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

J Chem Phys

Laboratory of Advanced Spectroelectrochemistry and Li-ion Batteries, Dalian Institute of Chemical Physics, Chinese Academy of Sciences, Dalian 116023, China.

Published: May 2023

AI Article Synopsis

  • A new analytical method combining differential electrochemical mass spectrometry and infrared absorption spectroscopy has been developed to study the electrode-electrolyte interface in electrochemical devices.
  • This method allows for real-time detection of both solid and gas species during electrochemical reactions, particularly in non-aqueous electrolyte energy devices.
  • The research showcased the method's effectiveness by analyzing reactions in lithium-ion and lithium-oxygen batteries, providing valuable insights into their reaction mechanisms and potentially advancing energy storage technologies.

Article Abstract

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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http://dx.doi.org/10.1063/5.0144635DOI Listing

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