All‐Organic Battery Based on Deep Eutectic Solvent and Redox‐Active Polymers**

Author:

Uhl Matthias1ORCID,Sadeeda 1ORCID,Penert Philipp2ORCID,Schuster Philipp A.3ORCID,Schick Benjamin W.1ORCID,Muench Simon45ORCID,Farkas Attila1,Schubert Ulrich S.45ORCID,Esser Birgit2ORCID,Kuehne Alexander J. C.3ORCID,Jacob Timo167ORCID

Affiliation:

1. Institute of Electrochemistry Ulm University Albert-Einstein-Allee 47 89081 Ulm Germany

2. Institute of Organic Chemistry II and Advanced Materials Ulm University Albert-Einstein-Allee 11 89081 Ulm Germany

3. Institute of Organic and Macromolecular Chemistry Ulm University Albert-Einstein-Allee 11 89081 Ulm Germany

4. Laboratory of Organic and Macromolecular Chemistry Friedrich Schiller University Jena Humboldtstrasse 10 07743 Jena Germany

5. Center for Energy and Environmental Chemistry Jena (CEEC Jena) Friedrich Schiller University Jena Philosophenweg 7 07743 Jena Germany

6. Helmholtz-Institute Ulm (HIU) for Electrochemical Energy Storage Helmholtzstr. 11 89081 Ulm Germany

7. Karlsruhe Institute of Technology (KIT) P.O. Box 3640 76021 Karlsruhe Germany

Abstract

AbstractSustainable battery concepts are of great importance for the energy storage demands of the future. Organic batteries based on redox‐active polymers are one class of promising storage systems to meet these demands, in particular when combined with environmentally friendly and safe electrolytes. Deep Eutectic Solvents (DESs) represent a class of electrolytes that can be produced from sustainable sources and exhibit in most cases no or only a small environmental impact. Because of their non‐flammability, DESs are safe, while providing an electrochemical stability window almost comparable to established battery electrolytes and much broader than typical aqueous electrolytes. Here, we report the first all‐organic battery cell based on a DES electrolyte, which in this case is composed of sodium bis(trifluoromethanesulfonyl)imide (NaTFSI) and N‐methylacetamide (NMA) alongside the electrode active materials poly(2,2,6,6‐tetramethylpiperidin‐1‐yl‐oxyl methacrylate) (PTMA) and crosslinked poly(vinylbenzylviologen) (X‐PVBV2+). The resulting cell shows two voltage plateaus at 1.07 V and 1.58 V and achieves Coulombic efficiencies of 98 %. Surprisingly, the X‐PVBV/X‐PVBV+ redox couple turned out to be much more stable in NaTFSI : NMA 1 : 6 than the X‐PVBV+/X‐PVBV2+ couple, leading to asymmetric capacity fading during cycling tests.

Funder

Center of Excellence for Learning in Education, Science and Technology

Deutsche Forschungsgemeinschaft

Publisher

Wiley

Subject

General Energy,General Materials Science,General Chemical Engineering,Environmental Chemistry

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