4.8 Article

Elucidating anionic oxygen activity in lithium-rich layered oxides

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NATURE COMMUNICATIONS
卷 9, 期 -, 页码 -

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NATURE RESEARCH
DOI: 10.1038/s41467-018-03403-9

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  1. Assistant Secretary for Energy Efficiency and Renewable Energy, Office of Vehicle Technologies of the U.S. Department of Energy [DE-AC02-05CH11231]
  2. Department of Defense (DOD) through the National Defense Science & Engineering Graduate Fellowship (NDSEG) Program
  3. DOE Office of Science User Facility [DE-AC02-05CH11231]
  4. Radiation Lightsource, SLAC National Accelerator Laboratory
  5. U.S. Department of Energy, Office of Science, Office of Basic Energy Sciences [DE-AC02-76SF00515, DE-AC02-06CH11357]
  6. Use of the Advanced Photon Source at Argonne National Laboratory
  7. U.S. Department of Energy (DOE), Office of Basic Energy Science [DE-SC0012704]

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Recent research has explored combining conventional transition-metal redox with anionic lattice oxygen redox as a new and exciting direction to search for high-capacity lithium-ion cathodes. Here, we probe the poorly understood electrochemical activity of anionic oxygen from a material perspective by elucidating the effect of the transition metal on oxygen redox activity. We study two lithium-rich layered oxides, specifically lithium nickel metal oxides where metal is either manganese or ruthenium, which possess a similar structure and discharge characteristics, but exhibit distinctly different charge profiles. By combining X-ray spectroscopy with operando differential electrochemical mass spectrometry, we reveal completely different oxygen redox activity in each material, likely resulting from the different interaction between the lattice oxygen and transition metals. This work provides additional insights into the complex mechanism of oxygen redox and development of advanced high-capacity lithium-ion cathodes.

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