Volume 58, Issue 44 pp. 15680-15684
Communication

Tuning the Chemistry of Organonitrogen Compounds for Promoting All-Organic Anionic Rechargeable Batteries

Dr. Alia Jouhara

Dr. Alia Jouhara

Institut des Matériaux Jean Rouxel (IMN), UMR CNRS 6502, Université de Nantes, 2 rue de la Houssinière, B.P. 32229, 44322 Nantes Cedex 3, France

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Dr. Eric Quarez

Dr. Eric Quarez

Institut des Matériaux Jean Rouxel (IMN), UMR CNRS 6502, Université de Nantes, 2 rue de la Houssinière, B.P. 32229, 44322 Nantes Cedex 3, France

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Dr. Franck Dolhem

Dr. Franck Dolhem

Laboratoire de Glycochimie, des Antimicrobiens et des Agroressources (LG2A), UMR CNRS 7378, Université de Picardie Jules Verne, 33 rue Saint-Leu, 80039 Amiens Cedex, France

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Dr. Michel Armand

Dr. Michel Armand

CIC Energigune, Parque Tecnológico de Alava, Miñano, Alava, 01510 Spain

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Dr. Nicolas Dupré

Dr. Nicolas Dupré

Institut des Matériaux Jean Rouxel (IMN), UMR CNRS 6502, Université de Nantes, 2 rue de la Houssinière, B.P. 32229, 44322 Nantes Cedex 3, France

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Prof. Philippe Poizot

Corresponding Author

Prof. Philippe Poizot

Institut des Matériaux Jean Rouxel (IMN), UMR CNRS 6502, Université de Nantes, 2 rue de la Houssinière, B.P. 32229, 44322 Nantes Cedex 3, France

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First published: 19 August 2019
Citations: 46

Graphical Abstract

Charging ahead: The development of anion–ion batteries is possible by combining the benefits of p-type organic redox-active materials and molecular engineering to tune their working potentials. The pairing of an aromatic diamine as the positive electrode with a zwitterionic bipyridinium carboxylate compound as the negative electrode resulted in the assembly of an all-organic anionic battery.

Abstract

The ever-increasing demand for rechargeable batteries induces significant pressure on the worldwide metal supply, depleting resources and increasing costs and environmental concerns. In this context, developing the chemistry of anion-inserting electrode organic materials could promote the fabrication of molecular (metal-free) rechargeable batteries. However, few examples have been reported because little effort has been made to develop such anionic-ion batteries. Here we show the design of two anionic host electrode materials based on the N-substituted salts of azaaromatics (zwitterions). A combination of NMR, EDS, FTIR spectroscopies coupled with thermal analyses and single-crystal XRD allowed a thorough structural and chemical characterization of the compounds. Thanks to a reversible electrochemical activity located at an average potential of 2.2 V vs. Li+/Li, the coupling with dilithium 2,5-(dianilino)terephthalate (Li2DAnT) as the positive electrode enabled the fabrication of the first all-organic anionic rechargeable batteries based on crystallized host electrode materials capable of delivering a specific capacity of ≈27 mAh/gelectrodes with a stable cycling over dozens of cycles (≈24 Wh/kgelectrodes).

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