Hyphenated DEMS and ATR-SEIRAS techniques for in situ multidimensional analysis of lithium-ion batteries and beyond

电化学 电解质 锂(药物) 表征(材料科学) 化学 储能 电化学电池 电极 分析化学(期刊) 材料科学 纳米技术 物理化学 有机化学 物理 医学 内分泌学 功率(物理) 量子力学
作者
Long Pang,Zhiwei Zhao,Xian‐Yin Ma,Wen‐Bin Cai,Limin Guo,Shaojun Dong,Chuntai Liu,Zhangquan Peng
出处
期刊:Journal of Chemical Physics [American Institute of Physics]
卷期号:158 (17) 被引量:21
标识
DOI:10.1063/5.0144635
摘要

A wide spectrum of state-of-the-art characterization techniques have been devised to monitor the electrode-electrolyte interface that dictates the performance of electrochemical devices. However, coupling multiple characterization techniques to realize in situ multidimensional analysis of electrochemical interfaces remains a challenge. Herein, we presented a hyphenated differential electrochemical mass spectrometry and attenuated total reflection surface enhanced infrared absorption spectroscopy analytical method via a specially designed electrochemical cell that enables a simultaneous detection of deposited and volatile interface species under electrochemical reaction conditions, especially suitable for non-aqueous, electrolyte-based energy devices. As a proof of concept, we demonstrated the capability of the homemade setup and obtained the valuable reaction mechanisms, by taking the tantalizing reactions in non-aqueous lithium-ion batteries (i.e., oxidation and reduction processes of carbonate-based electrolytes on Li1+xNi0.8Mn0.1Co0.1O2 and graphite surfaces) and lithium-oxygen batteries (i.e., reversibility of the oxygen reaction) as model reactions. Overall, we believe that the coupled and complementary techniques reported here will provide important insights into the interfacial electrochemistry of energy storage materials (i.e., in situ, multi-dimensional information in one single experiment) and generate much interest in the electrochemistry community and beyond.
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