AI Article Synopsis

  • Electrolyte decomposition reactions on Li-ion battery electrodes lead to the formation of solid electrolyte interphase (SEI) layers, which cause loss of battery voltage and capacity during charge/discharge cycles.
  • The study uses density functional theory (DFT) to analyze the early decomposition steps of ethylene carbonate (EC) on the surface of a common NMC cathode in Li-ion batteries, focusing on the effects of dissolved Li ions and surface terminations with hydroxyl (-OH) or fluorine (-F) species.
  • The researchers found that the EC ring-opening reaction occurs quickly and is driven purely by chemical interactions, while -OH and -F species can somewhat inhibit this reaction, particularly -OH when bonded to a transition metal atom.

Article Abstract

Electrolyte decomposition reactions on Li-ion battery electrodes contribute to the formation of solid electrolyte interphase (SEI) layers. These SEI layers are one of the known causes for the loss in battery voltage and capacity over repeated charge/discharge cycles. In this work, density functional theory (DFT)-based ab initio calculations are applied to study the initial steps of the decomposition of the organic electrolyte component ethylene carbonate (EC) on the (101̅4) surface of a layered Li(Ni,Mn,Co)O (NMC) cathode crystal, which is commonly used in commercial Li-ion batteries. The effects on the EC reaction pathway due to dissolved Li ions in the electrolyte solution and different NMC cathode surface terminations containing adsorbed hydroxyl -OH or fluorine -F species are explicitly considered. We predict a very fast chemical reaction consisting of an EC ring-opening process on the bare cathode surface, the rate of which is independent of the battery operation voltage. This EC ring-opening reaction is unavoidable once the cathode material contacts with the electrolyte because this process is purely chemical rather than electrochemical in nature. The -OH and -F adsorbed species display a passivation effect on the surface against the reaction with EC, but the extent is limited except for the case of -OH bonded to a surface transition metal atom. Our work implies that the possible rate-limiting steps of the electrolyte molecule decomposition are the reactions on the decomposed organic products on the cathode surface rather than on the bare cathode surface.

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Source
http://dx.doi.org/10.1021/acsami.7b03435DOI Listing

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