PNF222 (high-mobility, n-type polymer)

Order Code: M2052A1
MSDS sheet

Price

(excluding Taxes)

£369.60


PNF222 is now available, featuring:

  • High molecular weight and high purity - PNF222 is purified by soxhlet extraction with methanol, hexane and chlorobenzene under argon atmosphere
  • Batch-specific GPC data - for confidence in your material and useful information for your thesis and publications
  • Larger-quantity orders - so that you can plan your experiments with polymer from the same batch

Pricing

Batch Quantity Price
M2052A1 100 mg £369.6
M2052A1 250 mg £739.2
M2052A1 500 mg £1330.6
M2052A1 1 g £2262
M2052A1 5 g / 10 g* Please enquire

 *for 5 - 10 grams order quantity, the lead time is 4-6 weeks.

Batch Details

Batch Mw Mn PDI Stock Info
M2052A1 98,436 55,594 1.77 In stock

 

General Information

Full name Poly[[1,​2,​3,​6,​7,​8-​hexahydro-​2,​7-​bis(2-​octyldodecyl)​-​1,​3,​6,​8-​tetraoxobenzo[lmn]​[3,​8]​phenanthroline-​4,​9-​diyl]​(3,​3'-​difluoro[2,​2'-​bithiophene]​-​5,​5'-​diyl)​]
Synonyms PNDI-2F, P(NDI2OD-T2F), PNDI(2OD)2T-2F
CAS number 1773524-46-1
Chemical formula (C62H86F2N2O4S2)n
Molecular weight See Batch Details table above
HOMO / LUMO HOMO = - 5.99 eV, LUMO = - 3.90 eV [1]
Suggesting solvents Chlorobenzene, dichlorobenzene
Classification / Family Bithiophene, Heterocyclic five-membered ring, Organic semiconducting materials, Low band gap polymers, Organic photovoltaics, Polymer solar cells, OFETs
pndi-2f, fn2200, pndi2od2t-2f (pnf222) chemical structure, 1773524-46-1
Chemical structure of PNF222, Chemical formula (C62H86F2N2O4S2)n.

Applications

PNF222, poly[[1,​2,​3,​6,​7,​8-​hexahydro-​2,​7-​bis(2-​octyldodecyl)​-​1,​3,​6,​8-​tetraoxobenzophenanthroline-​4,​9-​diyl]​(3,​3'-​difluoro[2,​2'-​bithiophene]​-​5,​5'-​diyl)​], is commonly used as polymer acceptor in all polymer solar cells or OFETs material.

Compared to PNDI(2OD)2T, with the introduction of the fluorine atoms on the electronic structure of the polymer, PNF222 has lower electronic energy levels due to the strong electronegativity of its fluorine atoms. In turn, this results in higher Voc, Jsc and FF for OPV devices.

It has also been reported that PCE of Si-PEDOT:PSS solar cells was promoted from 12.6% to 14.5% while a PNF222 polymer interlayer was incorporated, with the polymer orientation playing a critical role on the polymer–Si contact quality [3].

Literature and Reviews

  1. Controlling Energy Levels and Blend Morphology for All-Polymer Solar Cells via Fluorination of a Naphthalene Diimide-Based Copolymer Acceptor,  M. A. Uddin et al., Macromolecules, 49 (17), 6374–6383 (2016); DOI: 10.1021/acs.macromol.6b01414.
  2. Fluoro-Substituted n-Type Conjugated Polymers for Additive-Free All-Polymer Bulk Heterojunction Solar Cells with High Power Conversion Efficiency of 6.71%,  J. Jung et al., Adv. Mater., 27, 3310–3317 (2015); DOI: 10.1002/adma.20150121.
  3. Naphthalene Diimide-Based n-Type Polymers: Efficient Rear Interlayers for High-Performance Silicon–Organic Heterojunction Solar Cells, Y. Han et al., ACS Nano, 11 (7), 7215–7222 (2017); DOI: 10.1021/acsnano.7b03090.