Rocking-Chair Proton Batteries with Conducting Redox Polymer Active Materials and Protic Ionic Liquid Electrolytes
Author(s) -
Huan Wang,
Rikard Emanuelsson,
Christoffer Karlsson,
Patric Jannasch,
Maria Strömme,
Martin Sjödin
Publication year - 2021
Publication title -
acs applied materials and interfaces
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.535
H-Index - 228
eISSN - 1944-8252
pISSN - 1944-8244
DOI - 10.1021/acsami.1c01353
Subject(s) - redox , materials science , electrolyte , polymerization , ionic liquid , polymer , battery (electricity) , anode , organic radical battery , dissolution , chemical engineering , cathode , inorganic chemistry , polymer chemistry , electrode , chemistry , organic chemistry , composite material , power (physics) , catalysis , physics , quantum mechanics , engineering , metallurgy
Rechargeable batteries that use redox-active organic compounds are currently considered an energy storage technology for the future. Functionalizing redox-active groups onto conducting polymers to make conducting redox polymers (CRPs) can effectively solve the low conductivity and dissolution problems of redox-active compounds. Here, we employ a solution-processable postdeposition polymerization (PDP) method, where the rearrangements ensured by partial dissolution of intermediated trimer during polymerization were found significant to produce high-performance CRPs. We show that quinizarin (Qz)- and naphthoquinone (NQ)-based CRPs can reach their theoretical capacity through optimization of the polymerization conditions. Combining the two CRPs, with the Qz-CRP as a cathode, the NQ-CRP as an anode, and a protic ionic liquid electrolyte, yields a 0.8 V proton rocking-chair battery. The conducting additive-free all-organic proton battery exhibits a capacity of 62 mAh/g and a capacity retention of 80% after 500 cycles using rapid potentiostatic charging and galvanostatic discharge at 4.5 C.
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