Enhanced Electrochemical Doping Kinetics in Conjugated Polymers by Blending with Hydrophilic Block Copolymers

Author(s):  
Micah Barker ◽  
Tommaso Nicolini ◽  
Georges Hadziioannou ◽  
Natalie Stingelin
Author(s):  
Ilaria Bargigia ◽  
Lisa R. Savagian ◽  
Anna M. Österholm ◽  
John R. Reynolds ◽  
Carlos Silva

2020 ◽  
Author(s):  
Ilaria Bargigia ◽  
Lisa R. Savagian ◽  
Anna M. Österholm ◽  
John R. Reynolds ◽  
Carlos Silva

In this work, we address the nature of electrochemically induced charged states in conjugated polymers, their evolution as a function of electrochemical potential, and their coupling to their local environment by means of transient absorption and Raman spectroscopies synergistically performed in situ throughout the electrochemical doping process. In particular, we investigate the fundamental mechanism of electrochemical doping in an oligoether-functionalized 3,4-propylenedioxythiophene (ProDOT) copolymer. The changes embedded in both linear and transient absorption features allow us to identify a precursor electronic state with charge-transfer (CT) character that precedes polaron formation and bulk electronic conductivity. This state is shown to contribute to the ultrafast quenching of both neutral molecular excitations and polarons. Raman spectra relate the electronic transition of this precursor state predominantly to the C<sub>β</sub> -C<sub>β</sub> stretching mode of the thiophene heterocycle. We characterize the coupling of the CT-like state with primary excitons and electrochemically induced charge separated states, providing insight into the energetic landscape of a heterogeneous polymer-electrolyte system and demonstrate how such coupling depends on environmental parameters, such as polymer structure, electrolyte composition, and environmental polarity.<br>


2020 ◽  
Vol 8 (17) ◽  
pp. 5934-5940 ◽  
Author(s):  
Tharindu A. Ranathunge ◽  
Duong T. Ngo ◽  
Dilan Karunarathilaka ◽  
Nuwan H. Attanayake ◽  
Indika Chandrasiri ◽  
...  

Using electro-copolymerization as a versatile tool in synthesizing alternating and block copolymers, we have designed conjugation polymers with unique optical properties and excellent conductivities in comparison to conventional conjugated polymers.


2014 ◽  
Vol 89 (20) ◽  
Author(s):  
S. van Reenen ◽  
M. V. Vitorino ◽  
S. C. J. Meskers ◽  
R. A. J. Janssen ◽  
M. Kemerink

Polymers ◽  
2020 ◽  
Vol 13 (1) ◽  
pp. 110
Author(s):  
Lin-Lin Xiao ◽  
Xu Zhou ◽  
Kan Yue ◽  
Zi-Hao Guo

In the past two decades, conjugated polymers (CPs) have drawn great attention due to their excellent conductivity and charge mobility, rendering them broad applications in organic electronics. Controlling over the morphologies and nanostructures of CPs is very important to improve the performance of CP-based devices, which is still a tremendously difficult task. Conjugated block copolymers (cBCPs), composed of different CP blocks or CP coupled with coiled polymeric blocks, not only maintain the advantages of high conductivity and mobility but also demonstrate features of morphological versatility and tunability. Due to the strong π–π interaction and crystallinity of the conjugated backbones, the self-assembly behaviors of cBCPs are very complicated and largely remain to be explored. In this tutorial review, we first summarize the general synthetic methods for different types of cBCPs. Then, recent studies on the self-assembly behaviors of cBCPs are discussed, with an emphasis on the structural factors that affect the morphologies of cBCPs both in bulk and thin film states. Finally, we briefly provide our outlook on the future research of the self-assembly of cBCPs.


2020 ◽  
Vol 11 (25) ◽  
pp. 6383-6392 ◽  
Author(s):  
Garion E. J. Hicks ◽  
Charles N. Jarrett-Wilkins ◽  
Jenny R. Panchuk ◽  
Joseph G. Manion ◽  
Dwight S. Seferos

Conjugated block copolymers, where each block contains a unique electroactive group, allows selective block-oxidation in solution, which promotes reversible, redox-controlled self-assembly.


2020 ◽  
Author(s):  
Ilaria Bargigia ◽  
Lisa R. Savagian ◽  
Anna M. Österholm ◽  
John R. Reynolds ◽  
Carlos Silva

In this work, we address the nature of electrochemically induced charged states in conjugated polymers, their evolution as a function of electrochemical potential, and their coupling to their local environment by means of transient absorption and Raman spectroscopies synergistically performed in situ throughout the electrochemical doping process. In particular, we investigate the fundamental mechanism of electrochemical doping in an oligoether-functionalized 3,4-propylenedioxythiophene (ProDOT) copolymer. The changes embedded in both linear and transient absorption features allow us to identify a precursor electronic state with charge-transfer (CT) character that precedes polaron formation and bulk electronic conductivity. This state is shown to contribute to the ultrafast quenching of both neutral molecular excitations and polarons. Raman spectra relate the electronic transition of this precursor state predominantly to the C<sub>β</sub> -C<sub>β</sub> stretching mode of the thiophene heterocycle. We characterize the coupling of the CT-like state with primary excitons and electrochemically induced charge separated states, providing insight into the energetic landscape of a heterogeneous polymer-electrolyte system and demonstrate how such coupling depends on environmental parameters, such as polymer structure, electrolyte composition, and environmental polarity.<br>


Author(s):  
Tine Hardeman ◽  
Marie-Paule Van Den Eede ◽  
Lize Verheyen ◽  
Guy Koeckelberghs

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