4.8 Article

Mn(II) deposition on anodes and its effects on capacity fade in spinel lithium manganate-carbon systems

Journal

NATURE COMMUNICATIONS
Volume 4, Issue -, Pages -

Publisher

NATURE PUBLISHING GROUP
DOI: 10.1038/ncomms3437

Keywords

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Funding

  1. Department of Energy (DOE) Office of Energy Efficiency and Renewable Energy (EERE) Postdoctoral Research Award under the EERE Vehicles Technology Program
  2. DOE [DE-AC05-06OR23100]
  3. Center for Electrical Energy Storage, an Energy Frontier Research Center
  4. U.S. Department of Energy, Office of Science, Office of Basic Energy Sciences
  5. Applied Battery Research for Transportation (ABR) Program from the U. S. DOE-EERE Office of Vehicle Technologies
  6. U.S. DOE [DE-AC02-06CH11357]
  7. 973 Program of China [2009CB220105]
  8. Beijing Natural Science Foundation [2120001]
  9. National Natural Science Foundation of China [21273129]
  10. Bosch (China) Ltd.
  11. Human Resources Development of the Korea Institute of Energy Technology Evaluation and Planning (KETEP) grant
  12. Korean government, Ministry of Trade, Industry and Energy [20124010203310]
  13. National Research Foundation of Korea (NRF)
  14. Korea government (MEST) [2009-0092780]

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Dissolution and migration of manganese from cathode lead to severe capacity fading of lithium manganate-carbon cells. Overcoming this major problem requires a better understanding of the mechanisms of manganese dissolution, migration and deposition. Here we apply a variety of advanced analytical methods to study lithium manganate cathodes that are cycled with different anodes. We show that the oxidation state of manganese deposited on the anodes is +2, which differs from the results reported earlier. Our results also indicate that a metathesis reaction between Mn(II) and some species on the solid-electrolyte interphase takes place during the deposition of Mn(II) on the anodes, rather than a reduction reaction that leads to the formation of metallic Mn, as speculated in earlier studies. The concentration of Mn deposited on the anode gradually increases with cycles; this trend is well correlated with the anodes rising impedance and capacity fading of the cell.

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