4.8 Article

Insights on the Mechanism of Na-Ion Storage in Soft Carbon Anode

Journal

CHEMISTRY OF MATERIALS
Volume 29, Issue 5, Pages 2314-2320

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.chemmater.6b05474

Keywords

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Funding

  1. U.S. National Science Foundation [1507391]
  2. U.S. Department of Energy [DE-AR0000297TDD]
  3. Assistant Secretary for Energy Efficiency and Renewable Energy, Office of Vehicle Technologies of the U.S. Department of Energy under the advanced Battery Materials Research (BMR) program [DE-AC02-05CH11231, 6951379]
  4. DOE's Office of Biological and Environmental Research
  5. DOE [DE-AC05-76RLO1830]
  6. National Science Foundation [ACI-1053575]
  7. Scientific User Facilities Division, Office of Basic Energy Sciences of the U.S. DOE
  8. Direct For Mathematical & Physical Scien
  9. Division Of Materials Research [1507391] Funding Source: National Science Foundation

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Graphite is the commercial anode for lithium-ion batteries; however, it fails to extend its success to sodium-ion batteries. Recently, we demonstrated that a low-cost amorphous carbon soft carbon exhibits remarkable rate performance and stable cycling life of Na-ion storage. However, its Na-ion storage mechanism has remained elusive, which has plagued further development of such carbon anodes. Here, we remedy this shortfall by presenting the results from an integrated set of experimental and computational studies that, for the first time, reveal the storage mechanism for soft carbon. We find that sodium ions intercalate into graphenic layers, leading to an irreversible quasi-plateau at similar to 0.5 V versus Na+/Na as well as an irreversible expansion seen by in situ transmission electron microscopy (TEM) and X-ray diffraction (XRD). Such a high-potential plateau is correlated to the defective local structure inside the turbostratic stacking of soft carbon and the associated high-binding energies with Na ions, suggesting a trapping mechanism. On the other hand, soft carbon exhibits long sloping regions above and below the quasi-plateau during the first sodiation, where the sloping regions present highly reversible behavior. It is attributed to the more defects contained by soft carbon revealed by neutron total scattering and the associated pair distribution function studies.

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