On-Line Electrochemical Mass Spectrometry Investigations on Gassing Behavior of Li₄Ti₅O₁₂ Electrodes and Its Origins

Abstract

Advanced lithium ion batteries with the use of Li 4 Ti 5 O 12 (LTO) as unhazardous, thermal stable and “zero-strain” anode material are promising candidates for applications in the field of long-term energy storage systems. However, it is known from post-mortem gas analysis [1, 2] that LTO and organic carbonate electrolytes containing pouch bag cells swell during charging and storage due to evolving significant amounts of hydrogen gas. However, a correlation between gas evolution and cell chemistry couldn’t be formulated yet. In our study, we analyzed LTO-LiFePO 4 (LFP) full-cells and LTO-Li half-cells with three different water contents of the electrolyte in-operando with On-Line Electrochemical Mass Spectroscopy [3] to detect evolved gases followed by post-mortem ATR-FTIR and x-ray diffraction analysis of charged LTO electrodes. The main focus of this work is on the side reactions promoted by added moisture to the electrolyte solution to evaluate proposed mechanisms given by He et al. as well as Amine and coworkers [1, 2]. As an example, Figure 1 shows the charging profile of an in-operando LTO/LFP full-cell containing 4000 ppm H 2 O. The voltage profile (green, left axis) follows the typical trend with its charge/discharge plateau at ≈ 2 V. Here, it is observed that the charging time takes longer than the expected 5 hours at a rate of C/5, equating to an overall “charge capacity” of 193,9 mAh/g LTO . The red and blue line (right axis) gives in-operando concentrations for hydrogen and carbon dioxide, respectively. During the preliminary OCV step, hydrogen or carbon dioxide evolution is not detected. Both gases evolve upon charging, whereas the H 2 concentration approaches a plateau and the CO 2 concentration decreases after reaching an initial peak value. The hydrogen amount after the charging process was calculated to be 6x10 -6 mol after charging. If one considers the reduction potential for water and LTO in the Pourbaix diagram, the redox potential of the latter is below that of the H 2 evolution reaction, which implies that water can be reduced in contact with a charged LTO anode. Thus, the evolution of hydrogen is enabled by a parasitic reduction reaction of water while reducting the Ti 4+ species of LTO during Li + -ion intercalation in the charging step, which leads to an increase of the apparent “charging capacity” of LTO beyond its theoretically expected value. We propose a reaction mechanism [4] which corresponds to i) the H 2 O reduction process proposed by Belharouk et al. [2] and ii) the solvent reactions published by D. Aurbach [5] and P. Bruce and coworkers [6], respectively. The parasitic one-electron reduction of water leads to hydrogen gas evolution and the additional formation of solid carbonate compounds. These compounds were analyzed by FTIR-ATR and assigned to oligomers of general formula LiO 2 C(OC2H 4 ) n OCO 2 Li. As a result, reduction of water triggers a decomposition reaction of the solvent. Moreover, gassing can only occur in charged batteries, wherein the LTO anode's potential is lower than that for the reduction of water (potential of pristine LTO electrodes with ≈3 V vs. Li/Li + is above the H 2 O reduction potential). This is in accord with the evidence that no hydrogen can be detected in stored pouch bag cells without preliminary charge ([1]). References: [1] Y.-B. He et al., Scientific Reports 2-913 (2012) [2] I. Belharouak, et al., J. Electrochem. Soc. 158 , A1165 (2012) [3] N. Tsiouvaras et al., J. Electrochem. Soc. 160 ,A471 (2013) [4] R. Bernhard et al., in preparation [5] D. Aurbach, Nonaqueous Electrochemistry , pp. 145, Marcel Dekker Inc., New York/Basel (1999) [6] S. A. Freunberger et al., J. Am. Chem. Soc. 133 , 8040 (2011) Acknowledgements: Stiftung Nagelschneider München is gratefully acknowledged by RB for scholary and financial support. BASF SE is gratefully acknowledged for financial support by TUM. Figure caption: Fig. 1: In-operando full-cell: galvanostatic charge of a LTO/LFO full-cell (6.21 mg LTO cm -2 ) at 0.22 mAcm -2 using 1 M LiTFSI in EC/EMC 3/7 wt./wt. with the addition of 4000 ppm H 2 O and real-time hydrogen (red line) and CO 2 (blue line) gas concentration.