Two‐Step Redox in Polyimide: Witness by In Situ Electron Paramagnetic Resonance in Lithium‐ion Batteries

Author:

Bai Yunfei1,Wang Zhen1,Qin Ning2,Ma Detian1,Fu Wenbin3,Lu Zhouguang2ORCID,Pan Xiaobo1

Affiliation:

1. State Key Laboratory of Applied Organic Chemistry Lanzhou University) Key Laboratory of Nonferrous Metal Chemistry and Resources Utilization of Gansu Province College of Chemistry and Chemical Engineering 730000 Lanzhou Gansu P. R. China

2. Department of Materials Science and Engineering Shenzhen Key Laboratory of Interfacial Science and Engineering of Materials Guangdong-Hong Kong-Macao Joint Laboratory for Photonic-Thermal-Electrical Energy Materials and Devices Southern University of Science and Technology 518055 Shenzhen Guangdong P. R. China

3. School of Materials Science and Engineering Georgia Institute of Technology 30332 Atlanta GA United States

Abstract

AbstractOrganic materials are promising candidates for future rechargeable batteries, owing to their high natural abundance and rapidly redox reaction. Elaborating the charge/discharge process of organic electrode is critical to unveil the fundamental redox mechanism of lithium‐ion batteries (LIBs), but monitoring of this process is still challenging. Here, we report a nondestructive electron paramagnetic resonance (EPR) technique to real‐time detect the electron migration step within polyimide cathode. From in situ EPR tests, we vividly observe a classical redox reaction along with two‐electron transfer which only shows one pair of peaks in the cyclic voltammetry curve. The radical anion and dianion intermediates are detailed delineation at redox sites in EPR spectra, which can be further confirmed through density functional theory calculations. This approach is especially crucial to elaborate the correlation behind electrochemical and molecular structure for multistep organic‐based LIBs.

Funder

National Natural Science Foundation of China

Publisher

Wiley

Subject

General Chemistry,Catalysis

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