4.8 Article

Full Energy Range Resonant Inelastic X-ray Scattering of O2 and CO2: Direct Comparison with Oxygen Redox State in Batteries

Journal

JOURNAL OF PHYSICAL CHEMISTRY LETTERS
Volume 11, Issue 7, Pages 2618-2623

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.jpclett.0c00423

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Funding

  1. DOE Office of Science User Facility [DE-AC02-05CH11231]
  2. LDRD of Lawrence Berkeley National Laboratory
  3. Guangdong Key-lab Project [2017B0303010130]
  4. Shenzhen Science and Technology Research Grant [ZDSYS20170728102618]
  5. Advanced Light Source

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The evolving oxygen state plays key roles in the performance and stability of highenergy batteries involving oxygen redox reactions. Here, high-efficiency full energy range O-K mapping of resonant inelastic X-ray scattering (mRIXS) was collected from O-2 (O-0) and CO2 (O2- with strong covalency) molecules and compared directly with Li2O2 (O-) and the oxidized oxygen state in representative Na/Li-ion battery electrodes. Our results confirm again that the critical mRIXS feature around the 523.7 eV emission energy is from intrinsically oxidized oxygen, but not from the highly covalent oxygen state (CO2). The comparison of the mRIXS profile of the four different oxygen states, i.e., O2-, O-, On- (0 < n < 2), and O-0, reveals that oxygen redox states in batteries have distinct widths and positions along the excitation energy compared with Li2O2 and O-2. The nature of the oxidized oxygen state in oxide electrodes is thus beyond a simple molecular configuration of either peroxide or O-2.

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