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

• 作者: Mingxue Tang Nhat N.Bui Jin Zheng Likai Song Yan-Yan Hu
• 来源期刊: 能源化学
• 年，卷（期）: 2021,（9）
• 页码范围: 9-15
• 页数: 7页
• 语种: 英文

摘要

Organic electrodes are advantageous for rechargeable lithium-ion batteries owing to their high theoret-ical 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 reac-tion is delineated for TCNQ.TCNQ dimers form during the first electron injection upon lithiation and fol-lowed by the break-down of the dimers and associated 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 fundamen-tal understanding of how organic electrodes work and for informed design of high-performance organic materials for energy storage.