Issue 32, 2016

Solvation, exchange and electrochemical intercalation properties of disodium 2,5-(dianilino)terephthalate

Abstract

The development of intercalation chemistry in the early 70s has particularly enabled the deployment of novel and efficient electrode materials for electrochemical storage. A striking example is the commercialization of the first lithium-ion (rocking-chair) battery in 1991. Recently, a resurgence of new intercalation structures has occurred with the development of sodium-ion batteries, and therefore materials able to reversibly accommodate sodium ions in layered or porous solids (e.g., 3d transition-metal oxides). However, not only metal cations can be incorporated into multi-dimensional structures but also polar molecules and anions especially in 2-D host lattices where they can be accommodated through chemical or electrochemical reactions, respectively. Herein, we specifically report on disodium 2,5-(dianilino)terephthalate as a multifunctional organic intercalation material able to chemically exchange metal cations and accommodate organic polar molecules as well as host anions under electrochemical charging conditions. Powder X-ray diffraction measurements coupled with other analytical techniques were performed for evidencing the Na/Li exchange reaction as well as the solvent intercalation. Moreover, galvanostatic cycling tests and impedance spectroscopy measurements were performed to demonstrate the occurrence of anion intercalation process and the resulting effect on the conductivity of the analogous dilithium 2,5-(dianilino)terephthalate compound.

Graphical abstract: Solvation, exchange and electrochemical intercalation properties of disodium 2,5-(dianilino)terephthalate

Supplementary files

Article information

Article type
Paper
Submitted
11 May 2016
Accepted
30 Jun 2016
First published
30 Jun 2016

CrystEngComm, 2016,18, 6076-6082

Solvation, exchange and electrochemical intercalation properties of disodium 2,5-(dianilino)terephthalate

É. Deunf, N. Dupré, É. Quarez, P. Soudan, D. Guyomard, F. Dolhem and P. Poizot, CrystEngComm, 2016, 18, 6076 DOI: 10.1039/C6CE01112H

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