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Redox-Active Polymeric Ionic Liquids with Pendant N-Substituted Phenothiazine.

Authors :
Oh S
Nikolaev A
Tagami K
Tran T
Lee D
Mukherjee S
Segalman RA
Han S
Read de Alaniz J
Chabinyc ML
Source :
ACS applied materials & interfaces [ACS Appl Mater Interfaces] 2021 Feb 03; Vol. 13 (4), pp. 5319-5326. Date of Electronic Publication: 2021 Jan 22.
Publication Year :
2021

Abstract

Polymers that are elastic while supporting charge transport are desirable for flexible and soft electronics. Many polymers with bulky and conjugated redox-active pendant units have high glass transition temperatures ( T <subscript>g</subscript> ) in their neutral form that will not lead to elasticity at room temperature. Their behavior in charged form in the solid state without an electrolyte has not been extensively studied. Here, the design strategy of polymeric ionic liquid where two weakly interacting ionic groups are used to maintain a low T <subscript>g</subscript> is shown to lead to flexible redox active polymers. The use of a flexible ethylene backbone and redox-active phenothiazine (PTZ)-based pendant group resulted in polymers with relatively low T <subscript>g</subscript> that are electrically conductive. PTZ that was N-substituted with 2-(2-ethoxyethoxy)ethoxy)ethyl was found to promote solubility of the polymer and lower the T <subscript>g</subscript> of the neutral polymer by ∼150 °C relative to that of the T <subscript>g</subscript> of a variant without the N-substituent. Doping with trifluoromethanesulfonimide leads to an electrically conductive polymer without significantly increasing the T <subscript>g</subscript> . Physical characterization by UV-vis-NIR spectroscopy, electron spin resonance spectroscopy, and impedance spectroscopy verified that the molecular design leads to an efficient charge hopping between the PTZ groups.

Details

Language :
English
ISSN :
1944-8252
Volume :
13
Issue :
4
Database :
MEDLINE
Journal :
ACS applied materials & interfaces
Publication Type :
Academic Journal
Accession number :
33480673
Full Text :
https://doi.org/10.1021/acsami.0c20462