4.8 Article

Antisite occupation induced single anionic redox chemistry and structural stabilization of layered sodium chromium sulfide

Journal

NATURE COMMUNICATIONS
Volume 8, Issue -, Pages -

Publisher

NATURE PUBLISHING GROUP
DOI: 10.1038/s41467-017-00677-3

Keywords

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Funding

  1. National Natural Science Foundation of China [U1430104, 51622207, 51502039, U1630134, 51372228]
  2. National Key Research and Development Program of China [2016YFB0901504, 2017YFB0701600]
  3. Science & Technology Commission of Shanghai Municipality [11JC 1400500]
  4. Shanghai Pujiang Program [14PJ1403900]
  5. U.S. Department of Energy through the Advanced Battery Materials Research (BMR) Program [DE-SC0012704]
  6. U.S. Department of Energy [DE-AC02-06CH11357]

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The intercalation compounds with various electrochemically active or inactive elements in the layered structure have been the subject of increasing interest due to their high capacities, good reversibility, simple structures, and ease of synthesis. However, their reversible intercalation/deintercalation redox chemistries in previous compounds involve a single cationic redox reaction or a cumulative cationic and anionic redox reaction. Here we report an anionic redox chemistry and structural stabilization of layered sodium chromium sulfide. It was discovered that the sulfur in sodium chromium sulfide is electrochemically active, undergoing oxidation/reduction rather than chromium. Significantly, sodium ions can successfully move out and into without changing its lattice parameter c, which is explained in terms of the occurrence of chromium/sodium vacancy antisite during desodiation and sodiation processes. Our present work not only enriches the electrochemistry of layered intercalation compounds, but also extends the scope of investigation on high-capacity electrodes.

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