聚酰亚胺
氧化还原
电子顺磁共振
化学
锂(药物)
离子
原位
证人
电子
材料科学
纳米技术
有机化学
核磁共振
核物理学
计算机科学
冶金
程序设计语言
内分泌学
物理
医学
图层(电子)
作者
Yunfei Bai,Zhen Wang,Ning Qin,Detian Ma,Wenbin Fu,Zhouguang Lu,Xiaobo Pan
标识
DOI:10.1002/anie.202303162
摘要
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.
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