Bai Yunfei, Wang Zhen, Qin Ning, Ma Detian, Fu Wenbin, Lu Zhouguang, Pan Xiaobo
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.
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.
Angew Chem Int Ed Engl. 2023 Apr 24;62(18):e202303162. doi: 10.1002/anie.202303162. Epub 2023 Mar 27.
Organic 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.
由于有机材料具有高天然丰度和快速的氧化还原反应,它们是未来可充电电池的有前途的候选材料。阐明有机电极的充放电过程对于揭示锂离子电池(LIBs)的基本氧化还原机制至关重要,但监测这一过程仍然具有挑战性。在此,我们报告一种非破坏性电子顺磁共振(EPR)技术,用于实时检测聚酰亚胺阴极内的电子迁移步骤。通过原位EPR测试,我们生动地观察到一个经典的氧化还原反应以及双电子转移,该反应在循环伏安曲线中仅显示一对峰。在EPR光谱中对氧化还原位点处的自由基阴离子和二价阴离子中间体进行了详细描述,这可以通过密度泛函理论计算进一步证实。这种方法对于阐明基于多步有机的LIBs的电化学和分子结构之间的相关性尤为关键。