4.6 Article

Suppressing the chromium disproportionation reaction in O3-type layered cathode materials for high capacity sodium-ion batteries

Journal

JOURNAL OF MATERIALS CHEMISTRY A
Volume 5, Issue 11, Pages 5442-5448

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/c6ta10818k

Keywords

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Funding

  1. NSAF [51502039, U1430104]
  2. National Key Scientific Research Project [2016YFB090150]
  3. 1000 Youth Talents Plan and Science & Technology Commission of Shanghai Municipality [08DZ2270500]
  4. Energy Efficiency and Renewable Energy, Office of Vehicle Technologies of the U.S. Department of Energy through the Advanced Battery Materials Research (BMR) Program [DE-SC0012704]
  5. U.S. Department of Energy, Basic Energy Science [DE-AC02-06CH11357]

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Chromium-based layered cathode materials suffer from the irreversible disproportionation reaction of Cr4+ to Cr3+ and Cr6+, which hinders the reversible multi-electron redox of Cr ions in layered cathodes, and limits their capacity and reversibility. To address this problem, a novel O3-type layer-structured transition metal oxide of NaCr1/3Fe1/3Mn1/3O2 (NCFM) was designed and studied as a cathode material. A high reversible capacity of 186 mA h g (-1) was achieved at a current rate of 0.05C in a voltage range of 1.5 to 4.2 V. X-ray diffraction revealed an O3 -> (O3 + P3) -> (P3 + O3 '') -> O3 '' phase-transition pathway for NCFM during charge. X-ray absorption, X-ray photoelectron and electron energy-loss spectroscopy measurements revealed the electronic structure changes of NCFM during Na+ deintercalation/intercalation processes. It is confirmed that the disproportionation reaction of Cr4+ to Cr3+ and Cr6+ can be effectively suppressed by Fe3+ and Mn4+ substitution. These results demonstrated that the reversible multi-electron oxidation/reduction of Cr ions can be achieved in NCFM during charge and discharge accompanied by CrO6 octahedral distortion and recovery.

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