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

Author:

Pang Long12ORCID,Zhao Zhiwei3ORCID,Ma Xian-Yin4,Cai Wen-Bin4ORCID,Guo Limin5ORCID,Dong Shaojun12ORCID,Liu Chuntai6ORCID,Peng Zhangquan37ORCID

Affiliation:

1. State Key Laboratory of Electroanalytical Chemistry, Changchun Institute of Applied Chemistry, Chinese Academy of Science 1 , Changchun 130022, China

2. University of Science and Technology of China 2 , Hefei 230026, China

3. Laboratory of Advanced Spectroelectrochemistry and Li-ion Batteries, Dalian Institute of Chemical Physics, Chinese Academy of Sciences 3 , Dalian 116023, China

4. Shanghai Key Laboratory of Molecular Catalysis and Innovative Materials, Collaborative Innovation Center of Chemistry for Energy Materials, Department of Chemistry, Fudan University 4 , Shanghai 200438, China

5. College of Environment and Chemical Engineering, Dalian University 5 , Dalian 116622, China

6. Key Laboratory of Materials Processing and Mold (Zhengzhou University), Ministry of Education, National Engineering Research Center for Advanced Polymer Processing Technology, Zhengzhou University 6 , Zhengzhou 450002, China

7. School of Applied Physics and Materials, Wuyi University 7 , Jiangmen 529020, China

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.

Funder

National Natural Science Foundation of China

China Postdoctoral Science Foundation

National Key Research and Development Program of China

Dalian High-Level Talent Innovation Program

Publisher

AIP Publishing

Subject

Physical and Theoretical Chemistry,General Physics and Astronomy

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