Potential Dependent Dual Ion Transport of Conducting Polymer: Redox Polymer Bilayers

1995 ◽  
Vol 99 (20) ◽  
pp. 8249-8254 ◽  
Author(s):  
Myoungho Pyo ◽  
John R. Reynolds
Author(s):  
U. L. ZAINUDEEN ◽  
M. A. CAREEM ◽  
S. SKAARUP

2016 ◽  
Vol 4 (18) ◽  
pp. 3942-3947 ◽  
Author(s):  
Sahika Inal ◽  
George G. Malliaras ◽  
Jonathan Rivnay

Spectroscopic investigation of electrochromic moving fronts enables the study of ion transport in complex conducting polymer film morphologies.


2019 ◽  
Vol 10 (20) ◽  
pp. 2570-2578 ◽  
Author(s):  
Noémie Hergué ◽  
Bruno Ernould ◽  
Andrea Minoia ◽  
Julien De Winter ◽  
Pascal Gerbaux ◽  
...  

Coupling a conjugated P3HT block to a radical polymer block leads to improved PTMA battery performances.


2009 ◽  
Vol 1212 ◽  
Author(s):  
Yunfeng Li ◽  
Chin-Che Tin ◽  
Vince Cammarata

AbstractSpectroelectrochemistry was used to study the electron trapping and rectifying behavior in several diphenylamine endgroup polymeric bilayers. Various combinations of the following monomers were pairwise sequentially electropolymerized onto ITO transparent electrodes: FD, DNTD, DPTD and Cl4DPTD. Poly(FD) is a p-type material while poly(DNTD), poly(DPTD) and poly(Cl4DPTD) are bipolar materials being both n-type and p-type. Bilayers of ITO|poly(FD)|poly (DNTD) or ITO|poly (FD)|poly (DPTD), block electrons from reducing the outer layer even at -1.0 V vs Ag/AgCl, yet holes effectively oxidize both layers. The LUMO differences between poly(DNTD) and poly(Cl4DPTD) or poly(DPTD) and poly(Cl4DPTD) provide a large enough electronic barrier that electron trapping can occur between these n-type materials. The visible spectra results imply that these polymers, poly(DPTD) or poly(Cl4DPTD) can be used as photovoltaic materials.


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