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Real-time monitoring of the lithiation process in organic electrode 7,7,8,8-tetracyanoquinodimethane by in situ EPR

By Tang, Mingxue; Bui, Nhat N.; Zheng, Jin; Song, Likai; Hu, Yan-Yan
Published in Journal of Energy Chemistry Journal of Energy Chemistry 2020

Abstract

Organic electrodes are advantageous for rechargeable lithium-ion batteries owing to their high theoretical capacities, diverse functionalities, and environmental compatibility. Understanding the working mechanism of organic electrodes is vital to strategic materials design. However, due to lack of suitable characterization tools, it has been challenging to probe the reaction processes of organic electrodes in real-time. Here, non-destructive in situ electron paramagnetic resonance (EPR) was performed on a model organic electrode, 7,7,8,8-tetracyanoquinodimethane (TCNQ) used in rechargeable lithium-ion batteries, to directly follow the redox reactions in real-time. In order to minimize interfering signals from other parts of the batteries than the TCNQ electrode of interest, two sets of batteries are fabricated and studied with in situ EPR: (1) a LiCoO2//Li4Ti5O12 full-cell battery to determine the EPR signal evolution of additives and electrolytes; (2) a LiCoO2//TCNQ battery, and the difference in the observed EPR signals reflects purely the redox reactions of TCNQ upon lithiation and delithiation. A two-electron reversible redox reaction is delineated for TCNQ. TCNQ dimers form during the first electron injection upon lithiation and followed by the break-down of dimer-forming electron-coupling to produce massive delocalized electrons, resulting in increased EPR signal during the 2nd electron injection. Reversible trends are observed during electron ejection upon delithiation. In situ EPR is very sensitive to electron activities, thus is a powerful tool to follow redox reactions of organic electrodes, allowing for improved fundamental understanding of how organic electrodes work and informed design of high-performance organic materials for energy storage.

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