Conducting Redox Polymer as a Robust Organic Electrode-Active Material in Acidic Aqueous Electrolyte towards Polymer-Air Secondary Batteries.

ChemSusChem

Nanotechnology and Functional Materials, Materials Science and Engineering, The Ångström Laboratory, Uppsala University, Box 534, 751 21, Uppsala, Sweden.

Published: May 2020

AI Article Synopsis

  • Organic materials like conducting redox polymers (CRPs) are gaining attention for their environmentally friendly and sustainable use in batteries.
  • The CRP discussed is made from poly(3,4-ethylenedioxythiophene) with naphthoquinone groups, allowing for easy coating onto current collectors using techniques like roll-to-roll processing or ink-jet printing.
  • When tested, this CRP anode achieved a capacity of 76 mAh/g, a discharge voltage of 0.50 V in a polymer-air battery, and maintained 97% capacity after 100 cycles, demonstrating its potential in high-performance energy storage applications.

Article Abstract

Organic materials receive increasing attention as environmentally benign and sustainable electrode-active materials. We present a conducting redox polymer (CRP) based on poly(3,4-ethylenedioxythiophene) with naphthoquinone pendant group, which is formed from a stable suspension of a trimeric precursor and an oxoammonium cation as oxidant. This suspension allows us to easily coat the polymer onto a current collector, opening up use of roll-to-roll processing or ink-jet printing for electrode preparation. The CRP showed a full capacity of 76 mAh g even at a high C rate of 100 C in acidic aqueous electrolyte. These properties make the CRP a promising candidate as anode-active material; a polymer-air secondary battery was fabricated with the CRP as anode, a conventional Pt/C catalyst as cathode, and sulfuric acid aqueous solution as electrolyte. This battery yielded a discharge voltage of 0.50 V and showed good cycling stability with 97 % capacity retention after 100 cycles and high rate capabilities up to 20 C.

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Source
http://dx.doi.org/10.1002/cssc.202000627DOI Listing

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