4.8 Article

Formation of Surface Impurities on Lithium-Nickel-Manganese-Cobalt Oxides in the Presence of CO2 and H2O

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JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
卷 143, 期 27, 页码 10261-10274

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AMER CHEMICAL SOC
DOI: 10.1021/jacs.1c03812

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资金

  1. INL Laboratory Directed Research & Development (LDRD) Program under DOE Idaho Operations Office [DE-AC07-05ID14517]
  2. U.S. Department of Energy, Office of Energy Efficiency and Renewable Energy (EERE), Advanced Manufacturing Office Next Generation RD Projects [DE-AC0705ID14517]
  3. Robert Ramsay Chair Fund of The University of Alabama
  4. Office of Nuclear Energy of the U.S. Department of Energy
  5. Nuclear Science User Facilities [DE-AC07-05ID14517]

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Surface impurities in high nickel content LiNixMnyCozO2 (NMC) cathode materials are degraded by parasitic reactions and gas evolution.The reactivity and CO2 uptake of different NMC materials vary depending on the nickel content, with moisture pretreatment affecting the CO2 adsorption process. The electronic structure and surface properties of NMC materials play a role in the adsorption of CO2 and H2O, influencing the formation of surface impurities.
Surface impurities involving parasitic reactions and gas evolution contribute to the degradation of high Ni content LiNixMnyCozO2 (NMC) cathode materials. The transient kinetic technique of temporal analysis of products (TAP), density functional theory, and infrared spectroscopy have been used to study the formation of surface impurities on varying nickel content NMC materials (NMC811, NMC622, NMC532, NMC433, NMC111) in the presence of CO2 and H2O. CO2 reactivity on a clean surface as characterized by CO2 conversion rate in the TAP reactor follows the order: NMC811 > NMC622 > NMC532 > NMC433 > NMC111. The capacity of CO2 uptake follows a different order: NMC532 > NMC433 > NMC622 > NMC811 > NMC111. Moisture pretreatment slows down the direct CO2 adsorption process and creates additional active sites for CO2 adsorption. Electronic structure calculations predict that the (012) surface is more reactive than the (1014) surface for CO2 and H2O adsorption. CO2 adsorption leading to carbonate formation is exothermic with formation of ion pairs. The average CO2 binding energies on the different materials follow the CO2 reactivity order. Water hydroxylates the (012) surface and surface OH groups favor bicarbonate formation. Water creates more active sites for CO2 adsorption on the (1014) surface due to hydrogen bonding. The composition of surface impurities formed in ambient air exposure is dependent on water concentration and the percentage of different crystal planes. Different surface reactivities suggest that battery performance degradation due to surface impurities can be mitigated by precise control of the dominant surfaces in NMC materials.

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