Design of a Scavenging Pyrrole Additive for High Voltage Lithium-Ion Batteries

  • Jianzhong Yang
  • , Marco Tulio Fonseca Rodrigues
  • , Zhou Yu
  • , Seoung Bum Son
  • , Kewei Liu
  • , L. Nancy
  • , Dietz Rago
  • , Lei Cheng
  • , Zhengcheng Zhang
  • , Daniel Abraham
  • , Chen Liao

Research output: Contribution to journalArticlepeer-review

10 Scopus citations

Abstract

We report 1-(dimethylamino) pyrrole (PyDMA) as an electrolyte additive for high voltage lithium-ion batteries based on LiNi0.6Mn0.2Co0.2O2(NMC622)//Graphite with an upper cutoff voltage of 4.4 V. Density Functional Theory (DFT) modeling indicates that the unique structure of PyDMA could be effective in preventing the hydrolysis of LiPF6in a carbonate electrolyte, mitigating issues related to HF formation. The calculations also indicated that the additive would oxidize at lower potentials than typical electrolyte solvents, which could lead to protective films at the cathode surface. These expectations were tested using Nuclear Magnetic Resonance (NMR) and extensive electrochemical characterization. NMR studies confirmed the superb dehydrating capability of PyDMA, which successfully prevents HF formation even at high water content. Addition of 0.5 wt% PyDMA resulted in improved capacity retention in full-cells, and also in lower levels of transition metal dissolution from the cathode. Incremental capacity (dQ/dV) analysis indicates that benefits of PyDMA at low concentration (0.5-1 wt%) are associated with decreased rates of Li+-trapping reactions, and that higher concentrations of the additive can lead to isolation of cathode domains. Our study indicates that PyDMA could be a promising electrolyte additive for high voltage lithium-ion batteries at a low concentration.

Original languageEnglish
Article number040507
JournalJournal of the Electrochemical Society
Volume169
Issue number4
DOIs
StatePublished - Apr 1 2022
Externally publishedYes

Funding

Support from the Vehicle Technologies Office (VTO), David Howell (Manager), Battery R&D, Peter Faguy (Technology Manager), at the U.S. Department of Energy, Office of Energy Efficiency and Renewable Energy, is gratefully acknowledged. The electrodes and electrolytes used in this article are from Argonne’s Cell Analysis, Modeling and Prototyping Facility. This research is also partially supported by the Joint Center for Energy Storage Research (JCESR), an Energy Innovation Hub funded by the U.S. Department of Energy, Office of Science, and Basic Energy Sciences. We thank the Laboratory Computing Resource Center at Argonne National Laboratory for the generous allocation of computing time on the Bebop cluster. The submitted manuscript has been created by UChicago Argonne, LLC, Operator of Argonne National Laboratory (“Argonne”). Argonne, a U.S. Department of Energy Office of Science laboratory, is operated under Contract No. DE-AC02-06CH11357.

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