In Situ Electropolymerized Ambipolar Copolymers for Vertical OECTs

Kód výsledku v IS VaVaI

<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216305%3A26620%2F26%3A0198784" target="_blank" >RIV/00216305:26620/26:0198784 - isvavai.cz</a>

Výsledek na webu

<a href="https://onlinelibrary.wiley.com/doi/10.1002/smll.202411219" target="_blank" >https://onlinelibrary.wiley.com/doi/10.1002/smll.202411219</a>

DOI - Digital Object Identifier

<a href="http://dx.doi.org/10.1002/smll.202411219" target="_blank" >10.1002/smll.202411219</a>

Jazyk výsledku

angličtina

Název v původním jazyce

In Situ Electropolymerized Ambipolar Copolymers for Vertical OECTs

Popis výsledku v původním jazyce

A novel approach is reported for obtaining ambipolar electroactive polymers via in situ electropolymerization for vertical organic electrochemical transistor (vOECT) applications. It is shown that electropolymerization is a practical and efficient method to obtain copolymers without contamination from chemical polymerization processes. To this end, two monomers, G-DTP-Bu-NDI and G-DTP-G-NDI, are proposed, comprising naphthalene diimide (NDI) as the acceptor core and dithienopyrrole (DTP) as the donor unit, capable of forming carbon-carbon bonds under the influence of an electric current. The incorporation of oligo(oxyethylene) (OEG) side groups ensures their amphiphilicity. Both compounds underwent successful electrochemical polymerization, resulting in thin, porous, uniform polymer layers on the electrode surface. The synthesized polymers are further examined using electrochemical and spectroelectrochemical techniques in both organic and aqueous electrolytes. Regardless of the electrolyte medium (aqueous or non-aqueous), poly(G-DTP-Bu-NDI), and poly(G-DTP-G-NDI) exhibit stable electroactivity, as demonstrated by numerous scans showing ambipolar redox behavior. Both polymers are tested as components of vertical OECTs, following in situ electrochemical deposition within a 350 nm channel. The recorded transfer characteristics suggest that the fabricated donor-acceptor (D-A) compounds hold promise for developing a new generation of ambipolar ECT devices.

Název v anglickém jazyce

In Situ Electropolymerized Ambipolar Copolymers for Vertical OECTs

Popis výsledku anglicky

A novel approach is reported for obtaining ambipolar electroactive polymers via in situ electropolymerization for vertical organic electrochemical transistor (vOECT) applications. It is shown that electropolymerization is a practical and efficient method to obtain copolymers without contamination from chemical polymerization processes. To this end, two monomers, G-DTP-Bu-NDI and G-DTP-G-NDI, are proposed, comprising naphthalene diimide (NDI) as the acceptor core and dithienopyrrole (DTP) as the donor unit, capable of forming carbon-carbon bonds under the influence of an electric current. The incorporation of oligo(oxyethylene) (OEG) side groups ensures their amphiphilicity. Both compounds underwent successful electrochemical polymerization, resulting in thin, porous, uniform polymer layers on the electrode surface. The synthesized polymers are further examined using electrochemical and spectroelectrochemical techniques in both organic and aqueous electrolytes. Regardless of the electrolyte medium (aqueous or non-aqueous), poly(G-DTP-Bu-NDI), and poly(G-DTP-G-NDI) exhibit stable electroactivity, as demonstrated by numerous scans showing ambipolar redox behavior. Both polymers are tested as components of vertical OECTs, following in situ electrochemical deposition within a 350 nm channel. The recorded transfer characteristics suggest that the fabricated donor-acceptor (D-A) compounds hold promise for developing a new generation of ambipolar ECT devices.

Druh

J_imp - Článek v periodiku v databázi Web of Science

CEP obor

—

OECD FORD obor

10400 - Chemical sciences

Projekt

—

Návaznosti

I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Rok uplatnění

2025

Kód důvěrnosti údajů

S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Název periodika

Small

ISSN

1613-6810

e-ISSN

1613-6829

Svazek periodika

21

Číslo periodika v rámci svazku

30

Stát vydavatele periodika

DE - Spolková republika Německo

Počet stran výsledku

14

Strana od-do

—

Kód UT WoS článku

001478805700001

EID výsledku v databázi Scopus

2-s2.0-105004199353