Published May 1, 2017 | Version v1
Journal article

Characterization of PEDOT-Quinone Conducting Redox Polymers for Water Based Secondary Batteries

  • 1. Nanotechnology and Functional Materials, Department of Engineering Sciences, The Ångström Laboratory, Uppsala University, Box 534, SE-751 21 Uppsala (Sweden)
  • 2. Department of Chemistry-BMC, Biomedical Centre, Uppsala University, Box 576, SE-751 23 Uppsala (Sweden)

Description

Lithium-ion technologies show great promise to meet the demands that the transition towards renewable energy sources and the electrification of the transport sector put forward. However, concerns regarding lithium-ion batteries, including limited material resources, high energy consumption during production, and flammable electrolytes, necessitate research on alternative technologies for electrochemical energy storage. Organic materials derived from abundant building blocks and with tunable properties, together with water based electrolytes, could provide safe, inexpensive and sustainable alternatives. In this study, two conducting redox polymers based on poly(3,4-ethylenedioxythiophene) (PEDOT) and a hydroquinone pendant group have been synthesized and characterized in an acidic aqueous electrolyte. The polymers were characterized with regards to kinetics, pH dependence, and mass changes during oxidation and reduction, as well as their conductance. Both polymers show redox matching, i.e. the quinone redox reaction occurs within the potential region where the polymer is conducting, and fast redox conversion that involves proton cycling during pendant group redox conversion. These properties make the presented materials promising candidates as electrode materials for water based all-organic batteries.

Availability note (English)

Available from http://dx.doi.org/10.1016/j.electacta.2017.03.068

Additional details

Identifiers

DOI
10.1016/j.electacta.2017.03.068;
PII
S0013-4686(17)30534-0;

Publishing Information

Journal Title
Electrochimica Acta
Journal Volume
235
Journal Page Range
p. 356-364
ISSN
0013-4686
CODEN
ELCAAV

Optional Information

Copyright
Copyright (c) 2017 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.