Materials, OPV Polymers, Semiconducting Polymers
Compared to PffBT4T-2OD (PCE11), PffBT4T-C9C13 has larger side chains which help promote better solubility and film morphology. When using PffBT4T-C9C13 as a polymer donor and PC71BM as electron acceptor (with trimethylbenzene (TMB) as host solvent), a higher device performance of 11.7% was achieved [2].
Due to its broader absorption of the solar spectrum in the visible light region (with an absorption edge at about 800 nm), PffBT4T-C9C13 is also ideal for use as a donor material for all-polymer solar cells and NFA-polymer solar cells
Additionally, its higher solubility means that PffBT4T-C9C13 can be processed with non-halogenated solvents. There are great opportunities with this polymer for inkjet printing on an industrial scale - an environment-friendly approach for alternative renewable energy.
| Full name | Poly[(5,6-difluoro-2,1,3-benzothiadiazol-4,7-diyl)-alt-(3,3’’’-di(2-nonyltridecyl)-2,2’;5’,2’’;5’’,2’’’-quaterthiophen-5,5’’’-diyl)] |
| Synonyms | PffBT4T-C9C13, PCE12 |
| Chemical formula | (C66H97F2N2S5)n |
| CAS number | n/a |
| HOMO / LUMO | HOMO = -5.34 eV LUMO = -3.69 eV [1] |
| Solubility/processing solvents | Trimethylbenzene (TMB), chlorobenzene |
| Classification / Family | Benzothiadiazole, Fluorinated benzothiadiazole, Heterocyclic five-membered ring, Organic semiconducting materials, Low band gap polymers, Organic photovoltaics, All polymer solar cells, NFA-polymer solar cells |
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