymer electrolyte used as interficial layer in high performance organic photovoltaic cells (OPV) and organic light emitting diodes (OLED) to improve the interfacial properties.[1][2][3]

OPV devices with PFN-Br interfacial layer showed overall enhanced short-circuit current density, open-circuit voltage, fill factor and corresponding high efficiency in the inverted OPVs.[3] This was attributed to the good contact between ZnO electron extraction layer and the active layer, good interface adhesion between the electron extraction layer and active layer, and enhanced charge transport via suppressed bimolecular recombination.

Recent report of OPV with a record energy conversion efficiency of 17.3% also utilized PFN-Br, spin-coated on top of ZnO to improve the interfacial properties.[1]

Tandem Cell Device performance:
ITO/ZnO/PFN-Br/PBDB-T:F-M/M-PEDOT/ZnO/PTB7- Th:O6T-4F:PC71BM/MoO3/Ag
Voc=1.642 V
Jsc=14.35 mA/cm2
FF=73.7%
PCE=17.3%

PFN-Br finds application in a wide range of areas:
  • OPV interficial layer (metalic oxide compact layer)
  • OLED electron transport layer
  • Perovskite solar cells
  • Flexible printed electronics
  • Cationic polymer electrolyte
  • Anion exchange material
  • Light emitting electrochemical cells

Inne uwagi

Recommend to use 0.2 mg/ml concentration for electron-transport interfacial layer in OPV.
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Kod klasy składowania

11 - Combustible Solids

Klasa zagrożenia wodnego (WGK)

WGK 3

Temperatura zapłonu (°F)

Not applicable

Temperatura zapłonu (°C)

Not applicable


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Klienci oglądali również te produkty

Inverted polymer solar cells with 8.4% efficiency by conjugated polyelectrolyte
Yang T, et al.
Energy & Environmental Science, 5, 8208-8214 (2012)
Simultaneous enhancement of the molecular planarity and the solubility of non-fullerene acceptors: Effect of aliphatic side-chain substitution on the photovoltaic performance.
Z Zhang, et al.
Journal of Material Chemistry A, 5, 7776-7783 (2017)
Lingxian Meng et al.
Science (New York, N.Y.), 361(6407), 1094-1098 (2018-08-11)
Although organic photovoltaic (OPV) cells have many advantages, their performance still lags far behind that of other photovoltaic platforms. A fundamental reason for their low performance is the low charge mobility of organic materials, leading to a limit on the

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Explore the eco-friendly potential of organic thin film transistors (OTFTs) for detecting chemical analytes, identifying viruses, and assisting in health diagnostics. This mini-review highlights challenges of achieving sustainability, safety, and biodegradability of each component of an OTFT sensor.

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%.

Questions

1–3 of 3 Questions  
  1. How can I determine the shelf life / expiration / retest date of this product?

    1 answer
    1. If this product has an expiration or retest date, it will be shown on the Certificate of Analysis (COA, CofA). If there is no retest or expiration date listed on the product's COA, we do not have suitable stability data to determine a shelf life. For these products, the only date on the COA will be the release date; a retest, expiration, or use-by-date will not be displayed.
      For all products, we recommend handling per defined conditions as printed in our product literature and website product descriptions. We recommend that products should be routinely inspected by customers to ensure they perform as expected.
      For products without retest or expiration dates, our standard warranty of 1 year from the date of shipment is applicable.
      For more information, please refer to the Product Dating Information document: https://www.sigmaaldrich.com/deepweb/assets/sigmaaldrich/marketing/global/documents/449/386/product-dating-information-mk.pdf

      Helpful?

  2. How is shipping temperature determined? And how is it related to the product storage temperature?

    1 answer
    1. Products may be shipped at a different temperature than the recommended long-term storage temperature. If the product quality is sensitive to short-term exposure to conditions other than the recommended long-term storage, it will be shipped on wet or dry-ice. If the product quality is NOT affected by short-term exposure to conditions other than the recommended long-term storage, it will be shipped at ambient temperature. As shipping routes are configured for minimum transit times, shipping at ambient temperature helps control shipping costs for our customers. For more information, please refer to the Storage and Transport Conditions document: https://www.sigmaaldrich.com/deepweb/assets/sigmaaldrich/marketing/global/documents/316/622/storage-transport-conditions-mk.pdf

      Helpful?

  3. What are the end-capping groups on this polymer?

    1 answer
    1. There is no termination group attached to the ends of the polymer. It is simply hydrogen attached to the aromatic ring, rather than another monomeric unit.

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