Electrolyte and SEI Decomposition Reactions of Transition Metal Ions Investigated by On-Line Electrochemical Mass Spectrometry

作者：Sophie Solchenbach, Gloria Hong, Anna T.S. Freiberg, Roland Jung, Hubert Andreas Gasteiger · 发表于：Journal of The Electrochemical Society · 年份：2018 · DOI：10.1149/2.0511814jes · 被引用次数：205 · 研究领域：Advancements in Battery Materials、Advanced Battery Materials and Technologies、Advanced Battery Technologies Research

We use on-line electrochemical mass spectrometry (OEMS) to elucidate and quantify the electrolyte reduction on graphite caused by transition metal ions. To have a controlled system, we use ethylene carbonate (EC) with 1.5 M LiPF 6 and representative amounts of Ni(TFSI) 2 or Mn(TFSI) 2 as model electrolytes, combined with a 2-compartment cell in which anolyte and catholyte are separated by an impermeable solid lithium ion conductor. Focusing on C 2 H 4 evolution as a marker for EC reduction, we find that both Ni 2+ and Mn 2+ lead to enhanced gas evolution on pristine graphite electrodes once the potential is decreased to below the TM 2+ /TM 0 redox potential, demonstrating that the reduced transition metals are active toward electrolyte reduction. If the electrodes are preformed in a TM-free electrolyte and subsequently cycled in an electrolyte containing either Mn 2+ or Ni 2+ , the activity of nickel toward electrolyte decomposition is greatly reduced, whereas the electrolyte with manganese still shows a strong ongoing C 2 H 4 generation. The use of vinylene carbonate during formation partially suppresses the gas evolution from manganese. Using OEMS and post-mortem ATR-FTIR, we finally show that reduced manganese can decompose organic SEI components into Li 2 CO 3 , thereby compromising the integrity of the SEI and enabling the additional reduction of electrolyte.