Naphthalene diimide-based non-fullerene acceptors flanked by open-ended and aromatizable acceptor functionalitiesElectronic supplementary information (ESI) available: Experimental details, synthetic procedures, theoretical optical absorption, PESA, CV, TGA, DSC, IPCE and experimental spectra. See DOI: 10.1039/c7cc06369e
Herein we present the design, synthesis and characterization of two novel, naphthalene diimide (NDI) core-based non-fullerene acceptors, N5 and N6 , comprising respectively 2-methoxyethyl-2-cyanoacetate and cyanopyridone acceptor functionalities at the terminals. The influence of terminal units on o...
Gespeichert in:
Hauptverfasser: | , , , , , , , |
---|---|
Format: | Artikel |
Sprache: | eng |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
Zusammenfassung: | Herein we present the design, synthesis and characterization of two novel, naphthalene diimide (NDI) core-based non-fullerene acceptors,
N5
and
N6
, comprising respectively 2-methoxyethyl-2-cyanoacetate and cyanopyridone acceptor functionalities at the terminals. The influence of terminal units on optoelectronic and photovoltaic properties was studied. The target chromophore bearing cyanopyridone acceptor units (
N6
) afforded a power conversion efficiency of 6.10% when paired with the conventional donor polymer poly(3-hexylthiophene), a result that is the highest for the NDI core-based non-fullerene acceptors.
Herein we report synthesis and characterization of two NDI core-substituted non-fullerene acceptors,
N5
and
N6
, the chromophore (
N6
) bearing cyanopyridone acceptor units afforded a PCE of 6.10%. |
---|---|
ISSN: | 1359-7345 1364-548X |
DOI: | 10.1039/c7cc06369e |